{"title":"AGS Awareness","description":"\u003cp\u003e\u003cspan\u003eSeptember is Leukodystrophy Awareness Month, and we are asking our community to help us turn awareness into action for someone incredibly special—our cousin, Abbie. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e Aicardi-Goutières syndrome, or AGS, is a rare inherited disease that affects the brain, immune system, and skin. Genetic changes cause the immune system to mistake the body’s own DNA or RNA for a virus, creating ongoing inflammation. This can damage the brain’s white matter and affect development, movement, communication, feeding, vision, and many other parts of daily life. AGS affects every person differently, but its challenges can be lifelong and devastating. Abbie was diagnosed with AGS in October 2021. Since that day, she has battled courageously to live the fullest and most normal life possible. She is so much more than her diagnosis—she is brave, deeply loved, and worth fighting for every single day. To honor Abbie and spread awareness this September, we have created special AGS shirts and drinkware. The most meaningful part of every design is that the letters “AGS” are written in Abbie’s own handwriting. When you wear one of these shirts or carry one of these cups, you are carrying a piece of Abbie’s story and helping introduce others to a disease that far too few people know about. Everyone knows what our family means to us; that we will go to boundless lengths to do whatever they need. Yesterday, on Ashley’s birthday, we had the honor of sharing these designs with her. Our family has always surrounded Abbie, Ashley, and their family with tremendous love, support, and prayer. Now, we would love to see our community stand beside them too. Buy a shirt. Carry a cup. Start a conversation. Say the name “Aicardi-Goutières syndrome.” Share Abbie’s story. Educate yourself. Most importantly, please pray for Abbie’s strength and comfort, for more good days, for wisdom for her doctors, and for research to bring better treatments to everyone living with AGS. If you are unable to purchase, sharing this post is completely free and incredibly powerful. Your share may reach someone learning about AGS for the first time, another family walking this road, or someone connected to research and advocacy. The more we talk about AGS, the more people will hear its name. Knowledge creates understanding, understanding creates advocacy, and advocacy creates hope. Abbie deserves a world that understands her disease and continues fighting for better treatments and a brighter future. Let’s show her that her community sees her, loves her, prays for her, and stands with her. Local pickup and shipping are available. Feel free to purchase a shirt or drinkware item, share Abbie’s story, and help us spread as much AGS awareness as possible this September. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003c\/p\u003e","products":[{"product_id":"warriors-against-ags","title":"Warriors Against AGS - White Letters","description":"\u003cp\u003e\u003cspan\u003eSeptember is Leukodystrophy Awareness Month, and we are asking our community to help us turn awareness into action for someone incredibly special—our cousin, Abbie. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003cspan\u003e Aicardi-Goutières syndrome, or AGS, is a rare inherited disease that affects the brain, immune system, and skin. Genetic changes cause the immune system to mistake the body’s own DNA or RNA for a virus, creating ongoing inflammation. This can damage the brain’s white matter and affect development, movement, communication, feeding, vision, and many other parts of daily life. AGS affects every person differently, but its challenges can be lifelong and devastating. Abbie was diagnosed with AGS in October 2021. Since that day, she has battled courageously to live the fullest and most normal life possible. She is so much more than her diagnosis—she is brave, deeply loved, and worth fighting for every single day. To honor Abbie and spread awareness this September, we have created special AGS shirts and drinkware. The most meaningful part of every design is that the letters “AGS” are written in Abbie’s own handwriting. When you wear one of these shirts or carry one of these cups, you are carrying a piece of Abbie’s story and helping introduce others to a disease that far too few people know about. Everyone knows what our family means to us; that we will go to boundless lengths to do whatever they need. Yesterday, on Ashley’s birthday, we had the honor of sharing these designs with her. Our family has always surrounded Abbie, Ashley, and their family with tremendous love, support, and prayer. Now, we would love to see our community stand beside them too. Buy a shirt. Carry a cup. Start a conversation. Say the name “Aicardi-Goutières syndrome.” Share Abbie’s story. Educate yourself. Most importantly, please pray for Abbie’s strength and comfort, for more good days, for wisdom for her doctors, and for research to bring better treatments to everyone living with AGS. If you are unable to purchase, sharing this post is completely free and incredibly powerful. Your share may reach someone learning about AGS for the first time, another family walking this road, or someone connected to research and advocacy. The more we talk about AGS, the more people will hear its name. Knowledge creates understanding, understanding creates advocacy, and advocacy creates hope. Abbie deserves a world that understands her disease and continues fighting for better treatments and a brighter future. Let’s show her that her community sees her, loves her, prays for her, and stands with her. Local pickup and shipping are available. Feel free to purchase a shirt or drinkware item, share Abbie’s story, and help us spread as much AGS awareness as possible this September. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan style=\"color: rgb(21, 20, 20);\"\u003e\u003cstrong\u003eBleaching is not an option for this design\u003c\/strong\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eEvery color may not be available in every size. You will be emailed if the color you choose is out of stock in your size. \u003c\/span\u003e\u003c\/p\u003e","brand":"Oh My Ginger","offers":[{"title":"S","offer_id":50103855087864,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"M","offer_id":50103855120632,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"L","offer_id":50103855153400,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"XL","offer_id":50103855186168,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"2X","offer_id":50103855218936,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"3X","offer_id":50103855251704,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"4X","offer_id":50103855284472,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"5X","offer_id":50103855317240,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0501\/1357\/7128\/files\/IMG-2001.jpg?v=1785815520"},{"product_id":"abbies-warriors-white-letters","title":"AGS Pink Shield - White Letters","description":"\u003cp\u003e\u003cspan\u003eSeptember is Leukodystrophy Awareness Month, and we are asking our community to help us turn awareness into action for someone incredibly special—our cousin, Abbie. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003cspan\u003e Aicardi-Goutières syndrome, or AGS, is a rare inherited disease that affects the brain, immune system, and skin. Genetic changes cause the immune system to mistake the body’s own DNA or RNA for a virus, creating ongoing inflammation. This can damage the brain’s white matter and affect development, movement, communication, feeding, vision, and many other parts of daily life. AGS affects every person differently, but its challenges can be lifelong and devastating. Abbie was diagnosed with AGS in October 2021. Since that day, she has battled courageously to live the fullest and most normal life possible. She is so much more than her diagnosis—she is brave, deeply loved, and worth fighting for every single day. To honor Abbie and spread awareness this September, we have created special AGS shirts and drinkware. The most meaningful part of every design is that the letters “AGS” are written in Abbie’s own handwriting. When you wear one of these shirts or carry one of these cups, you are carrying a piece of Abbie’s story and helping introduce others to a disease that far too few people know about. Everyone knows what our family means to us; that we will go to boundless lengths to do whatever they need. Yesterday, on Ashley’s birthday, we had the honor of sharing these designs with her. Our family has always surrounded Abbie, Ashley, and their family with tremendous love, support, and prayer. Now, we would love to see our community stand beside them too. Buy a shirt. Carry a cup. Start a conversation. Say the name “Aicardi-Goutières syndrome.” Share Abbie’s story. Educate yourself. Most importantly, please pray for Abbie’s strength and comfort, for more good days, for wisdom for her doctors, and for research to bring better treatments to everyone living with AGS. If you are unable to purchase, sharing this post is completely free and incredibly powerful. Your share may reach someone learning about AGS for the first time, another family walking this road, or someone connected to research and advocacy. The more we talk about AGS, the more people will hear its name. Knowledge creates understanding, understanding creates advocacy, and advocacy creates hope. Abbie deserves a world that understands her disease and continues fighting for better treatments and a brighter future. Let’s show her that her community sees her, loves her, prays for her, and stands with her. Local pickup and shipping are available. Feel free to purchase a shirt or drinkware item, share Abbie’s story, and help us spread as much AGS awareness as possible this September. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan style=\"color: rgb(21, 20, 20);\"\u003e\u003cstrong\u003eBleaching is not an option for this design\u003c\/strong\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eEvery color may not be available in every size. You will be emailed if the color you choose is out of stock in your size. \u003c\/span\u003e\u003c\/p\u003e","brand":"Oh My Ginger","offers":[{"title":"S","offer_id":50103874289912,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"M","offer_id":50103874322680,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"L","offer_id":50103874355448,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"XL","offer_id":50103874388216,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"2X","offer_id":50103874420984,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"3X","offer_id":50103874453752,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"4X","offer_id":50103874486520,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"5X","offer_id":50103874519288,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0501\/1357\/7128\/files\/IMG-1995.png?v=1785815520"},{"product_id":"abbies-warriors-black-letters","title":"AGS Green Shield - Black Letters","description":"\u003cp\u003e\u003cspan\u003eSeptember is Leukodystrophy Awareness Month, and we are asking our community to help us turn awareness into action for someone incredibly special—our cousin, Abbie. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003cspan\u003e Aicardi-Goutières syndrome, or AGS, is a rare inherited disease that affects the brain, immune system, and skin. Genetic changes cause the immune system to mistake the body’s own DNA or RNA for a virus, creating ongoing inflammation. This can damage the brain’s white matter and affect development, movement, communication, feeding, vision, and many other parts of daily life. AGS affects every person differently, but its challenges can be lifelong and devastating. Abbie was diagnosed with AGS in October 2021. Since that day, she has battled courageously to live the fullest and most normal life possible. She is so much more than her diagnosis—she is brave, deeply loved, and worth fighting for every single day. To honor Abbie and spread awareness this September, we have created special AGS shirts and drinkware. The most meaningful part of every design is that the letters “AGS” are written in Abbie’s own handwriting. When you wear one of these shirts or carry one of these cups, you are carrying a piece of Abbie’s story and helping introduce others to a disease that far too few people know about. Everyone knows what our family means to us; that we will go to boundless lengths to do whatever they need. Yesterday, on Ashley’s birthday, we had the honor of sharing these designs with her. Our family has always surrounded Abbie, Ashley, and their family with tremendous love, support, and prayer. Now, we would love to see our community stand beside them too. Buy a shirt. Carry a cup. Start a conversation. Say the name “Aicardi-Goutières syndrome.” Share Abbie’s story. Educate yourself. Most importantly, please pray for Abbie’s strength and comfort, for more good days, for wisdom for her doctors, and for research to bring better treatments to everyone living with AGS. If you are unable to purchase, sharing this post is completely free and incredibly powerful. Your share may reach someone learning about AGS for the first time, another family walking this road, or someone connected to research and advocacy. The more we talk about AGS, the more people will hear its name. Knowledge creates understanding, understanding creates advocacy, and advocacy creates hope. Abbie deserves a world that understands her disease and continues fighting for better treatments and a brighter future. Let’s show her that her community sees her, loves her, prays for her, and stands with her. Local pickup and shipping are available. Feel free to purchase a shirt or drinkware item, share Abbie’s story, and help us spread as much AGS awareness as possible this September. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eEvery color may not be available in every size. You will be emailed if the color you choose is out of stock in your size. \u003c\/span\u003e\u003c\/p\u003e","brand":"Oh My Ginger","offers":[{"title":"Small","offer_id":50103874617592,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"Medium","offer_id":50103874650360,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"Large","offer_id":50103874683128,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"X-Large","offer_id":50103874715896,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"2X","offer_id":50103874748664,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"3X","offer_id":50103874781432,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"4X","offer_id":50103874814200,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"5X","offer_id":50103874846968,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0501\/1357\/7128\/files\/IMG-2003.jpg?v=1785815520"},{"product_id":"warriors-against-ags-black-letters","title":"Warriors Against AGS - Black Letters","description":"\u003cp\u003e\u003cspan\u003eSeptember is Leukodystrophy Awareness Month, and we are asking our community to help us turn awareness into action for someone incredibly special—our cousin, Abbie. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003cspan\u003e Aicardi-Goutières syndrome, or AGS, is a rare inherited disease that affects the brain, immune system, and skin. Genetic changes cause the immune system to mistake the body’s own DNA or RNA for a virus, creating ongoing inflammation. This can damage the brain’s white matter and affect development, movement, communication, feeding, vision, and many other parts of daily life. AGS affects every person differently, but its challenges can be lifelong and devastating. Abbie was diagnosed with AGS in October 2021. Since that day, she has battled courageously to live the fullest and most normal life possible. She is so much more than her diagnosis—she is brave, deeply loved, and worth fighting for every single day. To honor Abbie and spread awareness this September, we have created special AGS shirts and drinkware. The most meaningful part of every design is that the letters “AGS” are written in Abbie’s own handwriting. When you wear one of these shirts or carry one of these cups, you are carrying a piece of Abbie’s story and helping introduce others to a disease that far too few people know about. Everyone knows what our family means to us; that we will go to boundless lengths to do whatever they need. Yesterday, on Ashley’s birthday, we had the honor of sharing these designs with her. Our family has always surrounded Abbie, Ashley, and their family with tremendous love, support, and prayer. Now, we would love to see our community stand beside them too. Buy a shirt. Carry a cup. Start a conversation. Say the name “Aicardi-Goutières syndrome.” Share Abbie’s story. Educate yourself. Most importantly, please pray for Abbie’s strength and comfort, for more good days, for wisdom for her doctors, and for research to bring better treatments to everyone living with AGS. If you are unable to purchase, sharing this post is completely free and incredibly powerful. Your share may reach someone learning about AGS for the first time, another family walking this road, or someone connected to research and advocacy. The more we talk about AGS, the more people will hear its name. Knowledge creates understanding, understanding creates advocacy, and advocacy creates hope. Abbie deserves a world that understands her disease and continues fighting for better treatments and a brighter future. Let’s show her that her community sees her, loves her, prays for her, and stands with her. Local pickup and shipping are available. Feel free to purchase a shirt or drinkware item, share Abbie’s story, and help us spread as much AGS awareness as possible this September. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003eEvery color may not be available in every size. If your chosen color isn’t available, we will email you. \u003c\/p\u003e","brand":"Oh My Ginger","offers":[{"title":"Small","offer_id":50103874912504,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"Medium","offer_id":50103874945272,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"Large","offer_id":50103874978040,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"X-Large","offer_id":50103875010808,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"2X","offer_id":50103875043576,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"3X","offer_id":50103875076344,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"4X","offer_id":50103875109112,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"5X","offer_id":50103875141880,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0501\/1357\/7128\/files\/IMG-1999.jpg?v=1785815520"},{"product_id":"warriors-against-ags-colorful-lion","title":"Watercolor Lion AGS","description":"\u003cp\u003e\u003cspan\u003eSeptember is Leukodystrophy Awareness Month, and we are asking our community to help us turn awareness into action for someone incredibly special—our cousin, Abbie. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003cspan\u003e Aicardi-Goutières syndrome, or AGS, is a rare inherited disease that affects the brain, immune system, and skin. Genetic changes cause the immune system to mistake the body’s own DNA or RNA for a virus, creating ongoing inflammation. This can damage the brain’s white matter and affect development, movement, communication, feeding, vision, and many other parts of daily life. AGS affects every person differently, but its challenges can be lifelong and devastating. Abbie was diagnosed with AGS in October 2021. Since that day, she has battled courageously to live the fullest and most normal life possible. She is so much more than her diagnosis—she is brave, deeply loved, and worth fighting for every single day. To honor Abbie and spread awareness this September, we have created special AGS shirts and drinkware. The most meaningful part of every design is that the letters “AGS” are written in Abbie’s own handwriting. When you wear one of these shirts or carry one of these cups, you are carrying a piece of Abbie’s story and helping introduce others to a disease that far too few people know about. Everyone knows what our family means to us; that we will go to boundless lengths to do whatever they need. Yesterday, on Ashley’s birthday, we had the honor of sharing these designs with her. Our family has always surrounded Abbie, Ashley, and their family with tremendous love, support, and prayer. Now, we would love to see our community stand beside them too. Buy a shirt. Carry a cup. Start a conversation. Say the name “Aicardi-Goutières syndrome.” Share Abbie’s story. Educate yourself. Most importantly, please pray for Abbie’s strength and comfort, for more good days, for wisdom for her doctors, and for research to bring better treatments to everyone living with AGS. If you are unable to purchase, sharing this post is completely free and incredibly powerful. Your share may reach someone learning about AGS for the first time, another family walking this road, or someone connected to research and advocacy. The more we talk about AGS, the more people will hear its name. Knowledge creates understanding, understanding creates advocacy, and advocacy creates hope. Abbie deserves a world that understands her disease and continues fighting for better treatments and a brighter future. Let’s show her that her community sees her, loves her, prays for her, and stands with her. Local pickup and shipping are available. Feel free to purchase a shirt or drinkware item, share Abbie’s story, and help us spread as much AGS awareness as possible this September. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003eEvery color may not be available in every size. If your chosen color isn’t available, we will email you. \u003c\/p\u003e","brand":"Oh My Ginger","offers":[{"title":"Small","offer_id":50103875272952,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"Medium","offer_id":50103875305720,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"Large","offer_id":50103875338488,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"X-Large","offer_id":50103875371256,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"2X","offer_id":50103875404024,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"3X","offer_id":50103875436792,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"4X","offer_id":50103875469560,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"5X","offer_id":50103875502328,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0501\/1357\/7128\/files\/IMG-1997.jpg?v=1785815520"},{"product_id":"abbies-warriors-black-letters-1","title":"AGS Pink Shield - Black Letters","description":"\u003cp\u003e\u003cspan\u003eSeptember is Leukodystrophy Awareness Month, and we are asking our community to help us turn awareness into action for someone incredibly special—our cousin, Abbie. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003cspan\u003e Aicardi-Goutières syndrome, or AGS, is a rare inherited disease that affects the brain, immune system, and skin. Genetic changes cause the immune system to mistake the body’s own DNA or RNA for a virus, creating ongoing inflammation. This can damage the brain’s white matter and affect development, movement, communication, feeding, vision, and many other parts of daily life. AGS affects every person differently, but its challenges can be lifelong and devastating. Abbie was diagnosed with AGS in October 2021. Since that day, she has battled courageously to live the fullest and most normal life possible. She is so much more than her diagnosis—she is brave, deeply loved, and worth fighting for every single day. To honor Abbie and spread awareness this September, we have created special AGS shirts and drinkware. The most meaningful part of every design is that the letters “AGS” are written in Abbie’s own handwriting. When you wear one of these shirts or carry one of these cups, you are carrying a piece of Abbie’s story and helping introduce others to a disease that far too few people know about. Everyone knows what our family means to us; that we will go to boundless lengths to do whatever they need. Yesterday, on Ashley’s birthday, we had the honor of sharing these designs with her. Our family has always surrounded Abbie, Ashley, and their family with tremendous love, support, and prayer. Now, we would love to see our community stand beside them too. Buy a shirt. Carry a cup. Start a conversation. Say the name “Aicardi-Goutières syndrome.” Share Abbie’s story. Educate yourself. Most importantly, please pray for Abbie’s strength and comfort, for more good days, for wisdom for her doctors, and for research to bring better treatments to everyone living with AGS. If you are unable to purchase, sharing this post is completely free and incredibly powerful. Your share may reach someone learning about AGS for the first time, another family walking this road, or someone connected to research and advocacy. The more we talk about AGS, the more people will hear its name. Knowledge creates understanding, understanding creates advocacy, and advocacy creates hope. Abbie deserves a world that understands her disease and continues fighting for better treatments and a brighter future. Let’s show her that her community sees her, loves her, prays for her, and stands with her. Local pickup and shipping are available. Feel free to purchase a shirt or drinkware item, share Abbie’s story, and help us spread as much AGS awareness as possible this September. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003eEvery color may not be available in every size. If your chosen color isn’t available, we will email you. \u003c\/p\u003e","brand":"Oh My Ginger","offers":[{"title":"Small","offer_id":50103875731704,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true},{"title":"Medium","offer_id":50103875764472,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true},{"title":"Large","offer_id":50103875797240,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true},{"title":"XLarge","offer_id":50103875830008,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true},{"title":"2XLarge","offer_id":50103875862776,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true},{"title":"3XLarge","offer_id":50103875895544,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true},{"title":"4XLarge","offer_id":50103875928312,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true},{"title":"5XLarge","offer_id":50103875961080,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0501\/1357\/7128\/files\/IMG-2002.jpg?v=1785815520"},{"product_id":"abbies-warriors-white-letters-1","title":"AGS Pink Shield - White Letters","description":"\u003cp\u003e\u003cspan\u003eSeptember is Leukodystrophy Awareness Month, and we are asking our community to help us turn awareness into action for someone incredibly special—our cousin, Abbie. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003cspan\u003e Aicardi-Goutières syndrome, or AGS, is a rare inherited disease that affects the brain, immune system, and skin. Genetic changes cause the immune system to mistake the body’s own DNA or RNA for a virus, creating ongoing inflammation. This can damage the brain’s white matter and affect development, movement, communication, feeding, vision, and many other parts of daily life. AGS affects every person differently, but its challenges can be lifelong and devastating. Abbie was diagnosed with AGS in October 2021. Since that day, she has battled courageously to live the fullest and most normal life possible. She is so much more than her diagnosis—she is brave, deeply loved, and worth fighting for every single day. To honor Abbie and spread awareness this September, we have created special AGS shirts and drinkware. The most meaningful part of every design is that the letters “AGS” are written in Abbie’s own handwriting. When you wear one of these shirts or carry one of these cups, you are carrying a piece of Abbie’s story and helping introduce others to a disease that far too few people know about. Everyone knows what our family means to us; that we will go to boundless lengths to do whatever they need. Yesterday, on Ashley’s birthday, we had the honor of sharing these designs with her. Our family has always surrounded Abbie, Ashley, and their family with tremendous love, support, and prayer. Now, we would love to see our community stand beside them too. Buy a shirt. Carry a cup. Start a conversation. Say the name “Aicardi-Goutières syndrome.” Share Abbie’s story. Educate yourself. Most importantly, please pray for Abbie’s strength and comfort, for more good days, for wisdom for her doctors, and for research to bring better treatments to everyone living with AGS. If you are unable to purchase, sharing this post is completely free and incredibly powerful. Your share may reach someone learning about AGS for the first time, another family walking this road, or someone connected to research and advocacy. The more we talk about AGS, the more people will hear its name. Knowledge creates understanding, understanding creates advocacy, and advocacy creates hope. Abbie deserves a world that understands her disease and continues fighting for better treatments and a brighter future. Let’s show her that her community sees her, loves her, prays for her, and stands with her. Local pickup and shipping are available. Feel free to purchase a shirt or drinkware item, share Abbie’s story, and help us spread as much AGS awareness as possible this September. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003eEvery color may not be available in every size. If your chosen color isn’t available, we will email you. \u003c\/p\u003e","brand":"Oh My Ginger","offers":[{"title":"Small","offer_id":50103876059384,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true},{"title":"Medium","offer_id":50103876092152,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true},{"title":"Large","offer_id":50103876124920,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true},{"title":"XLarge","offer_id":50103876157688,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true},{"title":"2XLarge","offer_id":50103876190456,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true},{"title":"3XLarge","offer_id":50103876223224,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true},{"title":"4XLarge","offer_id":50103876255992,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true},{"title":"5XLarge","offer_id":50103876288760,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0501\/1357\/7128\/files\/IMG-2016.jpg?v=1785819996"},{"product_id":"abbies-warriors-black-letters-pink","title":"AGS Pink Shield - Black Letters","description":"\u003cspan\u003eEvery color may not be available in every size. You will be emailed if the color you choose is out of stock in your size. \u003c\/span\u003e","brand":"Oh My Ginger","offers":[{"title":"Small","offer_id":50103890051320,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"Medium","offer_id":50103890084088,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"Large","offer_id":50103890116856,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"X-Large","offer_id":50103890149624,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"2X","offer_id":50103890182392,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"3X","offer_id":50103890215160,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"4X","offer_id":50103890247928,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"5X","offer_id":50103890280696,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0501\/1357\/7128\/files\/IMG-2019.jpg?v=1785819996"},{"product_id":"abbies-warriors-white-letters-brown","title":"AGS Green Shield - White Letters","description":"\u003cp\u003e\u003cspan\u003eSeptember is Leukodystrophy Awareness Month, and we are asking our community to help us turn awareness into action for someone incredibly special—our cousin, Abbie. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003cspan\u003e Aicardi-Goutières syndrome, or AGS, is a rare inherited disease that affects the brain, immune system, and skin. Genetic changes cause the immune system to mistake the body’s own DNA or RNA for a virus, creating ongoing inflammation. This can damage the brain’s white matter and affect development, movement, communication, feeding, vision, and many other parts of daily life. AGS affects every person differently, but its challenges can be lifelong and devastating. Abbie was diagnosed with AGS in October 2021. Since that day, she has battled courageously to live the fullest and most normal life possible. She is so much more than her diagnosis—she is brave, deeply loved, and worth fighting for every single day. To honor Abbie and spread awareness this September, we have created special AGS shirts and drinkware. The most meaningful part of every design is that the letters “AGS” are written in Abbie’s own handwriting. When you wear one of these shirts or carry one of these cups, you are carrying a piece of Abbie’s story and helping introduce others to a disease that far too few people know about. Everyone knows what our family means to us; that we will go to boundless lengths to do whatever they need. Yesterday, on Ashley’s birthday, we had the honor of sharing these designs with her. Our family has always surrounded Abbie, Ashley, and their family with tremendous love, support, and prayer. Now, we would love to see our community stand beside them too. Buy a shirt. Carry a cup. Start a conversation. Say the name “Aicardi-Goutières syndrome.” Share Abbie’s story. Educate yourself. Most importantly, please pray for Abbie’s strength and comfort, for more good days, for wisdom for her doctors, and for research to bring better treatments to everyone living with AGS. If you are unable to purchase, sharing this post is completely free and incredibly powerful. Your share may reach someone learning about AGS for the first time, another family walking this road, or someone connected to research and advocacy. The more we talk about AGS, the more people will hear its name. Knowledge creates understanding, understanding creates advocacy, and advocacy creates hope. Abbie deserves a world that understands her disease and continues fighting for better treatments and a brighter future. Let’s show her that her community sees her, loves her, prays for her, and stands with her. Local pickup and shipping are available. Feel free to purchase a shirt or drinkware item, share Abbie’s story, and help us spread as much AGS awareness as possible this September. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan style=\"color: rgb(21, 20, 20);\"\u003e\u003cstrong\u003eBleaching is not an option for this design\u003c\/strong\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eEvery color may not be available in every size. You will be emailed if the color you choose is out of stock in your size. \u003c\/span\u003e\u003c\/p\u003e","brand":"Oh My Ginger","offers":[{"title":"S","offer_id":50103892148472,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"M","offer_id":50103892181240,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"L","offer_id":50103892214008,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"XL","offer_id":50103892246776,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"2X","offer_id":50103892279544,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"3X","offer_id":50103892312312,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"4X","offer_id":50103892345080,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true},{"title":"5X","offer_id":50103892377848,"sku":null,"price":21.5,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0501\/1357\/7128\/files\/IMG-2004.jpg?v=1785815520"},{"product_id":"abbies-warriors-black-letters-kids","title":"AGS Pink Shield (Black Letters) - Kids","description":"\u003cp\u003e\u003cspan\u003eSeptember is Leukodystrophy Awareness Month, and we are asking our community to help us turn awareness into action for someone incredibly special—our cousin, Abbie. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003cspan\u003e Aicardi-Goutières syndrome, or AGS, is a rare inherited disease that affects the brain, immune system, and skin. Genetic changes cause the immune system to mistake the body’s own DNA or RNA for a virus, creating ongoing inflammation. This can damage the brain’s white matter and affect development, movement, communication, feeding, vision, and many other parts of daily life. AGS affects every person differently, but its challenges can be lifelong and devastating. Abbie was diagnosed with AGS in October 2021. Since that day, she has battled courageously to live the fullest and most normal life possible. She is so much more than her diagnosis—she is brave, deeply loved, and worth fighting for every single day. To honor Abbie and spread awareness this September, we have created special AGS shirts and drinkware. The most meaningful part of every design is that the letters “AGS” are written in Abbie’s own handwriting. When you wear one of these shirts or carry one of these cups, you are carrying a piece of Abbie’s story and helping introduce others to a disease that far too few people know about. Everyone knows what our family means to us; that we will go to boundless lengths to do whatever they need. Yesterday, on Ashley’s birthday, we had the honor of sharing these designs with her. Our family has always surrounded Abbie, Ashley, and their family with tremendous love, support, and prayer. Now, we would love to see our community stand beside them too. Buy a shirt. Carry a cup. Start a conversation. Say the name “Aicardi-Goutières syndrome.” Share Abbie’s story. Educate yourself. Most importantly, please pray for Abbie’s strength and comfort, for more good days, for wisdom for her doctors, and for research to bring better treatments to everyone living with AGS. If you are unable to purchase, sharing this post is completely free and incredibly powerful. Your share may reach someone learning about AGS for the first time, another family walking this road, or someone connected to research and advocacy. The more we talk about AGS, the more people will hear its name. Knowledge creates understanding, understanding creates advocacy, and advocacy creates hope. Abbie deserves a world that understands her disease and continues fighting for better treatments and a brighter future. Let’s show her that her community sees her, loves her, prays for her, and stands with her. Local pickup and shipping are available. Feel free to purchase a shirt or drinkware item, share Abbie’s story, and help us spread as much AGS awareness as possible this September. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003eEvery color may not be available in every size. If your chosen color isn’t available, we will email you. \u003c\/p\u003e","brand":"Oh My Ginger","offers":[{"title":"Default Title","offer_id":50103909351672,"sku":null,"price":16.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0501\/1357\/7128\/files\/IMG-2018.jpg?v=1785819996"},{"product_id":"abbies-warriors-white-letters-pink-kids","title":"AGS Pink Shield (White Letters) - Kids","description":"\u003cp\u003e\u003cspan\u003eSeptember is Leukodystrophy Awareness Month, and we are asking our community to help us turn awareness into action for someone incredibly special—our cousin, Abbie. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003cspan\u003e Aicardi-Goutières syndrome, or AGS, is a rare inherited disease that affects the brain, immune system, and skin. Genetic changes cause the immune system to mistake the body’s own DNA or RNA for a virus, creating ongoing inflammation. This can damage the brain’s white matter and affect development, movement, communication, feeding, vision, and many other parts of daily life. AGS affects every person differently, but its challenges can be lifelong and devastating. Abbie was diagnosed with AGS in October 2021. Since that day, she has battled courageously to live the fullest and most normal life possible. She is so much more than her diagnosis—she is brave, deeply loved, and worth fighting for every single day. To honor Abbie and spread awareness this September, we have created special AGS shirts and drinkware. The most meaningful part of every design is that the letters “AGS” are written in Abbie’s own handwriting. When you wear one of these shirts or carry one of these cups, you are carrying a piece of Abbie’s story and helping introduce others to a disease that far too few people know about. Everyone knows what our family means to us; that we will go to boundless lengths to do whatever they need. Yesterday, on Ashley’s birthday, we had the honor of sharing these designs with her. Our family has always surrounded Abbie, Ashley, and their family with tremendous love, support, and prayer. Now, we would love to see our community stand beside them too. Buy a shirt. Carry a cup. Start a conversation. Say the name “Aicardi-Goutières syndrome.” Share Abbie’s story. Educate yourself. Most importantly, please pray for Abbie’s strength and comfort, for more good days, for wisdom for her doctors, and for research to bring better treatments to everyone living with AGS. If you are unable to purchase, sharing this post is completely free and incredibly powerful. Your share may reach someone learning about AGS for the first time, another family walking this road, or someone connected to research and advocacy. The more we talk about AGS, the more people will hear its name. Knowledge creates understanding, understanding creates advocacy, and advocacy creates hope. Abbie deserves a world that understands her disease and continues fighting for better treatments and a brighter future. Let’s show her that her community sees her, loves her, prays for her, and stands with her. Local pickup and shipping are available. Feel free to purchase a shirt or drinkware item, share Abbie’s story, and help us spread as much AGS awareness as possible this September. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003eEvery color may not be available in every size. If your chosen color isn’t available, we will email you. \u003c\/p\u003e","brand":"Oh My Ginger","offers":[{"title":"Default Title","offer_id":50103910990072,"sku":null,"price":16.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0501\/1357\/7128\/files\/IMG-2014.jpg?v=1785819996"},{"product_id":"abbies-warriors-black-letters-pink-kids","title":"AGS Green Shield (White Letters) - Kids","description":"\u003cp\u003e\u003cspan\u003eSeptember is Leukodystrophy Awareness Month, and we are asking our community to help us turn awareness into action for someone incredibly special—our cousin, Abbie. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003cspan\u003e Aicardi-Goutières syndrome, or AGS, is a rare inherited disease that affects the brain, immune system, and skin. Genetic changes cause the immune system to mistake the body’s own DNA or RNA for a virus, creating ongoing inflammation. This can damage the brain’s white matter and affect development, movement, communication, feeding, vision, and many other parts of daily life. AGS affects every person differently, but its challenges can be lifelong and devastating. Abbie was diagnosed with AGS in October 2021. Since that day, she has battled courageously to live the fullest and most normal life possible. She is so much more than her diagnosis—she is brave, deeply loved, and worth fighting for every single day. To honor Abbie and spread awareness this September, we have created special AGS shirts and drinkware. The most meaningful part of every design is that the letters “AGS” are written in Abbie’s own handwriting. When you wear one of these shirts or carry one of these cups, you are carrying a piece of Abbie’s story and helping introduce others to a disease that far too few people know about. Everyone knows what our family means to us; that we will go to boundless lengths to do whatever they need. Yesterday, on Ashley’s birthday, we had the honor of sharing these designs with her. Our family has always surrounded Abbie, Ashley, and their family with tremendous love, support, and prayer. Now, we would love to see our community stand beside them too. Buy a shirt. Carry a cup. Start a conversation. Say the name “Aicardi-Goutières syndrome.” Share Abbie’s story. Educate yourself. Most importantly, please pray for Abbie’s strength and comfort, for more good days, for wisdom for her doctors, and for research to bring better treatments to everyone living with AGS. If you are unable to purchase, sharing this post is completely free and incredibly powerful. Your share may reach someone learning about AGS for the first time, another family walking this road, or someone connected to research and advocacy. The more we talk about AGS, the more people will hear its name. Knowledge creates understanding, understanding creates advocacy, and advocacy creates hope. Abbie deserves a world that understands her disease and continues fighting for better treatments and a brighter future. Let’s show her that her community sees her, loves her, prays for her, and stands with her. Local pickup and shipping are available. Feel free to purchase a shirt or drinkware item, share Abbie’s story, and help us spread as much AGS awareness as possible this September. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003eEvery color may not be available in every size. If your chosen color isn’t available, we will email you. \u003c\/p\u003e","brand":"Oh My Ginger","offers":[{"title":"Default Title","offer_id":50103922295032,"sku":null,"price":16.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0501\/1357\/7128\/files\/IMG-2020.jpg?v=1785819996"},{"product_id":"abbies-warriors-black-letters-brown-kids","title":"AGS Green Shield (Black Letters) - Kids","description":"\u003cp\u003e\u003cspan\u003eSeptember is Leukodystrophy Awareness Month, and we are asking our community to help us turn awareness into action for someone incredibly special—our cousin, Abbie. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003cspan\u003e Aicardi-Goutières syndrome, or AGS, is a rare inherited disease that affects the brain, immune system, and skin. Genetic changes cause the immune system to mistake the body’s own DNA or RNA for a virus, creating ongoing inflammation. This can damage the brain’s white matter and affect development, movement, communication, feeding, vision, and many other parts of daily life. AGS affects every person differently, but its challenges can be lifelong and devastating. Abbie was diagnosed with AGS in October 2021. Since that day, she has battled courageously to live the fullest and most normal life possible. She is so much more than her diagnosis—she is brave, deeply loved, and worth fighting for every single day. To honor Abbie and spread awareness this September, we have created special AGS shirts and drinkware. The most meaningful part of every design is that the letters “AGS” are written in Abbie’s own handwriting. When you wear one of these shirts or carry one of these cups, you are carrying a piece of Abbie’s story and helping introduce others to a disease that far too few people know about. Everyone knows what our family means to us; that we will go to boundless lengths to do whatever they need. Yesterday, on Ashley’s birthday, we had the honor of sharing these designs with her. Our family has always surrounded Abbie, Ashley, and their family with tremendous love, support, and prayer. Now, we would love to see our community stand beside them too. Buy a shirt. Carry a cup. Start a conversation. Say the name “Aicardi-Goutières syndrome.” Share Abbie’s story. Educate yourself. Most importantly, please pray for Abbie’s strength and comfort, for more good days, for wisdom for her doctors, and for research to bring better treatments to everyone living with AGS. If you are unable to purchase, sharing this post is completely free and incredibly powerful. Your share may reach someone learning about AGS for the first time, another family walking this road, or someone connected to research and advocacy. The more we talk about AGS, the more people will hear its name. Knowledge creates understanding, understanding creates advocacy, and advocacy creates hope. Abbie deserves a world that understands her disease and continues fighting for better treatments and a brighter future. Let’s show her that her community sees her, loves her, prays for her, and stands with her. Local pickup and shipping are available. Feel free to purchase a shirt or drinkware item, share Abbie’s story, and help us spread as much AGS awareness as possible this September. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003eEvery color may not be available in every size. If your chosen color isn’t available, we will email you. \u003c\/p\u003e","brand":"Oh My Ginger","offers":[{"title":"Default Title","offer_id":50103923736824,"sku":null,"price":16.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0501\/1357\/7128\/files\/IMG-2015.jpg?v=1785819996"},{"product_id":"warriors-against-ags-black-letters-kids","title":"Warriors Against AGS (Black Letters) - Kids","description":"\u003cp\u003e\u003cspan\u003eSeptember is Leukodystrophy Awareness Month, and we are asking our community to help us turn awareness into action for someone incredibly special—our cousin, Abbie. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003cspan\u003e Aicardi-Goutières syndrome, or AGS, is a rare inherited disease that affects the brain, immune system, and skin. Genetic changes cause the immune system to mistake the body’s own DNA or RNA for a virus, creating ongoing inflammation. This can damage the brain’s white matter and affect development, movement, communication, feeding, vision, and many other parts of daily life. AGS affects every person differently, but its challenges can be lifelong and devastating. Abbie was diagnosed with AGS in October 2021. Since that day, she has battled courageously to live the fullest and most normal life possible. She is so much more than her diagnosis—she is brave, deeply loved, and worth fighting for every single day. To honor Abbie and spread awareness this September, we have created special AGS shirts and drinkware. The most meaningful part of every design is that the letters “AGS” are written in Abbie’s own handwriting. When you wear one of these shirts or carry one of these cups, you are carrying a piece of Abbie’s story and helping introduce others to a disease that far too few people know about. Everyone knows what our family means to us; that we will go to boundless lengths to do whatever they need. Yesterday, on Ashley’s birthday, we had the honor of sharing these designs with her. Our family has always surrounded Abbie, Ashley, and their family with tremendous love, support, and prayer. Now, we would love to see our community stand beside them too. Buy a shirt. Carry a cup. Start a conversation. Say the name “Aicardi-Goutières syndrome.” Share Abbie’s story. Educate yourself. Most importantly, please pray for Abbie’s strength and comfort, for more good days, for wisdom for her doctors, and for research to bring better treatments to everyone living with AGS. If you are unable to purchase, sharing this post is completely free and incredibly powerful. Your share may reach someone learning about AGS for the first time, another family walking this road, or someone connected to research and advocacy. The more we talk about AGS, the more people will hear its name. Knowledge creates understanding, understanding creates advocacy, and advocacy creates hope. Abbie deserves a world that understands her disease and continues fighting for better treatments and a brighter future. Let’s show her that her community sees her, loves her, prays for her, and stands with her. Local pickup and shipping are available. Feel free to purchase a shirt or drinkware item, share Abbie’s story, and help us spread as much AGS awareness as possible this September. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003eEvery color may not be available in every size. If your chosen color isn’t available, we will email you. \u003c\/p\u003e","brand":"Oh My Ginger","offers":[{"title":"Default Title","offer_id":50103927963896,"sku":null,"price":16.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0501\/1357\/7128\/files\/IMG-1998.png?v=1785815521"},{"product_id":"warriors-against-ags-white-letters-kids","title":"Warriors Against AGS (White Letters) - Kids","description":"\u003cp\u003e\u003cspan\u003eSeptember is Leukodystrophy Awareness Month, and we are asking our community to help us turn awareness into action for someone incredibly special—our cousin, Abbie. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003cspan\u003e Aicardi-Goutières syndrome, or AGS, is a rare inherited disease that affects the brain, immune system, and skin. Genetic changes cause the immune system to mistake the body’s own DNA or RNA for a virus, creating ongoing inflammation. This can damage the brain’s white matter and affect development, movement, communication, feeding, vision, and many other parts of daily life. AGS affects every person differently, but its challenges can be lifelong and devastating. Abbie was diagnosed with AGS in October 2021. Since that day, she has battled courageously to live the fullest and most normal life possible. She is so much more than her diagnosis—she is brave, deeply loved, and worth fighting for every single day. To honor Abbie and spread awareness this September, we have created special AGS shirts and drinkware. The most meaningful part of every design is that the letters “AGS” are written in Abbie’s own handwriting. When you wear one of these shirts or carry one of these cups, you are carrying a piece of Abbie’s story and helping introduce others to a disease that far too few people know about. Everyone knows what our family means to us; that we will go to boundless lengths to do whatever they need. Yesterday, on Ashley’s birthday, we had the honor of sharing these designs with her. Our family has always surrounded Abbie, Ashley, and their family with tremendous love, support, and prayer. Now, we would love to see our community stand beside them too. Buy a shirt. Carry a cup. Start a conversation. Say the name “Aicardi-Goutières syndrome.” Share Abbie’s story. Educate yourself. Most importantly, please pray for Abbie’s strength and comfort, for more good days, for wisdom for her doctors, and for research to bring better treatments to everyone living with AGS. If you are unable to purchase, sharing this post is completely free and incredibly powerful. Your share may reach someone learning about AGS for the first time, another family walking this road, or someone connected to research and advocacy. The more we talk about AGS, the more people will hear its name. Knowledge creates understanding, understanding creates advocacy, and advocacy creates hope. Abbie deserves a world that understands her disease and continues fighting for better treatments and a brighter future. Let’s show her that her community sees her, loves her, prays for her, and stands with her. Local pickup and shipping are available. Feel free to purchase a shirt or drinkware item, share Abbie’s story, and help us spread as much AGS awareness as possible this September. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003eEvery color may not be available in every size. If your chosen color isn’t available, we will email you. \u003c\/p\u003e","brand":"Oh My Ginger","offers":[{"title":"Default Title","offer_id":50103928422648,"sku":null,"price":16.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0501\/1357\/7128\/files\/IMG-2021.png?v=1785819997"},{"product_id":"abbies-warriors-white-letters-brown-1","title":"AGS Green Shield - White Letters","description":"\u003cp\u003e\u003cspan\u003eSeptember is Leukodystrophy Awareness Month, and we are asking our community to help us turn awareness into action for someone incredibly special—our cousin, Abbie. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003cspan\u003e Aicardi-Goutières syndrome, or AGS, is a rare inherited disease that affects the brain, immune system, and skin. Genetic changes cause the immune system to mistake the body’s own DNA or RNA for a virus, creating ongoing inflammation. This can damage the brain’s white matter and affect development, movement, communication, feeding, vision, and many other parts of daily life. AGS affects every person differently, but its challenges can be lifelong and devastating. Abbie was diagnosed with AGS in October 2021. Since that day, she has battled courageously to live the fullest and most normal life possible. She is so much more than her diagnosis—she is brave, deeply loved, and worth fighting for every single day. To honor Abbie and spread awareness this September, we have created special AGS shirts and drinkware. The most meaningful part of every design is that the letters “AGS” are written in Abbie’s own handwriting. When you wear one of these shirts or carry one of these cups, you are carrying a piece of Abbie’s story and helping introduce others to a disease that far too few people know about. Everyone knows what our family means to us; that we will go to boundless lengths to do whatever they need. Yesterday, on Ashley’s birthday, we had the honor of sharing these designs with her. Our family has always surrounded Abbie, Ashley, and their family with tremendous love, support, and prayer. Now, we would love to see our community stand beside them too. Buy a shirt. Carry a cup. Start a conversation. Say the name “Aicardi-Goutières syndrome.” Share Abbie’s story. Educate yourself. Most importantly, please pray for Abbie’s strength and comfort, for more good days, for wisdom for her doctors, and for research to bring better treatments to everyone living with AGS. If you are unable to purchase, sharing this post is completely free and incredibly powerful. Your share may reach someone learning about AGS for the first time, another family walking this road, or someone connected to research and advocacy. The more we talk about AGS, the more people will hear its name. Knowledge creates understanding, understanding creates advocacy, and advocacy creates hope. Abbie deserves a world that understands her disease and continues fighting for better treatments and a brighter future. Let’s show her that her community sees her, loves her, prays for her, and stands with her. Local pickup and shipping are available. Feel free to purchase a shirt or drinkware item, share Abbie’s story, and help us spread as much AGS awareness as possible this September. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003eEvery color may not be available in every size. If your chosen color isn’t available, we will email you. \u003c\/p\u003e","brand":"Oh My Ginger","offers":[{"title":"Small","offer_id":50103932518648,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true},{"title":"Medium","offer_id":50103932551416,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true},{"title":"Large","offer_id":50103932584184,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true},{"title":"XLarge","offer_id":50103932616952,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true},{"title":"2XLarge","offer_id":50103932649720,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true},{"title":"3XLarge","offer_id":50103932682488,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true},{"title":"4XLarge","offer_id":50103932715256,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true},{"title":"5XLarge","offer_id":50103932748024,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0501\/1357\/7128\/files\/IMG-2017.jpg?v=1785819996"},{"product_id":"abbies-warriors-black-letters-brown","title":"AGS Green Shield - Black Letters","description":"\u003cp\u003e\u003cspan\u003eSeptember is Leukodystrophy Awareness Month, and we are asking our community to help us turn awareness into action for someone incredibly special—our cousin, Abbie. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003cspan\u003e Aicardi-Goutières syndrome, or AGS, is a rare inherited disease that affects the brain, immune system, and skin. Genetic changes cause the immune system to mistake the body’s own DNA or RNA for a virus, creating ongoing inflammation. This can damage the brain’s white matter and affect development, movement, communication, feeding, vision, and many other parts of daily life. AGS affects every person differently, but its challenges can be lifelong and devastating. Abbie was diagnosed with AGS in October 2021. Since that day, she has battled courageously to live the fullest and most normal life possible. She is so much more than her diagnosis—she is brave, deeply loved, and worth fighting for every single day. To honor Abbie and spread awareness this September, we have created special AGS shirts and drinkware. The most meaningful part of every design is that the letters “AGS” are written in Abbie’s own handwriting. When you wear one of these shirts or carry one of these cups, you are carrying a piece of Abbie’s story and helping introduce others to a disease that far too few people know about. Everyone knows what our family means to us; that we will go to boundless lengths to do whatever they need. Yesterday, on Ashley’s birthday, we had the honor of sharing these designs with her. Our family has always surrounded Abbie, Ashley, and their family with tremendous love, support, and prayer. Now, we would love to see our community stand beside them too. Buy a shirt. Carry a cup. Start a conversation. Say the name “Aicardi-Goutières syndrome.” Share Abbie’s story. Educate yourself. Most importantly, please pray for Abbie’s strength and comfort, for more good days, for wisdom for her doctors, and for research to bring better treatments to everyone living with AGS. If you are unable to purchase, sharing this post is completely free and incredibly powerful. Your share may reach someone learning about AGS for the first time, another family walking this road, or someone connected to research and advocacy. The more we talk about AGS, the more people will hear its name. Knowledge creates understanding, understanding creates advocacy, and advocacy creates hope. Abbie deserves a world that understands her disease and continues fighting for better treatments and a brighter future. Let’s show her that her community sees her, loves her, prays for her, and stands with her. Local pickup and shipping are available. Feel free to purchase a shirt or drinkware item, share Abbie’s story, and help us spread as much AGS awareness as possible this September. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003eEvery color may not be available in every size. If your chosen color isn’t available, we will email you. \u003c\/p\u003e","brand":"Oh My Ginger","offers":[{"title":"Small","offer_id":50103933501688,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true},{"title":"Medium","offer_id":50103933534456,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true},{"title":"Large","offer_id":50103933567224,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true},{"title":"XLarge","offer_id":50103933599992,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true},{"title":"2XLarge","offer_id":50103933632760,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true},{"title":"3XLarge","offer_id":50103933665528,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true},{"title":"4XLarge","offer_id":50103933698296,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true},{"title":"5XLarge","offer_id":50103933731064,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0501\/1357\/7128\/files\/IMG-2022.jpg?v=1785819996"},{"product_id":"warriors-against-ags-colorful-lion-kids","title":"AGS Watercolor Lion - Kids","description":"\u003cp\u003e\u003cspan\u003eSeptember is Leukodystrophy Awareness Month, and we are asking our community to help us turn awareness into action for someone incredibly special—our cousin, Abbie. \u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e Aicardi-Goutières syndrome, or AGS, is a rare inherited disease that affects the brain, immune system, and skin. Genetic changes cause the immune system to mistake the body’s own DNA or RNA for a virus, creating ongoing inflammation. This can damage the brain’s white matter and affect development, movement, communication, feeding, vision, and many other parts of daily life. AGS affects every person differently, but its challenges can be lifelong and devastating. Abbie was diagnosed with AGS in October 2021. Since that day, she has battled courageously to live the fullest and most normal life possible. She is so much more than her diagnosis—she is brave, deeply loved, and worth fighting for every single day. To honor Abbie and spread awareness this September, we have created special AGS shirts and drinkware. The most meaningful part of every design is that the letters “AGS” are written in Abbie’s own handwriting. When you wear one of these shirts or carry one of these cups, you are carrying a piece of Abbie’s story and helping introduce others to a disease that far too few people know about. Everyone knows what our family means to us; that we will go to boundless lengths to do whatever they need. Yesterday, on Ashley’s birthday, we had the honor of sharing these designs with her. Our family has always surrounded Abbie, Ashley, and their family with tremendous love, support, and prayer. Now, we would love to see our community stand beside them too. Buy a shirt. Carry a cup. Start a conversation. Say the name “Aicardi-Goutières syndrome.” Share Abbie’s story. Educate yourself. Most importantly, please pray for Abbie’s strength and comfort, for more good days, for wisdom for her doctors, and for research to bring better treatments to everyone living with AGS. If you are unable to purchase, sharing this post is completely free and incredibly powerful. Your share may reach someone learning about AGS for the first time, another family walking this road, or someone connected to research and advocacy. The more we talk about AGS, the more people will hear its name. Knowledge creates understanding, understanding creates advocacy, and advocacy creates hope. Abbie deserves a world that understands her disease and continues fighting for better treatments and a brighter future. Let’s show her that her community sees her, loves her, prays for her, and stands with her. Local pickup and shipping are available. Feel free to purchase a shirt or drinkware item, share Abbie’s story, and help us spread as much AGS awareness as possible this September. \u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eEvery color may not be available in every size. You will be emailed if the color you choose is out of stock in your size. \u003c\/span\u003e\u003c\/p\u003e","brand":"Oh My Ginger","offers":[{"title":"Default Title","offer_id":50103934845176,"sku":null,"price":16.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0501\/1357\/7128\/files\/IMG-1996.png?v=1785815521"},{"product_id":"ags-green-shield","title":"AGS Green Shield 40oz Tumbler","description":"\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eSeptember is Leukodystrophy Awareness Month, and we are asking our community to help us turn awareness into action for someone incredibly special—our cousin, Abbie. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003cspan\u003e Aicardi-Goutières syndrome, or AGS, is a rare inherited disease that affects the brain, immune system, and skin. Genetic changes cause the immune system to mistake the body’s own DNA or RNA for a virus, creating ongoing inflammation. This can damage the brain’s white matter and affect development, movement, communication, feeding, vision, and many other parts of daily life. AGS affects every person differently, but its challenges can be lifelong and devastating. Abbie was diagnosed with AGS in October 2021. Since that day, she has battled courageously to live the fullest and most normal life possible. She is so much more than her diagnosis—she is brave, deeply loved, and worth fighting for every single day. To honor Abbie and spread awareness this September, we have created special AGS shirts and drinkware. The most meaningful part of every design is that the letters “AGS” are written in Abbie’s own handwriting. When you wear one of these shirts or carry one of these cups, you are carrying a piece of Abbie’s story and helping introduce others to a disease that far too few people know about. Everyone knows what our family means to us; that we will go to boundless lengths to do whatever they need. Yesterday, on Ashley’s birthday, we had the honor of sharing these designs with her. Our family has always surrounded Abbie, Ashley, and their family with tremendous love, support, and prayer. Now, we would love to see our community stand beside them too. Buy a shirt. Carry a cup. Start a conversation. Say the name “Aicardi-Goutières syndrome.” Share Abbie’s story. Educate yourself. Most importantly, please pray for Abbie’s strength and comfort, for more good days, for wisdom for her doctors, and for research to bring better treatments to everyone living with AGS. If you are unable to purchase, sharing this post is completely free and incredibly powerful. Your share may reach someone learning about AGS for the first time, another family walking this road, or someone connected to research and advocacy. The more we talk about AGS, the more people will hear its name. Knowledge creates understanding, understanding creates advocacy, and advocacy creates hope. Abbie deserves a world that understands her disease and continues fighting for better treatments and a brighter future. Let’s show her that her community sees her, loves her, prays for her, and stands with her. Local pickup and shipping are available. Feel free to purchase a shirt or drinkware item, share Abbie’s story, and help us spread as much AGS awareness as possible this September. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e40oz Metal Tumbler\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eSturdy handle\u003c\/li\u003e\n\u003cli\u003eMetal, double insulated\u003c\/li\u003e\n\u003cli\u003eShimmer glittery coating\u003c\/li\u003e\n\u003cli\u003eIncludes screw on lid and straw\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003cstrong\u003e40oz Metal Tumbler White with colored handle\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eSturdy Handle \u003c\/li\u003e\n\u003cli\u003eMetal, double insulated \u003c\/li\u003e\n\u003cli\u003eColored handle and lid\u003c\/li\u003e\n\u003cli\u003eIncludes screw on lid and straw\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"Oh My Ginger","offers":[{"title":"White Shimmer \/ Standard","offer_id":50114598076664,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"White Shimmer \/ Leakproof","offer_id":50114598109432,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"Light Pink Shimmer \/ Standard","offer_id":50114598142200,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"Light Pink Shimmer \/ Leakproof","offer_id":50114598174968,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"Pink Shimmer \/ Standard","offer_id":50114598207736,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"Pink Shimmer \/ Leakproof","offer_id":50114598240504,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"Light Purple Shimmer \/ Standard","offer_id":50114598273272,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"Light Purple Shimmer \/ Leakproof","offer_id":50114598306040,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"Teal Shimmer \/ Standard","offer_id":50114598338808,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"Teal Shimmer \/ Leakproof","offer_id":50114598371576,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"White\/White Handle \/ Standard","offer_id":50114598404344,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"White\/White Handle \/ Leakproof","offer_id":50114598437112,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"White\/Black Handle \/ Standard","offer_id":50114598469880,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"White\/Black Handle \/ Leakproof","offer_id":50114598502648,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"White\/Purple Handle \/ Standard","offer_id":50114598535416,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"White\/Purple Handle \/ Leakproof","offer_id":50114598568184,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"White\/Pink Handle \/ Standard","offer_id":50114598600952,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"White\/Pink Handle \/ Leakproof","offer_id":50114598633720,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"White\/Teal Handle \/ Standard","offer_id":50114598666488,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"White\/Teal Handle \/ Leakproof","offer_id":50114598699256,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0501\/1357\/7128\/files\/BA029454-8E51-4DD4-8E01-CBDE3C576094.png?v=1785958612"},{"product_id":"ags-pink-shield","title":"AGS Pink Shield 40oz Tumbler","description":"\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eSeptember is Leukodystrophy Awareness Month, and we are asking our community to help us turn awareness into action for someone incredibly special—our cousin, Abbie. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003cspan\u003e Aicardi-Goutières syndrome, or AGS, is a rare inherited disease that affects the brain, immune system, and skin. Genetic changes cause the immune system to mistake the body’s own DNA or RNA for a virus, creating ongoing inflammation. This can damage the brain’s white matter and affect development, movement, communication, feeding, vision, and many other parts of daily life. AGS affects every person differently, but its challenges can be lifelong and devastating. Abbie was diagnosed with AGS in October 2021. Since that day, she has battled courageously to live the fullest and most normal life possible. She is so much more than her diagnosis—she is brave, deeply loved, and worth fighting for every single day. To honor Abbie and spread awareness this September, we have created special AGS shirts and drinkware. The most meaningful part of every design is that the letters “AGS” are written in Abbie’s own handwriting. When you wear one of these shirts or carry one of these cups, you are carrying a piece of Abbie’s story and helping introduce others to a disease that far too few people know about. Everyone knows what our family means to us; that we will go to boundless lengths to do whatever they need. Yesterday, on Ashley’s birthday, we had the honor of sharing these designs with her. Our family has always surrounded Abbie, Ashley, and their family with tremendous love, support, and prayer. Now, we would love to see our community stand beside them too. Buy a shirt. Carry a cup. Start a conversation. Say the name “Aicardi-Goutières syndrome.” Share Abbie’s story. Educate yourself. Most importantly, please pray for Abbie’s strength and comfort, for more good days, for wisdom for her doctors, and for research to bring better treatments to everyone living with AGS. If you are unable to purchase, sharing this post is completely free and incredibly powerful. Your share may reach someone learning about AGS for the first time, another family walking this road, or someone connected to research and advocacy. The more we talk about AGS, the more people will hear its name. Knowledge creates understanding, understanding creates advocacy, and advocacy creates hope. Abbie deserves a world that understands her disease and continues fighting for better treatments and a brighter future. Let’s show her that her community sees her, loves her, prays for her, and stands with her. Local pickup and shipping are available. Feel free to purchase a shirt or drinkware item, share Abbie’s story, and help us spread as much AGS awareness as possible this September. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e40oz Metal Tumbler\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eSturdy handle\u003c\/li\u003e\n\u003cli\u003eMetal, double insulated\u003c\/li\u003e\n\u003cli\u003eShimmer glittery coating\u003c\/li\u003e\n\u003cli\u003eIncludes screw on lid and straw\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003cstrong\u003e40oz Metal Tumbler White with colored handle\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eSturdy Handle \u003c\/li\u003e\n\u003cli\u003eMetal, double insulated \u003c\/li\u003e\n\u003cli\u003eColored handle and lid\u003c\/li\u003e\n\u003cli\u003eIncludes screw on lid and straw\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"Oh My Ginger","offers":[{"title":"White Shimmer \/ Standard","offer_id":50114599092472,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"White Shimmer \/ Leakproof","offer_id":50114599125240,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"Light Pink Shimmer \/ Standard","offer_id":50114599158008,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"Light Pink Shimmer \/ Leakproof","offer_id":50114599190776,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"Pink Shimmer \/ Standard","offer_id":50114599223544,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"Pink Shimmer \/ Leakproof","offer_id":50114599256312,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"Light Purple Shimmer \/ Standard","offer_id":50114599289080,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"Light Purple Shimmer \/ Leakproof","offer_id":50114599321848,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"Teal Shimmer \/ Standard","offer_id":50114599354616,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"Teal Shimmer \/ Leakproof","offer_id":50114599387384,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"White\/White Handle \/ Standard","offer_id":50114599420152,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"White\/White Handle \/ Leakproof","offer_id":50114599452920,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"White\/Black Handle \/ Standard","offer_id":50114599485688,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"White\/Black Handle \/ Leakproof","offer_id":50114599518456,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"White\/Purple Handle \/ Standard","offer_id":50114599551224,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"White\/Purple Handle \/ Leakproof","offer_id":50114599583992,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"White\/Pink Handle \/ Standard","offer_id":50114599616760,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"White\/Pink Handle \/ Leakproof","offer_id":50114599649528,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"White\/Teal Handle \/ Standard","offer_id":50114599682296,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"White\/Teal Handle \/ Leakproof","offer_id":50114599715064,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0501\/1357\/7128\/files\/54BDFDD9-60B7-46D5-A6F7-01D49363A743.png?v=1785958611"},{"product_id":"watercolor-lion","title":"AGS Watercolor Lion 40oz Tumbler","description":"\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eSeptember is Leukodystrophy Awareness Month, and we are asking our community to help us turn awareness into action for someone incredibly special—our cousin, Abbie. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003cspan\u003e Aicardi-Goutières syndrome, or AGS, is a rare inherited disease that affects the brain, immune system, and skin. Genetic changes cause the immune system to mistake the body’s own DNA or RNA for a virus, creating ongoing inflammation. This can damage the brain’s white matter and affect development, movement, communication, feeding, vision, and many other parts of daily life. AGS affects every person differently, but its challenges can be lifelong and devastating. Abbie was diagnosed with AGS in October 2021. Since that day, she has battled courageously to live the fullest and most normal life possible. She is so much more than her diagnosis—she is brave, deeply loved, and worth fighting for every single day. To honor Abbie and spread awareness this September, we have created special AGS shirts and drinkware. The most meaningful part of every design is that the letters “AGS” are written in Abbie’s own handwriting. When you wear one of these shirts or carry one of these cups, you are carrying a piece of Abbie’s story and helping introduce others to a disease that far too few people know about. Everyone knows what our family means to us; that we will go to boundless lengths to do whatever they need. Yesterday, on Ashley’s birthday, we had the honor of sharing these designs with her. Our family has always surrounded Abbie, Ashley, and their family with tremendous love, support, and prayer. Now, we would love to see our community stand beside them too. Buy a shirt. Carry a cup. Start a conversation. Say the name “Aicardi-Goutières syndrome.” Share Abbie’s story. Educate yourself. Most importantly, please pray for Abbie’s strength and comfort, for more good days, for wisdom for her doctors, and for research to bring better treatments to everyone living with AGS. If you are unable to purchase, sharing this post is completely free and incredibly powerful. Your share may reach someone learning about AGS for the first time, another family walking this road, or someone connected to research and advocacy. The more we talk about AGS, the more people will hear its name. Knowledge creates understanding, understanding creates advocacy, and advocacy creates hope. Abbie deserves a world that understands her disease and continues fighting for better treatments and a brighter future. Let’s show her that her community sees her, loves her, prays for her, and stands with her. Local pickup and shipping are available. Feel free to purchase a shirt or drinkware item, share Abbie’s story, and help us spread as much AGS awareness as possible this September. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e40oz Metal Tumbler\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eSturdy handle\u003c\/li\u003e\n\u003cli\u003eMetal, double insulated\u003c\/li\u003e\n\u003cli\u003eShimmer glittery coating\u003c\/li\u003e\n\u003cli\u003eIncludes screw on lid and straw\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003cstrong\u003e40oz Metal Tumbler White with colored handle\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eSturdy Handle \u003c\/li\u003e\n\u003cli\u003eMetal, double insulated \u003c\/li\u003e\n\u003cli\u003eColored handle and lid\u003c\/li\u003e\n\u003cli\u003eIncludes screw on lid and straw\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"Oh My Ginger","offers":[{"title":"White Shimmer \/ Standard","offer_id":50114601058552,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"White Shimmer \/ Leakproof","offer_id":50114601091320,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"Light Pink Shimmer \/ Standard","offer_id":50114601124088,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"Light Pink Shimmer \/ Leakproof","offer_id":50114601156856,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"Pink Shimmer \/ Standard","offer_id":50114601189624,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"Pink Shimmer \/ Leakproof","offer_id":50114601222392,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"Light Purple Shimmer \/ Standard","offer_id":50114601255160,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"Light Purple Shimmer \/ Leakproof","offer_id":50114601287928,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"Teal Shimmer \/ Standard","offer_id":50114601320696,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"Teal Shimmer \/ Leakproof","offer_id":50114601353464,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"White\/White Handle \/ Standard","offer_id":50114601386232,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"White\/White Handle \/ Leakproof","offer_id":50114601419000,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"White\/Black Handle \/ Standard","offer_id":50114601451768,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"White\/Black Handle \/ Leakproof","offer_id":50114601484536,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"White\/Purple Handle \/ Standard","offer_id":50114601517304,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"White\/Purple Handle \/ Leakproof","offer_id":50114601550072,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"White\/Pink Handle \/ Standard","offer_id":50114601582840,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"White\/Pink Handle \/ Leakproof","offer_id":50114601615608,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"White\/Teal Handle \/ Standard","offer_id":50114601648376,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true},{"title":"White\/Teal Handle \/ Leakproof","offer_id":50114601681144,"sku":null,"price":42.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0501\/1357\/7128\/files\/FullSizeRender_a2693739-38e6-4b51-8494-830a2f223dbf.jpg?v=1785958761"},{"product_id":"16oz-glass-can-watercolor-lion","title":"AGS Watercolor Lion 16oz Glass Can","description":"\u003cp\u003e\u003cspan\u003eSeptember is Leukodystrophy Awareness Month, and we are asking our community to help us turn awareness into action for someone incredibly special—our cousin, Abbie. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003cspan\u003e Aicardi-Goutières syndrome, or AGS, is a rare inherited disease that affects the brain, immune system, and skin. Genetic changes cause the immune system to mistake the body’s own DNA or RNA for a virus, creating ongoing inflammation. This can damage the brain’s white matter and affect development, movement, communication, feeding, vision, and many other parts of daily life. AGS affects every person differently, but its challenges can be lifelong and devastating. Abbie was diagnosed with AGS in October 2021. Since that day, she has battled courageously to live the fullest and most normal life possible. She is so much more than her diagnosis—she is brave, deeply loved, and worth fighting for every single day. To honor Abbie and spread awareness this September, we have created special AGS shirts and drinkware. The most meaningful part of every design is that the letters “AGS” are written in Abbie’s own handwriting. When you wear one of these shirts or carry one of these cups, you are carrying a piece of Abbie’s story and helping introduce others to a disease that far too few people know about. Everyone knows what our family means to us; that we will go to boundless lengths to do whatever they need. Yesterday, on Ashley’s birthday, we had the honor of sharing these designs with her. Our family has always surrounded Abbie, Ashley, and their family with tremendous love, support, and prayer. Now, we would love to see our community stand beside them too. Buy a shirt. Carry a cup. Start a conversation. Say the name “Aicardi-Goutières syndrome.” Share Abbie’s story. Educate yourself. Most importantly, please pray for Abbie’s strength and comfort, for more good days, for wisdom for her doctors, and for research to bring better treatments to everyone living with AGS. If you are unable to purchase, sharing this post is completely free and incredibly powerful. Your share may reach someone learning about AGS for the first time, another family walking this road, or someone connected to research and advocacy. The more we talk about AGS, the more people will hear its name. Knowledge creates understanding, understanding creates advocacy, and advocacy creates hope. Abbie deserves a world that understands her disease and continues fighting for better treatments and a brighter future. Let’s show her that her community sees her, loves her, prays for her, and stands with her. Local pickup and shipping are available. Feel free to purchase a shirt or drinkware item, share Abbie’s story, and help us spread as much AGS awareness as possible this September. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eGlass Can Cup\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eFrosted or Glass\u003c\/li\u003e\n\u003cli\u003e16 ounces\u003c\/li\u003e\n\u003cli\u003eIncludes bamboo lid with silicone ring and stopper and plastic straw\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003cb\u003eNote\u003c\/b\u003e: Colors may vary across computer or phone screens, therefore colors may be slightly different than they appear on your screen.\u003c\/p\u003e","brand":"Oh My Ginger","offers":[{"title":"Frosted","offer_id":50114717090040,"sku":null,"price":26.0,"currency_code":"USD","in_stock":true},{"title":"Clear","offer_id":50114717122808,"sku":null,"price":26.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0501\/1357\/7128\/files\/42E539AB-2FF7-4D87-8B9B-B2A389CC5686.png?v=1785958611"},{"product_id":"ags-shield-pink-20oz-tumbler","title":"AGS Shield Pink 20oz Tumbler","description":"\u003cp\u003e\u003cspan\u003eSeptember is Leukodystrophy Awareness Month, and we are asking our community to help us turn awareness into action for someone incredibly special—our cousin, Abbie. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003cspan\u003e Aicardi-Goutières syndrome, or AGS, is a rare inherited disease that affects the brain, immune system, and skin. Genetic changes cause the immune system to mistake the body’s own DNA or RNA for a virus, creating ongoing inflammation. This can damage the brain’s white matter and affect development, movement, communication, feeding, vision, and many other parts of daily life. AGS affects every person differently, but its challenges can be lifelong and devastating. Abbie was diagnosed with AGS in October 2021. Since that day, she has battled courageously to live the fullest and most normal life possible. She is so much more than her diagnosis—she is brave, deeply loved, and worth fighting for every single day. To honor Abbie and spread awareness this September, we have created special AGS shirts and drinkware. The most meaningful part of every design is that the letters “AGS” are written in Abbie’s own handwriting. When you wear one of these shirts or carry one of these cups, you are carrying a piece of Abbie’s story and helping introduce others to a disease that far too few people know about. Everyone knows what our family means to us; that we will go to boundless lengths to do whatever they need. Yesterday, on Ashley’s birthday, we had the honor of sharing these designs with her. Our family has always surrounded Abbie, Ashley, and their family with tremendous love, support, and prayer. Now, we would love to see our community stand beside them too. Buy a shirt. Carry a cup. Start a conversation. Say the name “Aicardi-Goutières syndrome.” Share Abbie’s story. Educate yourself. Most importantly, please pray for Abbie’s strength and comfort, for more good days, for wisdom for her doctors, and for research to bring better treatments to everyone living with AGS. If you are unable to purchase, sharing this post is completely free and incredibly powerful. Your share may reach someone learning about AGS for the first time, another family walking this road, or someone connected to research and advocacy. The more we talk about AGS, the more people will hear its name. Knowledge creates understanding, understanding creates advocacy, and advocacy creates hope. Abbie deserves a world that understands her disease and continues fighting for better treatments and a brighter future. Let’s show her that her community sees her, loves her, prays for her, and stands with her. Local pickup and shipping are available. Feel free to purchase a shirt or drinkware item, share Abbie’s story, and help us spread as much AGS awareness as possible this September. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e20oz Metal Skinny Tumbler\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e20 ounces\u003c\/li\u003e\n\u003cli\u003eGlossy coating\u003c\/li\u003e\n\u003cli\u003eIncludes plastic lid with silicone ring and straw\u003c\/li\u003e\n\u003c\/ul\u003e","brand":"Oh My Ginger","offers":[{"title":"Default Title","offer_id":50115119677688,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0501\/1357\/7128\/files\/19969617-7BC4-45CC-9CB5-B63718EBF7F3.png?v=1785958610"},{"product_id":"ags-shield-green-20oz-tumbler","title":"AGS Shield Green 20oz Tumbler","description":"\u003cp\u003e\u003cspan\u003eSeptember is Leukodystrophy Awareness Month, and we are asking our community to help us turn awareness into action for someone incredibly special—our cousin, Abbie. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003cspan\u003e Aicardi-Goutières syndrome, or AGS, is a rare inherited disease that affects the brain, immune system, and skin. Genetic changes cause the immune system to mistake the body’s own DNA or RNA for a virus, creating ongoing inflammation. This can damage the brain’s white matter and affect development, movement, communication, feeding, vision, and many other parts of daily life. AGS affects every person differently, but its challenges can be lifelong and devastating. Abbie was diagnosed with AGS in October 2021. Since that day, she has battled courageously to live the fullest and most normal life possible. She is so much more than her diagnosis—she is brave, deeply loved, and worth fighting for every single day. To honor Abbie and spread awareness this September, we have created special AGS shirts and drinkware. The most meaningful part of every design is that the letters “AGS” are written in Abbie’s own handwriting. When you wear one of these shirts or carry one of these cups, you are carrying a piece of Abbie’s story and helping introduce others to a disease that far too few people know about. Everyone knows what our family means to us; that we will go to boundless lengths to do whatever they need. Yesterday, on Ashley’s birthday, we had the honor of sharing these designs with her. Our family has always surrounded Abbie, Ashley, and their family with tremendous love, support, and prayer. Now, we would love to see our community stand beside them too. Buy a shirt. Carry a cup. Start a conversation. Say the name “Aicardi-Goutières syndrome.” Share Abbie’s story. Educate yourself. Most importantly, please pray for Abbie’s strength and comfort, for more good days, for wisdom for her doctors, and for research to bring better treatments to everyone living with AGS. If you are unable to purchase, sharing this post is completely free and incredibly powerful. Your share may reach someone learning about AGS for the first time, another family walking this road, or someone connected to research and advocacy. The more we talk about AGS, the more people will hear its name. Knowledge creates understanding, understanding creates advocacy, and advocacy creates hope. Abbie deserves a world that understands her disease and continues fighting for better treatments and a brighter future. Let’s show her that her community sees her, loves her, prays for her, and stands with her. Local pickup and shipping are available. Feel free to purchase a shirt or drinkware item, share Abbie’s story, and help us spread as much AGS awareness as possible this September. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e20oz Metal Skinny Tumbler\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e20 ounces\u003c\/li\u003e\n\u003cli\u003eGlossy coating\u003c\/li\u003e\n\u003cli\u003eIncludes plastic lid with silicone ring and straw\u003c\/li\u003e\n\u003c\/ul\u003e","brand":"Oh My Ginger","offers":[{"title":"Default Title","offer_id":50115123544312,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0501\/1357\/7128\/files\/10B9C66A-4C83-4822-9AC9-513B0D2AA360.png?v=1785958610"},{"product_id":"watercolor-lion-20oz-tumbler","title":"AGS Watercolor Lion 20oz Tumbler","description":"\u003cp\u003e\u003cspan\u003eSeptember is Leukodystrophy Awareness Month, and we are asking our community to help us turn awareness into action for someone incredibly special—our cousin, Abbie. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003cspan\u003e Aicardi-Goutières syndrome, or AGS, is a rare inherited disease that affects the brain, immune system, and skin. Genetic changes cause the immune system to mistake the body’s own DNA or RNA for a virus, creating ongoing inflammation. This can damage the brain’s white matter and affect development, movement, communication, feeding, vision, and many other parts of daily life. AGS affects every person differently, but its challenges can be lifelong and devastating. Abbie was diagnosed with AGS in October 2021. Since that day, she has battled courageously to live the fullest and most normal life possible. She is so much more than her diagnosis—she is brave, deeply loved, and worth fighting for every single day. To honor Abbie and spread awareness this September, we have created special AGS shirts and drinkware. The most meaningful part of every design is that the letters “AGS” are written in Abbie’s own handwriting. When you wear one of these shirts or carry one of these cups, you are carrying a piece of Abbie’s story and helping introduce others to a disease that far too few people know about. Everyone knows what our family means to us; that we will go to boundless lengths to do whatever they need. Yesterday, on Ashley’s birthday, we had the honor of sharing these designs with her. Our family has always surrounded Abbie, Ashley, and their family with tremendous love, support, and prayer. Now, we would love to see our community stand beside them too. Buy a shirt. Carry a cup. Start a conversation. Say the name “Aicardi-Goutières syndrome.” Share Abbie’s story. Educate yourself. Most importantly, please pray for Abbie’s strength and comfort, for more good days, for wisdom for her doctors, and for research to bring better treatments to everyone living with AGS. If you are unable to purchase, sharing this post is completely free and incredibly powerful. Your share may reach someone learning about AGS for the first time, another family walking this road, or someone connected to research and advocacy. The more we talk about AGS, the more people will hear its name. Knowledge creates understanding, understanding creates advocacy, and advocacy creates hope. Abbie deserves a world that understands her disease and continues fighting for better treatments and a brighter future. Let’s show her that her community sees her, loves her, prays for her, and stands with her. Local pickup and shipping are available. Feel free to purchase a shirt or drinkware item, share Abbie’s story, and help us spread as much AGS awareness as possible this September. \u003c\/span\u003e\u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e20oz Metal Skinny Tumbler\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e20 ounces\u003c\/li\u003e\n\u003cli\u003eGlossy coating\u003c\/li\u003e\n\u003cli\u003eIncludes plastic lid with silicone ring and straw\u003c\/li\u003e\n\u003c\/ul\u003e","brand":"Oh My Ginger","offers":[{"title":"Default Title","offer_id":50115127902456,"sku":null,"price":30.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0501\/1357\/7128\/files\/DF0B8D43-5795-4966-AEEA-9BC588DDE0D6.png?v=1785958610"},{"product_id":"ags-pink-shield-mug","title":"AGS Pink Shield Mug","description":"\u003cp\u003e\u003cspan\u003eSeptember is Leukodystrophy Awareness Month, and we are asking our community to help us turn awareness into action for someone incredibly special—our cousin, Abbie. \u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e Aicardi-Goutières syndrome, or AGS, is a rare inherited disease that affects the brain, immune system, and skin. Genetic changes cause the immune system to mistake the body’s own DNA or RNA for a virus, creating ongoing inflammation. This can damage the brain’s white matter and affect development, movement, communication, feeding, vision, and many other parts of daily life. AGS affects every person differently, but its challenges can be lifelong and devastating. Abbie was diagnosed with AGS in October 2021. Since that day, she has battled courageously to live the fullest and most normal life possible. She is so much more than her diagnosis—she is brave, deeply loved, and worth fighting for every single day. To honor Abbie and spread awareness this September, we have created special AGS shirts and drinkware. The most meaningful part of every design is that the letters “AGS” are written in Abbie’s own handwriting. When you wear one of these shirts or carry one of these cups, you are carrying a piece of Abbie’s story and helping introduce others to a disease that far too few people know about. Everyone knows what our family means to us; that we will go to boundless lengths to do whatever they need. Yesterday, on Ashley’s birthday, we had the honor of sharing these designs with her. Our family has always surrounded Abbie, Ashley, and their family with tremendous love, support, and prayer. Now, we would love to see our community stand beside them too. Buy a shirt. Carry a cup. Start a conversation. Say the name “Aicardi-Goutières syndrome.” Share Abbie’s story. Educate yourself. Most importantly, please pray for Abbie’s strength and comfort, for more good days, for wisdom for her doctors, and for research to bring better treatments to everyone living with AGS. If you are unable to purchase, sharing this post is completely free and incredibly powerful. Your share may reach someone learning about AGS for the first time, another family walking this road, or someone connected to research and advocacy. The more we talk about AGS, the more people will hear its name. Knowledge creates understanding, understanding creates advocacy, and advocacy creates hope. Abbie deserves a world that understands her disease and continues fighting for better treatments and a brighter future. Let’s show her that her community sees her, loves her, prays for her, and stands with her. Local pickup and shipping are available. Feel free to purchase a shirt or drinkware item, share Abbie’s story, and help us spread as much AGS awareness as possible this September. \u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eCeramic mug, 11oz\u003c\/span\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eMicrowave safe!\u003c\/li\u003e\n\u003cli\u003eDesign on both sides\u003c\/li\u003e\n\u003cli\u003eDishwasher safe\u003c\/li\u003e\n\u003cli\u003eShips in a plain white gift box\u003c\/li\u003e\n\u003c\/ul\u003e","brand":"Oh My Ginger","offers":[{"title":"Default Title","offer_id":50115222798584,"sku":null,"price":16.5,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0501\/1357\/7128\/files\/F8A5099E-863F-4306-AE42-4C1E80E40940.png?v=1785958610"},{"product_id":"ags-green-shield-mug","title":"AGS Green Shield Mug","description":"\u003cp\u003e\u003cspan\u003eSeptember is Leukodystrophy Awareness Month, and we are asking our community to help us turn awareness into action for someone incredibly special—our cousin, Abbie. \u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e Aicardi-Goutières syndrome, or AGS, is a rare inherited disease that affects the brain, immune system, and skin. Genetic changes cause the immune system to mistake the body’s own DNA or RNA for a virus, creating ongoing inflammation. This can damage the brain’s white matter and affect development, movement, communication, feeding, vision, and many other parts of daily life. AGS affects every person differently, but its challenges can be lifelong and devastating. Abbie was diagnosed with AGS in October 2021. Since that day, she has battled courageously to live the fullest and most normal life possible. She is so much more than her diagnosis—she is brave, deeply loved, and worth fighting for every single day. To honor Abbie and spread awareness this September, we have created special AGS shirts and drinkware. The most meaningful part of every design is that the letters “AGS” are written in Abbie’s own handwriting. When you wear one of these shirts or carry one of these cups, you are carrying a piece of Abbie’s story and helping introduce others to a disease that far too few people know about. Everyone knows what our family means to us; that we will go to boundless lengths to do whatever they need. Yesterday, on Ashley’s birthday, we had the honor of sharing these designs with her. Our family has always surrounded Abbie, Ashley, and their family with tremendous love, support, and prayer. Now, we would love to see our community stand beside them too. Buy a shirt. Carry a cup. Start a conversation. Say the name “Aicardi-Goutières syndrome.” Share Abbie’s story. Educate yourself. Most importantly, please pray for Abbie’s strength and comfort, for more good days, for wisdom for her doctors, and for research to bring better treatments to everyone living with AGS. If you are unable to purchase, sharing this post is completely free and incredibly powerful. Your share may reach someone learning about AGS for the first time, another family walking this road, or someone connected to research and advocacy. The more we talk about AGS, the more people will hear its name. Knowledge creates understanding, understanding creates advocacy, and advocacy creates hope. Abbie deserves a world that understands her disease and continues fighting for better treatments and a brighter future. Let’s show her that her community sees her, loves her, prays for her, and stands with her. Local pickup and shipping are available. Feel free to purchase a shirt or drinkware item, share Abbie’s story, and help us spread as much AGS awareness as possible this September. \u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eCeramic mug, 11oz\u003c\/span\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eMicrowave safe!\u003c\/li\u003e\n\u003cli\u003eDesign on both sides\u003c\/li\u003e\n\u003cli\u003eDishwasher safe\u003c\/li\u003e\n\u003cli\u003eShips in a plain white gift box\u003c\/li\u003e\n\u003c\/ul\u003e","brand":"Oh My Ginger","offers":[{"title":"Default Title","offer_id":50115225714936,"sku":null,"price":16.5,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0501\/1357\/7128\/files\/3ADB289C-EE74-414D-87FD-73F61B2A7DDA.png?v=1785958610"},{"product_id":"ags-watercolor-lion-mug","title":"AGS Watercolor Lion Mug","description":"\u003cp\u003e\u003cspan\u003eSeptember is Leukodystrophy Awareness Month, and we are asking our community to help us turn awareness into action for someone incredibly special—our cousin, Abbie. \u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e Aicardi-Goutières syndrome, or AGS, is a rare inherited disease that affects the brain, immune system, and skin. Genetic changes cause the immune system to mistake the body’s own DNA or RNA for a virus, creating ongoing inflammation. This can damage the brain’s white matter and affect development, movement, communication, feeding, vision, and many other parts of daily life. AGS affects every person differently, but its challenges can be lifelong and devastating. Abbie was diagnosed with AGS in October 2021. Since that day, she has battled courageously to live the fullest and most normal life possible. She is so much more than her diagnosis—she is brave, deeply loved, and worth fighting for every single day. To honor Abbie and spread awareness this September, we have created special AGS shirts and drinkware. The most meaningful part of every design is that the letters “AGS” are written in Abbie’s own handwriting. When you wear one of these shirts or carry one of these cups, you are carrying a piece of Abbie’s story and helping introduce others to a disease that far too few people know about. Everyone knows what our family means to us; that we will go to boundless lengths to do whatever they need. Yesterday, on Ashley’s birthday, we had the honor of sharing these designs with her. Our family has always surrounded Abbie, Ashley, and their family with tremendous love, support, and prayer. Now, we would love to see our community stand beside them too. Buy a shirt. Carry a cup. Start a conversation. Say the name “Aicardi-Goutières syndrome.” Share Abbie’s story. Educate yourself. Most importantly, please pray for Abbie’s strength and comfort, for more good days, for wisdom for her doctors, and for research to bring better treatments to everyone living with AGS. If you are unable to purchase, sharing this post is completely free and incredibly powerful. Your share may reach someone learning about AGS for the first time, another family walking this road, or someone connected to research and advocacy. The more we talk about AGS, the more people will hear its name. Knowledge creates understanding, understanding creates advocacy, and advocacy creates hope. Abbie deserves a world that understands her disease and continues fighting for better treatments and a brighter future. Let’s show her that her community sees her, loves her, prays for her, and stands with her. Local pickup and shipping are available. Feel free to purchase a shirt or drinkware item, share Abbie’s story, and help us spread as much AGS awareness as possible this September. \u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eCeramic mug, 11oz\u003c\/span\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eMicrowave safe!\u003c\/li\u003e\n\u003cli\u003eDesign on both sides\u003c\/li\u003e\n\u003cli\u003eDishwasher safe\u003c\/li\u003e\n\u003cli\u003eShips in a plain white gift box\u003c\/li\u003e\n\u003c\/ul\u003e","brand":"Oh My Ginger","offers":[{"title":"Default Title","offer_id":50115234267384,"sku":null,"price":16.5,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0501\/1357\/7128\/files\/37BA3EA3-0F07-4166-A0CC-6A597DA8D4E6.png?v=1785958610"},{"product_id":"warriors-against-ags-mug","title":"Warriors Against AGS Mug","description":"\u003cp\u003e\u003cspan\u003eSeptember is Leukodystrophy Awareness Month, and we are asking our community to help us turn awareness into action for someone incredibly special—our cousin, Abbie. \u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e Aicardi-Goutières syndrome, or AGS, is a rare inherited disease that affects the brain, immune system, and skin. Genetic changes cause the immune system to mistake the body’s own DNA or RNA for a virus, creating ongoing inflammation. This can damage the brain’s white matter and affect development, movement, communication, feeding, vision, and many other parts of daily life. AGS affects every person differently, but its challenges can be lifelong and devastating. Abbie was diagnosed with AGS in October 2021. Since that day, she has battled courageously to live the fullest and most normal life possible. She is so much more than her diagnosis—she is brave, deeply loved, and worth fighting for every single day. To honor Abbie and spread awareness this September, we have created special AGS shirts and drinkware. The most meaningful part of every design is that the letters “AGS” are written in Abbie’s own handwriting. When you wear one of these shirts or carry one of these cups, you are carrying a piece of Abbie’s story and helping introduce others to a disease that far too few people know about. Everyone knows what our family means to us; that we will go to boundless lengths to do whatever they need. Yesterday, on Ashley’s birthday, we had the honor of sharing these designs with her. Our family has always surrounded Abbie, Ashley, and their family with tremendous love, support, and prayer. Now, we would love to see our community stand beside them too. Buy a shirt. Carry a cup. Start a conversation. Say the name “Aicardi-Goutières syndrome.” Share Abbie’s story. Educate yourself. Most importantly, please pray for Abbie’s strength and comfort, for more good days, for wisdom for her doctors, and for research to bring better treatments to everyone living with AGS. If you are unable to purchase, sharing this post is completely free and incredibly powerful. Your share may reach someone learning about AGS for the first time, another family walking this road, or someone connected to research and advocacy. The more we talk about AGS, the more people will hear its name. Knowledge creates understanding, understanding creates advocacy, and advocacy creates hope. Abbie deserves a world that understands her disease and continues fighting for better treatments and a brighter future. Let’s show her that her community sees her, loves her, prays for her, and stands with her. Local pickup and shipping are available. Feel free to purchase a shirt or drinkware item, share Abbie’s story, and help us spread as much AGS awareness as possible this September. \u003cspan class=\"html-span xexx8yu xyri2b x18d9i69 x1c1uobl x1hl2dhg x16tdsg8 x1vvkbs x3nfvp2 x1j61x8r x1fcty0u xdj266r xat24cr xm2jcoa x1mpyi22 xxymvpz xlup9mm x1kky2od\"\u003e\u003cimg height=\"16\" width=\"16\" class=\"xz74otr x15mokao x1ga7v0g x16uus16 xbiv7yw\" alt=\"💙\" src=\"https:\/\/static.xx.fbcdn.net\/images\/emoji.php\/v9\/t6c\/1\/16\/1f499.png\"\u003e\u003c\/span\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eCeramic mug, 11oz\u003c\/span\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eMicrowave safe!\u003c\/li\u003e\n\u003cli\u003eDesign on both sides\u003c\/li\u003e\n\u003cli\u003eDishwasher safe\u003c\/li\u003e\n\u003cli\u003eShips in a plain white gift box\u003c\/li\u003e\n\u003c\/ul\u003e","brand":"Oh My Ginger","offers":[{"title":"Default Title","offer_id":50115255304440,"sku":null,"price":16.5,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0501\/1357\/7128\/files\/DA5F9CA1-1546-4A0C-A3A3-016C9087498E.png?v=1785958610"}],"url":"https:\/\/ohmygingertx.com\/collections\/ags-awareness.oembed","provider":"Oh My Ginger","version":"1.0","type":"link"}