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This #EBAwarenessWeek, #INmuneBio honors those living with RDEB, a rare condition causing fragile skin and chronic wounds. We thank @debraOfAmerica & @EBResearch for their advocacy and support. Together, we’re advancing better treatments and brighter futures. #EBweek #WeFightEB
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We stand with the epidermolysis bullosa (EB) community in recognizing and raising awareness for #EBAwarenessWeek. Join us in supporting the cause and help us bring visibility to this rare and painful genetic disorder. #EBWeek #WeFightEB
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Throughout the year and especially during #EBAwarenessWeek, Krystal Biotech recognizes and supports all those impacted by #EB. #EBWeek #EpidermolysisBullosa
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Throughout the year and especially during #EBAwarenessWeek, #KrystalBio and our leadership team recognizes and supports all those impacted by #DEB. Read more about this #RareDisease: krys.bio/j3o #LivingWithDEB. #EBWeek #EBAwarenessWeek #DEB
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🅰️: At any age. EB can be diagnosed prenatally with genetic testing. Many infants are diagnosed shortly after birth & have been many who were diagnosed much later in life. This #EBweek, debra is tackling Google's TOP SEARCHED EB questions➡️ debra.pulse.ly/3l3wbh1jut
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"その先へ" 10月25日〜31日は国際的な #表皮水疱症 啓発週間です🦋 本日は啓発週間最終日です🦋 まだ道の途中。 model : @igumoc #EBAwarenessWeek #EBAwarenessDay #EBWeek #WeFightEB #EpidermolysisBullosa
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"36" 10月25日〜31日は国際的な #表皮水疱症 啓発週間です🦋 36は表皮水疱症の指定難病の番号。 難病とは、発病の原因が明確でないために治療方法が確立しておらず、長期の療養を必要とする疾患です。 model : @igumoc #EBAwarenessWeek #EBAwarenessDay #EBWeek #WeFightEB #EpidermolysisBullosa
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We're rounding out #EBAwarenessWeek with an Abeona Sponsored Webinar, Gene Therapy for Large Chronic Wounds in Recessive Dystrophic Epidermolysis Bullosa, presented by Jean Tang, MD, PhD. Listen now ➡️ player.captivate.fm/episode/… #PeDRA #pedraresearch #EBWeek #EpidermolysisBullosa
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"36" 10月25日〜31日は国際的な #表皮水疱症 啓発週間です🦋 36は表皮水疱症の指定難病の番号。 難病とは、発病の原因が明確でないために治療方法が確立しておらず、長期の療養を必要とする疾患です。 model : @igumoc #EBAwarenessWeek #EBAwarenessDay #EBWeek #WeFightEB #EpidermolysisBullosa
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@KrystalBiotech is honored to celebrate the strength and determination of the #DEB community during #EBAwarenessWeek. Learn more about #LivingWithDEB and the incredible patients and their families to whom we are dedicated: krys.bio/j3o. #LivingWithDEB #EBWeek
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"36" 10月25日〜31日は国際的な #表皮水疱症 啓発週間です🦋 36は表皮水疱症の指定難病の番号。 難病とは、発病の原因が明確でないために治療方法が確立しておらず、長期の療養を必要とする疾患です。 model : @igumoc #EBAwarenessWeek #EBAwarenessDay #EBWeek #WeFightEB #EpidermolysisBullosa
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"36" 10月25日〜31日は国際的な #表皮水疱症 啓発週間です🦋 36は表皮水疱症の指定難病の番号。 難病とは、発病の原因が明確でないために治療方法が確立しておらず、長期の療養を必要とする疾患です。 model : @igumoc #EBAwarenessWeek #EBAwarenessDay #EBWeek #WeFightEB #EpidermolysisBullosa
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"36" 10月25日〜31日の一週間は国際的な #表皮水疱症 啓発週間です🦋 拡散のご協力よろしくお願いします🦋 model : @igumoc #EBAwarenessWeek #EBAwarenessDay #EBWeek #WeFightEB #EpidermolysisBullosa
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Approximately 200 children are born with #EpidermolysisBullosa every year in the United States. Join me for #EBAwarenessWeek (Oct 25-31) as I spread awareness of this debilitating rare connective tissue disorder. Learn more and take action at debra.org/ebweek#EBweek

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10月25日〜31日の一週間は国際的な #表皮水疱症 啓発週間です🦋 今日からこむぎさんの写真を投稿していきます📸 表皮水疱症について広く知っていただきたいので、拡散のご協力よろしくお願いします🦋 #EBAwarenessWeek #EBAwarenessDay #EBWeek #WeFightEB #EpidermolysisBullosa
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It’s #EBAwarenessWeek! join me in spreading awareness of #EpidermolysisBullosa, a rare connective tissue disorder that causes extremely fragile skin that blisters and tears with any friction. Learn more about EB and take action at debra.org/ebweek #EBweek #WeFightEB

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#EpidermolysisBullosa Awareness Week is just around the corner on October 25-31! 🦋 #EBweek is a special time to raise public awareness, promote the need for a cure, and spur advocacy on behalf of the thousands living with EB. ➡️ Get involved at debra.pulse.ly/546737hs4l
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For #EBweek (10/25-31), students at Stemley Road Elementary School in AL learned all about #EpidermolysisBullosa, crafted colorful posters, and came together to walk in honor of their fellow student, Adriana, who lives with EB. We LOVE to see these amazing awareness efforts! 🦋✊
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While #EBAwarenessWeek may be over for 2022, each patient's story is a year-long journey. Learn more and see patient stories here: bit.ly/3svogO8. #DEB #raredisease #EBWeek
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EB is a painful, #rare condition that profoundly impacts patients, families, & caregivers. As #EBWeek ends, we’d like to express our support for all those living w/ #EB & stress the importance of raising awareness of this #raredisease. #LivingWithDEB #EBWeek #dystrophicEB
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