Top Tweets for #FacesOfEB
"I hope that one day they find a cure for my baby’s condition and for all that have this painful disease."
Kit's mum tells us about finding out that Kit has Junctional Epidermolysis Bullosa when he was born: https://t.co/bgye5C9lgY
#CureEB #ResearchtheCure #EB #JEB #FacesofEB

Parents of children (up to 16) with EB, please consider this online survey. Study will develop a wellbeing toolkit for parents with EB @CharityDEBRA @EBResearch #CureEB #FacesofEB #EBStories #EpidermolysisBullosa
Survey: https://t.co/ah6XagFKwl
Info: https://t.co/vf9t49xaNI
Albi's mum & grandma tell us a bit about him💙🦋
To read more of his story, visit https://t.co/MBtMZX4V5G
#CureEB #ResearchtheCure #FacesofEB #EBStories #EBSmiles #EpidermolysisBullosa #EB #Research
Albi has recessive dystrophic epidermolysis bullosa. His mum, Erin, shares his story. https://t.co/MBtMZX4V5G 💙🦋
#CureEB #ResearchtheCure #FacesofEB #EBStories #EBSmiles #EpidermolysisBullosa #EB #Research

"I have not only survived to the age of 20, but grown into a person who gains confidence from what I endure... brushing the ash off my butterfly wings & continuing to live for as long as I can."
Read Sohana's story: https://t.co/6xKd3FHkzz
#CureEB #FacesofEB #MyEB #EBStories
"When I was born, not much about EB was known".
Thank you Jennifer for sharing your #myEB story. Visit https://t.co/qSSMCVmfEw to read more of her story or to share your own.
🦋🦋
#EBStories #FacesofEB #CureEB #ResearchtheCure #StopthePain #HealEB #FightEB #EBResearch #EBSimplex

"Living with EB has taught me how to be strong and tolerate severe pain... it will not stop me from chasing my dreams"
🦋💙 Ala'a shares her #EBStory with us: https://t.co/vAedvBnFX9
#myEB #EBStories #FacesofEB #CureEB #ResearchtheCure #StopthePain #HealEB #FightEB #EBResearch

Happy @rarediseaseday! #FacesOfEB #EBawareness
[photo credit: FACES OF EB © Ari Espay & https://t.co/ijaB0iQMXR]
![debraOfAmerica's tweet photo. Happy @rarediseaseday! #FacesOfEB #EBawareness
[photo credit: FACES OF EB © Ari Espay & https://t.co/ijaB0iQMXR] https://t.co/PgxWndhL1I](https://pbs.twimg.com/media/CcYx8GCXEAUNMwG.jpg)
Rafi has EB. Spread awareness for her on @rarediseaseday (2/29 - 3 days away!) photo credit: #FacesOfEB © #AriEspay

Ella has EB. Spread awareness for her on @rarediseaseday (2/29). [photo credit: #FacesOfEB © #AriEspay]
![debraOfAmerica's tweet photo. Ella has EB. Spread awareness for her on @rarediseaseday (2/29). [photo credit: #FacesOfEB © #AriEspay] https://t.co/J5xfZ9v8q4](https://pbs.twimg.com/media/Cb_rMWDUkAA4jaY.jpg)
Amelia has EB. Spread awareness for her on @rarediseaseday (2/29). [photo credit: #FacesOfEB © #AriEspay]
![debraOfAmerica's tweet photo. Amelia has EB. Spread awareness for her on @rarediseaseday (2/29). [photo credit: #FacesOfEB © #AriEspay] https://t.co/wBTsYez7fj](https://pbs.twimg.com/media/CbrGrj4UEAADCSS.jpg)
Gabrielle has EB. Spread awareness for her on @rarediseaseday (2/29). [photo credit: #FacesOfEB © #AriEspay]
![debraOfAmerica's tweet photo. Gabrielle has EB. Spread awareness for her on @rarediseaseday (2/29). [photo credit: #FacesOfEB © #AriEspay] https://t.co/yELvsdpITL](https://pbs.twimg.com/media/Cbgx45LW4AEGBhK.jpg)
Yann has EB. Spread awareness for him on @rarediseaseday (2/29). [photo credit: #FacesOfEB © #AriEspay]
![debraOfAmerica's tweet photo. Yann has EB. Spread awareness for him on @rarediseaseday (2/29). [photo credit: #FacesOfEB © #AriEspay] https://t.co/W7HzXNrAbF](https://pbs.twimg.com/media/CbWjKFeUMAAAEeM.jpg)
Kiba has EB. Spread awareness for him on @rarediseaseday (2/29). [photo credit: #FacesOfEB © #AriEspay]
![debraOfAmerica's tweet photo. Kiba has EB. Spread awareness for him on @rarediseaseday (2/29). [photo credit: #FacesOfEB © #AriEspay] https://t.co/Jx3nQ2rVFA](https://pbs.twimg.com/media/CbGfbRpUEAEEvhz.jpg)
Deja has EB. Spread awareness for her on @rarediseaseday (2/29). [photo credit: #FacesOfEB © #AriEspay]
![debraOfAmerica's tweet photo. Deja has EB. Spread awareness for her on @rarediseaseday (2/29). [photo credit: #FacesOfEB © #AriEspay] https://t.co/WstqSXzM1r](https://pbs.twimg.com/media/Ca8sqJ2WEAQ88jG.jpg)
Kayomurz has EB. Spread awareness for him on @rarediseaseday (2/29). [photo credit: #FacesOfEB © #AriEspay]
![debraOfAmerica's tweet photo. Kayomurz has EB. Spread awareness for him on @rarediseaseday (2/29). [photo credit: #FacesOfEB © #AriEspay] https://t.co/gMhRwK38wb](https://pbs.twimg.com/media/CayZlyhWIAA60o7.jpg)
Hayley has EB. Spread awareness for her on @rarediseaseday (2/29). [photo credit: #FacesOfEB © #AriEspay]
![debraOfAmerica's tweet photo. Hayley has EB. Spread awareness for her on @rarediseaseday (2/29). [photo credit: #FacesOfEB © #AriEspay] https://t.co/lHIhOYB5ZR](https://pbs.twimg.com/media/CaoAfTzWEAA7DcP.jpg)
Rafi (@Rafisrun) has EB. Spread awareness for her on @RareDiseaseDay (2/29). [photo credit: #FacesOfEB © #AriEspay]
![debraOfAmerica's tweet photo. Rafi (@Rafisrun) has EB. Spread awareness for her on @RareDiseaseDay (2/29). [photo credit: #FacesOfEB © #AriEspay] https://t.co/EKbwEZDikE](https://pbs.twimg.com/media/Cad7oRQXIAA_UQl.jpg)
Liam has EB. Spread awareness for him on Rare Disease Day (2/29). [photo credit: #FacesOfEB © Ari Espay]
![debraOfAmerica's tweet photo. Liam has EB. Spread awareness for him on Rare Disease Day (2/29). [photo credit: #FacesOfEB © Ari Espay] https://t.co/sPh4aWfofv](https://pbs.twimg.com/media/CaTfajdW0AAITBi.jpg)
Catt has EB. Spread awareness for her on Rare Disease Day (2/29). [photo credit: #FacesOfEB © Ari Espay]
![debraOfAmerica's tweet photo. Catt has EB. Spread awareness for her on Rare Disease Day (2/29). [photo credit: #FacesOfEB © Ari Espay] https://t.co/2tjAUwCVcf](https://pbs.twimg.com/media/CaJREZRWIAAjVgY.jpg)
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