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Tayma, 9, struggles with the most severe version of Epidermolysis Bullosa, a rare, agonizing disorder that causes skin to ...
How patients who are living with Epidermolysis Bullosa fight their daily pain and focus on empowerment across continents ...
Throughout, viewers also see EB patients receiving three promising new, FDA-approved medications for the first time and get a ...
Epidermolysis bullosa is a rare and severe skin disease where patients have fragile skin that blisters and tears. A Mt.
This month, the Holler family will be headed to the Tribeca Film Festival—which would normally be pretty heady stuff for a ...
Ashley Bergen says the healthcare system "helps in some ways" but there have been unexpected barriers to accessing care.
Dermaliq Therapeutics and global non-profit organisation DEBRA Research have entered into a partnership aimed at advancing ...
Eddie Vedder and wife Jill share why they’ve become so involved in awareness for a rare disease in an exclusive clip from new film 'Matter of Time' ...
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Dublin Live on MSNTalented Meath teen with rare skin condition designs unique bag to fundraise for charitySophia is raising money for a national charity that supports people living with an incurable genetic skin condition, often ...
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Independent.ie on MSNCork MACE Stores selling striking new bag devised by 14-year-old to support work of charity DebraMACE stores across Cork will play their part in a nationwide campaign to raise awareness of epidermolysis bullosa (EB).
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