PHOENIX (AZFamily) —As we head toward the new year, the medical advances just keep coming for the muscular dystrophy community. New treatments and therapies are being approved to help families ...
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AMISH KITCHEN: Daughter Verena discusses her disability
"Muscular dystrophy can take many things from me, but it will not take away my happiness, nor will it take away my faith." ...
Born with a rare form of muscular dystrophy, Peri Finkelstein has never let her disorder define her. Instead, the 24-year-old New Yorker has used her challenges as a springboard to make the world a ...
SEATTLE, Nov. 17, 2025 /PRNewswire/ -- Atossa Therapeutics, Inc. (Nasdaq: ATOS) ("Atossa" or the "Company"), a clinical-stage biopharmaceutical company developing innovative medicines in oncology, ...
Nila Morton was born with a rare form of muscular dystrophy called Ullrich, which requires her to rely on a wheelchair Nila Morton Nila Morton, a graduate student at Howard University, was excited to ...
New York, Jan. 26, 2026 (GLOBE NEWSWIRE) -- In recognition of Rare Disease Day on February 28, the Muscular Dystrophy Association (MDA) is sharing powerful community stories throughout the month that ...
"High clinical suspicion is important for this population of patients. Since muscular dystrophy is progressive in nature, monitoring disease progression in these patients is critical for timing ...
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Chilean woman with muscular dystrophy becomes face of euthanasia debate as bill stalls in Senate
SANTIAGO, Chile (AP) — As a child, Susana Moreira didn’t have the same energy as her siblings. Over time, her legs stopped walking and she lost the ability to bathe and take care of herself. Over the ...
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