Chris Anselmo, who has a rare form of muscular dystrophy, hopes to educate pharma on the patient journey and help new patients cope with a life-changing diagnosis. We spoke to him to find out more.
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E! News on MSNLeah Messer Gives Update on Daughter Ali's Muscular Dystrophy BattleMore than a decade after Leah Messer's daughter Ali was diagnosed with muscular dystrophy, she's thriving, the Teen Mom star ...
Johnny Quintana’s life changed at the age of 19 when he was diagnosed with a rare form of muscular dystrophy called Facioscapulohumeral muscular dystrophy (FSHD).
In a preview clip from the upcoming season (below), Leah and Ali -- who was diagnosed with a rare form of muscular dystrophy when she was only four years old -- get into an argument after the ...
He has been diagnosed with a rare form of muscular dystrophy and needs to use a mobility aid to get around. He woke up on Friday morning to discover that two of his scooters and his Can-Am bike ...
FSHD is the second most common form of muscular dystrophy after the Duchenne type, and affects around 1 million people worldwide, with no approved treatments. It tends to cause muscle wasting in ...
Scientists have discovered how to overcome the genetic defect that causes the most serious form of muscular dystrophy, it was revealed today. Although at an early stage, the research may lead to ...
Becker muscular dystrophy tends to appear later than the most common form of the disease, Duchenne MD (DMD). Symptoms may appear as late as age 25. Becker MD also progresses slower than DMD and is ...
LUBBOCK, Texas — Johnny Quintana’s life changed at the age of 19 when he was diagnosed with a rare form of muscular dystrophy called Facioscapulohumeral muscular dystrophy (FSHD). Now at 36 ...
For Julie Chaloupka, Katy’s Kloset was more than just a resource — it was a lifeline. Her daughter, Jennifer, had a form of muscular dystrophy, and the family often struggled to obtain the supplies ...
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