Cure FSHD For All

Imagine being told there’s a treatment that could change your life, only to be turned away because you don’t fit the criteria. Today, we’re launching the #CureFSHDForALL initiative, because every person living with FSHD deserves to have access to life-changing treatments.

This is what it’s like having #FSHD, according to a 12 year old.

Together, we can make sure no one is excluded from a future free of #FSHD. Sign the petition today: bit.ly/CureFSHDForAll

Imagine there is a treatment for your family member’s muscle wasting disease, but they can’t get access to it. Sign the petition demanding that every FSHD patient—regardless of age or mobility—has a fighting chance to access a cure: bit.ly/CureFSHDForAll

Time is muscle. We cannot afford to wait. Sign the petition now to demand a plan for access to therapies for ALL people with FSHD. Sign it here: bit.ly/CureFSHDForAll

We started #CureFSHDForALL, so that ALL people with FSHD, regardless of age or severity, have a fighting chance to access approved therapies. Learn who we are: curefshdforall.com/who-we-are

Sign the #CureFSHDForALL petition to help push the FDA and pharma companies to design trials that are inclusive for ALL people with FSHD. bit.ly/CureFSHDForAll

A cure for FSHD should be accessible to ALL. Join us in advocating for clinical trials that are inclusive and equitable for the entire FSHD community. Visit our website to learn more: curefshdforall.com

Sign this petition demanding that every FSHD patient—regardless of age or mobility—has a fighting chance to access a cure! change.org/p/access-to-th…

Imagine being told there’s a treatment that could change your life, only to be turned away because you don’t fit the criteria. Today, we’re launching the #CureFSHDForALL initiative, because every person living with FSHD deserves to have access to life-changing treatments.