It's World FSHD Day and FSHD Society has launched Project Mercury. This initiative is aimed at speeding the development of therapies to those affected by FSHD globally. Thanks for inviting our founder, Chip Wilson to share his #FSHD story.

Tomorrow is World FSHD Day! Chip Wilson, founder of lululemon athletica & SOLVE FSHD, talks about the significance of the Orange Slice Selfie campaign. Learn more about #WorldFSHDDay and how different countries around the globe are celebrating tomorrow: bit.ly/3JnoHTI

Chip Wilson, the creator of Lululemon and SOLVE FSHD, stands as a business innovator, philanthropist, and a person affected by rare disease. His passion for fitness led him to build a successful career in designing athletic wear, but a diagnosis FSHD altered his active lifestyle.

Have you listened to this month’s Community Profiles episode of #FSHD Radio? Chip Wilson, entrepreneur and philanthropist, discussed living with FSHD and shared the story behind SOLVE FSHD. Watch the interview here: bit.ly/3Mp7P1h or listen on your favorite podcast app!

(1/2) People around the world are living longer, but spend a longer period of life in poorer health. #XPRIZEHealthspan is here to change that. We’re grateful to Chip Wilson and his foundation SOLVE FSHD for bringing this prize to life as a co-title and bonus prize sponsor.

Today we announced our latest investment in Epic Bio. Epic's unique approach to correct the molecular pathology implicated in FSHD should lead to an effective treatment that prevents further muscle degeneration and thereby slows disease progression. solvefshd.com/news-updates/p…

It is always sweet to hear these words, but let us continue until we are healed.
FSHD Society FulcrumTx SOLVE FSHD LivingwithFSHD

On March 2 at 3pm PT, Amy Halseth, Executive Director Clinical Development, will take part in a group presentation titled ''Ongoing clinical trials in NMD' for our Phase 1/2 #FSHD program, FORTITUDE™, at the 2nd Annual #SolveFSHD Conference. Visit: solvefshd.com

Robert Grange, HNFE professor, was funded by SOLVE FSHD to work on a research project to assess skeletal muscle torque as a functional outcome measure in the TIC-DUX4 mouse model of Facioscapulohumeral Muscular Dystrophy (FSHD). 🧑‍🔬

Read more here ⤵️
tinyurl.com/4t7rxcaf

Important information for people with #FSHD . #Canadian FSHers register with cndr.org

#solvefshd #curefshd

Great news for people with #RareDiseases in #canada
canada.ca/en/health-cana…

#fshd #solvefshd #curefshd #musculardystrophy

medicalxpress.com/news/2023-09-c…

#fshd #curefshd #solvefshd #nmd #raredisease #musculardystrophy #muscle #hope

neurologylive.com/view/us-nation…

#fshd #solvefshd #nmd #RareDiseases #muscle

XPRIZE Healthspan is a global competition to restore function

Jamie Justice | Nature Aging

XPRIZE Hevolution Foundation SOLVE FSHD

rdcu.be/dwFz7

finance.yahoo.com/news/apples-pe…

#fshd #curefshd #solvefshd #technology #Disability #nmd #TechForGood

FSHD News FSHD Society neurologyindia.com/article.asp?is…
FSHDUK NEUROLOGY INDIA Neeraj Singh BJP Neta Raebareli SOLVE FSHD
#FSHD1 #FSHD2

#FSHD affects men, women & children & leads to progressive muscle wasting & weakness.

With support from @SolveFSHD, Vita is working hard to develop cell therapies for neuromuscular diseases like FSHD. #investor #RareDiseaseMonth

fredhutch.org/en/news/spotli…

Fred Hutchinson Cancer Center continues to unravel the mysterious and complex #DUX4

#fshd #solvefshd #curefshd #musculardystrophy #nmd

Jamie Justice XPRIZE ICFSRcongress Hevolution Foundation SOLVE FSHD Bummed I won’t be able to be there… :(