Carrino Foundation (@carrinofshd) 's Twitter Profile
Carrino Foundation

@carrinofshd

The Chris Carrino Foundation for FSHD, a 501(c)(3) dedicated to curing #FSHD and inspiring others thru @ChrisCarrino.

ID: 321567495

linkhttps://linktr.ee/CarrinoFoundation calendar_today21-06-2011 19:43:45

429 Tweet

603 Followers

172 Following

Carrino Foundation (@carrinofshd) 's Twitter Profile Photo

It’s World FSHD Day! #FSHD is the most prevalent form of Muscular Dystrophy. Approximately 1 million people worldwide have FSHD It’s a progressive disease with no treatment and no cure. But we’re getting close…. Please donate with the link in our bio

It’s World FSHD Day!

#FSHD is the most prevalent form of Muscular Dystrophy.  

Approximately 1 million people worldwide have FSHD

It’s a progressive disease with no treatment and no cure. 

But we’re getting close….

Please donate with the link in our bio
FSHD Society (@fshdsociety) 's Twitter Profile Photo

Don’t miss the newest episode of FSHD Straight Talk! Tim interviews Chris Carrino, voice of the Brooklyn Nets and founder of the Chris Carrino Foundation for FSHD Carrino Foundation! youtu.be/BRW-YuBnuu8

Carrino Foundation (@carrinofshd) 's Twitter Profile Photo

An open-label pilot study of losmapimod to evaluate the safety, tolerability, and changes in biomarker and clinical outcome assessments in participants with facioscapulohumeral muscular dystrophy type 1 - ScienceDirect #FSHD sciencedirect.com/science/articl…

Carrino Foundation (@carrinofshd) 's Twitter Profile Photo

🎬 Check out “Good Bad Things: Worldwide Virtual Premiere” on VEEPS This weekend only. FSHD portrayed on screen like never before by Danny Kurtzman in a poignant performance. 25% of the purchase thru this link will go to the foundation. veeps.com/goodbadthings/…

Carrino Foundation (@carrinofshd) 's Twitter Profile Photo

Today on #RareDiseaseDay, we stand with the 870,000 people living with FSHD. 💜 Awareness fuels research, and research leads to a cure. Share and support! 💪 #CureFSHD #FSHDawareness

Today on #RareDiseaseDay, we stand with the 870,000 people living with FSHD. 💜 Awareness fuels research, and research leads to a cure. Share and support! 💪 #CureFSHD #FSHDawareness
Carrino Foundation (@carrinofshd) 's Twitter Profile Photo

Epicrispr Biotechnologies Announces FDA Clearance of IND Application for EPI-321, A First-in-Class Epigenetic Therapy for FSHD businesswire.com/news/home/2025…

Carrino Foundation (@carrinofshd) 's Twitter Profile Photo

Avidity Biosciences Announces the Accelerated Approval Regulatory Pathway in the U.S. is Open for Del-Brax and Initiates the Global, Confirmatory Phase 3 FORWARD™ Study in FSHD aviditybiosciences.investorroom.com/2025-06-09-Avi…

Carrino Foundation (@carrinofshd) 's Twitter Profile Photo

On #WorldFSHDDay please lend your voice with a donation and help us continue the work of finding a treatment for #FSHD. app.donorview.com/Donation/Donat…

Lisa Marie Falbo (@lisamariefalbo) 's Twitter Profile Photo

📺 Watch “Your New Jersey” Saturdays at 6 AM and Sundays at 8 AM on MeTV WJLP New Jersey/New York! My guests this weekend are: 1️⃣: 🏀 Chris Carrino, longtime radio voice of the Brooklyn Nets and founder of Carrino Foundation 2️⃣: Highlights from Fanatics Fest with Make-A-Wish New Jersey 🌟 3️⃣: 🏟️

📺 Watch “Your New Jersey” Saturdays at 6 AM and Sundays at 8 AM on MeTV WJLP New Jersey/New York!

My guests this weekend are:
1️⃣: 🏀 <a href="/ChrisCarrino/">Chris Carrino</a>, longtime radio voice of the Brooklyn Nets and founder of <a href="/CarrinoFSHD/">Carrino Foundation</a> 
2️⃣: Highlights from Fanatics Fest with <a href="/wishnj/">Make-A-Wish New Jersey</a> 🌟
3️⃣: 🏟️