I still think of Labor Day as the day to raise money for the Muscular Dystrophy Association. Since they no longer have a telethon and want to still donate to a very good charity, you can go to the MDA website to donate.

Muscular Dystrophy Association

www.mda.org

#MDAstrong

GAL GADOT⭐ signed Wonder Woman ❤️💫 toy received by little girl Carmela 💛w/ Muscular Dystrophy
1/9/21 *5th anniversary!

YouTube link🎥here👉> youtu.be/MdTUItR-Ghs

#Cure4Carmela #MDAstrong
#MuscularDystrophyAwarenessMonth
#DianaPrince #Themyscira

@mdukcharity.bsky.social
@lyndacarter.bsky.social

🔍 Have you explored our first Rare Advocacy Spotlight LinkedIn Newsletter with exclusive insights, updates, and stories highlighting @mda.org's incredible work?

Read exclusive insights & stories: https://bit.ly/4oCspuB

Don't forget to subscribe 📬

#RareDisease #MDAStrong #RareAdvocacySpotlight

🏕️ A Week That Changes Lives

Discover how the @mda.org’s summer camp empowers those with neuromuscular conditions and how you can get involved.

Learn more: https://bit.ly/47gnMR3

#RareAdvocacySpotlight #RareDisease #RareAdvocacy #MDAStrong #MuscularDystrophyAssociation #RareSky

🤝 Connection & Community

The @mda.org brings together the neuromuscular community—locally and virtually—to share support, resources, and hope.

Learn more: https://bit.ly/47gnMR3

#RareAdvocacySpotlight #RareDisease #RareAdvocacy #MDAStrong #MuscularDystrophyAssociation #RareSky

💙 What does it mean to be #MDAStrong?

Strength is resilience. Strength is progress. Strength is community.

Learn more about @MDA.org: https://bit.ly/47gnMR3

#RareAdvocacySpotlight #RareDisease #RareAdvocacy #MuscularDystrophyAssociation #RareSky

🔎 Explore @MDA.org Advocacy

From national policy to local community efforts, MDA is improving access to care and opening doors for involvement.

See how you can advocate: https://bit.ly/47gnMR3

#RareAdvocacySpotlight #MDAStrong #MuscularDystrophyAssociation #RareSky

🌟 The Gold Standard in Care 🌟

The @MDA.org is widely considered the benchmark for multidisciplinary care in neuromuscular conditions.

Discover how MDA continues to lead the way.

👉 Explore here: https://bit.ly/47gnMR3

#RareAdvocacySpotlight #MDAStrong #RareSky

💡The Muscular Dystrophy Association @mda.org advances research, care & advocacy for 300+ neuromuscular conditions. 💙

Learn more: https://bit.ly/47gnMR3

#RareAdvocacySpotlight #RareSky #MDAStrong #MuscularDystrophyAssociation

🌟 Introducing the Rare Advocacy Spotlight Hub!

Our inaugural feature highlights the @mda.org—75 yrs advancing care, research & support for 300+ neuromuscular conditions.

Read now: https://bit.ly/3KVUheF

#RareAdvocacySpotlight #MDAStrong #RareDisease #PatientAdvocacy

💪 “Being strong is showing up and giving my all—even when I face challenges.” – Brayden, MDA Ambassador

This Sept, discover what it means to be #MDAstrong.

Donate $35.75+ & get our 75th anniversary tee: www.mda.org/Strong
What makes you strong? mda.org/MDAstrong