#Pyrographer With Usher Syndrome Wins National #RareArtist Award - Texas #pyrographer Krista Webb, living with #UsherSyndrome, named a national Rare Artist awardee by the #EveryLifeFoundation - www.disabled-world.com/communicatio...
Join us for Rare Disease Week on Capitol Hill, Feb 24–26, 2026! Educate Congress & apply for travel scholarships by Nov 8. Learn More: everylifefoundation.org/rare-advocates/rare-dise... #RareDiseaseWeek #LAMFoundation #EveryLifeFoundation #CapitolHill #RareDiseaseAdvocacy
Together we can Stronger.
#everylifefoundation
Let's comes to Join us on 30 September.
Together we are stronger...💪
#everylifefoundation
September is Muscular Dystrophy (MD) Awareness Month! 💚 Limb-Girdle Muscular Dystrophy (LGMD) is one form of muscular dystrophy.
Help raise awareness by sharing our posts! To learn more about LGMD.
#everylifefoundation
#LGMDawareness
#LgmdDay2025
#TogetherWeAreStronger
Let's count down 30 September and mark your calendar...
Join our hands to make event successful.
#musculardystrophypakistan #livingwithlgmd #LGMD2A #MuscularDystrophyAwareness #sarepta #everylifefoundation
Let's count down 30 September LGMD Awareness Day...
#everylifefoundation
Sending love to everyone living with a rare disease today. Sign this petition from the #EveryLifeFoundation to support funding for research for everyone impacted by a #RareDisease everylifefoundation.quorum.us/campaign/111...
#RareDiseaseDay #DisabilityAwareness #TakeAction