Spinal Muscular Atrophy Research Team
320284955
2009
LACKAWANNA, NY 14218
smarthope.com
smarthopedotcom
spinalmuscularatrophyresearchteam
Podobné organizace
Muscular Dystrophy Association |
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Spinal Muscular Atrophy Foundation |
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Joshua Joel Sma Life Foundation |
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Podobné organizace global
Spinal Muscular Atrophy UK |
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MULTIPLE SYSTEM ATROPHY TRUST |
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TREATSMA |
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CURE SMA CANADA SOCIETY |
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DEFEAT MULTIPLE SYSTEM ATROPHY AUSTRALIA LTD |
Podobně sociální sítě (1315)
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"Sdružení válečných veteránů ČR"1343 |
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Česká kardiologická společnost, z.s.1362 |
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Římskokatolická farnost Vrbno pod Pradědem1323 |
Novinky
RT @WNYTomPrince: Special Shout-out to @BishopTimonHigh @TimonAthletics Baseball Standout and D'Youville commit, Brendan Gossling. He has… (tw)
RT @sportsunionwny: Congrats goes out to Bishop Timon sophomore goaltender Cameron Chase on being named First Team All Fed. @BTSJHockey @… (tw)
Poslední komentáře
Absolutely inspired by the work you're doing! Every bit of support brings us one step closer to a cure for SMA. 💙 #SMARTSupportdetail |
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Sending love and strength to everyone affected by SMA! Together, we can make a difference and help create a brighter future. 🌟 #CureSMA #SMARTHopedetail |
Poslední diskuze
How can we better engage and educate communities about the importance of supporting research efforts for Spinal Muscular Atrophy and other neuromuscular diseases?Odpovědí: 3, Naposledy před 1 den detail |
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What innovative fundraising strategies have been successful in increasing awareness and financial support for organizations like the Spinal Muscular Atrophy Research Team (SMART)?Odpovědí: 3, Naposledy před 1 den detail |
V okolí
4.5
LACKAWANNA
O společnosti
- H125 -
Photos Home Dear Friends There are a great many worthwhile causes in need of your support and we at the Spinal Muscular Atrophy Research Team SMARTwould like to encourage you to become a SMART supporter consider it the SMART thing to do. What is Spinal Muscular Atrophy SMA. SMA is a genetic degenerative neuromuscular disease that debilitates muscle function. It is the 1 genetic cause of death in children less than 2 years old.