Smashsmard, Inc.
SMARD1 is an inherited condition that causes muscle weakness and respiratory failure typically beginning in infancy. We are on a mission for a CURE! smashSMARD was started to bring a permanent end to SMARD, CMT2S and IGHMBP2-related disorders. 100% of every donation is being used to develop a life-saving gene therapy for those affected. smashSMARD is a non-profit 501(c)3 organization which mission is to increase awareness of SMARD1 and the IGHMBP2 gene mutation in order to fund research that will lead to treatments and cures.
Founded
2018
3065
X (Twitter)
134
Address
Lincolnshire
smashSMARD | SMARD1 Let39s Make a Change Let39s Make a Change Home About About SMARD Research Blog More. smashSMARD Outside of Facebook Donate on Facebook no fees Exciting Announcement. smahSMARD is proud to make the most exciting announcement yet that the first ever therapy for IGHMBP2related disorders has been granted approval for a clinical trial to begin. In 2018 smashSMARD and smashSMARD.
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smashSMARD was started to bring a permanent end to SMARD, CMT2S and IGHMBP2-related disorders.
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Lincolnshire
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