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Families of Spinal Muscular Atrophy (FSMA SMA) - National Headquarters
LIFETIME AMOUNT RAISED
About Families of Spinal Muscular Atrophy (FSMA SMA) - National Headquarters
At Cure SMA, everything from our financing needs to our normal choices are determined by our vision, mission and qualities. Cure SMA drives the route to a world without spinal bulky decay, the most obvious hereditary reason for death for newborn children. We subsidize and immediate complete research that drives leaps forward in treatment and consideration, and we give families the help they requirement throughout today. Our Values Development Our dedication to a treatment and cure is not pretty much looking for arrangements its additionally about making them. We're working with some of today's most keen personalities to propel a differing qualities of methodologies and champion the most guaranteeing revelations and strategies. Offset As perseveringly as we seek after a treatment and cure, we are likewise vital. We know the speediest route to a future without SMA is to take an extensive, fair-minded methodology to research and keep up a parity of idealism and authenticity. Cooperation Our group is everything to us. We would not have made it this far in our battle without the important commitments of our analysts, specialists, and families. Regard There is no "right route" to live with a sickness like spinal brawny decay. Each individual's experience is diverse, and its each family's entitlement to choose what SMA implies for them. Sympathy Because of the Cure SMA group, no individual is ever alone in confronting this ailment. We offer unequivocal backing to individuals influenced by SMA and impart straightforwardly and genuinely, providing for them clear and exact data. Determination Our work is not done until we have a treatment and cure, and we'll stay solid in our battle regardless of what difficulties come our direction.
925 Busse Road, Elk Grove Village, IL 60007
TOGETHER, WE'VE RAISED
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