Recently, we announced that Dr. Lyndsay Murray at The University of Edinburgh will receive a a Cure SMA basic research grant of $80,000 over two years, to explore the reasons causing motor neuron cell death in SMA. Motor neurons are nerve cells in the brain stem and spinal cord that control muscle movement. We know […]
Cure SMA Announces Basic Research Funding for Dr. Lyndsay Murray Read More »
Cure SMA and Parent Project Muscular Dystrophy (PPMD) are conducting two different surveys about clinical trial participation. The goal is to find out more about how the neuromuscular community—individuals and families affected by conditions like spinal muscular atrophy or muscular dystrophy—thinks about potential therapeutics and clinical trials. All parents of children with SMA who live
At the end of last week, we announced the close of our for request for proposals (RFP) for clinical care research. A clinical care RFP is an invitation for scientists to submit their best ideas for projects that address the clinical, psychological or social aspects of SMA. They explain what they want to study, how
Funding Process Reaches Next Steps for Spinal Muscular Atrophy Clinical Care Research Read More »
Did you catch Cure SMA on Top Chef last week? Chef Takashi Yagihashi competed on behalf of Cure SMA for Bravo’s Top Chef Duels series. What a great opportunity to raise awareness of SMA, right on the heels of SMA Awareness Month! Chef Takashi and his family have been involved with Cure SMA for several
Chef Takashi Competes for Cure SMA Read More »
Cure SMA was featured in the July/August issue of Assay and Drug Development Technologies, a scientific journal that focuses on the development of new drugs. In honor of SMA Awareness Month, SMA was also featured on the front cover. Assay reaches scientists in 170 countries worldwide, making this a unique opportunity for us to influence
Cure SMA Featured in Assay and Drug Development Technologies Read More »
