Your contribution directly funds medical research and clinical trials targeting ASAH1 mutations that cause SMA-PME and Farber disease—ultra-rare genetic neurodegenerative conditions. We are a 501(c)(3) public charity, incorporated June 11, 2021, and approved as such on February 2, 2022.
For greatest convenience and optional fee (enter 0 at fee prompt), please consider a one-time or monthly recurring donation. Click the link to use any major credit card or transfer directly from your bank account.
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Thank you for your generosity. Donors receive special appreciation items based on contribution level.
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SMA-PME Research seeks corporations that are interested in matching funds from their employees. Many corporate employers offer giving programs that can double your impact.