Spinal Muscular Atrophy Foundation
At a glance
Key takeaways
- The foundation exists to accelerate treatments for spinal muscular atrophy and funds only work with an immediate impact on late translational research or clinical trials, so a small charity should apply only if its work sits in that area.
- Only principal investigators can apply, so an organisation without a principal investigator leading the request should not apply in its own name.
- Researchers send a letter of intent to info@smafoundation.org, and the filing gives its application method as rolling, although grant applications are accepted only by invitation.
- Its geographic focus is given as worldwide, and about 8 in 10 of its grants to organisations fall between $69,000 and $220,000, with a median of about $140,000, so a request in that region is realistic, though the largest grant was about $655,000 and that band is not a ceiling.
- In its latest filing, 53% of grant dollars to organisations went to organisations it had funded in earlier filings, so existing relationships with the foundation are likely to matter.
Overview
Spinal Muscular Atrophy Foundation is a US private foundation based in Jackson, WY.
What they fund
Profile derived from the foundation's IRS Form 990-PF filings (TY2024, TY2023, TY2022) and its website, with every statement checked against those sources. Sources read on 7 October 2026.
Priority Areas
The Spinal Muscular Atrophy Foundation’s mission is to accelerate the development of treatments for spinal muscular atrophy. Its strategies include funding novel preclinical and clinical research in the SMA field, building alliances with academic and industry collaborators, and developing research tools for researchers and industry collaborators. Its external funding is limited to work with an immediate impact on late translational research or clinical trials. Its research aims to expand basic knowledge of the disease and translate findings into therapeutic applications in the clinic; it also makes research tools and data available to the biomedical research community at minimal or no cost. Principal investigators submit a letter of intent, and full grant applications are by invitation.
Themes
- Treatments for SMA
- Late translational research
- Clinical trials
Geographic Focus
Priority: Worldwide.
How to apply
Researchers submit a letter of intent and direct it, along with inquiries, to info@smafoundation.org. Grant applications are accepted only by invitation.
Application success factors
- Repeat giving: In its TY2024 filing, 53% of its grant dollars to organisations went to organisations it had also funded in its TY2022 or TY2023 filing.
- Grant size: Across its TY2022, TY2023 and TY2024 filings, half of its 21 grants to organisations were about $140,000 or less.
What the foundation says:
- External funding is limited to work that will have an immediate impact on late translational research or clinical trials.
- Only principal investigators can apply for funding.
Where grants go
From grants to organisations in the foundation’s filings for tax years 2022–2024.
Grant dollars by state
Outside the US or with no state on the filing: 11%
- The largest single recipient received 70% of grant dollars to organisations.
- In tax year 2024, 53% of grant dollars went to organisations Spinal Muscular Atrophy Foundation had funded in earlier filings.
- 11% of grant dollars went directly to organisations outside the US (Switzerland, United Kingdom).
Grants
How much do they typically give?
Share of 11 grants in tax year 2024 by size
Median $141k (tax year 2024)
The largest grants to organisations in the foundation’s latest filing:
- Johns Hopkins University · Characterization of gene expression in motor neurons in sma$238,8142024 tax year
- Swiss Federal Institute of Technology Lausanne · Testing of mitochondrial modulators in sma models$218,0062024 tax year
- Stanford University · Generation of spinal cord motor neurons from pluripotent cells$207,0002024 tax year
- University of Florida · Characterization of muscle environment in sma$197,9072024 tax year
- Stanford University · Oversight on the stanford-sma foundation regenerative medicine program projects$167,8252024 tax year
- University of Edinburgh · Characterization of neuromuscular junctions in sma$141,2122024 tax year
- Stanford University · Characterization of neuron-glial-immune cell interactions in sma$117,4942024 tax year
- Boston Children's Hospital · Testing therapeutics that promote neuron growth in sma models$98,5712024 tax year
Grants to organisations listed in the foundation’s Form 990-PF filings. Grants to individuals are not shown.
Officers and directors
- Juli Oh Esq — Treasurer
- Loren Eng — President
- Story Landis — Director
- Simon Prisk Esq — Director
- Stephen Mikita Esq — Director
- Helen Meates — Director
- Jonathan Leff — Director
- Andrew Knight — Director
- Gerald Fischbach MD — Director
- Douglas Cole MD — Director
- Dinakar Singh — Board Chairman
From the latest Form 990-PF filing
3 years of tax filings
| Year | Total expenses | Grants paid | Assets | Filing document |
|---|---|---|---|---|
| 2022 tax year | $4,039,863 | $653,689 | $24,079,888 | Filing for 2022 tax year |
| 2023 tax year | $3,641,528 | $1,155,632 | $33,691,989 | Filing for 2023 tax year |
| 2024 tax year | $4,733,792 | $1,491,789 | $50,173,258 | Filing for 2024 tax year |
Figures from the foundation’s IRS Form 990-PF filings. Assets are at fair market value at year end. The document icon links to each year’s filing on ProPublica Nonprofit Explorer.
Sources
Registers and filings
Other sources
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At a glance

Applying to Spinal Muscular Atrophy Foundation?
Hinchilla drafts your answers around this funder's priorities, using your organisation's own documents.
No credit card required
Contact
- info@smafoundation.org
- Jackson, WY
- smafoundation.org

Applying to Spinal Muscular Atrophy Foundation?
Hinchilla drafts your answers around this funder's priorities, using your organisation's own documents.
No credit card required
Contact
- info@smafoundation.org
- Jackson, WY
- smafoundation.org