Make a difference.

Help us to find treatments and a cure for patients with MEF2C mutations. Mutations on the MEF2C gene cause a severe form of autism with absence of speech or profound issues with communication, along with critical motor skill deficiencies. We are grateful for your assistance in helping our children obtain treatments to provide a better quality of life with the greatest degree of self sufficiency possible.

The US MEF2C Foundation is a registered 501(c)(3) non profit corporation, EIN # 93-2224419. Your donation is fully tax deductible.

Zelle is our preferred method to transfer funds because there are no fees incurred, and you may transfer funds directly from your bank using your bank’s Zelle platform. For Zelle transactions please use our email address —info@usmef2cfoundation.org —for a direct and free transfer to our nonprofit fund.

If you would like to make a donation on behalf of a patient, please email us with the contact information of the patient’s family so we can let them know of your gift.

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Cowan Team at MUSC - Gene Therapy

Cowan Team at MUSC - Gene Therapy

Gene therapy investigations for patients with MEF2C mutations.

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Boston Children's Hospital - Clinical Assessments and Clinical Trial Readiness

Getting to clinical trial with any drugs or treatments that are deemed effective will include clinical assessments of our patients and the creation of solid biolmarkers with which to measure the efficacy of drugs on our patients. This process involves the coupling of clinical assessments with solid research.

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Unravel Biosciences - Collection and research on RNAseq data for our patients

Unravel is generating an RNAseq database for neurodevelopmental disorders. Help fund the collection and research of RNAseq samples of our patients to uncover potential therapeutic mechanisms for MHS.