Our Mission is simple: To find a cure for ALL FOXG1 patients in the world (all ages, all mutations)

FOXG1 Research Foundation strategy is to:
- Understand the impact of FOXG1 dysfunction on brain development and function
- Identify candidate strategies for drug development
- Evaluate the efficacy of candidate therapies
- Invest in both patient-derived induced pluripotent stem cells (iPSC), FOXG1 syndrome mouse models, and other modalities recommended by our Scientific Advisory Board

Then, we will identify and vet therapeutic strategies. Our scientists will seek to understand:
- If restoration of healthy FOXG1 expression can alleviate symptoms of FOXG1 syndrome
- If downstream targets of FOXG1 are good candidates for drug development
- What time points are most effective to initiate treatment
- If a therapy would no longer be effective after a certain age
- If a candidate therapy can be delivered safely
- If a candidate therapy can be modified to treat other common neurologic disorders
- Key symptoms that contribute to quality of life.

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We will share our process and progress and results publicly through this Facebook page and on our website www.FOXG1Research.org

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Donations to the FOXG1 Research Foundation are 501(c)3 tax exempt.