Our Story
The 16P Genetic Syndrome Foundation was founded by Dr. Nika Akid and her husband after their son was diagnosed with 16p11.2 deletion syndrome in 2014. This foundation is dedicated to providing support and promoting research for families navigating the challenges of this rare genetic condition.
Impact
By offering up-to-date information and guidance, the foundation helps children and individuals with 16p11.2 deletion syndrome reach their full potential while celebrating their unique variations.
Why Donate?
Your donations are vital in supporting the foundation's mission to provide essential resources and information for families affected by 16p11.2 deletion syndrome.
Make a Difference Today
Join the fight against 16p11.2 deletion syndrome by donating cryptocurrency or cash. Your contribution will empower families and advance research, ensuring a brighter future for those affected.
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