THANK YOU FOR YOUR DONATION

The ADNP Kids Research Foundation is a recognized 501(c)3 non-profit organization; Federal ID number (EIN) 30-0964243

Thank you for your generous donation to the ADNP Kids Research Foundation.  Your support is helping our mission of Awareness, Research, Support and Hope for those affected with ADNP Syndrome.

Your support is helping with important projects such as the largest study of ADNP Syndrome and the first ever drug trial for ADNP Syndrome.  We could not do the work that we do without support from donors like you.

Our organization is 100% volunteer ran grassroots organization.  If you have any questions about your donation or what we are working on, please feel free to contact us anytime at admin@adnpfoundation.org.

Thank you for your support,
Sandra Sermone
Founder/President
ADNP Kids Research Foundation
sandra@adnpfoundation.org
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All rights reserved. No portion of the content of this website may be reproduced in any manner without the written permission of the author/creator.   Any information used from this website must also have credit noted to ADNP Kids Research Foundation / www.adnpfoundation.org. The information on this website is not substitute for personal diagnosis or medical care advise. Families and patients should consult a medically qualified clinician in all matters relating to genetic diagnosis, management and health. Information on ADNP changes is a very fast-moving field and while the information in this guide is believed to be the best available at the time of publication, some facts may later be updated or change. Please see additional disclosures on our PRIVACY POLICY page.