ADNP Kids Research Foundation
  • About Us
    • What is ADNP
    • Our Story
    • Our Mission
    • Our Team
    • Medical and Scientific Advisory Board
    • Inclusivity Statement
  • RESEARCH
    • Research Strategy
    • Research Projects
    • Ketamine Update
    • Path to a cure
    • publications
  • Connect
    • Newly Diagnosed
    • Contact Registry
    • Worldwide Parent Ambassadors
    • contact us
    • ADNP Family Conference >
      • HIGHLIGHTS- ADNP Syndrome Family Conference
      • TSA Travel Help
      • #CureADNP
  • NEWS
    • Ketamine Trial Phase 2 Announcement
    • Mount Sinai Launches First Drug Trial for ADNP Syndrome
    • Seaver Midtown Partnership
    • Biomarker Discovered
    • NEWS - p.Tyr719* Case Study
    • NEWS HIGHLIGHTS- ADNP Syndrome Family Conference
  • ADNP STORE
  • DONATE/SUPPORT
    • WARRIOR FUN RUN >
      • WARRIOR FUN RUN PHOTO RELEASE
    • Boston Marathon
    • Third Party Fundraising

Because we don't know what's possible unless we try.

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ADNP Kids Research Foundation is an IRS accredited 501(c)(3) non-profit charitable organization.
Tax ID (EIN) 30-0964243 - Public Charity 
DONATE!
RESEARCH IS AT THE HEART OF OUR MISSION:
It is our goal to advance the scientific understanding of ADNP syndrome, so that effective treatments can be developed to improve the lives of individuals with ADNP syndrome.   High-quality research can lead to more effective treatments, greater understanding of the disease, and an eventual CURE for this disorder. 

Your tax-deductible donation funds life-changing research and provides for education, advocacy and support for ADNP Syndrome.  Please donate today!

DONATE VIA PAYPAL HERE
​WITHPAYPAL ACCOUNT or WITH CREDIT CARD AS GUEST
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QR CODE OPTION TO DONATE
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Alternative to credit card payment
DONATE by CHECK
MAIL TO:
ADNP Kids Research Foundation
24500 NE 132nd Circle
Brush Prairie, WA 98606
 ADDITIONAL INFORMATION:
If you have any questions or concerns, please contact our foundation 
​by emailing admin@adnpfoundation.org ​or by calling (360) 831-3069.
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Privacy Policy  |  Terms of Services  |  Other Policies  
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.
  • About Us
    • What is ADNP
    • Our Story
    • Our Mission
    • Our Team
    • Medical and Scientific Advisory Board
    • Inclusivity Statement
  • RESEARCH
    • Research Strategy
    • Research Projects
    • Ketamine Update
    • Path to a cure
    • publications
  • Connect
    • Newly Diagnosed
    • Contact Registry
    • Worldwide Parent Ambassadors
    • contact us
    • ADNP Family Conference >
      • HIGHLIGHTS- ADNP Syndrome Family Conference
      • TSA Travel Help
      • #CureADNP
  • NEWS
    • Ketamine Trial Phase 2 Announcement
    • Mount Sinai Launches First Drug Trial for ADNP Syndrome
    • Seaver Midtown Partnership
    • Biomarker Discovered
    • NEWS - p.Tyr719* Case Study
    • NEWS HIGHLIGHTS- ADNP Syndrome Family Conference
  • ADNP STORE
  • DONATE/SUPPORT
    • WARRIOR FUN RUN >
      • WARRIOR FUN RUN PHOTO RELEASE
    • Boston Marathon
    • Third Party Fundraising