ADNP Kids Research Foundation
  • About Us
    • What is ADNP
    • Our Story
    • Our Mission
    • Our Team >
      • Families >
        • Newly Diagnosed
        • ADNP Patient Registry
        • Contact Registry
        • Worldwide Parent Ambassadors
        • contact us
        • ADNP Family Conference >
          • HIGHLIGHTS- ADNP Syndrome Family Conference
          • TSA Travel Help
          • #CureADNP
    • Medical and Scientific Advisory Board
    • Inclusivity Statement
  • RESEARCH
    • Research Projects
    • Research Strategy
    • Ketamine Trial
    • Ketamine Trial Publication
    • Ketamine Update
    • Path to a cure
    • publications
  • NEWS
    • NET Collaboration Study
    • 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
    • Boston Marathon
    • Third Party Fundraising
  • Warrior Fun Run 2022
    • Past Fun Run Pictures
    • Sponsorship Opportunity
  • Link Page
  • New Page

INCLUSIVITY STATEMENT

The ADNP Kids Research Board of Directors condemns racism and the impact it has on the communities we serve. We would not stand for discrimination on the basis of disability, nor will we stand for discrimination on the basis of race.

Furthermore, we recognize that words without action are empty. Our mission is to promote research, find curative treatments, and improve the lives of all individuals living with ADNP syndrome. As we work to fulfill that mission, we commit to take inventory of our current policies, ensure that we hear diverse voices, address unconscious bias, and provide an inclusive culture. 
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 >
      • Families >
        • Newly Diagnosed
        • ADNP Patient Registry
        • Contact Registry
        • Worldwide Parent Ambassadors
        • contact us
        • ADNP Family Conference >
          • HIGHLIGHTS- ADNP Syndrome Family Conference
          • TSA Travel Help
          • #CureADNP
    • Medical and Scientific Advisory Board
    • Inclusivity Statement
  • RESEARCH
    • Research Projects
    • Research Strategy
    • Ketamine Trial
    • Ketamine Trial Publication
    • Ketamine Update
    • Path to a cure
    • publications
  • NEWS
    • NET Collaboration Study
    • 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
    • Boston Marathon
    • Third Party Fundraising
  • Warrior Fun Run 2022
    • Past Fun Run Pictures
    • Sponsorship Opportunity
  • Link Page
  • New Page