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
Picture
If someone you know and love has ADNP Syndrome please help us spread awareness of our mission to find a cure!

Please print out the PDF below
Take a picture and post on social media with the hashtags seen on the sign and also hashtag where the picture is taken.

Example:
If you take a photo with the sign at Disneyworld you would hashtag:
#CureADNP #JourneyToCureADNP #Florida #Disneyworld

or take a photo and tag where you live
#CureADNP #JourneyToCureADNP #Switzerland

WE NEED AWARENESS
If you know a celebrity please have them post a photo holding our sign and ask them to post on their social media accounts. 

Click on the PDF below to open a PRINTABLE form.
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