WE ARE LIVE!!
Bridge the Gap –The Largest-Ever Study of SYNGAP1 (MRD5)
Beckett's Portrait representing SYNGAP1 in "Beyond the Diagnosis" Washington DC at the NIH. A Big Thank You to Patricia Weltin, artist Ian Mohon and Rare Disease United Foundation
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New Video Rare Disease Report
WHAT ARE SYNGAP MUTATIONS?
Interview with Monica Weldon, President
September 24, 2015
Scripps Florida Scientists Win $3.3 Million Grant to Accelerate Development of Treatments for Intellectual Disability, Autism, Epilepsy
CLICK HERE to Read the Article
Check out the New Brochure on Living with SYNGAP from
UNIQUE UK
Congratulations to Monica Weldon
and the Bridge the Gap Team
on the nomination for the
2015 & 2016 Champion Of Hope
RARE Champion in Advocacy Award
from Global Genes
Check out Noah Coughlan's Run AcrossAmerica for Rare Disease.
Thank You Noah!!
CLICK HERE TO READ HIS STORY
Day 119- So hot my phone malfunctions. Running for 7 year old Beckett from#Texas. For #SYNGAP @bsyngap@mlweldon5pic.twitter.com/9p2NvP04G6
Check out our research tab for more information on how to enroll in the new study on Rare Epilepsy Network.
Thank you to Dr. Jacques Michaud, Dr. Gavin Rumbaugh and Dr. Thomas Creson who combined efforts to write a summary helping define SYNGAP for Physicians to better help diagnose patients. Thank you to the National Organization of Rare Disease for publishing SYNGAP to their data base.
SYNGAP NORD PAPER IS LIVE!
To find out more on how to partcipate in the Chromosome 6 Research Study at The University of Groningen with Dr. Conny, To Enroll Follow the Link