Mike has a son with SynGAP and he wants to make sure we are doing everything we can to help. So he created SRF with his wife, Ashley.
Here is a longer bio as well as images for head shots.
Also see, Mike's Nomination to the Rare Champions of Hope.
Rare Parents Tackling Rare Diseases a profile of SRF and Ashley & Mike's work in IPM on December 23, 2022
August 31, 2021 - Building the Connections with the SYNGAP Research Fund
September 1, 2021 - Dawn Blessing & Mike Graglia on the Speed of Change
November 1, 2021 - Mike interviewed by Mathew Passy of Causepods about SYNGAP10.
May 3, 2022 - Onno & Lyndsey interview Mike in the Rarebase Remarks Podcast.
June 3, 2022 - David Hirsch, founder of SFN interviews Mike about fatherhood and SRF.
December 30, 2022 - Kira Dineen of DNA Today interviews Mike & Elli Brimble for a conversation about SYNGAP1-related non-syndromic intellectual disability.
Thank you to the Epilepsy Foundation of America for convening this exceptional panel of Men in the Rare Epilepsies.
Global Genes 2021 Panel: Developing a Dynamic Plan for Impactful Advocacy and Storytelling
Thank you Ira for featuring SRF on Progress, Potential, and Possibilities.
Thank you to Billy for this interview and 10% off link. Syngap.Fund/Billy.
July 2021 article in Americans for Safe Access Newsletter regarding CBD.
Lacking guidance from doctors, parents lead the charge in treating children with CBD by Isabella Jibilian, December 20, 2018