EP4 – Lee Reavey, Co-Founder and CEO of the NCBRS Worldwide Foundation

Lee Reavey is the Co-Founder and CEO of the NCBRS Worldwide Foundation. He co-founded NCBRS Parent Support Group in May 2010. Lee’s son received a diagnosis Nicolaides-Baraitser Syndrome as only the seventh known case of NCBRS in the world. At that time, there was very little, if any, information available online. 

NCBRS is related to a gene variant of SMARCA2 but more research is needed. 

⬇️⬇️

NCBRS website – https://bit.ly/3S5S8uY 

NCBR patient registry – https://bit.ly/3D7FJ5g

Facebook – https://www.facebook.com/ncbrsworldwidefoundation

Twitter – https://twitter.com/ncbrsfoundation

Instagram – https://www.instagram.com/ncbrs/

Don’t miss an episode of Signalise! Be sure to ✔️FOLLOW or ✔️SUBSCRIBE via your podcast app of choice. You can also follow #Signalise news on @Dazzle4Rare on FacebookInstagramand Twitter. You can find host Kimberly on LinkedIn at @kattague.


Posted

in

by

Tags:

A white text-only logo for Dazzle4Rare which reads, "Dazzle4Rare. We are rare family. dazzle4rare.net"
Dazzle4Rare text-only logo on white background. It reads, "Dazzle4Rare We are Rare Family dazzle4rare.net"

site Search

Black text on white background. Signalise text-only logo reads, "Signalise a dazzle4rare podcast"