Monica Weldon, Syngap 1

Monica Weldon, SYNGAP 1

EveryLife Foundation for Rare Diseases

Monica Weldon Discusses SYNGAP and the Role of Advocacy

Five Minutes with Monica Weldon - President and Founder of Bridge the Gap - SYNGAP

Genetic Epilepsy Team Australia

Monica Weldon on Why She Attends Rare Disease Day in Washington, DC

What Are SYNGAP Mutations?

Rare Disease Report

Monica Weldon: Personal Story from the New Era of Patient Advocacy

National Organization for Rare Disorders (NORD)

Overcoming SYNGAP1: A Family's Journey of Hope & Resilience

Hatching For Health

Monica Weldon | Rare Voices S1E6 Highlight 1

MEC Global Events | Monica Weldon | Bridge the Gap – SYNGAP Education and Research Foundation | USA

MEC GLOBAL EVENTS

What it’s like living with 1 working SYNGAP1 Gene!

SYNGAP1 Foundation

Monica Weldon | Rare Voices S1E6 Highlight 2

Syngap Awareness Video

Bridge the Gap SYNGAP ERF

From Nothing to Now

SYNGAP1 Foundation

My Boy Beckett@ 7 Months Old - He Has A Genetic Mutation Called SYNGAP1

What are SYNGAP Mutations?

Rare Disease Report

Part 1 Instagram Live with Living Well With Epilepsy

UK Syngap1 Family Meetup 2019

SYNGAP1 Foundation

SYNGAP1 Full Presentation

Simons Searchlight

"Innovative Patient Education and Support Options: From Diagnosis to Next Steps."

Monica Weldon at the N O R D Conference in Washington D C

Chip Baker-The Success Chronicles