Enroll now... Join the Global Moyamoya Patient Registry Today

MoyaMoya Foundation
  • Home
  • Inspiration
  • Resources
  • Donate
  • Impact
  • Registry
  • Board of Directors
  • Medical Advisory Board
  • Privacy Policy
  • Financial Disclosure
  • Contact Us
  • Shop
  • More
    • Home
    • Inspiration
    • Resources
    • Donate
    • Impact
    • Registry
    • Board of Directors
    • Medical Advisory Board
    • Privacy Policy
    • Financial Disclosure
    • Contact Us
    • Shop
  • Sign In
  • My Account

  • Signed in as:

  • filler@godaddy.com

  • My Account

  • Sign out

MoyaMoya Foundation

Signed in as:

filler@godaddy.com

  • Home
  • Inspiration
  • Resources
  • Donate
  • Impact
  • Registry
  • Board of Directors
  • Medical Advisory Board
  • Privacy Policy
  • Financial Disclosure
  • Contact Us
  • Shop

Account

  • My Account

  • Sign out

  • Sign In
  • My Account

SEMINAR ON MOYAMOYA DISEASE FOR PATIENTS AND PROVIDERS

May 6, 2021 - Hybrid Event Live Streamed - Boston MA


Medical information, patient stories, support and networking event moderated by Dr. David M. Greer, MD from Boston Medical Center featuring Dr. Christopher S. Ogilvy, MD from Beth Israel Deaconess Medical Center, Dr. Edward R. Smith, MD from Boston Children's Hospital, Boston Medical Center and patients Corey Repucci, Samantha Houle and Lisa Bayha Deck.


YouTube Video Link:

 https://www.youtube.com/watch?v=KWnwYAej_jc&t=9s

The World of Rare Disease: Moyamoya Disease

The World of Rare Disease - March 1, 2021


In this episode host, Lisa Deck, interviews two patients with Moyamoya disease: Sam Houle and Catherine Stratton. They are also joined by Sam's father, Dean Houle, to discuss Moyamoya disease and the patient experience.


The World of Rare Disease - Moyamoya Foundation Co Facebook Live full interview

Zoom Webinar Video

Lenox Hill Hospital Neurosurgeons Coronavirus And The Brain Webinar

[Click the LINK above to view] On May 6th World Moyamoya Day,  honored patients affected by this rare neurovascular disease with Board President of Moyamoya Foundation  Dean Houle.

Making a difference

State of CT Officially Recognizes Moyamoya Awareness!

[Click Image Above] to view Senate Bill No. 1091

It's official in Connecticut as of July 1, 2019. Moyamoya Awareness Day Is on May 6th of each year, to align with World Moyamoya Day!

Moyamoya Foundation Co is a qualified 501(c)(3) charitable non-profit foundation.

  

Disclaimer: "We are not medical professionals, and this website is not intended to provide medical advice. Its content is for informational purposes only. Always consult with your physician or other qualified healthcare professional regarding any medical concerns or conditions, and refrain from making medical decisions solely based on information obtained from this website.". 


Copyright © 2026 MoyaMoya Foundation Co. - All Rights Reserved.

  • Home
  • Contact Us
  • Members Only Access
  • Terms and Conditions

Powered by

This website uses cookies.

We use cookies to analyze website traffic and optimize your website experience. By accepting our use of cookies, your data will be aggregated with all other user data.

DeclineAccept