The Mast Cell Disease Society, Inc.

11/27/2025

This Thanksgiving, our team at TMS wanted to share what makes this work so meaningful to us. Supporting our community and being part of your journey inspires everything we do. We’re so grateful for your trust, resilience, and dedication!

11/25/2025

Living with a mast cell disease can be overwhelming, but community can make a difference.

In partnership with Medicines, we’re hosting a Facebook Live panel discussion on December 10 at 3 PM ET, bringing together members of the community, including our very own Isabelle Charlot. You’ll hear more about building meaningful support systems with loved ones and care teams.

Find out more and RSVP here: https://buff.ly/yqiyHYR

11/24/2025

With Thanksgiving just a few days away, we know holiday gatherings can be tough for those managing mast cell disease or food sensitivities. Our Mast Cell Nutrition at the Holidays video with Bonnie Nasar shares helpful tips for navigating meals with confidence and care. Watch here: https://buff.ly/48NRV9C

11/22/2025

We’re so grateful to everyone who joined us for this year’s TMS Together Virtual Symposium. Just a reminder, everyone who registered has access to the Whova platform until January 30, 2026. After that date, session recordings will be available in the TMS Webinar Library on our website.

11/21/2025

Hello community! Thanksgiving is next week. What’s one tip for celebrating with mast cell disease? Share your thoughts below.

11/20/2025

Check out our Kids’ Corner at https://buff.ly/VpWT5RK a creative space for young artists in our mast cell disease community. Enjoy fun coloring pages like the Mighty MastCell Defenders and the new Awareness Ribbon Garden. We can’t wait to see your colorful creations

Kid’s Corner Welcome to the Kids’ Corner, a creative space for young artists in our […]

11/19/2025

Living with a mast cell disease can be overwhelming, but community can make a difference.

In partnership with Blueprint Medicines, we’re hosting a Facebook Live panel discussion on December 10 at 3 PM ET, bringing together members of the community, including our very own Isabelle Charlot. You’ll hear more about building meaningful support systems with loved ones and care teams.

Find out more and RSVP here: https://buff.ly/yqiyHYR

11/18/2025

Resource shoutout from us at TMS! The Ehlers Danlos Society offers helpful tools, education, and community connections for those living with EDS and related conditions including members of our mast cell community. Explore their resources here: https://buff.ly/9oic1xE

The Ehlers-Danlos syndromes (EDS) are a group of 13 heritable connective tissue disorders. The conditions are caused by genetic changes that affect connective tissue. Each type of EDS has its own set of features with distinct diagnostic criteria. Some features are seen across all types of EDS, inclu...

11/17/2025

You can explore past TMS webinars in our online library, featuring expert presentations on mast cell disease care, research, and patient experiences. Watch and learn at your own pace:

TMS Webinar & Event Library 2025 Webinars September 2025 July 2025 May 2025 2024 Webinars […]

11/16/2025

Weekly Upcoming Support Groups!

- 11/18, 4:00–5:00 PM ET – General Support Group with Calla
- 11/18, 6:30–7:30 PM ET – Undiagnosed Only Support Group
- 11/19, 8:00–9:00 PM ET – Positivity Support Group
- 11/19, 8:00–9:00 PM ET – Sexuality Support Group
- 11/20, 1:00–3:00 PM ET – Mastocytosis Support Group with Pam Hodge
- 11/21, 1:00–2:30 PM ET – MCAS Support Group (3rd Fridays)
- 11/23, 2:00–3:00 PM ET – Fiber Arts with the ED

Sign up to join: https://buff.ly/YXgViEw

11/15/2025

Shonna Snyder, Ph.D., represented The Mast Cell Disease Society at the 2025 ECNM Meeting in London, where experts from around the world gathered to share new insights and strengthen collaboration in mast cell disease research and care! Read her full reflection here:

TMS Attends the European Competence Network on Mastocytosis (ECNM) Meeting By Shonna Snyder, Ph.D. When […]

11/14/2025

Calling all Facebook connoisseurs! If you’re passionate about connection and making a difference, email Isabelle.Charlot@tmsforacure.org or Info@tmsforacure.org with the subject line “Facebook Moderator Interest.”