The Mast Cell Disease Society, Inc.

The Mast Cell Disease Society, Inc. If you are having any medical emergency such as anaphylaxis, chest pain, difficulty breathing, severe abdominal pain, you must call 911.

We are dedicated to providing multi-faceted support to patients, families and medical professionals in our community and to leading the advancement of knowledge and research in mast cell diseases through education, advocacy and collaboration. The Mast Cell Disease Society, Inc (TMS) volunteers are not doctors and not on call 24/7. TMS is not liable for emergency posts on this FB page. The Mast Cell Disease Society, Inc. is a nonprofit organization dedicated to supporting patients affected by Mast Cell Disorders as well as their families, caregivers, and physicians through research, education, and advocacy. We are here on this forum to support you and give you a safe place to find information and communicate with others in similar situations. We are not liable for any posting from our membership. TMS does not accept responsibility for content of any external links posted on this FB page. We are unable to monitor the content of third-party websites.

03/16/2026

A look back at our ISM Patient and Family Seminar in Mountain View, CA. In partnership with Medscape Education and the American Initiative on Mast Cell Diseases, this event brought patients and families together for education and connection.

Watch the full recording in our webinar library at tmsforacure.org

The Mast Cell Disease Society is partnering with Project ECHO to support healthcare professionals through the Mast Cell ...
03/12/2026

The Mast Cell Disease Society is partnering with Project ECHO to support healthcare professionals through the Mast Cell Disease TeleECHO program. This series provides case based learning and expert guidance to strengthen the evaluation and treatment of mast cell diseases. Continuing education credit is available for physicians and other members of the healthcare team.

Learn more: https://buff.ly/bA9sSUN

Some webinars in our library are available for purchase and help support our work.Explore the library here: https://buff...
03/11/2026

Some webinars in our library are available for purchase and help support our work.

Explore the library here: https://buff.ly/UQ4Go42

Share in the comments what webinar topics you would like to see next!

03/10/2026

Growing our team helps us continue expanding patient education and community support. We’re grateful for the people who contribute their time and expertise to help strengthen the work of TMS.

Please join us in welcoming Robin in the comments.

Join Cogent Biosciences and TMS on March 18th at 6:30 PM EST for Finding Your Rhythm: Managing Life with Systemic Mastoc...
03/09/2026

Join Cogent Biosciences and TMS on March 18th at 6:30 PM EST for Finding Your Rhythm: Managing Life with Systemic Mastocytosis. A virtual webinar offering practical approaches to help with the day-to-day unpredictability of systemic mastocytosis and supporting daily life in ways that feel realistic and manageable. Register here: https://buff.ly/zD6MDEV

TMS support groups provide a welcoming space for patients and caregivers to connect and feel understood. View the full s...
03/08/2026

TMS support groups provide a welcoming space for patients and caregivers to connect and feel understood. View the full schedule and join a group here: https://buff.ly/iPS3BQo

03/05/2026

Thank you to everyone who participated in our February community poll. Your feedback helps guide the education, advocacy, and support we prioritize throughout the year. If you are not already receiving our newsletter and community updates, you can sign up here:
https://buff.ly/XdgtFtP

The Colors of SM program connects artists and individuals living with or caring for someone with systemic mastocytosis (...
03/04/2026

The Colors of SM program connects artists and individuals living with or caring for someone with systemic mastocytosis (SM) to bring their journey to life.

Together, the duo translates the experiences of living with SM into a beautiful and personal work of art.

Learn more about the program and apply to participate at www.ColorsofSM.com.

To be considered, you must be a U.S. resident aged 18 or older. There is no cost to participate.

by: The Colors of SM program connects artists and individuals living with or caring for someone with systemic mastocy...
02/26/2026

by:

The Colors of SM program connects artists and individuals living with or caring for someone with systemic mastocytosis (SM) to bring their journey to life.

Together, the duo translates the experiences of living with SM into a beautiful and personal work of art.

Learn more about the program and apply to participate at www.ColorsofSM.com.

To be considered, you must be a U.S. resident aged 18 or older. There is no cost to participate.

We asked members of our community how The Mast Cell Disease Society has impacted their healthcare journey. Their respons...
02/25/2026

We asked members of our community how The Mast Cell Disease Society has impacted their healthcare journey. Their responses reflect the importance of credible patient education and informed clinical conversations in shaping safer, more confident care experiences. Learn more at https://buff.ly/DMcEabi

Address

PO Box 416
Sterling, MA

Opening Hours

Monday 8am - 5am
Tuesday 8am - 5pm
Wednesday 8am - 5pm
Thursday 8am - 5pm
Friday 8am - 5pm

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