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    COVID-19 Statements from the The Mast Cell Disease Society, INC. (TMS) and Physicians from TMS Medical Advisory Board.

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The Mast Cell Disease Society

is a non-profit organization 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.

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Announcement

Announcement

September 2021, TMS engaged the FDA to speak on the impact systemic mastocytosis and its variants has on the quality of life.

FDA Patient Listening Session

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Infographics

Infographics

Printable Infographics and brochures! Use these for handouts and display.

Printable Resources!

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Donate

Donate

TMS works tirelessly for those people affected by Mast Cell Disorders. Your support allows us to assist and support patients, fund research and raise awareness. Join us as we look for a cure and provide hope to so many.

Donate Now

Donate Now

Emergency room guide

This is a handy reference guide to provide everything you need for emergency room visits as a patient with a Mast Cell Disease. (INCLUDING EMERGENCY RESPONSE PLAN & PREMEDICATION FOR MAJOR & MINOR PROCEDURES)

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latest news

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FDA Patient Listening Session on Mastocytosis

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TMS 2020 Needs Assessment Survey

The Mast Cell Disease Society, Inc. 2020 Needs Assessment Survey This survey was conducted from August 2020 – February 2021, and…

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Get Support

Get Support

It takes a village. Join a support group in your area and get love and support from others who are dealing with mast cell diseases.

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Virtual Conference

Virtual Conference

Join us this October 13-20, 2021 for our 24th National Patient & Caregiver Conference!

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