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.

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

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

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
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)
latest news

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…
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.
Virtual Conference

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