We are The Mast Cell Disease Society.Learn More
24th National Virtual ConferenceRegister Now!
for patients and caregivers. October 13-20, 2021
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COVID-19 Statementsfrom the The Mast Cell Disease Society, INC. (TMS) and Physicians from TMS Medical Advisory BoardLearn More
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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.
AnnouncementTMS has become aware that over the weekend, the FDA has quietly announced changes in how food labels are going to be listing ingredients. These changes will include LOOSENING guidelines on naming ingredients in a given food...
Food Label Policy Changes
InfographicsPrintable Infographics and brochures! Use these for handouts and display.
DonateTMS 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.
Emergency room guide
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…
Executive Director – Lauren Denton
It is with great excitement, that we announce the arrival of The Mast Cell Disease Society’s first-ever Executive Director –…
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.
Join us this October 13-20, 2021 for our 24th National Patient & Caregiver Conference!