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Please join us on Tuesday, 10 January 2023, to celebrate and congratulate Valerie Slee as she retires from her long tenure as the Chair of the TMS Board. The on-line Zoom event will be held from 6:30 - 8 pm EST, with a special presentation at 7:00 pm.
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2022 TMS Patient & Provider Symposium - Join us virtually October 15th as we come together to focus on addressing needs of our global community.
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Join a Network of 20,000+ - Stay up to date on education, resources and events with TMS Speaks Monthly eNewsletters
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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.
Announcement
Announcement
The Mechanisms Behind Hypermobile Ehlers-Danlos Syndrome, Mast Cell Activation Syndrome, and Dysautonomia.Joint Research Funding Announcement
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
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TMS Wants You… To Be Health Literate
TMS Wants You… To Be Health Literate In recognition of Health Literacy in October, TMS presents Health Literacy Series: Blog…
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!