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The Mastocytosis Society
is a non-profit organization dedicated to supporting patients affected by Mastocytosis and Mast Cell Activation Disorders as well as their families, caregivers and physicians through research, education and advocacy.
Our CommunityA mother discovers her own difficult journey has been one of preparation for comforting her daughter who was also diagnosed with a mast cell disease. A story of love and commitment for all of us.
Princess Among Soldiers
TMS CaregiversFamily members often serve as the first line of medical support for individuals living with Mast Cell Disorders. It's a love and dedication that often can be a lifesaver.
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
The Mastocytosis Society, Inc. Announces Three Research Grants
The Mastocytosis Society, Inc. Announces Three Research Grants (Sterling, MA, February 14, 2018) The Mastocytosis Society, Inc. (TMS) has awarded…
Announcing the new TMS Physician Database!
NEWS UPDATE FROM TMS! Exciting News! TMS proudly announces the opening of the new TMS PHYSICIAN DATABASE!!! This online tool,…
It Takes a Village
It Takes a Village
Join a support group in your area and get love and support from others who are dealing with Mast Cell Disorders.
The Mastocytosis Society, Inc. will hold its next large scientific and support conference for patients, families and health care professionals in 2019, in Northern California. In 2018, we will host six regional one-day conferences with a presentation by a mast cell specialist and a support group session. Stay tuned for updates!