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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 Community
Our Community
A 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 Caregivers
TMS Caregivers
Family 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.Incredible Caregivers
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
latest news
TMS Research Grant Offering
Research Grant-Request for Proposals on Pediatric Mastocytosis, including Related Disorders of Pediatric Mast Cell Activation: The Mastocytosis Society, Inc. (TMS) is…
Summer 2017 Chronicles, Letter and Updates from the Chair
Summer Greetings! Here within TMS, there is so much going on that I hardly know where to start. The new…
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.
2018-2019 Conferences
2018-2019 Conferences
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!
