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We are The Mastocytosis Society.
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Exciting News - TMS Membership is now FREE!
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Participate in the 2017 Walk-A-Thon. Let's make a difference together.
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Community is what keeps us together.
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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
Letter and Updates from the Chair, July 2017
Summer Greetings! Here within TMS, there is so much going on that I hardly know where to start. The new…
The Stony Brook Chronic Illness Project-Patient Survey
DO YOU HAVE A CHRONIC ILLNESS? Scientists at Stony Brook University are conducting one of the largest, most important research…
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 CONFERENCE
2018 CONFERENCE
The Mastocytosis Society, Inc will hold its next large scientific and support conference for patients, families and health care professionals in 2018. Various sites are under consideration. In 2017, we will be hosting video conferences by mast cell specialists on selected topics. Stay tuned for updates!
