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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
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
latest news
Mast Cell Activation Syndrome Patient Survey
Calling all MCAS Patients! Mast Cell Activation Syndrome Patient Survey Click HERE to take the survey! This survey will be…
TMS Mast Cell Activation Syndrome Initiatives Update
Good day, The Board and committee volunteers at TMS have been increasingly aware of frustrations arising in several areas, specifically…
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!