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.

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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

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Infographics

Infographics

Printable Infographics and brochures! Use these for handouts and display.

Printable Resources!

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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.

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Emergency room guide

This is a handy reference guide to provide everything you need for emergency room visits as a patient with a Mast Cell Disorder. (INCLUDING EMERGENCY RESPONSE PLAN & PREMEDICATION FOR MAJOR & MINOR PROCEDURES)

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latest news

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Deciphera Pharmaceuticals Presents: Living with Systemic Mastocytosis (SM) WebEx

On Tuesday, October 9, 2018, at 11 AM, EDT, Deciphera Pharmaceuticals will be hosting a webinar for the Systemic Mastocytosis…

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Epi Pen Shortage

There is an ongoing shortage of epinephrine auto-injectors causing a crisis for mast cell disease patients attempting to fill their…

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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.

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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!

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