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Mission2018-03-23T11:28:20+00:00

OUR MISSION

The mission of Super T’s Mast Cell Foundation is to increase awareness through education and support for the mast cell community, medical professionals and the public. Additionally, providing financial assistance for patients diagnosed with Mast Cell Activation Disorder.

OUR VISION

To improve the quality of life of patients and families affected by Mast Cell. We will offer physician based medical literature for patients and caregivers, resources within the mast cell community such as social media links, foundations and support outlets.  Additionally, we will offer yearly events to raise funds so STMCF may provide grants in order to support those diagnosed and suffering with mast cell.

TOGETHER WE CAN 

When you think you can’t do something to help, you are wrong. If this is the first time you have heard of mast cell activation disorder then you are probably not alone. Tell somebody else. Spread the word. Make a difference.

  • Share this website

  • Join us on Facebook

  • Go to an event

  • Ask us a question

If yesterday you knew less about mast cell activation disorder than today, we have made progress. If tomorrow you tell two people about what you learned, we can move mountains.

HOSPITALS

Hospitals need better information on how to treat patients. Share best practices and resources around the globe.

DIAGNOSIS

Small symptoms compound fast. Here is what to look for so that you can get diagnosed correctly and quickly

EDUCATION

A gathering of all resources and links to those combatting Mass Cell Syndrom

TREATMENTS

Gathering of treatment options from emergency procedures to long term care.

CHANGE A LIFE TODAY

As long as rare diseases exist, there will be people out there to help. It doesn’t take much to change a life, Get in touch today and start making the difference.

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