At Super T’s Mast Cell Foundation, it our mission to be a resource for patients suffering with Mast Cell Disease through our grant giving program offered twice a year. STMCF is the only foundation globally providing financial support along with physician created resources provided to patients diagnosed with Mast Cell Disease.

We are committed to those affected by Mast Cell Disease, while using our passion to make a difference. We will always have an open-minded approach when raising awareness, financial support, and educating opportunities for mast cell patients.


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.


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.

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


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


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


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


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.