Super T's Mast Cell Foundation

Super T’s Mast Cell Foundation is the only nonprofit globally recognized for providing financial support to mast cell patients. In addition, it is our mission to continue creating and providing necessary educational and medical resources to best equip patients and their communities with the necessary information explaining how to manage and treat mast cell diseases.

Condition Awareness & Advocacy

Here is a list of conditions this partner raises awareness and advocacy for:

Resources & Support

Connect With Super T's Mast Cell Foundation

Patient Worthy Posts on Mast Cell Disease

My Life with Rare Chronic Illnesses

Hello, my name is Megan. I have been diagnosed with postural orthostatic tachycardia syndrome (POTS), Ehlers-Danlos syndrome (EDS), mast cell activation syndrome (MCAS), small fiber

This Little Light of Mine

I recall the day, almost six years ago, when I observed the liveliness of joy in one who paraded around in a pink frilly skirt,

New Report Demonstrates How Dental Complications with Systemic Mastocytosis Should be Managed

Mastocytosis refers to an entire group of disorders. All of these conditions are characterized by a rapid production of mast cells (MCs), which are abnormal.

Rare Classroom: Mast Cell Activation Syndrome

Welcome to the Rare Classroom, a new series from Patient Worthy. Rare Classroom is designed for the curious reader who wants to get informed on

HT-KIT Granted Orphan Drug Designation for Mastocytosis

In the United States, Orphan Drug designation is granted to drugs or biologics intended to treat, prevent, or diagnose rare diseases or conditions. Rare conditions

Woman With EDS, MCAS, and POTS Gets a Service Dog After Helping Others

Crystal Goodwin, from South Portland, Maine, was diagnosed with mast cell activation syndrome (MCAS) back in 2011. A rare disease diagnosis can turn one’s life