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.
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.
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.