My Nonprofit Reviews

My husband was diagnosed with inclusion body myositis over 20 years ago. TMA was the only source of information at that time.(pre internet) We have watched it take on more in the way of creating awareness and advocacy for these diseases. In recent years the amount of funding for research and the grants given are a great step forward toward understqnding and curing this rare disease. My family believes so strongly in TMA that we fundraise every year.

More Feedback