Welcome to the CT Myeloma Fighters Information Group (CTMMFIG)!
Our Mission
Since 2001, our mission has been to bring myeloma patients and care partners together through trusted education, shared experience, and peer support—fostering hope and living well with myeloma.
Learning together. Supporting one another.
For any additional info, please contact:
Michael Tuohy: 203-206-3889
Robin Tuohy: 203-206-3536
Email: [email protected]
Where Shared Journeys Become Shared Strength: When you or a loved one is diagnosed with myeloma, the path ahead can feel uncertain, but you don’t have to walk it alone. Our group is part of the International Myeloma Foundation’s educationally supported network of myeloma specific groups. Whether you’re newly diagnosed, navigating a relapse, or supporting a loved one, we are here for you.
Connecticut Multiple Myeloma Fighters Information Group Leaders receiving an award at the International Myeloma Foundation's 25th Anniversary Support Group Leaders Summit on September 14, 2024 in recognition of the dedication and resilience of the group celebrating 23 years supporting their myeloma coMMunity.
Upcoming events
IMF Events
Support Group Events
About Us
Michael and Robin Tuohy started the CT Multiple Myeloma Fighters Information Group in the Spring of 2001 with the help of the International Myeloma Foundation. Michael was diagnosed with multiple myeloma in 2000 at the age of 36. Our support group was the 1st support group specifically for multiple myeloma patients in the State of CT. Myeloma patients, caregivers, family and friends are welcome to attend our meetings.
Our mission is to be an ongoing resource for information, support, shared experiences and hope for persons with multiple myeloma, their family and friends.
Our focus is to reach out to the myeloma community and empower them through education, provide support, and let them know they are not alone. Education is key in the fight against myeloma. Although we are not medical professionals, we strive to provide the most current information in myeloma treatment, clinical trials, side effects, pain management and quality of life issues by our affiliation with the International Myeloma Foundation. Patients talk about things that doctors don’t – like insurance, bills, assistance, work and how to go about life in general. Our shared experiences help each other!
CURE magazine interview with Robin Tuohy, Vice President Patient Support, International Myeloma Foundation
