Hybrid Meetings: In-Person OR Virtual
- In-Person: We will meet at the Prospect Public Library, 17 Center Street, Prospect, CT 06712 in the Community Room.
If you are sick, we ask that you please stay home, as many in our group have compromised immune systems. You are welcome to join the meeting virtually.
Masks at meetings will be optional.
The Community Room has special air purifiers installed to help with safety precautions. - Virtual: We will continue to provide group members with a Zoom link to join meetings virtually.
For details, please contact Robin Tuohy ([email protected]).
Welcome to the CT Myeloma Fighters Information Group!
For any additional info, please contact:
Michael Tuohy: 203-206-3889
Robin Tuohy: 203-206-3536
Email: [email protected] or [email protected]
41.5008174, -72.9785104
Why attend our Information Group?
Support groups bring together myeloma patients, caregivers, family members & friends. Patients involved in a support group experience more positive outcomes due to their understanding of treatment options and enables them to have key conversations with their healthcare team.
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!
If you would like to share your story please contact us. By sharing our experiences we can help each other. Knowledge is Power!