If you are living with DM1 or DM2, or are the caregiver of an adult or child with the disease, we invite you to join us for a group conversation to help shape the future of MDF. Your perspectives and experiences will directly inform our strategic planning work moving forward. The conversations will run for 60 - 90 minutes and space is limited. If you are interested in participating please sign up using the links below.

• Living with DM1: March 25th at 10am PST/ 1pm EST or March 30th at 4:30pm PST/7:30 pm EST
   
• Living with DM2: March 23rd at 12pm PST/ 3pm EST or March 29th at 4:30 pm PST/7:30 pm EST
   
• Caregivers of children with the disease: March 26th, 1pm PST/ 4pm EST
   
• Caregivers of adults with the disease: March 24th, 3pm PST/6 pm EST
   

If you are interested in contributing, but the times below do not work with your calendar, we hope you will participate in our community survey!