Community Webinar: Navigating Your Emotional Journey Following Genetic Diagnosis

When:
March 13, 2025 1:00PM

Join Jett Foundation’s Community Webinar Series to hear from Mary-Frances Garber on how to best navigate your emotional journey after a genetic diagnosis, such as Duchenne muscular dystrophy.

Navigating Your Emotional Journey Following Genetic Diagnosis
Thursday, March 13, 2025
1pm ET | 12pm CT | 11am MT | 10am PT

 

Mary-Frances Garber, MS, CGC

Guest Speaker

Mary-Frances Garber is a board certified, licensed genetic counselor with a private practice, Listening, Reflecting, Healing, where she provides supportive genetic counseling and bereavement services. Her belief is that individuals and families need a place to process their emotions associated with their genetic issues. She worked as a prenatal genetic counselor in the Maternal Fetal Medicine department at Newton Wellesley Hospital and as a consultant with Genome Medical providing counseling for those with family histories or diagnoses of cancer and other conditions. Earlier in her career, she was the Executive Director for NERGG, Inc., The New England Regional Genetics Group and worked at Brigham and Women’s Hospital in the Antenatal Diagnostic Center. Mary-Frances attended the University of Rochester, graduating with a BS in Molecular Genetics, and Sarah Lawrence College where she earned a MS in Human Genetics. Mary-Frances is a member of the National Society of Genetic Counselors and has served as Region I Representative on the Board of Directors. In her spare time, MF enjoys being a mother to her three adult daughters and playing and coaching tennis.

Our Community Webinar Series is focused on ensuring that our Duchenne and rare disease community is better prepared for those unexpected moments, challenging medical decisions, and difficult stages when on a Duchenne journey.

No one ever expects Duchenne and there is no correct way to tackle a diagnosis, but we can always better prepare. This webinar series is an opportunity to equip yourself with more knowledge, resources, and tools for those real-life, often unanticipated, scenarios.

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How is the rare disease community accomplishing goals?

Tune in on February 29 to hear from our panel and moderators on how they are accomplishing goals and living life to the fullest!

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