Community Webinar: Cardiac Imaging, Treatment, and Therapy in Duchenne, Becker, and Carriers

July 18, 2024 1:00PM

Join Jett Foundation’s Community Webinar Series to hear from Dr. Jonathan Soslow on cardiac imaging, treatment, and therapy for individuals living with Duchenne, Becker, or are carriers.

Cardiac Imaging, Treatment, and Therapy
Thursday, July 18, 2024
1pm ET | 12pm CT | 11am MT | 10am PT


Dr. Jonathan Soslow

Guest Speaker

Dr. Jonathan Soslow is a Professor of Pediatrics in the Division of Pediatric Cardiology at Vanderbilt University Medical Center. He has advanced training in cardiac imaging, including transthoracic echocardiography, transesophageal echocardiography, and cardiac magnetic resonance imaging (CMR). His research focuses on the assessment of serum and imaging biomarkers in Duchenne muscular dystrophy (DMD) cardiomyopathy and after heart transplant.

His current funding includes R01s from the Food and Drug Administration and the National Institutes of Health. He is the Director of Clinical Research and the Director of Cardiac MRI for the Division of Pediatric Cardiology at Vanderbilt University Medical Center (VUMC). He helped found and now co-directs the DMD Multispecialty Clinic at Vanderbilt University Medical Center and has also helped found the Pediatric Gene Therapy Clinic at Vanderbilt University Medical Center.

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.

Experience the magic this summer!

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!

Your gift helps Jett Foundation provide programming and opportunities, such as Camp Promise, to many families impacted by Duchenne muscular dystrophy each year.

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