Be a light of hope this holiday season. Ignite more progress, restore more freedom, and inspire more hope for families living with neuromuscular disease.
We use cookies to improve your experience.
Innovations in Care
We provide access to support and programs that empower the lives of people living with neuromuscular diseases.
2020 MDA Engage Pompe Disease Symposium
July 12, 2020
Time: 11:00am - 4:45pm ET
Virtual, online event
There is no cost to members of the MDA community or clinicians to attend the event, however, registration is required.
Event Chair: Dr. Heather A. Lau, Director of the Lysosomal Storage Disease Program, NYU Langone Health
Agenda
Welcome (11:00am ET)
Elise Qvale, MDA
The COVID-19 Impact (11:05am ET)
Dr. Heather A. Lau, NYU Langone Health
Research and Clinical Trials (11:25am ET)
Dr. Heather A. Lau, NYU Langone Health
Drug Development Roundtable (12:20pm ET)
Moderator: Dr. Heather A. Lau, NYU Langone Health
Panelist: Dr. Barry Byrne (UF Health), Sean Doerr (family), Mark Lyles, MD (Amicus), Amy Fisher (Spark Therapeutics)
Best Practices and Future Considerations for Clinical Care of Pompe
Stephanie Austin, MS, MA, CGC, Duke University Medical Center
Genetics and Pompe (2:15pm ET)
Kara Anstett, MS, CGS, NYU Langone Health
PT and Exercise (3:00pm ET)
Laura Case, PT, DPT, MS, PCS, C/NDT, Duke University Medical Center
Nutritional Considerations in Pompe (3:30pm ET)
Surekha Pendyal, Msc, MEd, RD, FAND, Duke University Medical Center
MDA Spotlight (4:00pm ET)
Elise Qvale, MDA
Raise your voice through grassroots advocacy (4:15pm ET)
Brittany Johnson Hernandez and Mark Fisher, MDA
On Monday, July 13, the MDA will be hosting a Pompe disease Patient Focused Drug Development (PFDD) Meeting virtually online. We encourage Engage attendees to also attend the PFDD meeting. For information on the PFDD meeting, and to register, click here.
Thank you to our supporters:
For questions reach out to: mdaengage@mdausa.org | 1-833-ASK-MDA1 (1-833-275-6321)