Join Shawna N.M. Barnes, writer, disabled veteran, and MG patient advocate, as she hosts “Pushing Back at MG From Getting Informed to Taking Action,” a virtual event on Oct. 23 at 6 p.m. EST. Hear from fellow patients and a leading doctor about finding reliable information, daily management strategies, and working with your care team to feel confident in treatment decisions.
Interested in joining the virtual event? Click the link to register today!
Transcript
Living with myasthenia gravis can bring up a lot of questions. Where do you find reliable information? How do you manage energy and your daily routine? How do you work with your care team to feel confident about the decisions that are being made for your treatment?
That’s why Myasthenia Gravis News is hosting a special live event called “Pushing Back at MG from Getting Informed to Taking Action.” And I’m the host.
It’s happening virtually on Thursday, Oct. 23, at 6 p.m. Eastern Standard Time. During this event, you’ll hear from two MG patients who know these challenges firsthand, plus a leading doctor who works with patients every day.
Together, they’ll talk about how to find trustworthy information, what daily tools and practices really do actually make a difference, and how to approach care and treatment options and decisions with confidence.
This won’t just be another webinar. It’s going to be an honest conversation shaped by patients, for patients — with practical insights that you can use right away.
So mark your calendar and RSVP today. Yeah — you today.
Join us live on Oct. 23, and let’s push back at MG together. Hope to see you there.