Latest Post
My Journey Living with Myasthenia Gravis: Gloria’s MG Story
"Little by little, I learned to listen to myself, recognize my limits, and understand that asking for help is not a sign of weakness but an act of courage."
LATEST FROM THE MGFA INSIDER BLOG
Caregiving: The Struggle is Real
Navigating the complex journey of caring for your spouse
– and remembering to care for yourself.
Miss America Program Titleist Audrey Getman Doesn’t Let MG Stop Her
Miss Kingston Audrey Getman shares her MG story.
Tips for Traveling with Myasthenia Gravis
Traveling with an illness like myasthenia gravis can be challenging,
but with some planning and the right tricks up your sleeve, you can enjoy your trip
safely.
Healthy Green Smoothies from MGFA
Green smoothies give you a dose of veggies with your fruit and are a great way to start the morning or provide an afternoon snack. People with MG may find that smoothies are an easier way to ensure you receive healthy, nutritious foods even when you are having difficulty chewing and swallowing.
Pediatric MG: Listen to This Podcast Episode
MGFA’s Meridith O’Connor talks with Dr.
Jonathan Strober, director of the Neuromuscular Clinic at Benioff Children’s
Hospital.
Rare Disease Week: Highlighting Seronegative MG, a “Rare-of-the-Rare” Disease
The struggle seronegative myasthenia gravis patients face for
diagnosis and treatment.
How to Be an Advocate for Yourself and Others with Myasthenia Gravis
Rare Disease Day happens once a year, but you can bring awareness to
myasthenia gravis any day of the week!
When Every Day is Rare Disease Day
Illuminating the support rare disease patients need 365 days of the
year.
Rare Disease Week – Advocacy at Home and on the Hill
Rare Disease Week starts on February 28. Learn how you can advocate
for people with MG.
MG patients discuss finding community at the MGFA Patient Conference
Hear from patients about why they are attending the MGFA National
Patient Conference in 2023.