Latest Post
My MG Story: Danielle’s Journey with Seronegative Myasthenia Gravis
Danielle wants to share her treatment journey to help others understand the challenges of finding the right approach.
LATEST FROM THE MGFA INSIDER BLOG
Our MG Story: Advice for Spouses and Caregivers
In this vlog, Cary asks her husband Zack some questions about his
experience as an MG caregiver.
Mistakes Caregivers Make and How to Avoid Them
Get started transforming the mistakes into your success
strategies.
Caregiving: The Struggle is Real
Navigating the complex journey of caring for your spouse
– and remembering to care for yourself.
MGFA Advocacy Update
Learn more about Rare Disease Week on Capitol Hill and hear the latest on our advocacy efforts.
MGFA and Bionews Partner to Deliver Myasthenia Gravis News to Wider MG Community
Myasthenia Gravis News, delivered by Bionews, is an online news source intended to provide the myasthenia gravis (MG) community with the most recent news and information about MG, as well as first-hand community perspectives from patient and caregiver columnists.
Preparing for a Medical Emergency When You Have Myasthenia Gravis
Find tools and advice to help you prepare for the worst.
The Snowflake Disease
Just like a snowflake, myasthenia gravis symptoms can appear one
minute and be gone the next.
Our MG Story: When Your Child Has Myasthenia Gravis
The Oronuga family’s life was turned upside down when
Teniola was diagnosed with MG at age three. They share what it is like to battle this
chronic autoimmune condition in Nigeria.
Remembering Tom Larsen, the Incomparable “Rocket Man”
In February the MGFA and the MG Community lost a dedicated volunteer
and champion advocate of patients and caregivers. Friends and staff remember his
legacy.
MGFA Invited to Participate in the INSPIRE Advisory Board and MSMilan Patient Community Day Conference
Collaborating with others to drive increased awareness about rare
disease around the world