Latest Post
My MG Story: Victoria Discusses Life and Work with Myasthenia Gravis
Nine years ago, Victoria woke up with MG symptoms. She shares her experience with diagnosis and treatment in a small town.
LATEST FROM THE MGFA INSIDER BLOG
Rituximab: Why B cell reduction therapy doesn’t work for all MG patients
Kevin O’Connor, PhD discusses why some MuSK MG
patients relapse after Rituximab.
Helping People Understand and Experience Myasthenia
MG patient Rebecca Molitoris demonstrates to others what it feels
like to have MG.
Sleep Right, Sleep Tight.
Sleep if vital to biological functioning and is critical for MG
patients. These tips can help you.
Myasthenia Gravis Can Be a Tough Act to Swallow
Eating can be hard work for MG patients but KJ Fallon provides some
good tips.
Hungarian MG Patients Use Social Media to Connect Across the Miles
Andrea Ujj is connecting Hungarian MG patients as part
of our global MG community.
Thymectomy and MG
Dr. Kevin O’Connor discusses Thymectomy and why
symptoms persist after the procedure.
Only 6 More Days Until the MGFA National Conference – and I Can Hardly Wait!
MGFA Board Chair Nancy Law Talks about her National Conference
Memories and the Importance of this Annual Global Event.
MGFA Partners with Rare Across America to Advocate for MG Patients
Volunteers Ensure Political Leaders Understand the Challenges of
Rare Diseases like Myasthenia.
CARE-MG Registry Will Help Us Understand How COVID-19 Affects MG Patients
Dr. Srikanth Muppidi Using CARE-MG to Understand how COVID-19
Impacts the MG Community