Latest Post
Walking for MG Awareness in Halifax
Struggling with MG symptoms but determined to make a difference, Nadine steps out of the shadows.
LATEST FROM THE MGFA INSIDER BLOG
We’re Not Alone: Creating a Spanish-Language Support Group
Leah Gaitan-Diaz conducts Spanish speaking support groups to close
the language gap for the MG Community.
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.