When MG Strikes… Learn More at the March Conference!

Myasthenia gravis is a chronic neurological autoimmune disorder that causes weakening of the voluntary muscles in the body. The most frequently affected muscles control eyelid movement, swallowing, and facial expression. In the past, people with MG didn’t have effective treatments–something that has thankfully changed. In fact, most MG patients today can expect to live a normal life span.

The first noticeable symptom of MG is usually a drooping eyelid, but some people may suddenly have trouble swallowing. The truth is, symptoms vary greatly from person-to-person. Often, if the symptoms are mild, it can be misdiagnosed because weakness is common to many other disorders. In very severe cases, however, doctors may recommend a thymectomy–the removal of the thymus gland–which has been found to be abnormal in many people with MG. Immunosuppressant drugs are another form of treatment that can help patients regain strength of weakened muscles.

The Myasthenia Gravis Foundation of America provides valuable resources for patients, their families, and caregivers. If you would like to get involved with the organization, why not attend their national conference? Here’s what you need to know:

The MGFA National Conference 2017
Astor Crowne Plaza
New Orleans, Lousiana
March 26 – 28, 2017


Erica Zahn

Erica Zahn

Erica Zahn is passionate about raising awareness of rare diseases and disorders and helping people connect with the resources that may ease their journey. Erica has been a caregiver, and is a patient, herself, so she completely relates to the rare disease community--on a deeply personal level.

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