June is Myasthenia Gravis Awareness Month

I don’t post on Tuesdays. But there’s a matter very close to my heart that I wanted to share.

June is Myasthenia Gravis Awareness month.

So, what is myasthenia gravis (MG)?

It’s a not too well known autoimmune neuromuscular disorder that usually takes 1-2 years to diagnose. It’s also called the snowflake disease because every case is different. It usually starts with a routine infection, like the cold or the flu, and then myasthenic symptoms start to appear, but are often misdiagnosed as something else. Anyone can get it, all ethnicities, all ages, both genders. Generally, MG involves muscle weakness. This can be localized to certain parts of the body, such as in ocular MG where only the eyes are affected, or generalized to all parts of the body. It usually doesn’t result in death, unless someone enters myasthenic crisis and doesn’t receive medical help right away, but does tend to limit the amount of activity someone can do. The more exertion, the more tired an MG patient becomes. It can be devastating to individuals and families when their loved one is no longer able to do the things they were once able to.

For more information, check out: http://www.myasthenia.org/

Why is this important?

Well, my mom was diagnosed with this about 10 years ago. At the time, she was the mother of two adolescents and one pre-adolescent, and we were all trying to figure ourselves out. It wasn’t an easy time, and finding our mother asleep on the couch in the middle of the day because she was just so exhausted was hard for us. I was, and still am, very close to my mom and was old enough to realize something was wrong. It took almost 2 years for her to be diagnosed. There were periods when she was better and periods when she was too tired to do anything. For awhile, it was hard on us because we didn’t know what was going on, didn’t know what MG was, didn’t know if Mom was going to be okay.

I’m happy to say that, 10 years later, my mom is very stable. Due to dietary changes that just happened to work in her case, she hardly feels the effects of MG and lives a relatively normal life.

So, wear teal and spread the word, because most people just don’t know what myasthenia gravis is.

Thank you for reading!

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