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“You don’t know where your gMG journey will take you, but don't quit. And don't lose that fighting spirit.”
Dale, living with gMG since 2015
MEET THE gMG AMBASSADORS
Watch how Dale and Greg manage daily life with generalized myasthenia gravis (gMG). See how they cope with symptoms, make modifications, and work with their doctors to manage their disease.
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MEET DALE
His favorite travel destination
“My absolute favorite place is Hawaii. I’d move there right now.”
A modification he’s made to manage gMG
“I get double vision in my left eye from working on the computer for 10 hours a day. I try to take breaks regularly, but closing my eyes for the rest of the day is something I do to ease my double vision.”
WATCH DALE'S STORY
"gMG is a silent disease. Unless you live with it, you can’t really understand it."
Greg, living with gMG since 2002
MEET GREG
His family
“I have a wife, 3 children, a beagle named Remy, and a canary named Woody.”
When he first knew he had gMG
“When I was first diagnosed, I was slurring a lot. I saw my dentist, a general practitioner, and a few neurologists. Fortunately, I had a test that said I have myasthenia gravis.”
WATCH GREG'S STORY
The community is here for you
Explore the tools and resources made just for you.
These resources can help you partner with your doctor to manage your gMG.
Antibodies usually attach to harmful things like bacteria. However, in gMG your body starts producing abnormal antibodies that instead attach to normal proteins in the NMJ. Most people with gMG make AChR antibodies. These antibodies activate the complement system (part of the immune system). Complement disrupts the structure of the neuromuscular junction itself and is one of the main causes of damage in AChR+ gMG.
Occurring suddenly and lasting for a short time. An acute disease is one with symptoms that only last for a short period of time. People with myasthenia gravis often experience both acute and chronic symptoms.
Long-lasting, persistent, or constant. A chronic disease is one with symptoms that occur over a long period of time. People with myasthenia gravis often experience both chronic and acute symptoms.
A chronic autoimmune, neuromuscular disease that causes weakness in the skeletal muscles, which can worsen after periods of activity and improve after periods of rest. This weakness can affect moving, eating, and breathing.
MuSK antibodies are a type of antibody. Normally, antibodies attach to harmful things like bacteria. However, in gMG your body starts producing antibodies that instead attach to normal proteins in the NMJ. MuSK antibodies prevent the muscles from receiving messages properly from the nerves. When your muscles don't receive the signal, you experience muscle weakness.
An 8-category questionnaire that allows you and your doctor to measure the symptoms that most affect your daily living. Each category is graded on a scale of 0 (normal) to 3 (most severe). An MG-ADL score can be between 0 and 24, with a higher score meaning your symptoms are more severe.
As gMG affects each person differently, uncontrolled disease can also vary person to person. The most common signs and symptoms that may indicate uncontrolled disease include:
Myasthenia Gravis Activities of Daily Living Profile (MG-ADL)—a tool your doctor may use to assess the extent of your symptoms)—greater than or equal to 6
Some but not all of the following: ongoing weakness, difficulty speaking, problems with chewing or swallowing, impaired vision or drooping eyelid, shortness of breath, or difficulty with activities such as brushing your teeth or combing your hair—which can impact your daily quality of life
Progression of symptoms requiring frequent treatment changes and/or increase in treatment dosing
It’s important to speak with your doctor if you are experiencing these signs and symptoms of gMG to understand if your disease may be uncontrolled.
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