Myasthenia Gravis Support Group
Myasthenia gravis (MG) is a neuromuscular disease leading to fluctuating muscle weakness and fatiguability. The hallmark of myasthenia gravis is muscle weakness that increases during periods of activity and improves after periods of rest. Although myasthenia gravis may affect any voluntary muscle, muscles that control eye and eyelid movement, facial expression, and...
I look forward to reading our other members answers!! Who knows between us we might come up with an answer!
Gez
One theory is that things like diabetes, thyroid diseases, lupus, etc come about from frequent emotional or physical stress. For instance, many elderly people are diagnosed with diabetes after the death of a loved one. That's not to say that they were not predisposed to the disease. The theory is that the emotional stress of these events changes our hormone output. The brain is a powerful organ and is constantly being signaled and sending out signals to maintain homeostasis (metabolic equilibrium). The more trauma or physical/emotional stress you are exposed to, the greater the chances that you will develop an autoimmune disease.
Having said that, I don't know if I believe that entirely. It doesn't explain teenagers that grew up happy/healthy and develop such diseases. Then there are the individuals that don't take care of themselves, eat poorly, smoke, etc and never develop them (even with a strong family history). That's why these autoimmune diseases are still such a mystery and many autoimmune diseases have strains that still haven't been identified. It's all such a mystery and I hope that I'm alive to see those discoveries, better treatments and more importantly, cures.
I can't wait to hear what everyone else has to say on this topic. Wishing everyone a nice weekend and a good week ahead.
Aloha,
Angie
That said, I had asthma as a child and have suffered with fatigue most of my adult life. Also, I had swallowing difficulty before 2011. So maybe the MG has been present for a while??
May this week be kind to us all!
Barbara
My first meeting with my neurologist was not for MG specifically as I came to him with a wide variety of symptoms.The first thing my neurologist did was do a general testing for heavy metals, ciiiac disease, and tests for a wide variety of things including different globulins and electrophoresis. He also did overnight oximetry which showed a severe apnea and ordered autonomic function studies which were positive. I also had a biopsy for small fiber neuropathy which was positive. My heavy metals testing was negative. Also cilicac was negative. Marie
I know for a fact that stress makes MG much worse. Rest and enough sleep also make a difference.
I hope you find what works for you!
Hugs,
Carly
But was anyone else on PPI's long term before MG? I'm relatively young. The only medicine I have ever taken, was I was on prilosec for a couple of years a few years ago because I couldn't keep GERD under control without it.
Just noticing I'm getting some GERD symptoms back now on prilosec.