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...
Of interest is that a type of eye twitching that is induced by a series of maneuvers has been used to point to MG by ophthalmologists. I had not heard of this before am enclosing a link.
I would think with eye muscle weakness twitching might happen sooner then later in any given circumstance.
http://www.ncbi.nlm.nih.gov/pubmed/21654336
My own personal experience was that is was mainly annoying....royally so....but usually stopped within three weeks or so. Wish I could say I knew of some magic drops for it but I don't! Marie
Not sure if you are on any of those meds. You should let you doctor beware of your problems and also consider the small possibility of a medication side effect.
I have also been having problems with feeling very fatigued as soon as I wake up. Many MG patients are diagnosed with sleep apnea. I use a PiPAP and still have problems in the morning feeling very fatigued.
I participated in a quality of sleep study done by PatientsLikeMe. They just release the results of the study, which showed a much higher frequency of sleep problems for people with chronic illnesses. You can find the results at;
http://patientslikeme_forum.s3.amazonaws.com/PatientsLikeMe_Sleep_Survey_Infographic.pdf
I have started tracking my quality of sleep using my fitbit. Many other similar devices also track sleep. The data shows problems falling asleep and waking up an average of 8 to 12 times a night. It rates my quality of sleep at 75%.
I will use the above information to discuss my concerns with my neuro and pulmonary doctors in a couple of weeks. It may be time for me to have a repeat sleep study.
I hope this may help in some way and you can get some answers very soon.
Wishing you the very best.
Bruce
You know what? Since starting mestinon all my muscle twitches went away. I don't even seem to get muscle twitches from mestinon, but will on rare occasion get a few when it starts to disappear from my system and my symptoms come back. I take more mestinon, my symptoms go away and my twitches stop, so it's not a result of too much mestinon.
Okay, so what I said was....
I have had eye twitching for many, many years. Long before I was ever consistently symptomatic or diagnosed. Sometimes it goes on for 4 or 5 months at a time. One of the doctors that I used to work for on the mainland always told me that it was due to lack of sleep. Even though I was sleeping all the time.
Working in a medical clinic is hard when you are winking at everyone. There is nothing more embarrassing than having a patient family member wink back at you when you leave the exam room. I didn't know if he was making fun of me or making a pass. lol
This is one of the most annoying things for me too because I can't get my eyes focused when it's happening. Any blurring or double vision is compounded by the twitching. If someone has a way to minimize this, I'm listening. Sometimes I just cover it with a patch to rest it which does seem to alleviate it to some degree. So I do that when I'm at home but I just don't see myself going to work with a pirate patch so I just struggle through it there. I'm anxious to hear what others have to say on this topic. Hugs!
The increased fatigue I would worry with and let your neuro know. There may be a change in you care in the offing.
Hope you get some relief, twitching can get annoying.