Anyone have twitching eyelids?

I know by your posts that many of you have muscle twitching throughout your body but do many of you have twitching eyelids? It is very annoying and I was wondering if Lyme causes it. I have read that magnesium deficiency could be involved,but I take plenty of  that (800 mg daily) Anyone? Thanks alot!  D

I had that the first few months when my illness reared it's ugly head. I don't anymore. I only had it in my right eye too.

I had it on and off for a few years before that I found out I had Lyme.

Dowa...
I had the twitching eyes..and it later turned into bells palsy. My whole rigth side of my face would drop. And my eye would drive me crazy. But it would still close. Luckily. But the eye would look bad...dropped and my right lip and I would look off.
And the Dr. and I had a long tak today about magnesium. And he said that is was proven to help the lyme build its big wall and that lyme thrived on it to protect itself against all abx.
So we are not allowed any of it at all.
This is also backed by Dr. Fry. And others.
Learn something new every dan day. We are the ginny pigs..but hey..we are paving the way for others.
This whole mistery is going to pop very soon. We are all going to wake up from this night mare very soon!

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2004 in Martha's Vineyard me and my two daughters then 11 mos and 6 all got Lyme Disease. This was only known to us because we found the tiny ticks on us and we got very ill. My dog also got lyme and he went lame.
We have fought it for 4 years to no avail.
We all got it again this summer is Texas.
I am now in treatment in Scottsdale Arizona at Envita.

"The eyes cannot see for for what the mind does not know."

My left eye twitches often. Now it looks different from my right. Theres puffieness underneath when I smile and I have crows feet on the left but not the right...weird.

Thanks everyone for your input. I dont understand NOT taking magnesium as most all of us are very deficient in it? How does that make any sense??  D

This is all so frustrating and quite maddening. My one eye suddenly (well the past few years) looks so much different than the other eye and I've also experienced twitching although not too often. I notice it much more in photos, especially when I'm smiling. I mentioned this and so many other symptoms to four different doctors over the past few years (2 neurologists, 2 internists) and it was just all brushed off as CFIDS. I have my first appointment with a lyme specialist next week. I also checked the supplements I've been taking for CFIDS/Fibro and three of them contain magnesium which I'm stopping until I see the specialist.