Cpnhelp.org

When I started the naci that was a new symptom both eyes more the left . I had never had this symptom before. It passed in about 2 weeks. I don't know if this helps or not but good luck.

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zero negative sjogren's diagnosed 2/03, 200mg minocin daily, biaxin,plaquinel mwf, flagyli every 3 weeks.

Colorbleu what are you taking the Lamasil and Fungizone for?  Are you taking antibioticsi.  When you say continue ipmrovement is this for CFSi.  Can you give more details please?

 This twitching of the eye and other areas is mentioned a lot in CFSi and FMSi literature. Theres some things I have read about oxygen deprivation to the area but Im not sure that is all there is too it. Some think it stress but again I dont think thats all there is to it.

  I have it happen to my eye, in my arm, on my chest.

  Could for sure be some vitamin or mineral deficiency since many of those cause muscle spasms. Seems to me I havent had it in my eye since I started b12 injections. I did have my arm doing it just yesterday.

 Might get the b12 checked anything under 540 (lab low is much lower and you will be told its normal) the specialists are treating with injections or oral sublingual.

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CAPi- zithro, flagyli, plaquenil - CPNi +, fibromyalgiai, endometriosis, b12 deficiency

I realise this is an old post, came across it whilst searching for eye twitches.

From all the tests I've had over the past 6 months, I'd recommend anyone with continuing twitches to go see an optician and ask for a full Medical Eye Test,not the standard vision test.

From personal experience these twitches could be due to tiredness or stress but it could also be something more serious such as Nystagmus. Don't hang around, get it checked.

Berkshire, UK. Diagnosed RRMSi Feb 4th 2008.

NACi 2400mg. All supplementsi. Doxyi 200mg. Zithi 250mg M/W/F.
No GP/Neuroi support. Self medicating with help from David Wheldoni.
Started CAPi 20th April 2008.

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Berkshire, UK. Diagnosed RRMSi Feb 4th 2008.

NACi 2400mg. All supps. Doxyi 200mg. Zithi 250mg. Metroi 400mg.
No GP/Neuroi support. Self medicating with help from David Wheldoni.
Started CAPi 20th April 2008. First pulse June 2008

Old posts are good posts, too, Andesine. Come to think of it, I experienced eye twitching about six months before the MSi diagnosis in 2005. It only happened when I was tired or very stressed. Of course, we all know what came behind it - optic neuritis in that same eye. To be honest, though, the eye doctor would never have determined the cause. Once the optic neuritis hit, he said MS within minutes of my walking into the office. (I've since returned the favor and educated him on chlamydia pneumoniae.)

The difference between what we do and what we are capable of doing would suffice to solve most of the world’s problems. Mohandas Gandhi

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The difference between what we do and what we are capable of doing would suffice to solve most of the world’s problems. Mohandas Gandhi

The reason I say go see an Optician is I had the twitch but under tests developed Double Vision and "pulsing" in my right eye. By pulsing I mean you could see my eyeball beating. I asked for a full medical eye exam and he put me through the wringer. At the end of it he told me my eyes were fine but he was very worried there was something more serious going on. He got straight on the phone to my GP and told him to send me to a Neurologist within the next week.

Prior to that I'd been diagnosed with Vertigo.

I think it needs to be a good optician though, not one of these chains that do cheap glasses where you get a 5 minute test. I went to an independent guy and the tests took almost 2 hours, with various different machines, eye drops for pupil dilation etc.

I must talk to him about Cpni.

Berkshire, UK. Diagnosed RRMSi Feb 4th 2008.

NACi 2400mg. All supplementsi. Doxyi 200mg. Zithi 250mg M/W/F.
No GP/Neuro support. Self medicating with help from David Wheldoni.
Started CAPi 20th April 2008.

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Berkshire, UK. Diagnosed RRMSi Feb 4th 2008.

NACi 2400mg. All supps. Doxyi 200mg. Zithi 250mg. Metroi 400mg.
No GP/Neuroi support. Self medicating with help from David Wheldoni.
Started CAPi 20th April 2008. First pulse June 2008

I agree; talk to him about cpni. Mine is one of the top three in Chicago and I was fortunate to get in on a couple hours' notice as a personal favor to the guy who makes my glasses. He was very dismissive of cpn when I first told him. I'm sure he thought I was hysterically grasping at straws, having been so newly diagnosed with MSi. By the time I left, though, he asked for the website info and made a point of making sure he had the stuff I'd printed out for him. I think he (and my regular eye doctor) are prime candidates for cpn enlightenment, as they so often come in contact with newly diagnosed MS patients. Both of them were my first inkling of MS due to the vision loss and optic neuritis and both gave me the thumbnail sketch of 'what to expect with MS'. Now, just think if both of them forevermore tell their suspected MS cases "and you can go to this website and it will educate you on how to kill off this pesky disease". What a sea-change in thinking THAT would be!

The difference between what we do and what we are capable of doing would suffice to solve most of the world’s problems. Mohandas Gandhi

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The difference between what we do and what we are capable of doing would suffice to solve most of the world’s problems. Mohandas Gandhi