Im trying not to get caught up with the miracle stories floating about but Ive come to a point where I feel that I have little choice other than to at least try aimspro.
Ive been on avonex (that was when my condition deteriorated substantially), Ive tried diet (didnt do a lot), tried the antibiotics (didnt do anything for me either) and Ive been on LDN coming up 3 years (isnt doing a lot to improve things but I seem to remaining reasonably stable at least) Oh and Ive also been turned down for campath as Im not suitable.
My neuro is about as helpful as a chocolate teapot so Ive researched and tried all this off my own back as Im not about to sit back and let this MonSter take over any more of my life than it has already.
Back to the point lol... Ive sent some aimspro info off to my gp to see of shes willing to rx it, if not then I'll go to one of the private gps that is rx it. Basically Ive made up my mind to try it but was just interested in hearing the experiences of anyone else thats tried it
Current research has shown it to have anti inflamatory properties as well as effects on the bbb. So possibly a double whammy. The original article i read on this site (for simvastatin) found a 44% reduction in MRI activity or something.
http://www.thisisms.com/article106.htmlA group of 30 patients with MS given 80 mg a day of Merck & Co Inc's Zocor, or simvastatin, had a 44 percent reduction in brain lesions after three months of treatment, their study showed.
I think in the UK, low dosage (10mg I think) can possibly be purchased without a prescription. ie yes its available in the UK.
My GP in Buckinghamshire has prescribed simvastatin for me and you can buy low-dose statins OTC. I have a real problem with understaning the science behind aimspro - like I dont believe there is any - and consider it to be an eloborate con - just my opinion shared by my neurologist. However you should decide for yourself.Ellenem wrote:I havent tried lipitor ... is it available in the UK?
PS I think I prefer snail poison to goat's blood
I am what I am
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Sorry Ellenem missed your post.Ellenem wrote:Hi John
What dose of simvastatin do you take and what effects has it had on your MS?
I take 20mg daily but has it had any effect on my condition I dont really know My approach is to take medication, including Betaferon, and supplements that seem to me to be likely to do me some good based on some reasonable research. I turned down the campath trial because I didnt fancy the potemtial side-effects - but that is looking v interesting.
So far against statistical expectation (men diagnosed late are expected to become disabled quite rapidly) I'm doing reasonably well.
I am what I am
I used to be on 80mg simvastatin. As soon as I got off rebif, and was only on the statin (and abx's I think), the tingling in my hands disapeared within about a month. I couldnt remember the last time that was the case. When I switched to lipitor, I could feel the tingling in my feet noticeably subside within an hour or two of taking a dose. This quick feedback left me with no question to stay with my switch from simvastatin to lipitor, and that the statins were helping. I felt the effect after taking a dose, for about a month or two.Ellenem wrote:What dose of simvastatin do you take and what effects has it had on your MS?
I havent herd of anyone else report a noticeable effect within hours of taking lipitor, but i am pretty sure it wasnt a placebo effect. I was actually scared of comming of simvastatin.