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RE M.S AND LYME DISEASE

Posted: Fri Jan 09, 2015 1:54 am
by seeva
HI FRIENDS a mother of three who spent 2 years being treated for m.s has been cured with simple course of antibiotics
please read for more information shttp://www.dailymail.co.uk/health/article-2343 ... -BITE.html
regards
seeva

Re: RE M.S AND LYME DISEASE

Posted: Fri Jan 09, 2015 10:06 am
by SarahLonglands
Thanks for this Seeva: I saw this a while back, but you know, sometimes lyme disease is mistaken for MS and some people actually think that all MS is lyme disease, but really since the same antibiotics work for both diseases, it doesn't really matter. I tested positive for C pn but negative for lyme yet I still got better. How are you doing?

Sarah

Re: RE M.S AND LYME DISEASE

Posted: Sat Jan 10, 2015 1:36 am
by seeva
Thanks Sara for your reply al my ms friends want to do the test and see is they have m.s or LYME disease We are not getting any good treatment from our drs. so we try all the possibility
regards
seeva

Re: RE M.S AND LYME DISEASE

Posted: Sat Jan 10, 2015 8:30 am
by SarahLonglands
Seeva, you seem to have not quite understood what I said: I have never had lyme disease but the antibiotics for C pn are the same as for lyme because they are all broad-based abx which will work for lots of things. I thought that you had started it once, before ccsvi came along, so you obviously didn't do it for long enough. You could always see Dr Thibault and start it again.

Sarah

Re: RE M.S AND LYME DISEASE

Posted: Sun Jan 11, 2015 6:07 am
by seeva
Dear Sarah thanks for the reply yes you are right that once i met dr. Thibault and had the drug few weeks nothing happened so i stop taking
thanks for riming me.
regards
seeva

Re: RE M.S AND LYME DISEASE

Posted: Sun Jan 11, 2015 11:18 am
by SarahLonglands
A few weeks? With this treatment and either of the progressive diseases, you need more time! Do try it again............Sarah

Re: RE M.S AND LYME DISEASE

Posted: Sun Jan 11, 2015 5:46 pm
by seeva
Dear Sarah thanks for your reply. soon I will do the test ELISA for CPN through my GP. and take the antibiotic for the bacterium should i have to do any other test please reply.
where are you living? who is your dr send you for the test? please reply
regards
seeva

Re: RE M.S AND LYME DISEASE

Posted: Mon Jan 12, 2015 7:20 am
by SarahLonglands
Hello Seeva, I live in the UK, not far from London and my doctor is also my husband: David Wheldon. I don't know for certain where I was tested: I think it might have been Southmead Hospital in Bristol.

I responded to the treatment very quickly because my disease was very active at the time. This tends not to happen with people who are just on a slow decline and may take quite a few months before they see any change. One person I know actually took nearly a year before she saw any change, but she was older than most people trying this: I don't know how relevant this is.

What you must realise though, is that you might be able to do no more than stop the progression, but that in itself is worthwhile I think. I did improve far more than simply stopping progression but I can't say for certan why this was: maybe it was just pure bloody-mindedness and determination because I did spend lots of hours trying to use a paintbrush and then throwing away the results. The first improvement both I and everyone else noticed though, was the return of clear thinking and of speech. So do please try the treatment again and let us all know how you are doing.

Sarah

Re: RE M.S AND LYME DISEASE

Posted: Tue Jan 13, 2015 4:56 am
by seeva
HI Sarah thanks for your reply. I will find local dr who can test for CPN. thanks for your help
regards
seeva