Wow Nancy! how inspired I am, is that all true?
Well it is the start of a huge experiment, I would love to walk the paths with Dave again, that is a truely amazing story unbeievable actually. I love that. Thanks so much for cheering me up. Please God help us here, we are so wanting to walk the paths again. I am overwhealmed ...
Luv Marie.![]()
>From: "nancymike" <
[email protected]>
>Reply-To:
[email protected]
>To: <
[email protected]>
>Subject: Re: CS>MS sufferer
>Date: Sat, 24 Apr 2004 00:24:53 -0500
>
>Hi Marie,
>Horay for yu and your husband,
> I cured my MS with CS. The main cautions with this is that it is NOT AN INSTANT cure. Obviously you husband has had tis for a long time. It will take some time to get better. The thing is that he will be getting better while not feeling uch of anything. The CS kills the MS virus, but it takes awhile for the myelin in that area to begin to heal. The other caution is that also, as the virus dies, it will aggrivate the nerves in the area surrounding it. There were times I thought I was having an exacerbation, BUT instead the virus was dying, but not wthout a fight. I call these "healing crisis". Some of them lasted a few hours, or a few days, or even a few weeks. But, after it was over, I never had that symptom again. and shortly after that I got oe of my lost feelings or ability back. Perhaps somethng was no longer numb, or my hearing improved, or I was able to walk long distances which I could definately not do before. Obviously all MS victims are different, but no matter how bad it may get, do not give up. It will absolutely get better.
> I would slowly wean him off all the medications, however, remember this is a slow process so don't stop everything at one time. For example, he will probably continue to get spasms for a time, but they will be fewer, and fewer as time goes by. REMEMBER, he will get slowly better, which is much better than getting slowly worse.
> If you have any more questions contact me off list at
[email protected].
> When I first started the CS, I could baely walk, and I could not step up on step without help. It took me forever just to turn over in bed. When I got out of bed in the am, I had to wait for the spasms to stop justso I could take a step. It was about 2 years later, but I could get around great, and now 3 1/2 years later I went hiking in the tropical rain forest just a few weeks ago, also went white water rafting, and flying through the tree tops with the monkeys. I am 60 years old and enjoying a life I thought I would never have. I am better than I was 20 years ago. The most implrtant thing is patience.
>Nancy DeLise
>PS: I recently had my last 4 MRI's checked and compared and my MS lesions are getting smaller!!!
> ----- Original Message -----
> From: Marie Hofman
> To:
[email protected]
> Sent: Thursday, April 22, 2004 3:49 AM
> Subject: CS>MS sufferer
>
>
> Hi it's Marie ... I posted for the first time one week ago about my husband who is paralized with MS and I have him on CS ... oh yes I do and I will not stop. I have already seen results, the first of which I have ever seen in his devilish disease, please can anybody help me with withdrawing from Prozac. He takes Fluox and this week I stopped one (of his two) daily pills, he is feeling pain down the right side, I will not stop taking him off this terrifying drug but will do it slowly. I need to know what you guys think about it, the doctors will hate it, but he needs them out of his system. Any answers. Thanks so much. xxxxxx luv me.
>
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