Re: good ccsvi video (another one)

[Guest guest]

You may not have seen this video put out by Ameds in Poland -

It was exactly like that.

It is 9 weeks since my treatment today and whilst I am still in my wheelchair

EVERYTHING else has returned 100% apart from incontinence which is fine most of

the tiime but I do still have the odd panic and I still have cold feet. I am

walking a few yards with my walker every day and balance is still not there.

People without MS would then wonder what on earth I was so ecstatic about.

Slurred speech, blurred vision, headaches, neck ache, (everything ache),

tinnitis, neuralgia, ON, dizziness.............. and that's just the head - get

the picture - it has all gone!

I have just had the best Christmas in over 15 years, being able to decorate the

tree without wondering what was going on every 2 seconds, wrapping up gifts

without getting the sellotape stuck to itself or me, writing labels not only

legibly but elegantly, and remembering what I'd put in each parcel.

, stick to your guns and continue refusing all the mainstream drugs - they

do more harm than good. Sorry I can't help on LDN - never took it.

Janet

To: mscured

From: sonia_butterfly@...

Date: Mon, 27 Dec 2010 18:59:46 +0000

Subject: good ccsvi video

Hi guys, I thought I would share this video with you, it summarizes everything

about the liberation treatment. Here in Czech Republic, they dont approve of

this procedure, or maybe some doc does but I havent found out yet.

_http://watch.ctv.ca/news/w5/the-liberation-treatment/#clip237617_

(http://watch.ctv.ca/news/w5/the-liberation-treatment/#clip237617)

And now a bit update on my ms relapse/lyme struggle.

I'm in remission since 21st Oct 2010, MRI has shown a big lesion between C 4 - 5

in the spinal cord and after a few weeks of getting better, symptoms came back

16th Dec. I have been on avonex since sept 2009 and now the doc gives me choice

between rebif and tysabri which both feel like a nightmare. I have stiff hands,

sore feet and unsensitivity issues with my belly. Tomorrow the doc is gonna

offer me steroids which I dont believe in aynmore. So there is this final step

of mine, going my own way and not doing what doc says, or trying these horrible

drugs. I havent had my take with LDN - Revia its called over here - yet, and I

would like to hear some of your insight. And yes Dudley, I am familiar with your

links, I just want some REAL advice.

Thanks a lot

[Guest guest]

Great site. I'm glad you're doing so well.

>

>

> You may not have seen this video put out by Ameds in Poland -

>

> It was exactly like that.

>

> It is 9 weeks since my treatment today and whilst I am still in my wheelchair

EVERYTHING else has returned 100%

[Guest guest]

>

> ,

>

I take LDN and it's been a miracle for me. I still have to stick to BBD and

avoid anything artificial, but on a typical day, I have few, if any

symptoms. Before LDN I had ON, no balance, no feeling in my left leg, brain

fog was horrible, I stuttered and slurred my speech badly enough that my own

children could barely understand me, couldn't drive, and was in constant

pain.

Since LDN, I have mild symptoms if eat something I shouldn't. I don't take

anything else, (except supplements) and I've never taken standard ms drugs.

I have SPMS and progression has stopped.

Yvette

>

> To: mscured

> From: sonia_butterfly@...

> Date: Mon, 27 Dec 2010 18:59:46 +0000

> Subject: good ccsvi video

>

>

>

>

>

>

> H So there is this final step of mine, going my own way and not doing what

> doc says, or trying these horrible drugs. I havent had my take with LDN -

> Revia its called over here - yet, and I would like to hear some of your

> insight. And yes Dudley, I am familiar with your links, I just want some

> REAL advice.

>

> Thanks a lot

>

>

>

>

>

>