Friend with multiple sclerosis

August 12, 2003

Hello everyone. My name's Jeff el. I am tired of slowing

progression trying to stop exacerbations and feeling bad as of

December 29. I made a decision to do my own research into multiple

sclerosis I found out tremendous things and have talked to some good

people , doctors herbalists , and I've read great articles. I

started testing things I read on myself. You can say I am a guinea

pig. The results so far , my fatigue is gone, my multiple sclerosis

pain is gone and I had this for seven years and fatigue also was a

problem. I did research on the blood brain barrier, free radical

damage, and oxidative stress , and I started testing some of the

supplements. Some of the herbs. What results have I had they are

pretty good my doctor is amazed and now I am ready to do the rest.

And I am using doctors , with certain types of knowledge and

herbalists. I am picking their brain. I am not going to be

another statistic. I'm not going into a nursing home before , I am

an old person because I have multiple sclerosis. I am going to fight

back. I do not trust doctors who give us drugs that cause side

effects worse than the problems itself. Some drugs are good , but

are they really necessary , shouldn't we all just ask questions I

have been asking for many years with no answers. They are out there

and I'm going to find it a share, It.

August 12, 2003

Jeff

Like you I was 12 yrs ago diagnosed and was told my MS was because of

my heavy metals. I did as you said all the brain picking and never

used the medicines out there for MS patients.

I removed metals and supplimented what did come out me or is low in my

blood with suppliments.

I even did detox for 6 yrs and watched my diet.

I was totaly well and started working in the country that was

poisioning me but I had to keep up the mercury protocol and keep

visiting my doctors here in US every few months.

Later my medicines were banned by my country and were banned because

MS Association didn't believe in mercury or amalgam or anything to do

with MS.

I got sicker and sicker till my medicines ran out and I was back to bed

in pain and agony but this time much worse and in bed. Where when I

first found out 16yrs ago I needed a wheel chair but did get around.

3 yrs being stuck near the source of my metals and my muscles died and

though i had no pain I couldnt get up to weak to stand to even use a

walker.

Now I am back here brought on an ambulance back with my doctors and

finaly getting some help. But sadly my cells have shut and I can't get

anything in that is needed and what is in is metals. If anything goes

out I get repoisioned and it gets recirculated in my system.

I did carry on with what ever I could back home but it wasn't available.

Now I cant push metals or anything. Don't have any minerals in my body

either and have to put them in by port.

My body doesn't keep it either so I have to do it daily. I have been

here a year trying to find a way to start my old treatment which was

great and worked so well and is now not so much of a weird thing and I

wasn't lynched talking about mercury this time.

I have many doctors on my case as it was very complicated but they are

amazing and will work with herbalists too. Though they are all

doctors, but also believe in alternative as they saw it work with me

for so long.

Now I cant sit on the wheel chair at times like heat, I will fall

flopping off it.

Need to be held all the time or I flop if its hot or humid.

Lucky I dont have muscle pain as I used to but that isn't a good thing

either.

I lost my bones and muscles and then my teeth cause bone won't hold.

Good luck to all of us and I pray you all get the relief I did get many

years ago, for 4 lovely years. Its been 4 yrs since I have been like

this too.

I guess 4 good and four bad balances out. But I am sure going to fight

and will research everything for my doctors too. And we all work

together and have been for 12 yrs. Good luck to you all.

Yes now I am diagnosed with MS but sadly could have avoided it had I

not gone back and got cut off for 3 yrs.

Mira

On Tuesday, Aug 12, 2003, at 12:34 US/Central, Jeff wrote:

> Hello everyone. My name's Jeff el. I am tired of slowing

> progression trying to stop exacerbations and feeling bad as of

> December 29. I made a decision to do my own research into multiple

> sclerosis I found out tremendous things and have talked to some good

> people , doctors herbalists , and I've read great articles. I

> started testing things I read on myself. You can say I am a guinea

> pig. The results so far , my fatigue is gone, my multiple sclerosis

> pain is gone and I had this for seven years and fatigue also was a

> problem. I did research on the blood brain barrier, free radical

> damage, and oxidative stress , and I started testing some of the

> supplements. Some of the herbs. What results have I had they are

> pretty good my doctor is amazed and now I am ready to do the rest.

> And I am using doctors , with certain types of knowledge and

> herbalists. I am picking their brain. I am not going to be

> another statistic. I'm not going into a nursing home before , I am

> an old person because I have multiple sclerosis. I am going to fight

> back. I do not trust doctors who give us drugs that cause side

> effects worse than the problems itself. Some drugs are good , but

> are they really necessary , shouldn't we all just ask questions I

> have been asking for many years with no answers. They are out there

> and I'm going to find it a share, It.

>

August 13, 2003

I agree with you wholeheartly Jeff. It took me a while cause I have had

this disease for 26 years but I am at the point that you are now. there are

ways of making yourself better. First, you need all the knowledge that you

can get your hands on. I have no education in the medical profession, so it

is hard for me but I do know my body and know that it doesn't want those

awful drugs. So I am fighting for my life. and you know what my body is

responding. It's slow but faster than I thought that it would be.

Keep me posted on how you are doing, I am very interested.

Marie

----- Original Message -----

From: " Jeff " <jeffalan19556@...>

Sent: Tuesday, August 12, 2003 1:34 PM

Subject: [low dose naltrexone] Friend with multiple sclerosis