Re: Was CFS or Heaptitis C Discussed atLDN Conference?

[Guest guest]

One of the

responses to CFS:

Do you have a

naturopath or a chiropractor in your area that practices kinesiology? If so,

you need to be tested for fungus and molds. You also need to be tested

for amino acids as when these are out of balance, CFS is a common thing.

It is treatable, but allopathic medicine practitioners are poorly equipped

and/or do not care to deal with it.

What are you doing

for your Lyme and MS? Part of what controls these is also part of what

will deal with CFS.

If you want to

invest in a phone call, give Tom Lahey a call. 949 492-6642 Tom is a chemist who has worked with MS for a

number of years. He also treats lyme. I deal only with terminal

cancer, but run into these other items all the time. Their offices are in

San Clemente, California, 3 hours behind eastern time.

Bruce Guilmette, Ph.D.

Survive Cancer Foundation, Inc.

http://www.survivecancer.net

From: low dose naltrexone [mailto:low dose naltrexone ] On Behalf Of cmrichards@...

Sent: Friday, July 15, 2005 7:53

PM

low dose naltrexone

Subject: Re: [low dose naltrexone]

Was CFS or Heaptitis C Discussed atLDN Conference?

No, this man has never heard of CFS. He asked me what it was.

I also have a family doctor, only for normal

things as he doesn't have a

clue. I was originally going to give him

immune, mycoplasma and other

oddities and his comment was he didn't want these

things as he knew

nothing about them. This is in Vero Beach.

I had a friend who was going to an infectious

disease doctor and he

stopped his practice to research AIDS. My

friend went to a doctor and

had told him she had CFS. When she started

having afternoon fevers he

told her to throw away her thermometer. Less

than a month later she was

dying from Non hodgkins lymphoma. The man

never took her seriously,

like many doctors concerning CFS. Most write

it in their notes and

never mention it again.

[Guest guest]

I know this wonderful alternative doctor in Sebastian!!! Isn't that close to you? He is so informed and caring . I can call my dentist and find out his name if you are interested. I went to him years ago for a chelation consult. Kathy

Re: [low dose naltrexone] Was CFS or Heaptitis C Discussed atLDN Conference?

No, this man has never heard of CFS. He asked me what it was.I also have a family doctor, only for normal things as he doesn't have aclue. I was originally going to give him immune, mycoplasma and otheroddities and his comment was he didn't want these things as he knewnothing about them. This is in Vero Beach.I had a friend who was going to an infectious disease doctor and hestopped his practice to research AIDS. My friend went to a doctor andhad told him she had CFS. When she started having afternoon fevers hetold her to throw away her thermometer. Less than a month later she wasdying from Non hodgkins lymphoma. The man never took her seriously,like many doctors concerning CFS. Most write it in their notes andnever mention it again.

[Guest guest]

Bruce,

I do have mold problems. Last years hurricanes to care of my carpets so

will replace with tile. I also had food sensitivites to 43 of 90

tested. I ran a search on food sensitivities and MS and found a group

there. Most were the normal things milk poducts, eggs, grains but beans

were a surprise to me. I show sensitivities to beans including green

beans.

Also all grains except oatmeal, even rice and soy.

Of course if the immune syster is depressed cancer can be a problem.

Mother died of breast cancer and dad of lung cancer. My father was an

alcholic. I met a friend in FL. from NC through a support group and she

has a CFS diagnoses. Her mother died of breast cancer, her father of

lung cancer and he was also an alcholic. She recently was diagnosed

with Mycobacteium Avium Complex. I mentioned another friend with CFS

diagnoses who died of Non hodgkins lymphoma in another post.

CFS is inteesting as most of the research is done by the little people

as opposed to big business. One researcher Kenny DeMehlier applied for

a patent on beta lactase antibiotics for all autoimmune disorders. They

supposedly

work on inflamation. Saw a recent study on minocycline with samo on

inflamation, an earlier one on doxy. Kenny DeMehlier and his testing of

an antiviral pathway says MS and CFS are somehow on the far ends of the

spectrum. I am not a medical person, just a parrot. FYI

When I went to an infectious disease doc. & he would do testing, but

without extensive travel cannot get anything other than normal done

anymore.

ME

[Guest guest]

You may be speaking of Dr. Ahner, pronounced like honor. He has treated

CFS and believes in it but no one I know has gotten well or that much

better.

[Guest guest]

" Dr Kenny DeMehlier and his testing ofan antiviral pathway says MS

and CFS are somehow on the far ends of the spectrum "

He has publicly said that CFS and MS, for which he has a patent are

basically 2 diseases that are on the oppoisite sides of the spectrum

due to a low molecular weight antiviral product called RnaseL which

has been implicated in CFS, and for which the drug Ampligen in its

final approval phase for CFS, treats. How different outcomes ouccur

between MS and CFS is unknown though there are some important

overlaps especially EBV, and HHV6 or CMV which will probably somehow

in the future be implicated in both and other diseases.

> Bruce,

> I do have mold problems. Last years hurricanes to care of my

carpets so

> will replace with tile. I also had food sensitivites to 43 of 90

> tested. I ran a search on food sensitivities and MS and found a

group

> there. Most were the normal things milk poducts, eggs, grains but

beans

> were a surprise to me. I show sensitivities to beans including

green

> beans.

> Also all grains except oatmeal, even rice and soy.

>

> Of course if the immune syster is depressed cancer can be a

problem.

> Mother died of breast cancer and dad of lung cancer. My father

was an

> alcholic. I met a friend in FL. from NC through a support group

and she

> has a CFS diagnoses. Her mother died of breast cancer, her father

of

> lung cancer and he was also an alcholic. She recently was

diagnosed

> with Mycobacteium Avium Complex. I mentioned another friend with

CFS

> diagnoses who died of Non hodgkins lymphoma in another post.

>

> CFS is inteesting as most of the research is done by the little

people

> as opposed to big business. One researcher Kenny DeMehlier

applied for

> a patent on beta lactase antibiotics for all autoimmune

disorders. They

> supposedly

> work on inflamation. Saw a recent study on minocycline with samo

on

> inflamation, an earlier one on doxy. Kenny DeMehlier and his

testing of

> an antiviral pathway says MS and CFS are somehow on the far ends

of the

> spectrum. I am not a medical person, just a parrot. FYI

>

> When I went to an infectious disease doc. & he would do testing,

but

> without extensive travel cannot get anything other than normal done

> anymore.

>

> ME

[Guest guest]

Ampligen is an alpha interferon inducer. It has been found to down

regulate the 2-5A R-Nase L antiviral pathway but I believe it

upregulates or somehow effects the PKR pathway which is bad for CFS. Of

course the company making Ampligen (Hemispherix Biopharm-something like

that) does not reveal that fact. Ampligen was also being tested on

Hepatitis C.