ALS

[Guest guest]

In Tuesday's Hartford Courant newspaper there was a short mention of new ALS

research findings:

Virus Found In ALS Victims

Scientists have identified a virus in the spinal-cord tissue of people who

died of amyotrophic lateral sclerosis, known as ALS and Lou Gehrig's disease,

providing evidence that the baffling and lethal motor-neuron disease could be

caused by an infection.

A viral theory of ALS has been around for decades but never proved. If

confirmed, the finding could have major implications for treatment. There

are 30,000 Americans living with the disease, which destroys neurons that

control movement.

[Guest guest]

SUSYDOG,

Thanks for the references. I appreciate that you have all these resources!

Barb

> Did the article in the Hartford Courant identify the virus?

<A HREF= " http://www.intelihealth.com/IH/ihtIH/EMIHC000/333/333/262140.html " >

I

nteliHealth : Health News</A>

http://www.intelihealth.com/IH/ihtIH/EMIHC000/333/333/262140.html

Virus Found In People With Lou Gehrig's Disease

January 11, 2000

Medical Tribune

A research team has discovered a virus in the spinal cords of victims of

amyotrophic lateral sclerosis (ALS), a fatal nervous system disorder also

known as Lou Gehrig's Disease.

Researchers at University of California, Irvine College of Medicine

(www.uci.edu) and at the Rockefeller University in Lyon, France, found that

15 of 17 victims of ALS showed evidence of a virus in the motor nerve cells

of their spinal cords. The virus was found in only one of 29 people who died

of other causes. The virus found is similar to Echovirus-7, an infectious

agent known to cause meningitis and rare cases of encephalitis.

The findings, which appear in the January issue of Neurology

(www.neurology.org) <A HREF= " http://www.neurology.org/ " >The American Academy

of Neurology</A> , provide the best evidence to date of a possible viral

cause of the disease and could result in new treatments for the disorder.

>>

[Guest guest]

I guess I will have to telephone and send for a copy, many thanks.

Did you have any luck on other paramedic online courses, that we both looked

into earlier, prior to my PC crashing. The Aussie one was a dead end.

JC

[] Re: ALS

>

> Re: [] More Welcomes !

>

>

>> No wonder I could not get them.

>

>

>I tried the web site today and got the same result ( other folks got the

>same)

>I have seen the new (?) training syllabus. Not a great deal new in it but

>worth a look all the same.

>

>Cheers

>Rod Eglin

>

>

>

>

>

>

[Guest guest]

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

From: JOHN CARPENTER <JOHN.CARPENTER.SNR@...>

> I guess I will have to telephone and send for a copy, many thanks.

> Did you have any luck on other paramedic online courses, that we both

looked

> into earlier, prior to my PC crashing. The Aussie one was a dead end.

> JC

> -----Original Message-----

> From: Rod Eglin <rodegg@...>

Nope. Not much info I'm afraid.

That Aussie one cost a lot and was no good unless you lived in Aussie land.

It's a bit like the UK isn't it!

A load of dingo's kidneys.

Take care

Rod

[Guest guest]

ALS

> To All,

> This may seem like a silly question but has anyone vaccinated from 1998

> been diagnosed with this illness? One more question. I have a problem

with

> the fluid in my left eye that is causing it to thicken. This causes dark

> spots in the fluid that resemble dirt on a lens and is quite annoying. has

> anyone else been experiencing this problem?

>

> V/R

> Bob

>

> Bob,

The study below was just released recently saying GWV's are twice as likely

to ge ALS as those that did not go to the Gulf.

Jim Rarey

DAV Praises VA Action for Persian Gulf Veterans with ALS

WASHINGTON-The Disabled American Veterans (DAV) is applauding the action

taken today by the Department of Veterans Affairs (VA) to grant immediate

service connection for Persian Gulf War veterans who suffer from amyotrophic

lateral sclerosis (ALS). Secretary of Veterans Affairs J.

Principi announced the unusual action citing the results of a new VA and

Department of Defense (DoD) study which found preliminary evidence that

veterans who served in Operation Desert Shield-Desert Storm are nearly twice

as likely as their non-deployed counterparts to develop ALS. Commonly

called

Lou Gehrig's Disease, ALS is a fatal neurological disease that destroys the

nerve cells that control muscle movement. Neither a cause nor an effective

treatment for ALS is known. " The DAV is pleased that Secretary

Principi acted swiftly to aid Gulf War veterans suffering from ALS, their

families, and their survivors, " said DAV National Commander H.

Steese,

Jr. " The decision to immediately grant presumptive service connection also

means that Gulf War veterans suffering from ALS can get immediate medical

treatment and care from the VA and that their families will be cared for. "

The Secretary's action covers members of the armed services who

deployed

to Southwest Asia from Aug. 2, 1990 through July 31, 1991. Southwest Asia

includes the countries of Oman, the United Arab Emirates, Bahrain, and other

nations in addition to Iraq and Saudi Arabia. The joint VA-DoD study, which

began in March 2000, involved nearly 700,000 service members deployed during

the Gulf War and 1.8 million who did not deploy during the designated

period.

It found 40 cases of ALS among deployed veterans, a statistically

significant greater number than would be normal. " We will compensate

veterans with ALS and their survivors, and we will do so quickly, " Secretary

Principi said. " We are giving compensation now because of the fatal nature

of the disease. Veterans need help now and they will get it. " " The

DAV is ready to lend assistance to Gulf War veterans and their families who

believe they may be eligible for compensation, " Commander Steese said.

" They

should contact their nearest DAV National Service Office. " The

Disabled American Veterans is a non-profit organization founded in 1920 and

chartered by the U.S. Congress in 1932. It is dedicated to one, single

purpose: building better lives for our nation's 2.3 million disabled

veterans

and their families. ###

[Guest guest]

Jim,

I read that. My question is if any non-deployed Vets vaccinated with the

questionable lots of Anthrax have become ill with this disease? In my

situation, I deployed to the Gulf in 1998 for Operation Southern Watch and

was vaccinated with three shots from Lot FAV020. I was not in the Gulf War

per se but fall under the Umbrella clause since I deployed to that region. I

now have GWS symptoms and have completed the Persian Gulf physical. Others

I know personally, did not deploy and are having similar problems.

V/R

Bob

Date: Fri, 14 Dec 2001 01:31:07 -0500

From: " Jim Rarey " <jimrarey@...>

Subject: Re: ALS

ALS

> To All,

> This may seem like a silly question but has anyone vaccinated from 1998

> been diagnosed with this illness? One more question. I have a problem

with

> the fluid in my left eye that is causing it to thicken. This causes dark

> spots in the fluid that resemble dirt on a lens and is quite annoying. has

> anyone else been experiencing this problem?

>

> V/R

> Bob

>

> Bob,

The study below was just released recently saying GWV's are twice as likely

to ge ALS as those that did not go to the Gulf.

Jim Rarey

DAV Praises VA Action for Persian Gulf Veterans with ALS

WASHINGTON-The Disabled American Veterans (DAV) is applauding the action

taken today by the Department of Veterans Affairs (VA) to grant immediate

service connection for Persian Gulf War veterans who suffer from amyotrophic

lateral sclerosis (ALS). Secretary of Veterans Affairs J.

Principi announced the unusual action citing the results of a new VA and

Department of Defense (DoD) study which found preliminary evidence that

veterans who served in Operation Desert Shield-Desert Storm are nearly twice

as likely as their non-deployed counterparts to develop ALS. Commonly

called

Lou Gehrig's Disease, ALS is a fatal neurological disease that destroys the

nerve cells that control muscle movement. Neither a cause nor an effective

treatment for ALS is known. " The DAV is pleased that Secretary

Principi acted swiftly to aid Gulf War veterans suffering from ALS, their

families, and their survivors, " said DAV National Commander H.

Steese,

Jr. " The decision to immediately grant presumptive service connection also

means that Gulf War veterans suffering from ALS can get immediate medical

treatment and care from the VA and that their families will be cared for. "

The Secretary's action covers members of the armed services who

deployed

to Southwest Asia from Aug. 2, 1990 through July 31, 1991. Southwest Asia

includes the countries of Oman, the United Arab Emirates, Bahrain, and other

nations in addition to Iraq and Saudi Arabia. The joint VA-DoD study, which

began in March 2000, involved nearly 700,000 service members deployed during

the Gulf War and 1.8 million who did not deploy during the designated

period.

It found 40 cases of ALS among deployed veterans, a statistically

significant greater number than would be normal. " We will compensate

veterans with ALS and their survivors, and we will do so quickly, " Secretary

Principi said. " We are giving compensation now because of the fatal nature

of the disease. Veterans need help now and they will get it. " " The

DAV is ready to lend assistance to Gulf War veterans and their families who

believe they may be eligible for compensation, " Commander Steese said.

" They

should contact their nearest DAV National Service Office. " The

Disabled American Veterans is a non-profit organization founded in 1920 and

chartered by the U.S. Congress in 1932. It is dedicated to one, single

purpose: building better lives for our nation's 2.3 million disabled

veterans

and their families. ###

[Guest guest]

> Anyone know any information on ALS, misdiagnosis, or

> cause, or alternative treatment, I have a client coming

> in diagnosed with ALS and wonder what else can be done,

> cause basically it isn't pretty what is ahead if he goes

> medical.

> thank you

> Antonia

um, actually, I suspect there is a connection to mercury

poisoning, or maybe other metals. I'd certainly get a

hair test done.

autism/files/HOW_TO_hair_test

best,

Moria

[Guest guest]

One source said Branched Chain Amino Acids helped 85% of sufferers with it.

That would be 12 grams leucine, 8 grams isoleucine, and 6.4 grams of valine

per day.

Threeonine is supposed to reduce symptoms too.

Also Phosphatidylcholine and vitamin E with B1 is supposed to improve

symptoms

with 95% success.

--- from Hyperhealth v98.1

jp

>

> > Anyone know any information on ALS, misdiagnosis, or

> > cause, or alternative treatment, I have a client coming

> > in diagnosed with ALS and wonder what else can be done,

> > cause basically it isn't pretty what is ahead if he goes

> > medical.

> > thank you

> > Antonia

[Guest guest]

There'a an ALS protocol at www.lef.org that I could recommend for

any neurodegenerative disorder.

Duncan Crow

>

> Anyone know any information on ALS, misdiagnosis, or

> cause, or alternative treatment, I have a client coming

> in diagnosed with ALS and wonder what else can be done,

> cause basically it isn't pretty what is ahead if he goes

> medical.

> thank you

> Antonia

> --

> Antonia

> Breakthrough Coaching

> http://www.Body-dynamics.com

> 920-868-9599

[Guest guest]

Antonia Go to Mercola.com and research. Nice web site

Dwight Munson

ALS

Anyone know any information on ALS, misdiagnosis, or

cause, or alternative treatment, I have a client coming

in diagnosed with ALS and wonder what else can be done,

cause basically it isn't pretty what is ahead if he goes

medical.

thank you

Antonia

--

Antonia

Breakthrough Coaching

http://www.Body-dynamics.com

920-868-9599

[Guest guest]

dear naturegirl,

i haven´t posted anything into the group for months now, i think.

but i have been very busy researching on the intestines.

i have come to the conclusion, that people, who suffer from allergies and

most important: from auto-immune diseases have a chronic inflammation.

where??? in the small intestine. as a consequence you suffer from leaky gut

syndrome, which means, that any food can be toxic for you.

the partly undigested proteins pass the intestinal wall, and that´s where

most immune cells are to be found. our intestines are the largest area of

our bodies, that is exposed to the " outside " , which means, there MUST be

most of our immune cells.

so, as soon as such a protein passes the leaky intestinal wall of the small

intestine, it contacts with an immune cell forming an

antibody-antigen-complex. this is the so-called food intolerance. not to be

mixed up with allergy reaction.

we have two different kinds of cells there: the mucous producing cells,

which produce more and more mucous in order to protect the blood from toxic

products, and the epithelial cells, who absorb nutrients into the blood

stream.

if you eat toxic food for years, you will begin to suffer from heavy

disease.

so, many people, especially the chronically ill, suffer from a subclinical

morbus crohn.

but: where´s the exit? i asked myself.

i have come across some doctor´s works about crohn´s disease. an alternative

approach to crohn´s disease is the treatment with high dosage l-glutamine.

why? l-glutamine is needed in large quantities by fast growing cells.

(that´s why it is given in cases of chemotherapy, where fast growing cells,

no matter if good or " bad " , are being killed)the epithelial cells of the

mucosa in the small intestine live only around three days. what we see as

bowel movement in the toilet, is largely made up by dead intestinal cells

from the small intestine. only a little part of our poo-poo is actually made

up by food remainders.

okay, so l-glutamine seems to be the answer.

sportspeople are told to take large quantities, in order to grow lean muscle

mass, not because they need these large amounts for the muscles, but because

the small intestines munges most of it away, before the muscles can get hold

of it.

we are talking about 30 - 40 grams per day here.

in order to repair the intestinal walls, we need between 20 and 30 grams per

day.

best taken along with omega 3 fatty acids, vitamins a,e,d and the b-complex.

for all, who are concerned: give this a try!!! and give me feedback.

(rheumatism, ms, als, lupus, crohn, autism, allergies......)

i think, i have found a major key for healing here.

of course, it makes sense to cleanse the guts first. i have also worked out

an intestinal cleanse, but the entire booklet is written in german. :-(

i am aware, that all of the above mentioned diseases come along with a wide

range of other things like fungi, metals, sugar regulation disorders, etc.

but the key really seems to be the chronic inflammation and porosity of the

small intestines.

mind you: the much talked about bowel flora is mostly only to be found in

the large intestine, but the actual metabolism happens in the small

intestine.

i would be very happy about your oppinion.

love and greetings

marlene

ALS

Hi All,

When performing a treatment on myself, ALS came up 3rd on the test

matrix in red. WHile I have had muscles spasms for the last 10

months it was thought to be viral induced benign fascitis syndrome.

I do not have muscle weakness at all, no visual, CNS, speech,

balance involvement. In fact I feel the best I have in a long time.

MS was ruled out long ago. I did the virtual doctor thing too. I

realize the power of the QXCI and how the technician must be a

competent interpreter of the results. I am seeking some input from

more experienced practitioners than I. Could this be my unconscious

fear of a fatal disease?

Thx-J

.............................................

[Guest guest]

Interestingly enough, several of the Rife frequencies for ALS is the

same for Lyme's disease and MS. I do believe that fear of ALS can

well bring it up on the test screen. I would also do the Emotional

Freedom Technique to overcome this fear; it works (search on the Web).

Craig has given Dr. Callahan's work to the world free of

charge much to the dismay of RC. You can also search ATTRACTOR FIELD

THERAPY for free protocols for nearly every illness tho ALS is one of

those that you have to call in about but you'll get the points to tap

within 24 hours via e mail from Dr. Kurt Ebert.

I trust you're doing the Individual Reaction for the entry? Does it

keep coming up over and over again? Best not to get too concerned if

you see it one time or even twice. Our minds can create mountains out

of ant hills. is Rotella M.Ac., Arnold, Md.

> Hi All,

> When performing a treatment on myself, ALS came up 3rd on the test

> matrix in red. WHile I have had muscles spasms for the last 10

> months it was thought to be viral induced benign fascitis syndrome.

> I do not have muscle weakness at all, no visual, CNS, speech,

> balance involvement. In fact I feel the best I have in a long time.

> MS was ruled out long ago. I did the virtual doctor thing too. I

> realize the power of the QXCI and how the technician must be a

> competent interpreter of the results. I am seeking some input from

> more experienced practitioners than I. Could this be my unconscious

> fear of a fatal disease?

> Thx-J

[Guest guest]

Do the 9-day intensive on the welcome page, with friends if possible.

http://www.immunics.org/index.html

At 09:42 AM 8/29/2005 -0700, you wrote:

>Hello Bayard,

>

>My sister has ALS, Lou Gerigs Disease, in an advanced stage. How could I

>possibly help her?

>

>Tordin

[Guest guest]

Would she be receptive to " experimentation " with Godzilla? It sure won't

hurt anything and who knows it might just be her " Miracle " .

Jack

ALS

Has anybody had any dealings with ALS (Lou Gherig's disease). The wife of a

friend of mine has been diagnosed with it.

She is having trouble with her throat - difficulty swallowing and talking.

Bernie

The group's main page has a menu to the left, with photos of Godzilla

devices and info. This is a discussion, free speech forum, not medical

advice. All info is free to members. Membership is free, but by joing, you

agree to hold harmless the posters, including moderator, from damages from

anything you find here whether jointly, severally, or individually. We are

interested in your results, but cannot say anything about repeatability, or

whether this might have medical benefits. Thanks, for your understanding,

good luck researching. --bG

[Guest guest]

I tried to start them out with a simple zapper, but I don't think she's even

tried that. Scared I guess. I'd really like to get her using a godzilla, or

a BE, or even a BT, which might be the most appropriate device, if the

problem lies in the brain. Her main problems are a lot of trouble swallowing

and talking. WHere would you place the electrodes?

I don't actually know her, but I've become friends with her husband.

Bernie Heere

From:

[mailto: ]On Behalf Of JACK

MILLIORN

Sent: Saturday, May 13, 2006 11:05 AM

Subject: Re: ALS

Would she be receptive to " experimentation " with Godzilla? It sure won't

hurt anything and who knows it might just be her " Miracle " .

Jack

ALS

Has anybody had any dealings with ALS (Lou Gherig's disease). The wife of

a

friend of mine has been diagnosed with it.

She is having trouble with her throat - difficulty swallowing and talking.

Bernie

The group's main page has a menu to the left, with photos of Godzilla

devices and info. This is a discussion, free speech forum, not medical

advice. All info is free to members. Membership is free, but by joing,

you

agree to hold harmless the posters, including moderator, from damages from

anything you find here whether jointly, severally, or individually. We

are

interested in your results, but cannot say anything about repeatability,

or

whether this might have medical benefits. Thanks, for your understanding,

good luck researching. --bG

[Guest guest]

Hi Jack,

Where would you place the electrodes.

The notion that ALS is actually Lymes disease makes me think that the salt/c

protocol might work as well. Or was that discussion on a different forum?

Bernie

Re: ALS

Would she be receptive to " experimentation " with Godzilla? It sure

won't

hurt anything and who knows it might just be her " Miracle " .

Jack

ALS

Has anybody had any dealings with ALS (Lou Gherig's disease). The wife

of

a

friend of mine has been diagnosed with it.

She is having trouble with her throat - difficulty swallowing and

talking.

Bernie

The group's main page has a menu to the left, with photos of Godzilla

devices and info. This is a discussion, free speech forum, not medical

advice. All info is free to members. Membership is free, but by joing,

you

agree to hold harmless the posters, including moderator, from damages

from

anything you find here whether jointly, severally, or individually. We

are

interested in your results, but cannot say anything about repeatability,

or

whether this might have medical benefits. Thanks, for your

understanding,

good luck researching. --bG

[Guest guest]

I would do a blood electrification then follow the protocol that Donna

outlines. I would do the blood electrification daily or several times a

day. It seems to me this ALS thing needs some intensive treatment.

Jack

ALS

Has anybody had any dealings with ALS (Lou Gherig's disease). The wife

of

a

friend of mine has been diagnosed with it.

She is having trouble with her throat - difficulty swallowing and

talking.

Bernie

The group's main page has a menu to the left, with photos of Godzilla

devices and info. This is a discussion, free speech forum, not medical

advice. All info is free to members. Membership is free, but by joing,

you

agree to hold harmless the posters, including moderator, from damages

from

anything you find here whether jointly, severally, or individually. We

are

interested in your results, but cannot say anything about repeatability,

or

whether this might have medical benefits. Thanks, for your

understanding,

good luck researching. --bG

[Guest guest]

What it means?

What next?

Bernie Heere wrote:

>

> I don't actually know her, but I've become friends with her husband.

> Bernie Heere

>

>

[Guest guest]

>It seems to me this ALS thing needs some intensive treatment.<

My aunt was dead in 3 months after being diagnosed with it, but she had a

lifelong history of many problems, including diabetes and being terribly

obese. DB

[Guest guest]

Hi Gail

I am sorry to hear of your diagnosis.

A long time ago I had a friend who got the same diagnosis. She was very quiet about it and so had less support than I hope you will have.

She didn't tell me much about what was happening, so I can't share as much as I wish I could with you. She went to only one ALS support group meeting too.

I think you are doing the most beneficial thing, looking for what is available.

There was a homeopath in Germany (?) who had had some success with ALS, I think the name is Timmerman. Alize maybe. He/she was willing to work with local homeopaths at that time.

Are you going to keep a journal of what happens for you, how it feels etc, both for yourself and perhaps also for others who may face what you are facing now?

Hope you also have some good help and support available where you are. What service does that clinic give? Do you like the practioners there? etc.

I need to get to bed now -- there's a conference on M.S. tomorrow morning (have to miss church unfortunately) -- want to see whether I like the new neurologist in my area.

Take good care! and keep finding good thoughts,

Jean

ALS

Does anyone in this group have ALS or care for someone with ALS?I'm just diagnosed, beginning at ALS clinic in Phoenix AZ. Would like to hear from anyone dealing with this.Gail

[Guest guest]

Hi Jean

Thanks for your kind words and thoughts.

I am vocal about what's going on with me. I have aloving family and

a deep circle of caring friends. I just started to think about

keeping a journal, something I have not done since I was a teenager,

but I think it could put some perspective on things. I'm still

working. I am a senior research technician for US Dept of

Agriculture. I have looked into a disability retirement but the

govt. must accomodate me before it will allow my to retire, something

I don't really want to do anyway as I love my job.

I really liked the neurologist who diagnosed me and I have been

referred to two other neurologists in town for the 2nd and third

opinions (required to get into the clinic). The clinic is supposed

to be full service but I don't go there until next week. Meanwhile I

am reading as much as I can online about this. But today, the most

important thing will be hugging my two young grandaughters. That's

the best medicine in the world.

Take care, Jean

Gail

disease. , " gettingthere35 "

<gettingthere35@...> wrote:

>

> Hi Gail

> I am sorry to hear of your diagnosis.

> A long time ago I had a friend who got the same diagnosis. She was

very quiet about it and so had less support than I hope you will have.

> She didn't tell me much about what was happening, so I can't share

as much as I wish I could with you. She went to only one ALS support

group meeting too.

> I think you are doing the most beneficial thing, looking for what

is available.

> There was a homeopath in Germany (?) who had had some success with

ALS, I think the name is Timmerman. Alize maybe. He/she was

willing to work with local homeopaths at that time.

>

> Are you going to keep a journal of what happens for you, how it

feels etc, both for yourself and perhaps also for others who may face

what you are facing now?

>

> Hope you also have some good help and support available where you

are. What service does that clinic give? Do you like the practioners

there? etc.

>

> I need to get to bed now -- there's a conference on M.S. tomorrow

morning (have to miss church unfortunately) -- want to see whether I

like the new neurologist in my area.

> Take good care! and keep finding good thoughts,

> Jean

>

> ALS

>

>

> Does anyone in this group have ALS or care for someone with ALS?

> I'm just diagnosed, beginning at ALS clinic in Phoenix AZ. Would

like

> to hear from anyone dealing with this.

> Gail

>

[Guest guest]

Hi Gail -- I'm sending MUCH love and energy to you!!

Just got back from that M.S. conference, and know that the neurologist who spoke is probably NOT a one for me, though local (good to know!)

Besides they had lots of freebies! - a great breakfast, a timer, an overtheshoulder bag and pens and hiliters! plus a chance, of course, to talk with others in their 'journey'

and it was great that the speaker and also the MS nurses went to each table for our individual concerns.... I did get some good help too.

More and more as life goes on, I see how very lucky I have been, despite being 'disabled' nearly fifty years....

I am EVER so glad to hear that you have a wide circle of support!!! That will mean so very much to you in the coming years. And probably some who want to help now, will give way to others who prefer to help later...

WOW that you are still working! and great that you are being careful so as to get best results re benefits.

Sounds like you have a job that will be great training for all this, too. You know how to find what you need to know. And at least to some extent you are able to be 'practical' and 'theoretical' and such, which for me at least is a huge help. Early on I decided to have 'me' as a client/patient, which helps a bit re the emotion. And then my mind/body/spirit therapist makes sure that the emotive part gets heard too!! also essential we think.

Hurray for the hugs from those grandchildren!! They too can be a source of joy and strength no matter what!!

And I am so very glad that you have a good relationship with that first neurologist. So many neurologist are more 'in their scientific head' I think. While it is great that they do research to try to get more of their patients well, I more than once have heard MSers complain that they are not seen as persons with other needs too. (And I left several neurologists before finding one I liked!) but that was years ago before docs learned they needed to be people too -- maybe more are 'nicer' now.

Do keep us informed!!

much love, Jean

ALS> > > Does anyone in this group have ALS or care for someone with ALS?> I'm just diagnosed, beginning at ALS clinic in Phoenix AZ. Would like > to hear from anyone dealing with this.> Gail>

[Guest guest]

...I don't think we've tried it out yet on ALS. you could be the first.

bG

>

> Has there been any research on using these devices on ALS

patients? I

> have a girlfriend who is expecting a diagnosis of ALS from her

biopsy.

> Too many traumatic procedures on her body these last 7 years.

>

> If any one can lead me to anything, would be appreciated. She

deals

> with alot of pain in the morning, preventing her getting out of bed

> without the use of crutches now. I believe there might be a use on

> either this group, or other groups doing similar research.

>

> Thanks!

> Graffer

>

[Guest guest]

AMIOTROFIESE LATERALE SKLEROSE

( ALS )

ALS is ‘n motorneuronsiekte wat gekenmerk word deur atrofie van die boonste ledemate en spierverswakking en verlamming van die onderste ledemate. Hierdie chroniese rugmurgsiekte eindig gewoonlik met verlamming van die breinstam.

OORSAKE

ALS word veroorsaak deur die degenerasie van die rugmurg, veral die voorste horingselle en die piramidale bane. ‘n Virus veroorsaak dat die mielenskede van senuweevesels vernietig word deur leukosiete.

BEHANDELING

Die behandeling is byna soortgelyk aan die van MS.

ALS moet aggressief en oor 'n lang tydperk behandel word. Hoe langer 'n pasient die siekte het, hoe swakker is die prognose. Behandeling bestaan uit:

Dieet

Aanvullings

Elektroterapie.

DIEET

Die dieet moet heeltemal vry wees van glutien, suiwel, koring en versadigde vette, m.a.w. volg 'n vegetariese dieet. Vermy alle vleis, suiwelprodukte, sojaprodukte, eiers,

gebraaide kosse, vette,gis, koffie, alkohol, sout, suiker,

sigarette, grondbone, grondboonbotter, brouersgis, verhitte kookolies, margarien, gebraaide kosse, glutien, byvoegings, insekdoders, gort,

sjokolade, speserye, hawermout, verfynde kosse, rog, geprosesseerde,- geblikte,- bevrore kosse, kleursels, asyn, verhitte koolhidrate, bv. brood, beskuit, aartappelskyfies, pasta, pizza, koek, tert, pasteie, koeldranke, roomys,

heuning, neutmuskaat, olywe, tamatie, eend, tiemie,

haringvis, avokado, rooi peper, sitrus, tee, kool, sampioene, dadels, groen peper, aarbeie, pere, mint, prei, tabak, pietersielie,

druiwe, spanspek, piesang, garnale, mostert,

mielies, kunsmatige versoeters, klapper, patat, aartappel en eiervrug.

Vermy verder stres en angs, blootstelling aan hitte, soos warm baddens, stortbaddens, sonbad, oorverhitting wanneer oefen, uitputting en virale infeksies.

Eet: ROU en lig gekookte groente,rou vrugte, vis,gespruite sade soos alfalfa, sonneblom, rooi klawer, gespruite bone, neute, sade soos pampoen, perske, appelkoos, bruinrys, millet en

olyfolie.

Eet net organiese groente en vrugte sonder enige byvoegings . Eet baie rou spruite , alfalfa , sauerkraut , donkergroen groente en drink vars uitgedrukte , organiese groente- en vrugtesappe , asook groen drankies wat baie chlorophyll bevat.

Drink 300 ml gesuiwerde water per elke 10 kg liggaamsgewig.

Periodes van rou groentesapvas vir 3 dae per maand moet gedoen word onder die toesig van 'n naturopatiese- of mediese dokter wat kennis het van naturopatie.

AANVULLINGS

Galium-Heel-10 druppels soggens

Hormeel- 10 druppels smiddae

Hepeel- 1 tablet saans 20 minute voor ete.

Schwef-Heel-10 druppels voor slaaptyd.

Vitamien B12-400mcg pd

Inositol-1000mg pd

Vitamien D-1500 ie pd

Procydin-1 kapsule 3x pd

Oktakosanol-40mg pd

Kolamien fosfaat-400mg van 'n 10 cc spuit-binne-aars- NIE intramuskuler nie.

Pankreatiese ensieme-6 g pd

EPA\DHA\Flaksolie-3 eetlepels pd

DHEA-50 mg pd.

Elektroterapie:

QXCI\SCIO- 3xpw

Kruiemiddels:

Sutherlandia, hypoxis, alfalfa, echinacea en valeriaan.

ALS

Hello,I have a client with progressive ALS. He cannot talk, walk and it is so difficult to swallow. His cell vitality is 1, V- 66, A- 45, R- 50, H- 49, O- 49, P-71, E-65, Imp- 1400The highest stress number is Environmental and it shows allopathic toxins.The doctor told him to eat more fats and more sugar to keep his heart working. I am concern that the white sugar he puts in his black tea is not a good idea. I think that the black tea and the sugar are not the best for him.I will appreciate any ideas with similar cases.ThanksKatia

[Guest guest]

He needs hormone support - urgently and to cut out wheat, starch, grains, sugar. The more caffeine the lower the adrenals. Bye Sue

ALS

Hello,I have a client with progressive ALS. He cannot talk, walk and it is so difficult to swallow. His cell vitality is 1, V- 66, A- 45, R- 50, H- 49, O- 49, P-71, E-65, Imp- 1400The highest stress number is Environmental and it shows allopathic toxins.The doctor told him to eat more fats and more sugar to keep his heart working. I am concern that the white sugar he puts in his black tea is not a good idea. I think that the black tea and the sugar are not the best for him.I will appreciate any ideas with similar cases.ThanksKatia