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Atkins/fat in diet

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I've been away and can't read all responses now, so sorry if this has

already been addressed...

It was established more than 30 yrs ago that MS patients benefit from

a LOW fat diet. Do a Google search for dr. Swank and you will find

all the info you need. It still amazes me that drs don't inform their

patients, but what else is new? I did not do well on the Swank diet.

I am thin and I lost almost 15 lbs and became weak... My savior has

been Prokarin, a histimine therapy. Histimine enables MSers to digest

protein (no restrictive diet and no exacerbations!). All of this

means, of course, whatever therapy you choose (LDN, histimine, diet)

DON'T take antacids if you have MS.

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> I've been away and can't read all responses now, so sorry if this

has

> already been addressed...

>

> It was established more than 30 yrs ago that MS patients benefit

from

> a LOW fat diet. Do a Google search for dr. Swank and you will find

> all the info you need. It still amazes me that drs don't inform

their

> patients, but what else is new? I did not do well on the Swank

diet.

> I am thin and I lost almost 15 lbs and became weak... My savior

has

> been Prokarin, a histimine therapy. Histimine enables MSers to

digest

> protein (no restrictive diet and no exacerbations!). All of this

> means, of course, whatever therapy you choose (LDN, histimine,

diet)

> DON'T take antacids if you have MS.

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If this is true then why didn't I know sooner? I live with my tums bottle allways have and thought I allways will! But now maybe not! Thanks........ Reg.

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

From: low dose naltrexone

Date: 01/29/04 17:36:44

low dose naltrexone

Subject: [low dose naltrexone] Atkins/fat in diet

I've been away and can't read all responses now, so sorry if this has already been addressed...It was established more than 30 yrs ago that MS patients benefit from a LOW fat diet. Do a Google search for dr. Swank and you will find all the info you need. It still amazes me that drs don't inform their patients, but what else is new? I did not do well on the Swank diet. I am thin and I lost almost 15 lbs and became weak... My savior has been Prokarin, a histimine therapy. Histimine enables MSers to digest protein (no restrictive diet and no exacerbations!). All of this means, of course, whatever therapy you choose (LDN, histimine, diet) DON'T take antacids if you have MS.

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my medical reading has purely come from being an MS patient. Each

person should do what works for him/her. That said, my reading leads

me to believe that MS patients need all the stomach acid they can

get. If you read back to Decem., you'll see an MSer taking papaya

enzymes. I take fresh pineapple. To learn a bit about why MSers

benefit from digestive enzymes, many naturopathic sites will have

info. I'd also call Key pharmacy in WA state (they have a toll free

number) and ask to speak to a pharmacist--Jim is very helpful there.

They have many MS patients. I bought a formulation called Similase

from them. It aided my digestion and I no longer need to use it, as I

am feeling better(with LDN and histimine)....In terms of doing

yourself harm, I am only a layperson, but I am inclined to say you

are making your body work very hard to process food.

Best of luck.

> > I've been away and can't read all responses now, so sorry if this

> has

> > already been addressed...

> >

> > It was established more than 30 yrs ago that MS patients benefit

> from

> > a LOW fat diet. Do a Google search for dr. Swank and you will

find

> > all the info you need. It still amazes me that drs don't inform

> their

> > patients, but what else is new? I did not do well on the Swank

> diet.

> > I am thin and I lost almost 15 lbs and became weak... My savior

> has

> > been Prokarin, a histimine therapy. Histimine enables MSers to

> digest

> > protein (no restrictive diet and no exacerbations!). All of this

> > means, of course, whatever therapy you choose (LDN, histimine,

> diet)

> > DON'T take antacids if you have MS.

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Helen Hecker is the expert I know on digestive enzymes. She has

covered every angle there, through her son. I saw your name on a

recent post here Helen ... and know you can help.

All the best

> > > I've been away and can't read all responses now, so sorry if

this

> > has

> > > already been addressed...

> > >

> > > It was established more than 30 yrs ago that MS patients

benefit

> > from

> > > a LOW fat diet. Do a Google search for dr. Swank and you will

> find

> > > all the info you need. It still amazes me that drs don't inform

> > their

> > > patients, but what else is new? I did not do well on the Swank

> > diet.

> > > I am thin and I lost almost 15 lbs and became weak... My savior

> > has

> > > been Prokarin, a histimine therapy. Histimine enables MSers to

> > digest

> > > protein (no restrictive diet and no exacerbations!). All of

this

> > > means, of course, whatever therapy you choose (LDN, histimine,

> > diet)

> > > DON'T take antacids if you have MS.

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before was diagnosed, i started taking tums like crazy. i kept

telling my docs that something was very wrong with my stomach. then,

when i got my MS diagnosis and asked about my stomach, they said it

was unrelated. i don't believe that's true, judging from what i hear

from patients. seems to me about half of us have digestive issues.

see a naturopath. they are not in the pocket of the pharma.

companies. my (university-based!!) docs didn't tell me about any

options--LDN, diet, histimine--they just said " go on avonex. "

--- In low dose naltrexone , " Reg Kreil " <regkreil@h...>

wrote:

> If this is true then why didn't I know sooner? I live with my tums

bottle

> allways have and thought I allways will! But now maybe not!

Thanks........

> Reg.

>

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

>

> From: low dose naltrexone

> Date: 01/29/04 17:36:44

> low dose naltrexone

> Subject: [low dose naltrexone] Atkins/fat in diet

>

> I've been away and can't read all responses now, so sorry if this

has

> already been addressed...

>

> It was established more than 30 yrs ago that MS patients benefit

from

> a LOW fat diet. Do a Google search for dr. Swank and you will find

> all the info you need. It still amazes me that drs don't inform

their

> patients, but what else is new? I did not do well on the Swank

diet.

> I am thin and I lost almost 15 lbs and became weak... My savior has

> been Prokarin, a histimine therapy. Histimine enables MSers to

digest

> protein (no restrictive diet and no exacerbations!). All of this

> means, of course, whatever therapy you choose (LDN, histimine,

diet)

> DON'T take antacids if you have MS.

>

>

>

>

>

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I would say that whether or not one takes antacids would depend very much on

the person in question. I suffer from an esophageal hernia, which is nothing

to mess around with. I *could* have a rather problematic surgery to correct

it, or I could make the lifestyle changes I have . . . along with sometimes

taking antacids. As an esophageal hernia can lead to Barrett's esophagus,

which in turn almost always leads to cancer, my money is on taking the

antacids.

And while we're at it, I wish two things. I wish people would stop telling

other people here to do this or don't do that. If people want to share their

own experiences or cite something they've read, for heaven's sake, do so.

But to cite something as gospel--particularly things as definitely

controversial as Prokarin and histamine--urging their beliefs on others, I

think that's wrong. And it's one of the things that makes people very leery

of giving LDN a chance.

And I'd also like to see more conversations about LDN and less about every

alternative therapy to come down the pike. That'w what the group is for.

Just my two cents.

Galoux

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