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>

> Same question as before but now I'm wondering about the

>

> Best Bet Diet, Ann Boroch and the Swank Diet

I've been on Best Bet Diet since Feb '06, after an attack of optic neuritis and

an MRI showing a few lesions. I've not had a relapse since. Doctors like to

pooh-pooh this, saying that I'm just in remission. I always point out that I do

not believe I'm in remission because whenever I eat something I shouldn't, my

symptoms immediately return (balance & coordination problems, numb hands, pins &

needles in my feet, etc). It's not easy to get an MD to acknowledge the use of

diet in managing/curing disease, but I want credit for the work I've put into

it!

Over the last couple years, I have developed new food intolerances that show up

on my ELISA test results and I avoid those foods as well. I have to say that

since I started L-glutamine supplementation, I don't have the same severity of

reactions (or none at all) to my cheats or accidents with food. Perhaps my gut

is finally healing!

Crystal

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I have been on the Best Bet Diet (BBD) getting on 5 years strictly, no cheating,

and feel amazing. Brain fog deminished within weeks (but didn't go completely

until CCSVI treatment).When first diagnosed 16 years ago I started the Swank

diet but kept giving in to dairy and gluten which I knew were no good for

me. MacDougall is the famous one who beat MS (neuros called it remission)

with 4 years on the Swank diet. He went from bedridden to running up and down

the stairs two at a time. I told myself I was not allowed to stray from

whichever diet I had chosen for 4 years.I had CCSVI treatment 11 months ago but

am still on the BBD and don't plan on stopping it. I'd have an ELISA food

intolerance test and from that decide which of the diets suit you and your

intolerances the best. I have always known gluten and dairy did not suit me and

chose the BBD for that main reason. I could not do it cold turkey and gave up

all gluten for a month and didn't move on to the next one until I knew I

wouldn't cheat on that one. Dairy next, legumes next, refined sugar last,

tomatoes not at home but will put up with them if included in a dish when

out.Two years ago a lesion disappeared (still not found luckily). The neuro put

it down to the equipment which is absolute rubbish as MRIs should be more rather

than less diserning in 16 years. I put it down to a) BBD 2) amalgam removal 3)

exercise and stress removal. Good luck. Janet

To: mscured

From: abbykohut@...

Date: Sun, 25 Sep 2011 13:25:41 +0000

Subject: Best Bet

Same question as before but now I'm wondering about the

Best Bet Diet, Ann Boroch and the Swank Diet

Thanks!

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, after eight years and thousands of out-of-pocket dollars for alt

treatments and diets that did nothing, I no longer have expectations for

anything. If you don't have them, you're not disappointed if they don't work,

and you're grateful if they do. ... I took a break on treatments for a year or

so (except for massage) and found myself continuing to progress. So I broke down

and got on Rebif and stopped progressing. No side effects if I take two NSAIDs

after the shot. It's a long, slippery slide with pharmaceuticals, so now I'm on

Ampyra and AM seeing results—more strength, better balance and I can stay on my

feet longer. (I just started physical therapy to improve my odds.) I'm getting

both meds free from the companies.

I AM moderate with my diet, eat a little cheese, very little dead animal, take

supplements and eat lots of organic produce. I FEEL good. I have an accessible

vegetable garden of cedar planters on my back deck. And I do take an herbal

liver support. I really think we should be open to anything to improve our

quality of life, and not obsess about a cure.

The thing I found that helps me the most physically is staying positive, and

through practice it isn't an effort anymore. When I'm cheerful, my body works

better. I NEVER talk about MS and disability negatively. My favorite quote is

from Neil Marcus: " Disability is not a brave struggle or `courage in the face of

adversity.' Disability is an art. It's an ingenious way to live. " Considering I

live alone, adaptation and figuring out how to do things from the scooter is a

necessity—and fun. Ky. Voc. Rehab paid for hand controls in my truck and a lift

for my scooter, so I have a social life. Considering that the scooter puts me

" on stage, " I always try to look snappy. People like me because I never complain

and have not made MS the focus of my life. Happiness is a choice. Life is good.

Martha

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> I completely agree. It's annoying and disappointing isn't it? I know that for

me, things don't generally pan out as they do for others, but I have great

affects from thing that others don't too. As you say Martha, one size doesn't

fit all.From that point, I think we all just look for what DOES work for us and

use our inner-ears to listen to what our instinct and bodies tell us they

need/want.

>

> 'What we do in life, echoes through eternity.'

> MARCUS AURELIUS (121 - 180 A.D.)

>

> To: mscured

> From: mburton.akod@...

> Date: Thu, 29 Sep 2011 12:41:57 +0000

> Subject: Re: Best Bet

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started eating gluten and dairy again. One size does not fit all.

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Bravo Martha! My journey has been similar and we seem to be in the same place

on this. In 2008, after diagnosis, MS is all I could think about, now I try not

to think about it and I talk about it as little as possible.

Faith, good " self talking " , and positive thoughts about the future seem to be

the best help for me. I still follow the Swank diet, although not so rigidly, I

still take supplements and exercise daily, but I don't sweat it so much anymore.

I saved your text so I can revisit your post every now and then. Thank you and

best wishes.

-Tim

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> > I completely agree. It's annoying and disappointing isn't it? I know that

for me, things don't generally pan out as they do for others, but I have great

affects from thing that others don't too. As you say Martha, one size doesn't

fit all.From that point, I think we all just look for what DOES work for us and

use our inner-ears to listen to what our instinct and bodies tell us they

need/want.

> >

> > 'What we do in life, echoes through eternity.'

> > MARCUS AURELIUS (121 - 180 A.D.)

> >

> > To: mscured

> > From: mburton.akod@

> > Date: Thu, 29 Sep 2011 12:41:57 +0000

> > Subject: Re: Best Bet

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> These diet approaches to health take a long time. Anything less than 3

months and you can't even tell if it is going to help. McDougall was the famous

one who after being on the Swank diet for 4 years went from bedridden to running

up and down the stairs.

>

The other issue here is individual food intolerances. I was fortunate that BBD

worked for me within 5 weeks or so. But when symptoms started coming back, I

knew that I was developing new intolerances. I couldn't figure them out

(because there were multiples, it wasn't clearcut from one day to the next) so I

had an ELISA done.

Unfortunately, using dietary therapy is pretty much " all-or-nothing " . Even if

you avoid everything that the BBD recommends, if you are still eating something

that *you* personally are sensitive to, you are keeping your immune system hyped

up and will have symptoms. So, if someone has been on BBD for weeks or months

without improvement, I would strongly recommend an ELISA to see if there's

something else that needs to be eliminated from one's diet. I'll be the first

to say that it sucks to restrict oneself so much. But the results I've

experienced make it soooooo worth it to me. :)

Crystal

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Hi Tammy,

Dairy is to be avoided because of the casein protein. You can find all of

Ashton Embry's research here:

http://www.direct-ms.org/

HTH!

Crystal

>

> I would like to know about the dairy avoidance of the BB Diet. If we

> avoid dairy because of the high cases of MS in areas where people rely on

> dairy. Is it the fat from the dairy? Or dairy? Some diets allow fat-free

> dairy. Any thoughts?

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