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Hi

I personally think that any pathogen that produes toxins, such as

those which you have tested for are worth eradicating, since

otherwise they are only a burden on our bodies.

With the MSH production, maybe in the longterm it will return to

normal - dont forget Shoemaker is still only into this in the short

term really. Or even maybe Cheney's HGH & growth factor protocol is

they way to go to rebuild this.

Dave

> I was doing some research on MSH online when I found this. I about

fell out

> of my chair!! I have had my hopes up so much and then I read that

end stage

> CFS don't recover from the shoemakers protocol!!!????? I have been

sick for

> over ten years and I am completely disabled, so I am in the bad

stages of

> this. Am I reading this correctly, are some of us just fooling

> ourselves?????? Someone please correct me if I am reading this

wrong, because

> I feel pretty depressed about this.

>

>

> Leptin stimulates the production of alpha melanocyte stimulating

hormone

> (MSH), which in turn controls production of endorphins (the body's

natural

> " opiates " ) and melatonin (which regulates sleep) in the

hypothalamus. CFS

> patients rarely have much MSH. Eradicating CNS does nothing to the

high

> leptin and low MSH levels in patients with " end-stage CFS, " says

Shoemaker,

> but it certainly does in patients who are diagnosed acutely and

treated

> aggressively, preventing irreversible damage to the

MSH-manufacturing pathway.

>

>

>

>

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Hey ,

It is far too early to get scared about " end stage " concepts. There is

simply not enough research. Keep yourself focused on finding out what

exactly you have, various infections???? Also, one thing I love about Cheney

is his idea to get into warm water up to your neck. If you can possibly do

this it helps tremendously. It helps the lymph system and it just feels

good. I know Cheney talks about 3 stages of this disease, but I have seen

people in what he would label stage 3 recover. I have certainly seen people

with brain fog recover. Don't give up.

a Carnes

> I was doing some research on MSH online when I found this. I about fell

out

> of my chair!! I have had my hopes up so much and then I read that end

stage

> CFS don't recover from the shoemakers protocol!!!????? I have been sick

for

> over ten years and I am completely disabled, so I am in the bad stages of

> this. Am I reading this correctly, are some of us just fooling

> ourselves?????? Someone please correct me if I am reading this wrong,

because

> I feel pretty depressed about this.

>

>

> Leptin stimulates the production of alpha melanocyte stimulating hormone

> (MSH), which in turn controls production of endorphins (the body's natural

> " opiates " ) and melatonin (which regulates sleep) in the hypothalamus. CFS

> patients rarely have much MSH. Eradicating CNS does nothing to the high

> leptin and low MSH levels in patients with " end-stage CFS, " says

Shoemaker,

> but it certainly does in patients who are diagnosed acutely and treated

> aggressively, preventing irreversible damage to the MSH-manufacturing

pathway.

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I'm contacting you to let you know that there is hope for you. I've been ill

since 1989. Call Dr Bihari in NYC for help. His # is 212 9294196. Haven't

met a person yet that he has not helped. He does phone conferences.

Naltraxone will help a lot. I am not cured. But I work full time and am self

supportive. I function at about 85% which is very, very good, amd acceptable.

Good luck.. Carol in LI, NY.

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Carol, would you summarize Bihari's approach to treatment. I try to keep an

updated list of doctors for cfs patients.

Thanks,

a Carnes

> I'm contacting you to let you know that there is hope for you. I've been

ill

> since 1989. Call Dr Bihari in NYC for help. His # is 212 9294196.

Haven't

> met a person yet that he has not helped. He does phone conferences.

> Naltraxone will help a lot. I am not cured. But I work full time and am

self

> supportive. I function at about 85% which is very, very good, amd

acceptable.

> Good luck.. Carol in LI, NY.

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I agree this is a bit of a shock. Maybe if MSH turns out to be

a key factor in recovery we will be able to supplement it in the form

of a hormone creme or patch.

At least you know you are low in msh. So far I cannot find anyone to

do the test for me in the UK.

Any suggestions team?

Still waiting for nasal swab results.

Regards

Dave x

> I was doing some research on MSH online when I found this. I about

fell out

> of my chair!! I have had my hopes up so much and then I read that

end stage

> CFS don't recover from the shoemakers protocol!!!????? I have been

sick for

> over ten years and I am completely disabled, so I am in the bad

stages of

> this. Am I reading this correctly, are some of us just fooling

> ourselves?????? Someone please correct me if I am reading this

wrong, because

> I feel pretty depressed about this.

>

>

> Leptin stimulates the production of alpha melanocyte stimulating

hormone

> (MSH), which in turn controls production of endorphins (the body's

natural

> " opiates " ) and melatonin (which regulates sleep) in the

hypothalamus. CFS

> patients rarely have much MSH. Eradicating CNS does nothing to the

high

> leptin and low MSH levels in patients with " end-stage CFS, " says

Shoemaker,

> but it certainly does in patients who are diagnosed acutely and

treated

> aggressively, preventing irreversible damage to the MSH-

manufacturing pathway.

>

>

>

>

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  • 2 years later...

Hi,

The company Zengen has developed MSH products and it seems they are

currently being trialled. Some info here:

http://www.zengen.com/technology.htm#czen

If you check the News--> Press Release section, you'll find news of

the most recent trials they've conducted.

So hopefully this means it will be released in the not-too-distant future.

>

> Deb,

>

> Dr. Shoemaker had told me to check with him in 6 months about MSH

and that

> will be in January. I think it will be a while before it is

approved, if it

> indeed is approved. Keep on chugging!!

>

> Lucy

>

>

>

>

>

>

> >hi lucy - have only been on recup a month - way too early to say if

> >anything is happening.....lab forgot to draw my c4, had it redrawn

> >yesterday.....it'll be so interesting if msh becomes available for

all of

> >us with no detectable amts..... .......

> >deb

>

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  • 3 years later...

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