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Please check out Ron Ritch's site on neurodegenerative disorders. He's put

alot of work into gathering information.

http://pspinformation.com

Regards,

Pam

Re: Digest Number 1486

> This is my first message to the group. My wife passed away in December

from

> PSP after a long period ending in a nursing home. My research suggested

> quite early that trying to increase the amount of glutathione the liver

> produced would be one of the paths we should proceed in trying to slow the

> progression of the disease. I still think it is one of the best paths with

> PSP and it may be the same with MSA.

>

> This can be done best by adding N-Acetyl-cysteine or cysteine to the diet.

> These are amino acids used by the liver to create glutathione. NAC is also

a

> sustance that helps dry up the mucus in the throat. My website at

> http://pspinformation.com has some of the information I've uncovered.

> Especially interesting is a study from the University of Florida on the

use

> of NAC with neurogical diseases.

>

> I think glutamine, creatine and lecithin have uses too. NAC needs the B

> vitamins, vitamin C and selenium to be effective. Magnesium also may be

> useful.

>

> What someone who is taking NAC or cysteine doesn't need is tylenol.

Tylenol

> and NAC work against each other. Tylenol poisoning from an overdose stops

> the liver from creating glutathione and if an antidote isn't given soon

> enough the patient's liver fails and the patient dies.

>

> But is tylenol dangerous in small doses? I don't think anyone knows for

sure

> but since tylenol works against the production of glutathione and if not

> enough glutathione is being produced and there is an alternative to

tylenol

> that could be used in its place - why take the chance?

>

> With PSP the main thing we can do is to try to slow the progression of the

> disease. Most drugs normally used to treat Alzheimer's or Parkinson's

appear

> to do more harm than good. They all treat symptoms and none slow or cure

the

> disease. In many cases they introduce new symptoms or side-effects of

their

> own. In most cases the best course of treatment is loving care, good

> nutrition, the best quality of life possible. patience and a very watchful

> eye on the prescription and over-the-counter medications given.

>

> PSPInformation.com also covers other conditions besides PSP. I think good

> arguments could be made that diseases such as PSP, MSA, etc; are

variations

> of some greater disease that so far is unnamed. If a name was used to

cover

> the " family " of diseases instead of the present individual branches, we

> would be a much bigger group and be able to get more funding for research.

> But now we are splintered into small groups and really have little clout.

>

> You are welcome to visit our website and to contribute information. If you

> have any ideas how we can be of use to you please let me know.

>

>

>

> Ron Ritch

> Charlotte NC

>

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