Fw: Glutathione- a cure for cystic fibrosis?

July 27, 2003

Hi,

I think this was meant to go to the whole list.

Welcome Angie! Glutathion is a bright ray of hope for pwcf. But is has to be

studied further and it can't replace antibiotics. If your god sister is coughing

up blood I would head to the ER as soon as possible.

Peace

Torsten, dad of Fiona 6wcf and Sebastian newborn wocf

e-mail: torstenkrafft@...

Glutathione- a cure for cystic fibrosis?

My name is Angie K, my god sister has Cystic Fibrosis. While doing research, my

mother found an article about Hudson. She has three sons that were born

with cystic fibrosis, she conducted her own research and found that people with

cystic fibrosis have little glutathione- it usually gets trapped inside the

patients cells. Glutathione is a protein. It helps regulate the immune system.

This contributes to the mucus that CF patients get. She gives her sons

Glutathione orally and says that they are all living well and hardly ever sick.

I have seen many testimonials online about this.

We recently started my god sister on this. This is her 4th week. I know that

you should take Glutathione for several weeks before it completely works. Has

anyone else tried this treatment? If so, I would greatly appreciate any info.

Also, she has had a very bad cough for the last month and a half to the point

where she can not sleep and is coughing up blood. Is this normal for CF

patients? Could this be a good sign- perhaps that she is letting up mucus from

her lungs. The cronic cough began before the Glutathione treatment so I do not

believe they are related.

Also, does anyone know of any good doctors in New York. The doctor my god

sister has now is horrible, he tells her horrible things and changes her

medication every week.

If anyone would like more info on Glutathione you can see this web site:

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