Amazing Results

anonymous

New member
hiI wrote a few weeks ago about Glutathione(gsh) and nac for CF. It has been one month now since I have been taking GSH and NAC by mouth and also using it for irrigation for my sinuses. I have been able to reduce the bacteria load to Light growth of psuedomonas by using this treatement. I got rid of Staph and klebsiella. I am a firm believe that GSH is the best treatment for my sinuses and for CF. I am sure in a few more weeks to another month, my psuedomonas will be undetectable. I will need to remain taking gsh forever as if I stop all these bugs can come back.Since I am a transplant patient, I am taking a low dose orally of GSh five hundred and about three hundred of NAC. I might increase but I need to be careful because of the drugs I take. I was able to decrease my anti-rejection meds by two miligrams.I have noticed other positive changes on my body. I also gained three pounds without trying.If you are interested, check out the UTAH Valley Institute of Cystic Fibrosis which has conducted a studyhttp://members.tripod.com/uvicf/index.htmFeel free to email meRisagans@cs.comGod BlessRisahttp://www.transplantbuddies.org
 

Murgie

New member
HI Risa, I could not access the exact information ont he Utah Web site, can you tell me if this is something you might recommend for a 5 year old with CF?I had read the article in Womans day and submitted that to my sons doctors, but I have not pursued it any further.
 

anonymous

New member
Hell MurgieI am sorry but I cannot tell you what to do with your child. I only talk from personal experience. I just wish I had this treatment when i was younger. I put this information out for others to think about and talk to their doctors about a new treatment that does work. I would check back with the website and read all the information on the research and then you can make the right decision for your child. The link does work.http://members.tripod.com/uvicf/index.htmtry this. I am going to try to make you a hyper link that you can click on. This site may or may not convert it. The above link does work if you can copy and paste. If your current browser does not work go to internet explorer<a href="http://members.tripod.com/uvicf/index.htm">The Utah Valley Institute of cystic Fibrosis</a>I hope your doctor is open minded and investigates this program.God Bless YouRisa
 

anonymous

New member
Hi NAC stands for N-acetyl-cysteine. Here is a link that will explain the benefits in more detail. NAC helps your body prepare for the Gluathione and helps your body to produce its own Glutathione. With CF we are unable to have our liver release the glutathione.http://www.rienstraclinic.com/info/Nutrients/N-acetylcysteine.htm
 
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