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IV glutathione

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Parkinson's Disease
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Posted 1/16/2011 2:41 AM (GMT -5)
Hi, I'm popping in from the Lyme and hep c forums looking for any Parkinsons people who have gotten IV glutathione.
I have done it and it helped a lot but I'm trying to buy it for home.
Anyone?
Posted 1/16/2011 3:21 PM (GMT -5)
bucci
I have never heard of it. Tell us about it. What does it help with? How did you find it? Anything else.....?

Dan
Posted 2/25/2011 3:40 PM (GMT -5)
Hi Bucci.

My mom is going to get IV Gluthatione. Supposidely there are good benefits from it but you have to do a whole bunch of treatments. I think you can also take Gluthatione by mouth but might not be as effective.

Can you tell us what benefits you saw? How many did you do?

Thanks
Chootik
Posted 2/28/2011 7:50 PM (GMT -5)
I had IV glutathione several years ago.  The results were good, but temporary and expensive.  If you can afford it, check it out.

My understanding is that oral glutathione does not make it through the gut.  I would be interested to hear if anyone has tried the nasal spray.

 

Posted 3/26/2011 11:19 PM (GMT -5)
 I did 6 IV glutathion. 1st one was amazing.  My feet didn 't shuffle anymore.  Hand tremors stopped .  Handwriting improved.

  two days later I got another IV.  2000mg each time.  I did even better the 3rd time,  but it does not last.  Just when you wonder why your doctor doesnot want you to do it,  you will notice that your systoms start to slowly return.  even when you are still doing the iv s....   Six treatments cost me $800.00  because a nurse practioner gave me 30 minutes of her time  and gave me the IV..glutathion is a very strong antioxident.  I gave it up because I could not afford it and I couldnt find anyone to give it to me,    

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