posted
Other than the expense is there a downside or risk to IV Glutathione ?
-------------------- You won't know how sick I was until you see me when I'm well ! Posts: 123 | From Colorado | Registered: Sep 2012
| IP: Logged |
Summer3
Frequent Contributor (1K+ posts)
Member # 35286
posted
I don't think so other than the very small risk of infection. It is the only reliably helpful thing that I've ever done but it only lasts temporarily for me.
posted
Hi LuluBelle, I'm very sensitive to glutathione. I've tried taking supplements but they were too strong and made me very ill. Dr. B put glutathione in an ultra violet IV treatment I was trying and I got very ill. I have detox issues! I did try the lipsomal glutathione and was able to tolerate a drop or two. It's been a while now. My advice to is to go slow. I see Dr. N tomorrow at 9:00am. C.P.
Posts: 106 | From Colorado | Registered: Jul 2012
| IP: Logged |
posted
You might also want to try glut suppositories. They're said to be more effective than oral liposomal.
Posts: 431 | From New England | Registered: Dec 2011
| IP: Logged |
lax mom
Frequent Contributor (1K+ posts)
Member # 38743
posted
I love, love, love Glutathione. Like Summer, it's the only things that makes me feel better.
I've tried: IV, suppository, oral, nebulized and transdermal cream.
I think one problem is if you have an allergy to sulfur.
I think I will try a glutathione patch first. And true to my ways I will probably cut the patch down to start. Tiny dose and work up. Since I don't know how I will react I am afraid to jump in with an IV.
Carmen, you say natural whey. I use NOW brand whey (dutch chocolate - Mmmmm!)Is there something specific you mean by "natural" whey ?
-------------------- You won't know how sick I was until you see me when I'm well ! Posts: 123 | From Colorado | Registered: Sep 2012
| IP: Logged |
Summer3
Frequent Contributor (1K+ posts)
Member # 35286
posted
I've heard that only the undenatured whey protein contributes to the production of glutathione.
The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:
The
Lyme Disease Network of New Jersey 907 Pebble Creek Court,
Pennington,
NJ08534USA http://www.lymenet.org/