LymeNet Flash: Any Glutathione Buddies out there?

LymeNet on Facebook

LymeNet on Twitter

Follow @LymeDiseaseNet

The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive

The Lyme Disease Network is a non-profit organization funded by individual donations.

»	LymeNet Flash » Questions and Discussion » Medical Questions » Any Glutathione Buddies out there?

UBBFriend: Email this page to someone!

Author

Topic: Any Glutathione Buddies out there?

Lymelighter
Frequent Contributor (1K+ posts)
Member # 5310

posted

As per Dr. H's new protocol, I had my 5th IV Glutahione treatment today. I've titrated up to 800 mgs on my way to 2000mgs. The drip takes about 30 minutes and I find if I talk to others in the clinic, the time passes quickly. While I don't feel anything yet, I will say that I get a dose of clarity after the treatment. According to my LLMD, chelation is an ancillary benefit of doing IV Glutathione.

I'm going to give it a month and see how things pan out. Any other Glutathione buddies out there have experiences to share?

[This message has been edited by Lymelighter (edited 28 May 2004).]

Posts: 1010 | From Mars | Registered: Feb 2004 | IP: Logged |

Beverly
Frequent Contributor (5K+ posts)
Member # 1271

posted

I didn't know you could do IV Glutathione. It's good to know you had some clarity after treatment, I hope it continues.

I haven't tried Glutathione...yet, but hopefully I will soon.

Good luck to you.

Posts: 6641 | From Michigan | Registered: Jun 2001 | IP: Logged |

solsearcher
LymeNet Contributor
Member # 4482

posted

I'm taking glutathione as recommended by my LLMD as a supplement called Immunocal. I've posted this before. I don't recommend their cost nor their multi-level marketing scheme. But the glutathione may be helping with my sinus and ear problems. The jury is still out. I'll post again when I know more.

Scott

Posts: 112 | From St. Petersburg, FL USA | Registered: Aug 2003 | IP: Logged |

BW Houston
Member
Member # 5085

posted

I have been taking 1cc Glutathione/ATP injections IM mixed with 1/2 cc Lydocaine. I get them from Dr. H and Dr. S in Houston. I have been taking one a week for over a year. I think they do help in reducing symptons or I would not be doing it at $11 a pop. I don't have a prescription and I usually buy 6-10 at a time. They will even ship them to you.

I was a little apprehensive about giving them to myself, but after a couple of times it became routine. I inject in the back hip area where the nurse first showed me. Never tried the thigh. I have done them with and without the lydocaine. It's a much better deal with the lydocaine ($1) more per syringe and less pain and soreness.

If anybody finds a cheaper source out there, let me know.

Posts: 43 | From Houston, TX, USA | Registered: Jan 2004 | IP: Logged |

Cheryl
Frequent Contributor (1K+ posts)
Member # 75

posted

BW,

Where do you order it from?

Thanks,
Cheryl

quote:
Originally posted by BW Houston:
I have been taking 1cc Glutathione/ATP injections IM mixed with 1/2 cc Lydocaine. BW

------------------
Lyme Disease Information Online:
http://www.lymeinfo.net
Lyme Disease Information By Email:
http://groups.yahoo.com/group/lymeinfo/

Posts: 1547 | From NY | Registered: Oct 2000 | IP: Logged |

liz28
Unregistered

posted

I'd love to hear more about your experiences. I started taking NAC (precursor to glutathione) about a month ago, on Dr. H's orders. My symptoms immediately reduced in intensity, but I also started having severe relapses. If it wasn't for the NAC, I'd have been stuck at home for weeks.

As it is, I'm able to work part-time but feel bad, with a new set of symptoms from what I had before. I've never had muscle aches, but now my arms and shoulders are constantly sore, and I have all the "flu" symptoms, like a sore throat, sweating, and general malaise. Again, this is much better than it could have been without the NAC.

If you have similar symptoms, maybe this is herxing. If not, I'm worried that the NAC stirs things up, or else my abx protocol is not strong enough to handle a busier life.

IP: Logged |

Printer-friendly view of this topic

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, NJ 08534 USA
http://www.lymenet.org/