posted
Hello all, I met with a Dr. today in AZ that sais he has a protocol for killing lyme and its co-infections. It's simply mega high doses of hydrogen peroxide with magnesium and zinc. He will also do DMPS injections. This is once a week for ten weeks.
He states, "the spirochete organism does not make the chemical Catalase. An organism which does not produce catalase, nor superoxide dismutase (or SOD), is able to be killed by hydrogen peroxide."
Does anyone have any experience with this, or has tried it??
Posts: 80 | From scottsdale | Registered: May 2011
| IP: Logged |
posted
Ive done IV Peroxide before, it didn't do much. I did a few of them, and have also done collodial silver and some over IVs.
It should be helpful, i just didn't notice anything. I have problems with Drs who decide they have the answer-- if they did, we'd all be cured. Open mindedness is key.
Posts: 844 | From CA | Registered: Apr 2010
| IP: Logged |
posted
I've tried it, although not for 10 weeks. It helped my arthritis, but not quite as much as the IV C I've done. Let us know if you try it. I think its probably a good idea. Whether it's "the" cure or not, I'm sure it wouldn't hurt.
Posts: 707 | From Colorado | Registered: Jul 2010
| IP: Logged |
posted
i did the HP IVs with HCL pushes. for some reason, if it wasn't diluted enough i would get INTENSE BONE CRUSHIN PAIN from them in the arm it was administered in.
Perhaps some of the other people who had their veins blown from either HP or HCL (can't remember which) will come on and give you more info. I didn't notice much except a dent in my pockets and bruises on my arms.
posted
I did IV Hydrogen Peroxide for CFS years ago. It was supposed to raise my Natural Killer Cells. It didn't do much other than blow out my veins. I regret ever doing it...
Posts: 964 | From san diego | Registered: Oct 2009
| IP: Logged |
Rumigirl
Frequent Contributor (1K+ posts)
Member # 15091
posted
Yes, IV h2o2 if not diluted enough is horrible on the veins. If diluted enough is fine. It is great for you. BUT it is NOT a cure for Lyme and co. Anyone who says so doesn't know what they are talking about. There is no one thing that is a cure all by itself. Beware.
Posts: 3792 | From around | Registered: Mar 2008
| IP: Logged |
posted
To all of you, thank you for the feedback , but now I'm ****ting my pants! lol I like my veins, I've blown enough other parts of my body out! I agree it's not a cure, and the doc is crazy for saying it but I do think it can help in conjunction with other protocols. I'm doing dmps with it so both should break up some biofilm, lower my viral load, and remove some mercury which is important. Still going to attack those lovely parasites and bacteria though:)
Posts: 80 | From scottsdale | Registered: May 2011
| IP: Logged |
philly78
Frequent Contributor (1K+ posts)
Member # 31069
posted
I have a question. I don't know much about this but am wondering if you could dilute a mixture in a spray bottle and spray it on your skin? Other things seem to work by getting absorbed through the skin.
I did a quick google search and don't see it mentioned but did find that you can use it in other ways. Hmm...now this got me thinking.
-------------------- When faced with pain you have two choices....either quit and accept the circumstances, OR make the decision to fight with all the resources you have at your disposal. Posts: 1000 | From PA | Registered: Mar 2011
| IP: Logged |
posted
As far as biofilm goes, I started using Detoxamin, which is an EDTA suppository with fabulous results. I can tell it is breaking barriers down where I had not had success.
Posts: 964 | From san diego | Registered: Oct 2009
| IP: Logged |
posted
Hey philly, I'm from Boston, sorry abt your flyers:) Hydrogen peroxide on your skin does have an affect, but not the same as putting it into the blood. I have heard of several people putting H2O2 in a bath with epsom salt, and seeing toxins getting pulled out but the point of the IV is to rush it through your blood. Putting it on your skin, it would get absorbed directly into the cells. Like hoew your thinking though, wish doctors tried to think like us:)
Posts: 80 | From scottsdale | Registered: May 2011
| IP: Logged |
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/
UBBFriend: Email this page to someone!
Printer-friendly view of this topic