IM Penicillin G

Hi Sunshine,

Welcome to the forum!

Are you currently treating Lyme or is this research?

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**You never know how STRONG you are....until being STRONG is the ONLY choice you have**

lymediseasethroughmyeyes.blogspot.com/

Co-Moderator Lyme Disease Forum

I know of one person who did IM Peniccilin three times a week for Lyme. It was after years of antibiotic treatments. She claims this was the final antibiotic treatment she did before she went into remission for 8 years now. She did treat with many other antibiotic first (the usual suspects), and she does a lot of vitamins and herbals even to this day to keep her immune system supported. I think IM Pennicilin it is a valid treatment, but expect to do it for several months. She also mentioned that after a while your butt hurts from the shots and it is painful.

Lyme,

Hey hun. How have you been?

Yes, IM(Intra Muscular) penicillian, are shots of penicillian into the muscle.

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**You never know how STRONG you are....until being STRONG is the ONLY choice you have**

lymediseasethroughmyeyes.blogspot.com/

Co-Moderator Lyme Disease Forum

You can find IM or injection form of Penicillan G on the net. It is less expensive than from a pharmacist, ususally.

I found it interesting that CMACAREN new someone who had gone into remission with 3 shots a week. I wonder how many weeks she was treated.

If that worked for her, then why aren't more people getting this treatment?

For +Lyme, if you could find someone in your area to give you injections, that would be one way to try it. A nurse can do this. I don't know how hard it is to do yourself. You probably can't inject into your bum very easily, as the video's I have seen showing how to inject intramuscular requres that you pull the needle out to check for blood just prior to pushing the injection into the muscle. However you could do this in your thigh.

Those are the only two places I have been told are where those injections should be made.

I don't listen to standard procedures all the time. For instance, if syphilis is caused by T Pallidum and it is a spirochete killed by Penicillin G, then why isn't the Lyme and Leptosporosis spirochete treated with the same medicine as syphillis?

I don't care that scientist have given spirochetes different names like Lyme, Syphilis, and Leptosporosis. I care that if a spiral uninvited guest is in your body and you want it gone, that you use what works.

Before I learned about spirochetes I did not know about syphilis and it's transmission. Did you know you can catch syphilis by kissing? I wonder how many ways you can catch Lyme.

I am not convinced that there is much or any difference between the spirochetes of those three named diseases.

I also have dificulty in refering to them as bacteria, as they are truly Flagella and act more like a parasite.

But, they can't be a parasite, since parasites are for people in other countries, the US doesn't have any parasites. (Just kidding, but that is the politically correct way to explain parasitic disease in the US). Most doctors don't know a darn thing about Lyme or other diseases.

Which is why I am leaning towards the perfect treatment being a penicillan G at high enough doses and an antiparasitic drug in combination.

Any opinions about antiparasitic drugs for Lyme?

http://www.youtube.com/watch?v=zTN0xJw7AoQ

I realize I have gone into a lot of different pieces of information but I truly agree with Mother Natures Child that will probably be figured out by people. Screw the scientist, they don't really care if you or I live, they just care if they live!

Good health to you all and thank you for your comments!

Sunshine,

Hi again:) Are you currently being treated for Lyme?

A lot of what you said does make sense. I think the reason they don't use penicillian as often is because so many people are allergic to it. I think, but don't quote me, that Rocephin is one antibiotic that replaced penicillian.

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**You never know how STRONG you are....until being STRONG is the ONLY choice you have**

lymediseasethroughmyeyes.blogspot.com/

Co-Moderator Lyme Disease Forum