IV support for lyme?

Hi All:

Popping in a new string here, Girlie made me do it

My LLMD started me on a different kind of IV mix, that I haven't seen to much discussion about (but I am a newbie). I am in the Chronic Lymes stage, misdiagnosed for 16 years. Body is really trashed and immune system was already really impacted by Chronic Lympostic Leukemia.

Results from a NutraEval by Genova Diagnostics are really off. Antioxidants a-lipoic Acid, B1, B9 and Omega 3 oils labeled as "high need". Vitamins A, C, E, B2, B3, B12 and Pancreatic Enzymes labeled as "border line".

So immediately LLMD has me on a "Super Immune Cocktail" once a week alternating with hydrogen peroxide IV. This treatment is for 4 weeks.

IV Therapy - "Super Immune" once a week alternating with hydrogen peroxide once a week for 4 weeks. Plus IV with Methyl Folate 1 mg, Alpha Lipoic Acid 150 mg, and Glutathione 600 mg.

Super Immune cocktail is .45% NS, Vit C 500 mg/ml, Calcium Gluconate 50 mg/ml, Magnesium Sulfate 500 mg/ml, B5 250 mg/ml, B6 100 mg/ml, Selenium 200 mcg/ml, B-complex 100 mg/ml, sodium Bicarbonate 84 mg/ml, Hydroxocobalamin 1 mg/ml.

The Alpha Lipoic Acid IV, something interesting happened, I stopped shaking and the neuro symptoms backed off. It helped for that day with nuero stuff enough to notice a change. Next day though neuro stuff back. But interesting result. I need to repeat this to see if something is really good here or I just experienced an anomaly...which I am schedule for.

Any thoughts/comments on this IV therapy?

This cocktail sounds great. I think it will help your body a lot.
I onlyheard about Myers cocktail, but it contains less elements. This cocktail is great. I like Alpha Lipoic Acid, I take it in capsule form and my LLMD told me it is the best thing for nerves. I could imagine how powerful it is when comes in IV form.
Where do you live? I really like your LLMD's approach.

Thank guys...sorry for the slow response, been on the herxing train today and with neurological stuff, wow thats a rough ride.

My LLMD is located in Temecula, CA. I can give you his name/number if you like (dont know the rules for sure on how to share doctor info?? Ugh brain fog. I will look

Girlie, thanks for the smile. I dont know sometimes what to share or push out for feedback. So please wake me up as needed ;-) Im trying not to overload you guys.

So I see a thumbs up. I will keep daily log of the treatment and what I experience.

You people are amazing, thank you again for the help

I did a few months of h202 .ketes and little bacteria was still in cells ..i heard it is better in dw5...and at double dose to lyse cells ..make sure you have enough superoxidedi****ase and catalase to process..if you get tired after this may be a sign.., the myers is great ..what stopped the shakes was iv magnisum push .like lots ... also iv curcumin was tasty for inflamation and protects blood vessels from h202...your doc should call my doc and have a pow wow...also watch your blood sugar with the ala ..eat before during and after ..spirulina has helped ..iv phosphatidylcholine has helped too..as per the patricia kane protocal..my nurse friend says she got remission efrom 2 yrs of h202 3x a week with bvt ...

Post Edited (bluelyme) : 7/9/2016 12:51:50 AM (GMT-6)

Good to hear you're not herxing as badly.