Lyme disease

Hi, I have just been diagnosed with Lyme disease and am wondering if the CAPi treatment for Cpni will also do th trick for Lyme?  I have been on the abxi treatment for Cpn coming up to 11 months now, just hoping I won'y have to add anything further due to the lyme diagnosis.

Thanks :)

Yes I have this too Melly and hope the people who know respond. I am also on CAPi Wheldon.


Yes I have this too Melly and hope the people who know respond. I am also on CAPi Wheldon.


It's the answer I have also been searching for. The CAPi is dsigned to attack cpni at all stages of development. It is based on research by Drs. Stratton and Wheldon. Surely people have been helped by it. It has slowed the progression of my neurological symptom but neither stopped nor reversed them. Whether borrelia, babesia and bartonella have exactly the same life cycle vulnerabilities as cpn has not, I believe, been studied and may be the reason that I am not one of the success stories.

My diagnosis is ppmsi. Is that yours as well?

PPMSi-misdiagnosed 2001-diagnosed 2006. Probably caught cpni in birth canal but it didn't pass BBBi until my 40s. Minocycline 7 mos.- resulting bronchitis 5 months.Go to private m.d. out-of-plan. Wheldon CAPi 3/2/07 Stopped 12/12; resumed 12/13

Don't know about Melly, but I have chlamydia p. and then all of the above - Lyme borrelia, babesia etc. all of the co-infectionsi. I am on CAPi since end of don't know more than that.

I didn't even know I was sick! I twitch less, less muscle/joint pain is all. But weird things in my abdomen now. No MSi diagnosis so far but they said I had numerous scattered white matter foci in my brain.... so who knows...I have been to a Lyme doc and he treated with doxyi. If you have heavy metal in your body it will let the infection be worse..all I know.


I was diagnosed with rrmsi...had 5 relapses last year which left me unable to walk without aid.  Since starting the CAPi I have not had a relapse so somethings working. I am just not sure whether this is enough for lyme also or whether I should do something else :/

The combination is effective for Bb and it is a delicate balance in going fast enough to make progress over time and treating so agressively with individuals with neurological involvment that it causes increased neuro symptoms which can scare them off or possibly kill of to many cells at one time for the body to heal all of them quickly enought to prevent the individual for becoming scared and stopping.  Also the concentration of the secondary ab is sometime higher in treating Bb.   Problem with the Bb treatment by  the so called literate practitioner is they underestimate the involvement or tenacity of the C.Pn. infectionsi in the mix.  The capacity of the C.Pn. to inhibit natural apoptosisi of the cell allows the mix of infections that are intracellulari in nature to survive as they shift shape and form in response to abxi tx.

For myself once I was stable on my dosage I increased my Roxi to 300 twice a day to be a bit more agressive in treatment.    I had not progress to neurological symptoms in any significant way nor had a dxi of ms  some folks said that I had a situation like they did early in their disease I think it all may be a continuum and various factors contribut to ones progression and symptomatology hence why everyone looks and displays different symptoms.

Not sure that is at all helpful but I am not willing to have a long discussion of this as I am too busy being back in a productive life thanks to the information I got being here in this community over the past 7 years this past Spring.    Louise

  • CAPi(TiniOnly): 06/07-02/09 for CFSi<
  • MethylationProtocolSupplements: Started08/08
  • Intermtnt CAP: 02/09-02/10
  • Full MethylProtocol & LDNi 02/09
  • Off CAP: 02/10, cont LDN & MethlyProtocol support
  • <

Brief comment whilst I'm at work:

Five relapses down to zero; is that significant?



“Don't believe everything you read on the internet.”

―    Abraham Lincoln<

Melly, I agree with Supaguy!

How were you diagnosed with lyme and who by?................................Sarah

Completed Stratton/Wheldon regime for aggressive secondary progressive MSi in June 2007, after four years, three of which intermittent.   Still improving bit by bit and no relapses since finishing treatment.

Good you are at work

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