I was first tested for Borrelia by KDM 2.5yrs ago and the result was negative. I started his treatment including GcMAF and a year ago he re-tested me and the result was now positive. He explained that there were three reasons why I was now positive (i) I had been under an incredible amount of stress in the previous year (son with a brain tumor; husband with a subdural haematoma; and very ill myself yet having to function); stress exacerbates the condition; (ii) I had been on GcMAF for 1.5yrs and this brings the sprochetes out of hiding; (iii) the testing he was using was now more sensitive. I tested positive by PCR and this was confirmed by DNA sequencing.
In my own country I managed to get a local infectious diseases specialist to treat me. Last June I was admitted into hospital and was administered IV Ceftriaxone 2mg daily (which of course was recommended by KDM). I was discharged after a few days and continued this treatment daily for four weeks on an out-patient basis. Within hours of the first dose I developed a fever and must have slept for about two days. It was very tough treatment with a lot of pain, particularly head pain in specific locations. By the end of the four weeks I was herxing and had "burnt tongue" sensation. Unfortunately my local doctor wouldn't treat any further and when the four weeks were up he just said that was the end of his treatment
On KDM's advice, I gave my body a break for a few weeks and in September I started 3 different oral abx: doxycycline, plaquenil and azithromycin. In January I was told to drop the plaquenil. In April I was told to exchange the doxycycline for minocycline. I found the minocycline very difficult to tolerate and by the 1st week of June, under KDM's advice, I stopped all abx. So I guess I was on abx for almost 11 months in total. I am still on a maintenance dose of GcMAF (2nano every 2 weeks) as well as other medications.
KDM wants me to detox from the abx for a couple of months, to then return to Brussels in September for re-testing. I was last in Brussels in February. My CD57 has improved considerably but other markers show that I have high levels of internal inflammation.
It has been a rough ride. I would say that there has been some overall improvement but I am still not well. I just wonder what the September testing will show and what the next stage will be.
Filfla4