I've been taking the Abx for just over a month. I felt a bit rough in the beginning but haven't experienced any of the horrendous die-off i've read about. Last Thursday, I got up and felt a bit different and had a shower (easily getting in and out of the bath without falling on to the floor! I walked around my flat without tripping and without my crutch. I left the flat and without thinking left the crutch behind. I walked from my car to the cashpoint and back almost completely normally! This only lasted for half a day and now I'm back to 'normal'.
Posts on Cpn in a specific disease: MS, FMS, CFS, Asthma, Prostatitus, Heart Disease, etc.
One of these weird things I didn't stop thinking about:
I cannot avoid feeling myself mirrored with people with MS. I find us direct, without a lot of patience, easily irritable, stressed... and extremely intelligent. (I feel cocky writing this...)
It seems all of us got the nervous system damaged, so no doubt we do not have time for stories... therefore... our brain has infected parts eaten.
Got to get worse before getting better, right?
only been taking abx for three days and my walking is terrible. I should expect things like this? Will doing Epsom salt foot baths help get rid of toxins?
I was given Augmentin recently as a result of a bronchial infection by my daughter who is a nurse practitioner. I noticed my MS symptoms got better when I started taking Augmentin. I started researching, thinking there had to be a reason the antibiotics were making me feel so much better at a time when I would usually flare. Getting sick always has made my MS flare, but not this time. I have historically avoided taking antibiotics as I thought they were so bad for me and destroyed my gut flora.
Hi, I just received a letter back from my GP after sending him information from David's website. He says that his theory seems to be very much a one-man theory and that I should seek neurological treatment options. I told him that I wanted to do an Elispot test offered by ArminLabs (i know it's not 100%) that I would finance. He has offered to take the blood but will not prescribe the antibiotics without a Neurologist's opinion
It's been a while that an idea is running through my head. I am no doctor, and my medicine knowledge comes all from this site (and Dr. Wheldon's), Internet, and what my mother defines as 'her own Diogenes Syndrome' by keeping the most of my medical reports.
Let's say it is just a shot to the Moon:
On the 20.XII.2013, I got a lymph node removed from my armpit. Once they did the biopsy, they told my lymph was blocking TOXOPLASMOSIS. I never cared much about it, but today I am wondering if it would not be worth considering:
Hi I've been taking Borax in a bid to resolve (what I thought was) candida overgrowth. Many people I know with MS are following a candida protocol, quite successfully. I've been less successful, but I get significant die-off symptoms when taking Borax. Borax is anti-fungal and anti-bacterial, so could the die-off actually be CPN??
Does any one have an opinion on this please?
Hi, could humidity intolerance experienced by people with MS be attributed the the respiratory nsturre of CPN? Dampness always makes my symptoms worse
I have MS and plan to do the NAC test shortly. If I see no flu-like symptoms do i defeinitely not have CPN??thanks
Salut,Je sais que Chlamydia pneumoniae peut augmenter le risque d'avoir Maladie d'Alzheimer.Comment pouvons-nous être sûrs que nous n'avons pas commencé la maladie d'Alzheimer?