I was treated for five years or so by psychiatrists for severe depression and moderate mood swings.  I went through many antidepressants some helped then about a year ago they put me on Lithium which helped greatly with the pain in a few days.  I am still on Lithium.  Several months ago I started to zero in on infectionsi [3] that I did not know I had, very high Cpni [4] antibodies, IgGi [5] and IgA, and have started the Wheldon Protocol, CAPi [6].  I have M.S..

This Fall I had the worst sinus infection of my life, and it took a long time to get over it. Even after the infection misery subsided, I was still left with a stopped-up ear and partial deafness for a few weeks, not to mention fatigue and and embarrassing stupor. This comes from someone who has had dozens of bad sinus infectionsi [3]. I'm fairly well convinced that Cpni [4] was NOT the culprit this time.

It just dawned on me that Steve's imbalance has been markedly worse since around the time I got the sinus infection. Hmmmmm.

Hi Gang,

my name is Eriks and I have been on CAPi [6] for 7 months.

Since starting I was carefully convinced of the actions of a Pathogen/Infection.

I am now more and more convinced due to a steady certain improvement.

QUESTION?

Is my wife at risk from infection from me???? or am I asking the obvious?

How widespread should our concerns go?

For the past week I have been struggling with what appears to feel like a chest cold (or those  CPNi [4] elementary bodies are reactivated?)  This is such a strange feeling, in that, even though I have been "sick" with all the repercussions of the protocol, I haven't had anything like a cold, flu, or viral type illness since being on CAPi [6].  I have been running a low grade fever, coughing and feeling very flu-like.  Considering I don't get out of the house much, if it is viral my husband probably brought it home.

My mobility is becoming worse and I am also having neuropathy-type foot drag -- occasionally the  toes on my right foot fold over and I don't feel them right away until I've scraped them on the floor or stairs! And my feet, (even though I  think they are "up") aren't and I trip... I am unsteady.  My husband is constantly having to steady me and help me maneuver on the occasions we leave the house or he pushes me in a transport chair.

These are NEW symptoms which have developed over the last two pulses.   I have had problems with my right knee since the beginning of capi [6] but these symptoms are different. My left knee and leg are now affected.

Why is it these studies appear to not always ask "all the right questions".   I found this one [31] (done in 2006) on the effects of Azith on CFSi [32] patients.

What's funny is, it was concluded:  "They (the patients) improved only to an estimated maximum of 80% of their premorbid capacity".. hey 80% is pretty good when you've got CFS.  And, this was on 500 mg of Azith for 3 consecutive days for (only)  6 weeks (monotherapy).  Of course, we don't really know how incapacitated  these patients were..... but it doesn't really matter, 80% is pretty significant.

I recently had a blood test done for Cpni [4] panel to see what I could learn. I realize these tests are not considered accurate. But I was curious & had the opportunity ... so why not?

The panel included C. trachomatis, C. pneumoniae & C. psittaci.

Both the C. trachomatis and C. psittaci results came back normal reference range and said "ANTIBODY NOT DETECTED".

However the C. pneumoniae came back marked high on two fronts.

IgG  1:512 H   (reference range: 1:64)

IgA   1:64  H    (reference range: 1:16)

IgM <1:10

Interpretation = PAST INFECTION

I've written about my sister before.  She asked to be tested for CPni [4] at Cleveland clinic and came back positive, something like 1/125 or close to that.  Cleveland Clinic asked her if she wanted to be treated with 1 abxi [22] for a few weeks. 

She has lung and sinus problemsi [47], fibromyalgiai [15], fatigue and serious heart and vein problems and inflammationi [24].  Basically the falling apart syndrome.  I tried to get her started on CAPi [6], but she didn't follow through, claiming she didn't have time to get sick.  She did take NACi [37] for awhile.  Now she is really sick, with pretty bad heart problems.  She has been diagnosed with everything under the sun over the years, but then they always end up changing their minds and saying it probably isn't what they thought it was.

Just a quick update.  Just got off the phone of Dr AW's clinic.

It appears that in the blood sample that Paula produced a couple of weeks ago, using his dark filter microscope, he found BORRELIA!

Paula was bitten by about half a dozen ticks in the summer of 2004!

When she first became bedridden, she was tested by the NHS for Lyme but nothing was found.  I wonder if the little blighters have been forced out of their slumber like a massive kick up the arse, by the Doxyi [49] and Roxyi [50]! - I bet if we did the NHS Lyme test again, it would be positive - I wonder if it is worth asking?

Prior to any abxi [22] or Samento, Dr AW using his blood test, only found CPni [4] in Paula.

Presently I have been on Minocycline for over two weeks. The inflammation has been increasing in small increments daily. I was not keeping on top of the load of toxins/porphyria with my usual doses of glucose, Emergen-C and charcoal. So a couple of days ago (9/20) my recent supplement order was delivered which included some Yaeyama Chlorella to try out. Only after two days of use before lunch I am impressed of how effect it seems for me. It is the perfect pre-lunch mopper. Which is a time of day I really need help. It is when it is not convenient to take any of the other moppers I use. But to be clear, I definitely will continue all of them at the usual times I take them as well.

Well, I don't have to tell you that I am pleased things turned out pretty good for me. The first few days of Minoi [36] were misery but then things began to settle down. The last couple days I haven't had to take extra Emergen-C but I am still stiff and achy. Plus my eyes are so red some folks at the store look at me as if I am crying OR stoned... sympathy or disdain. Of course either way I don't appreciate the vibes so quickly move on. Also I have daily coughing sessions and about gag at times trying to break loose the mucus stuck in my bronchial airways. (sorry) Sometimes it just feels like a hair stuck in my throat. It is worse for me in the mornings.

If Lyme can be caused though having a root canal done -as it is said by the Doctor Steven Harris, M.D, in the conference he presented - the link given here by lifeontheice [62]: and now I read in the website healingdaily an article called “Should you have root canals? Where they talk about this Doctor, expert in root canals, who then found that this “repair in the tooth” might be the biggest cause of bacteria in the mouth and then the body. The article says:

This is the news:  In England, possible antibioticsi [22] to be sold over the counter, to treat CHLAMYDIA!

This is the story form http://www.guardian.co.uk/society/2008/aug/06/health [110]

Oral antibiotics are to be made available for the first time without doctor's prescription under guidelines approved yesterday by the medicines regulator.

A pill to treat chlamydia, the most commonly diagnosed sexually transmitted infection, will become available for purchase in pharmacies across England later this year.

GOD BLESS YOU FOR DOING THIS SITE!

Hope everyone gets the answers that are looking for, and the needed support; this thanks to you guys making this site possible for all of us!!!

It's marvelous!

Maria 

Here is a patent that was filed for raising core body temp to kill herpes viruses. The procedure seems rather elaborate. I think I will stick with the FIRi [114] sauna for now.

http://www.patentstorm.us/patents/6415797/fulltext.html  [115]

Raven

 CAP since 8-05 for CPNi [4] and Mycoplasma P. for MS and/or CFSi [32]