For the past week I have been struggling with what appears to feel like a chest cold (or those  CPNi [11] 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 [12].  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 [12] but these symptoms are different. My left knee and leg are now affected.

This is the news:  In England, possible antibioticsi [15] to be sold over the counter, to treat CHLAMYDIA!

This is the story form http://www.guardian.co.uk/society/2008/aug/06/health [93]

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.

Surefire Ways to Strengthen Your Immunei [6] System

If you often get sick and want to boost your immunity long-term, try these tips from naturopath Jonathan Goodman, N.D.

Shock Your System. At the end of your shower, make the water as hot as you can comfortably tolerate for one minute and follow that with a minute of tepid water. Do this daily. The extreme change in temperature stimulates white blood cell production. Don't do this if you've had a heart attack or stroke.

I have been monitored for microscopic blood in my urine since early 2000. The doctor I was treating with back home always seemed to believe it was due to celiac/gluten intolerance as we could never find anything conclusive.... hmmm.. cpni [11]???

I am now out of state with a urologist who has been treating me for 4 years.  Every time I have had an appointment there has been blood in my urine.  

 I just came from a visit with her (my urologist).... all has been tested (cystoscopy, kidney x-rays, urine cytology). Today, I pushed her for a "what are we going to do or conclude" about this?  The only confirmation that we have is that:

1) there are no cancerous or squamous cells; (which is great)  and,

A few interesting Articles :

... same old bologna [101]

Hi to all!

Does anybody of you have or had before elevated Coxsackie and/or Echovirus titres?

I have them along with the cpni [11]i [103]. I hope the Enteroviruses will pass when CPN gets better!

Could it just be a viral henchman? Just thinking about what gives me more problems?

 

Greetings from hamburg / germany

 

Cesare

I asked Dr. Powell to comment directly on concerns that have been mentioned over time as to whether he uses the CAPi [12] with his new patients. I received his response a number of weeks ago but have had no time to put it together in a cogent context. But continued posts on these questions has mobilized me to get his comments to our readers here. But context is, as we say, everything.

FYI.

http://www.turnthecorner.org/grants_2007_recipients.htm [107]

has anyone had a diagnosis of chronic strep? If so what treatments/protocolsi [9] were you treated with.

This week has been one of depression/frustration.... probably due to my impatience and lack of control.  But also because I don't understand what is going on with my body and this bacteria!  Family members keep looking at me at asking "when are you going to get better"... I stopped trying to explain. Having to use a wheelchair this week -- I've experienced the stares from people and small children and now understand what those of you with MSi [18] must endure from society.

Checking through recent post I found this from Pinky, and as Mac commented it might not get the attention it deserves in the place in which she posted it.

"It has been a long time since I have checked the site. Dr. P took me off Flagyli [48]i [111]/zithro right away because of the extreme die off. Now I am on Vit D (5,000 per day) and the assortment of liver//kidney saving drugs. The last time I went in I bought the Infrared Light, but must confess I have not used it faithfully. I have been getting PT in a warm pool (92) and it has done more for the pain that anything in 15 years.

I haven't blogged my treatment for a while, as I've been waiting to see if I would stick with a shift in protocol. So far, still with it, so thought it might be time to report in and get other's thoughts. New folks, please read this as informational only. It does help clarify Dr. Stratton's use of the continuous rather than pulsed protocol, but the rest of the hypotheses here are presented as my own speculations, not scientific fact.

In the lyme disease topics their have been someone who is  adequate treatened for it in UK.

I have forgotten the name of the author and cannot find the posting- unfortunately.

Can the one please write a private message with name and adress of the physician? For a friend of mine? Would be very nice.

 Thx!!!!

 gitta