I have been researching this issue of hypertension and tachycardia issues with cpni [4] as it effects the vascular system. My doctor wants to put me on high blood pressurei [3] medication and I'm concerned going to statin medications. I was reading Dr. Wheldon's story and found myself going through the same symptoms. Could the high blood pressure be related to severe inflammationi [5] do to cpn die off? OR something I need to address with blood pressure meds.

My pressures are around 140/96.

anyone else going through something similar?

Bonnie

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 [17] for a few weeks. 

She has lung and sinus problemsi [18], fibromyalgiai [11], fatigue and serious heart and vein problems and inflammationi [5].  Basically the falling apart syndrome.  I tried to get her started on CAPi [19], but she didn't follow through, claiming she didn't have time to get sick.  She did take NACi [15] 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.

A word of encouragement?? I haven't checked in for quite a while. Been doing ok, but have been undergoing Vitamin C IV treatments for 4 weeks followed by Rifampin 150mg twice a day for 4 days.  My energy is zapped and the Rifampin feels like poision to my body.

Hello, everyone. I 've been experiencing a GREAT improvement in my hypertensioni [3] and decided it calls for a report here.

For a background info: I've been having high BP for about 10 years. It started around the same time with my hypothyrodism symptoms. I've been taking antihypertensives on a daily basis for the past 5 years. Last fall, prior to starting CAPi [19] in Jan'08 my BP went out hand and even on medications it was often 160/100.

I've been on Cap  since begining of Jan'08. On my current protocol (Rifampin 600mg /day + Doxyi [25] 100 mg x 2/day) since March. At first my BP was spiking a lot. Hypertension crises always were a part of my die-off reactions. My BP became more stable as I was improving in general with arthritis, fatigue, pains.

This is the news:  In England, possible antibioticsi [17] to be sold over the counter, to treat CHLAMYDIA!

This is the story form http://www.guardian.co.uk/society/2008/aug/06/health [95]

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.

Hello all! Im Wanda and Im an advocate for my hubby, who went from perfect health to progressive decline starting 2003, we have been married 27 years and still adding on. 3 kids (2 grown) 1 dog, 2 cats.

Im learning how to navigate this site and post, so please forgive me as I learn. Im not sure if I will find hope here, any input is appreciated!

2003 he started with flu like illness extreme fatigue few small bite? on chest, fever, which developed in to what appeared to be hives? Doctor said hive, stress...xanax!, prednisone does pack...Prednisone did nothing, Next doc drew blood for lymes etc. put hubby on Doxyi [25] for 10 days...

I was going to post updates with my progress monthly but having being overwhelmed with trying to keep up with life and treatment, I am way  behind.

Anyway, here I go. I started back in Jan'08 with big doses of CAPi [19] (3 abxi [17]) and after extremely severe die-off reactions and stopping a couple of times, I re-started nice and slow in Feb'08, adding 1 abxi [98] at the time, making small changes and ramping up.  

Finally on full doses of current protocol - Rifampin 600 mg/day and Doxyi [25] 100 mg x 2/day - since mid-March. 

I went to see my Lyme dr for a monthly appt. and came back home all disturbed and worried. This was my 4th appt with this dr and I am still in the beginning phase of the CAPi [19] tx. By this time my dr and I should be developing a working relationship but it's not happening. During appt he asked - Remind me, how long have you been sick? So I told him my story again very briefly. As I mentioned that I saw rheum dr before finding him, he asked - And Rheum didn't find anyhting? That surprised me completely b/c on my 1st appt with this dr I brought to him consult notes from the rheum dr stating the dx and plan of tx (not CAP, of course but prednisolone & Sulfasalazine). I felt he didn't remember my case at all.

When I saw my dr a few days ago we went over my labs results that had come back. The Western Blot for Lyme disease. IgGi [41] was negative. Good news, right? But strangely enough, IgM was positive by both standards - unconventional Igenex (where the labs were actually done) and CDC.

I was floored, I really didn't believe that I may have Lyme.  The dr told there may be a false positive and we ordered a confirmation test with Igenex.

The reason I think it is strange to have IgM (+) b/c my sxi [101] started so long ago and logically it's IgG that should be (+) if I have Lyme.

It was only three weeks ago that I wrote about my 30th pulse and how easy and 'pleasant' it had been, so easy in fact that I was able to carry on taking Flagyli [58] for 14 days.   Well it just goes to show that one good pulse does not a pattern make... Day two post pulse 31 and my mouth is still full of bitters, my maxilla still aches, my eyes are itchy, my ankles are swollen, my ears are throbbing and my urine is still dark.   But MIRACLE OF MIRACLES the pain in my gut is hardly there and I have regularly been sleeping 7 or 8 hours a night.

I think that my experience is an example of that Tipping Point that Jim and others talk about.   Enough Cpni [4] cells have died in the cell for apoptosisi [103] to take place...