(Originally posted at the now-defunct website cpnhelp.org.)

David Wheldon's story: Cpn Treatment of Cardiac & Myalgic symptoms

I was born in 1950; I’ve always been very active. As an adolescent I had recurrent and painful sinusitis; this vanished in my late teens. Amongst my activities I listed caving (spelaeology) which requires some physical fitness. I continued cave exploration until well into my forties.

In 1999 my wife, Sarah, and I both caught a respiratory infection which started off as a sore throat; in a fortnight it had become a mild pneumonia. Sarah developed frank asthma which required a Salbutamol inhaler. I also had a wheeziness, particularly on exertion. This eventually cleared. I also suffered with sinusitis again. I didn’t seek medical advice.

A few months later I began to find turning my head not only painful but difficult. As I cycle to work this grew to be problematic. I found that if I wished to turn right (UK) I had to dismount and walk across the road. At about this time I noticed that I was developing soft-tissue swellings in my neck; these began to grow quite quickly. Shortly after this I found I had myalgia in my shoulders and the long muscles of my back. Sarah noticed that I was walking very awkwardly; if I wished to turn my head I had to turn all my body. Flexion of the spine was difficult, too.

In 2002 I noticed that my resting heart-rate had increased, and there were increasing numbers of dropped beats. These were quite alarming in the dead of night. Sarah noted that my apex beat was really hard and actually audible at night. I was worried by this time, but was more concerned with Sarah’s aggressively advancing Multiple Sclerosis, which was much more troubling.

By 2003 All my symptoms increased in intensity; they now included constant pleuritic pain (a sharp pain in the side when breathing) on the right. Also there was an exquisitely painful longitudinal white streak along the nail of my left forefinger. I began to feel vertigo when moving suddenly: it was as though I were standing on either side of a small see-saw. My blood pressure was 150/95. I had my blood tested for Chlamydia pneumoniae antibodies; the IF titres were 1:128. This level is seen in many asymptomatic people. Low titres mean little; they certainly don’t exclude the infection. Borrelia antibodies (Western Blot) were negative.

I began a course of empirical antichlamydial treatment; it was very similar to Sarah’s, namely doxycycline 200mg daily and roxithromycin 300mg daily. (it doesn’t matter whether you take all the daily dose at once with these.) That night I felt sweaty and ill; this feeling carried on for five days; it was worse in the evenings, and was accompanied by an odd state of mind.  All kinds of visions went through my mind, and Sarah says that I was babbling, changing the subject almost in mid-sentence. But this subsided. After three months I began a short course of metronidazole in addition to doxycycline and roxithromycin. Towards the end of this course I had a rather ominous feeling that something was about to happen. Three weeks later I began another five-day course of metronidazole. On the fourth day I began to feel pain in the muscles of the back of the neck and in the soft tissue swellings to the side of my neck. That evening I began to sweat profusely, and had very strong muscle fasciculations over my torso. These continued for a week or so after stopping the metronidazole; again they reached their peak in the evening, so I was able to work during the day. (Evening fevers seem quite common with resolving intracellular infections.) They were followed by crushing pains in both upper limbs, which I take to be a mild form of Reflex Sympathetic Dystrophy. Fortunately these eased within weeks. My weight dropped from 95 to 81 Kilos within a few weeks. Within three months the neck swellings had almost subsided. Reactions to the third pulse of metronidazole were slight. Reactions to the fourth, fifth and sixth were negligible. My blood pressure dropped to a typical morning BP of 115/75; the apex beat became actually quite difficult to feel, and my pulse became very soft and even. All the ectopics had gone.

Now I am on intermittent antibiotics and supplementation; this includes N-acetyl cysteine 600mg twice daily for the purpose of bursting any chlamydial elementary bodies which remain. I still have a little trouble with vertigo and ringing in the ears, but not enough to stop me riding my bicycle. I’m pain-free and supple, and have full movement of my spine and head. There is an impression of ongoing soft-tissue remodelling.

Sarah and I had a similar respiratory infection; she developed frank asthma, and I an intermittent wheeziness. So though I have no hard evidence that we both had an infection with Chl. pneumoniae it seems clinically likely. No other known pathogen causes a respiratory infection after the pattern described. Often this is a clinical diagnosis. We have to accept that, on an individual basis, present-day laboratory tests may have little diagnostic value.

I managed to work full-time during this illness, coming home to cook for us both. We kept our household together. Some of our social friends were alarmed and lost touch, but, well, I don’t suppose they were really friends.

Sarah’s recovery from secondary progressive MS (where recovery is not a part of the natural history of the disease) is recounted elsewhere on this site.

DW before & after 

The photo to the left was taken in 2002. Note the soft tissue swelling round the neck; to a lesser extent round the mouth and eyes. The right photo shows a much-changed man in 2005. 


Update: Dorian Grey's picture - in reverse

Since starting treatment - antibiotics, NAC, antioxidants/vitamins and mitochondrial support - I've noticed profound changes in my body, in such a way as I would not have thought possible. Healing is far quicker; nails and hair grow faster; even the bald bit on the crown of my head is filled with a downy hair. Joints seem to work better; everything seems to function well. I'm a little taller (The same height that I was at 21) and my posture is better. My abdomen is flat. Muscle tone has improved. Deterioration of eye refraction has not only stopped but gone into reversal. Night vision is better and has much more contrast. Thinking is a great deal clearer. It suddenly struck me that a chronic widespread intracellular infection might well disturb the cells' positioning system; were that so, cell-replacement programmes would slowly go out of kilter. Of course, this is only speculation. But I find it astonishing that, the infection dealt with, this positioning system might be able to reassert itself so positively, and cell replacement programmes should guide cells to find their way to the right destination.

[The picture of Dorian Grey, by Oscar Wilde. A wealthy young man commissions a portrait of himself, and, when it is finished he grieves because it will never change, while, in himself, the slow effects of age will progress from day to day and year to year. 'I would give my soul for the portrait to suffer on my behalf and for me to live without ageing. . . ' And so, with this Faustian pact somehow sealed, the portrait ages on his behalf. His dark deeds are etched on the portrait's face, and, even though it is locked away, its presence troubles him. . .]

By D W at Sun, 2006-02-05 15:26

Very interesting observations, David.

I, too am experiencing some reconstruction. Most noticeable is the fluid under my skin. I was afraid I was getting a "dowagers hump" but it is gone. Must have been fluid. Overall puffiness under the skin is down. I look like I lost weight but I haven't kept track with a scale--my clothes just fit better. My body is starting to look like it did about 10 years ago. I just need to be on a regular exercise program. My cheekbones are back. My face just looks better--there's a blush under the skin. My hair seems to be growing faster. So here I am at 6 months into the treatment. I have been able to get back into exercising when I feel good. I look and feel better even though the treatment is rough at times. Did you see my post about finding my former neurologist's name on one of the papers listed on your web site? (Michael J. Olek) He is now in Texas at another center and I will contact him down the road and let him know how I am. This was a real confirmation for me finding him again and making this association. And yes, we could call ourselves the "Dorian Gray's Revenge Club". A favorite story--how odd that it crops up in this context. thank you for all the input to this site, Raven

By raven at Sun, 2006-02-05 16:02


One more member for the

One more member for the "Dorian Gray's Revenge Club" applying. David tells me I looked as though I was getting a "dowager's hump" but no longer.  Long-term puffy ankle have likewise vanished.  I also look like I have lost weight, but if anything I have put a bit on, due to the fact that muscle is heavier than fat.  My high cheekbones have returned from wherever they were hiding and my hair and nails are growing at a rate of knots.  I had my hair cut short because it was getting so limp and lifeless and I thought I was never going to be able to grow it long again.  I had reached the height of  68 inches when I was thirteen, then I stopped.  I seemed to have shrunk of recent years, probably because I was stooping, but now I am standing tall again.

I can verify David's hair reappearance: I made him shave it really short because it looked so sparse and skimpy, but now I shall take a new photograph of him with his "new hair", just in time for his new passport......Sarah

By Sarah at Sun, 2006-02-05 18:42


This is so timely, David,

This is so timely, David, as I am just starting to notice such 'body reconstruction' changes in myself.  I have only been on the Wheldon protocol for 3.5 mos!  It seemed that everything became more "puffy" for me around my MS dx 4 yrs ago.  I gained weight over the yrs from lack of exercise, so much that I barely recognized myself.  Friends with whom I had played yrs of competitive tennis were unable to recognize me.  The swelling of the neck, orbits, tops of my feet....all those things.

David, your attention to these easily overlooked subtleties are what keep me on track.  Especially in this case where I see it first hand.  Very interesting picture comparison.

Thank you!

KK2  :)

By kitkat2 at Sun, 2006-02-05 19:16


The sense of reconstruction

The sense of reconstruction continues. Here's a little observation: When I was nineteen I was knocked off my motorcycle by an oncoming car which turned in front of me. I had a premonition it was going to do this and I slowed down. It was a dead-straight rural road. I recall flying over the bonnet of the car. No bones broken, and a soft fall in a ditch. However, my right ankle was bruised, and this extensive bruising took a very long time to heal. When it healed it left a mass of tiny veins and a purplish colour to the skin. Every so often since then the whole area has had periods when it looked angry, and sometimes it has seemed on the point of breaking down; during those periods it became quite painful, too, with a deep pain as though periosteum were involved. After treatment with antibiotics all this has vanished. The skin is a normal colour, texture and tone. You would not now know that a lesion had been sited here for 30 years. I guess chlamydiae as well as blood filled that haematoma: I suffered with chronic sinusitis at the time. I note this small event just for the record. Might it in later life have become ulcerated and secondarily infected? Dorian's picture improves a little more. David

By D W at Tue, 2006-02-21 11:31


How utterly fascinating!

How utterly fascinating! Makes you wonder if that "contaminated site" has been the original site for you all this time. Has it been about a year since treatment for you? are you treating in pulses at this point? Marie

By mrhodes40 at Tue, 2006-02-21 13:57


Thanks, Marie. I'm quite

Thanks, Marie. I'm quite taken aback myself. I had always wondered why this bruise had healed badly, with vascular neogenesis and abnormal superficial veins with dilated and narrowed sections beneath paper-thin skin. And, after all this time, how it should have the ability to correct itself with treatment. I think this is just one site of many. It was just obvious because it was very superficial. One of the many pathologies of chronic cpn infection is a vasculitis.

I took 6 months of continuous treatment; reactions followed 2nd and 3rd go of metronidazole and then left off. I think I may be one of the lucky ones who, once their immune systems are adverted to the presence of the germ, are able to clear it out. Soft tissue improvements continued after antibiotics were stopped. I'm now on intermittent maintenance.

By D W at Tue, 2006-02-21 15:12