This Is MS Multiple Sclerosis Community: Knowledge & Support

I was looking at the Cpn site and was reading your husband's story. The change in his looks is amazing. I would have asked this over there, but am not familiar with blogs yet. The pictures really caught my attention, because it looks like my son's neck. Is swollen glands a part of what your husband was experiencing?

My son has had numerous gland's that would literally swell up huge over night. He was treated with various ABX short term but then I asked for Biaxan which seemed to reduced the glands more permanently, but his neck has remained swollen ever since.

It is amazing in reading this stuff, how much these infections over lap and look similar. I don't know Cpn, but I understand Mycoplasma and Lyme pretty well, so am familiar with stealthy pathogens.

I think rather than just swollen glands it was all round tissue swelling, which developed gradually, had started before we even met. The change does look amazing, but I didn't even notice it until it went. For a while he looked rather haggard. You ought to write to David about it. His email address is at the bottom of this first page: http://www.davidwheldon.co.uk/ms-treatment.html. Symptoms always tend to overlap a lot, with many things, but the two main CPn regimes are aimed at other stealth pathogens as well as just CPn. This is useful since stealth pathogens are aptly named and keep well hidden.

Sarah

_________________
An Itinerary in Light and Shadow Completed Dr Charles Stratton / Dr David Wheldon abx regime for aggressive secondary progressive MS in June 2007, after four years. Still improving with no relapses since starting. Can't run but can paint all day.

Thanks I will email him.