Has anyone hypothised how cpni [1] fits into the MSi [2] latitude theory? Is it simply that vitamin Di [3] have a critical neuroprotective effect on growing bodies? Is cpn is as equally distributed throughout latitudes but the only difference being that those growing up with higher vitamin D ( via sunshine) are protected from cpn brain invasion.....or does vitamin D maybe protect against or help kill cpn?
Can anyone explain the lattitide theory to me and how cpn probably fits into it?
Thanks
___________________________________________________________
CPNi [1] pcri [4]i [4] and antibody positive , treating MSi [2], CFSi [5]i [5], TMJ, trigeminal neuralgia, IBSi [6]i [6] neutropenia, pus found in facial bone, Doxyi [7]i [7] 100x2,Doxy 200x2 zithro 250x1 alternate days. Metroi [8]i [8] pulses each month.
Links:
[1] http://www.cpnhelp.org/glossary/term/167
[2] http://www.cpnhelp.org/taxonomy/term/6
[3] http://www.cpnhelp.org/chlamydia_pneumoniae/vita
[4] http://www.cpnhelp.org/taxonomy/term/54
[5] http://www.cpnhelp.org/glossary/term/163
[6] http://www.cpnhelp.org/taxonomy/term/19
[7] http://www.cpnhelp.org/taxonomy/term/39
[8] http://www.cpnhelp.org/taxonomy/term/44
[9] http://www.cpnhelp.org/print/4219#comment-30822
[10] http://www.cpnhelp.org/glossary/term/171
[11] http://www.cpnhelp.org/taxonomy/term/63
[12] http://www.cpnhelp.org/chlamydia_pneumoniae/supp
[13] http://www.cpnhelp.org/glossary/term/168
[14] http://www.cpnhelp.org/glossary/term/183
[15] http://www.cpnhelp.org/print/4219#comment-30869
To start with, someone [9]
To start with, someone must be genetically predisposed to get multiple sclerosis, then they must get the pathogen, which must then get into the central nervous system, then they are more likely to get it if they are low in vitamin Di [3].
The Inuit live very far north but tend to be protected from acquiring MSi [2] because of their diet. Perhaps this will change if they get addicted to hamburgers.............Sarah
An Itinerary in Light and Shadow by a real "Painter of Light"...........Completed Stratton/Wheldon regime for aggressive secondary progressive MS in June 2007, after four years, three of which intermittent. Still slowly improving and no exacerbation since starting. EDSSi [10] was 7, now 2, less on a good day.
___________________________________________________________
I think Sarah's said it
The difference between what we do and what we are capable of doing would suffice to solve most of the world’s problems. Mohandas Gandhi
___________________________________________________________
The difference between what we do and what we are capable of doing would suffice to solve most of the world’s problems. Mohandas Gandhi
I am from the far
I am from the far North, was born and grew up North of the 58th Parallel. At some time after my dx of MSi [2], I was told that there was some correlation between being born in the winter months and MS as the mothers were more than likely very short of Vitamin Di [3]. Well I was born in December and that for the North is a very dark month with very little sunlight. Makes sense I guess. So you take the location, add the infection (or virus) with whatever type it takes and some genetic tendency and there you have it. I think that the mainstream medical society still believes that it is the combination of those three things, they just don't believe that the infection still exists inside of the cells and that there is any curing it.
Supplementsi [11] & NACi [12], starting CAPi [13] soon.
___________________________________________________________
SPMSi [14]< Supplementsi [11] & NACi [12], Doxyi [7] 200 mg, Azith 250 mg 3X/wk, most suppliments, currently Flagyli [8] 1500 mg x 3 days once per month
Its just strange because I
Its just strange because I dont have anyone in my family with MSi [2] but I definatly have a whole slue of family members on my paternal side who all had severe lung problems and all died of lung cancer.
___________________________________________________________
CPNi [1] pcri [4] and antibody positive , treating MSi [2],
CFSi [5], TMJ, trigeminal neuralgia,IBSi [6]neutropenia, pus found in facial bone,Doxyi [7] 100x2,Doxy 200x2 zithro 250x1 alternate days. Metroi [8] pulses each month.I don't have anyone [15]
I don't have anyone in my family with MSi [2] either, but by "genetic" I mean that there is a genetic predisposition, not that MS is an autosomal disease. The gene HLA DR15 is one implicated in causing MS, so maybe I carry that one. I do know for certain, though, that I was born on a latitude as far north as the north of Newfoundland, though and until CAPi [13] I had been coughing and spluttering most of the time............Sarah
An Itinerary in Light and Shadow by a real "Painter of Light"....................Sarah
An Itinerary in Light and Shadow by a real "Painter of Light"...........Completed Stratton/Wheldon regime for aggressive secondary progressive MS in June 2007, after four years, three of which intermittent. Still slowly improving and no exacerbation since starting. EDSSi [10] was 7, now 2, less on a good day.
___________________________________________________________