Posted by kikkie2004 on
URL: https://www.es-forum.com/EMF-Sensitivity-Porphyria-tp2442216p2449257.html

Hi Marc

Normally it's genetic, and the symptoms are rather obvious (except for the skin one, where exposure to the sun can make the skin swell and ache, but without blistering and thus the diagnosis is often mised).

But infections, etc, can cause secondary porphyria. And the lab tests araare inaccurate and only test for some of them (there is about 8).  

And according to that professor these porphyrins are the root cause of the symptoms of CFS , MS, MCS, ES, etc.

And two of those links I posted have people getting better from ES - one treating Cpn with antibiotics and the secondary porphyria with gluose, activated charcoal, carbs, etc, and the other group were treating conventionally diagnozed porphyria with Tegamet.

--- In [hidden email], "Marc Martin" <marc@...> wrote:
>
> > Then I found a book by a professor Steven Rochlitz, who asserts that
> > porphyria is the root cause of CFS, MCS, ES etc
>
> I thought porphyria was merely a symptom of heavy metal poisoning,
> just like can be... (?)
>
> Marc
>