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porphyrias

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Hi- Im wondering if anyone is dealing with any of the porphyrias. I read recently about porphyria cutanea tarda (skin type) and Im almost positive it is what I am dealing with based on symptoms the last couple of yrs. Im wondering what treatments are an option. Is it possible to chelate w this ? It sounds like mercury and lead are the culprits in this condition and I had started chelating only to have my symptoms worsen last yr while taking EDTA. I cant find any info on the web regarding chelation with this condition. My LLND was tied up a the DK seminar this week and couldnt discuss this with me.

I want to get the lab testing ASAP.

http://www.labbio.net/ - but I understand the labs go to Paris and take some time.

Im concerned that I wont be able to handle most (including the 6 wk parasite protocol I am supposed to be starting) with this condition but I read somewhere that the skin type is a bit different and maybe it will still be possible.

thanks for any info this is a very new subject to me. Im trying not to be overly concerned. Im hoping I didnt pass this condition on to my son as lyme is enough of a burden.

be well~

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