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Questions for those with repeated high porphyrin tests

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Has anyone else been told that repeated high porphyrins combined with otherwise

unexplained GI symptoms,chronic malutrition or failure to thrive,and ascites,are

a possible sign of metabolic liver disease ? I was told this when I went in on

Friday.In fact,the doctor went so far as to say,that this might be a " new " type 

of metabolic liver disease.If this is the case then an awful lot of those with

" autism " have the very same thing.

When I asked my last Dr. (You know who.) why my porphyrins were so high,he

simply shrugged his shoulders,and said " who knows " .I think for many children on

the spectrum,with GI disease,and high porphyrins,metabolic liver disease would

be a lot more reasonable explanation than mercury in vaccines.It would certaily

explain the continued high porphyrins in children who have been on chelation for

a while.Somebody once said to me if all porphyrins are consisteinly high,this

means a genetic,not environmental,reaon why.

I don't think I ought to tell my doctors,that I was chelating,and stopped,and

that these more recent test were done weeks after I stopped chelating.Would

porphyrins that are caused by metabolic disease respond to chelation,albeit

temporarily?

I wonder if  doctors who have not looked at this as a possible explanation,have

not because they are trying to prove,or are going by Wakefield,and antivaccine

dogma,conciously or not.Are there those,especially parents,who would oppose or

deny this as an explanation of their children's problems,even if it were

true,because they are so devoted to vaccines as an explanation?

Why would they want to test my blood levels of creatine as well ?

I see that autoimmune liver disease can cause " whole body " joint pain,what about

metabolic?

I was tested years ago for CF and Alpha-1,and I do not have either of them.

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