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<blockquote data-quote="Vettester Chris" data-source="post: 4696" data-attributes="member: 696"><p>Nelson, unfortunately chelation treatment wasn't even put on the table, since technically I am only a carrier with a single hereditary mutated gene. I believe it's known better as the <em>HFE Gene</em>. There are variances in ferritin levels within my family; ranging from 400 with one of my brothers, to 700-800 with my day (the culprit), but mine being the highest over 1,400. Again, since they couldn't tag both genes on me with the biopsy, believe it or not the specialists that I was referred to just sent me packing, said I'm fine. I had to basically figure out a mono plan to manage this, my GP being supportive of course, but not overly in the know. On the sun ... I use MelanotanII during the summer and vacation time (works great!).</p></blockquote><p></p>
[QUOTE="Vettester Chris, post: 4696, member: 696"] Nelson, unfortunately chelation treatment wasn't even put on the table, since technically I am only a carrier with a single hereditary mutated gene. I believe it's known better as the [I]HFE Gene[/I]. There are variances in ferritin levels within my family; ranging from 400 with one of my brothers, to 700-800 with my day (the culprit), but mine being the highest over 1,400. Again, since they couldn't tag both genes on me with the biopsy, believe it or not the specialists that I was referred to just sent me packing, said I'm fine. I had to basically figure out a mono plan to manage this, my GP being supportive of course, but not overly in the know. On the sun ... I use MelanotanII during the summer and vacation time (works great!). [/QUOTE]
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