Thank you for your thorough response Dr. Ditah and especially the link you provided to the AASLD document. I am printing it out and will take it with me to my appointment later today. When I asked my doctor why she did not advise treatment, she said my levels were too low, and she thought my insurance would not authorize treatment, but that is my problem, not one that should interfere with her recommendations. She also said that
phlebotomy involves getting 'stuck' (which is no big deal to me) and that I might feel tired afterwards, so I didn't get an answer that satisfied my concerns. She told me to go to a
blood bank and just donate blood, and they would use the blood in their bank, but I had to tell her that despite the
Hemochromatosis Organization declaring HH blood as safe, very few centers actually did use the blood for donations, which surprised her. I would have two choices, either to not be transparent about having HH (which I wouldn't do) or pay for phlebotomies at the blood bank, which is not ideal as my care would be disconnected from my medical records at the hospital. My regular hemotologist/
oncologist was promoted to another position, so this Doctor is very young and brand new, and I am wondering if she is just not completely aware of the guidelines, so your reference material is very important. If I do not get satisfactory answers, I will
seek a second opinion at Mayo where I see the very capable and caring Dr. XXXXXXX Foran for my MGUS. Thank you!