← Return to Acute myeloid leukemia (AML): What can I expect?

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@JustinMcClanahan

Hello @nicollissa and welcome to Connect! Thank you for sharing so much with @dell060969 regarding your AML diagnosis, your words of encouragement and your willingness to answer and questions Dell has. I especially appreciated your tips on how to recognize and avoid depression while going through treatment.

@nicollissa, right off the bat you mentioned something that caught my eye, hemophilia. If you are comfortable sharing a bit more about yourself, were you born with hemophilia or were you told that because your platelets were so low that you had hemophilia like symptoms of bleeding risk? I only ask because hemophilia is a genetic disorder and believe it or not, I am actually a hemophiliac! Naturally, my ears always perk up a bit when I hear or see that words because it is a rare disease and I don't ever meet many people with hemophilia. Even if you were not diagnosed with hemophilia but experienced hemophilia like symptoms, I can certainly relate to that part of your experience.

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Replies to "Hello @nicollissa and welcome to Connect! Thank you for sharing so much with @dell060969 regarding your..."

thank you, Justin, I dont have "view and reply", only "reply". thx.

Justin, my reason for being on the discussion page my husband has MF, so one page leads to another. My husband has dear first cousins that are hemophiliacs. You probably all ready know this, hemophilia is passed thru females to their male children. It doesn’t mean every male child will have it or every female will pass it on. His cousins were tested to find which girls carry and boys would have it. He had a dear cousin that lived a sheltered life his family always afraid he would get hurt somehow, after he grew up he decided he would live his life to the fullest. Which he did, he died at the age of 75 for something else.