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When And How Did You Know Your CLL Was Changing.
I am not on any treatment. I was diagnosed in December of 2019. I feel fairly good now. When did any of you know your CLL was changing? My WBC has held steady for several years in (Phone number can only be seen by MyLeukemiaTeam users) range. I am more interested in what symptoms you noticed when knew there was a change happening.
I noticed the night sweats and the fatigue. Also the slow and steady rise of my blood work. Cold or other infections seemed to take longer to get over.
Thank you.
I Have Not Seen Information About Mutated Vs Unmutated CLL. I Am Unmutated. Has Anyone Else Dealt With This?
Why Does Blood Come To The Surface Of My Hands And Arms Every Time I Bump Something
I Have A Dual Diagnosis Of MDS And Hereditary Hemochromotosis. Any One Else? Looking For Some Answers. Thanks
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