← Return to Anyone have chronic lymphocytic leukemia (CLL)?

Discussion
Comment receiving replies
Profile picture for Lori, Volunteer Mentor @loribmt

Welcome to Connect, | @whatshallido59 |
Your original post in another group mentioned: “I have been diagnosed with cronic lukemia is there any one that has the same.” I thought I’d bring you right over to this CLL (Chronic lymphocytic leukemia) support group so that you could meet up with some of the members who also have CLL.

If you wouldn’t mind sharing a little more about yourself, when were you diagnosed with the Chronic lymphocytic leukemia? What has your hematologist told you about your disease? CLL tends to be a very slowly developing form of leukemia and often patients can go years without any treatment. Are you in a watch and wait period or are you expected to start some treatments?

Jump to this post


Replies to "Welcome to Connect, | @whatshallido59 | Your original post in another group mentioned: “I have been..."

@loribmt my doctor here didn't say anything to me , I found out that I have CLL when I was in Germany.

@loribmt
My blood pressure was very low so my daughter took me to the doctor and after blood test they suggested that I go to the hospital. My white blood cell count was 97000 they called a hemotogist and he told me that I have CLL, my hemotologist at home told me nothing and I saw him two weeks before we went to Germany and my white blood cell count was 87000.