1,123 total results
Discussion
Bruising with CLL
Hello Everyone, About a month ago, I posted a few questions for my husband concerning his recent diagnosis of CLL. He is 72 years old....
Discussion
CLL, Spontaneous Regression
Diagnosed with CLL at age 50 from blood tests and bone marrow my disease progressed slowly for 10 years without treatment. After 10 years my...
Discussion
Hot Flashes with CLL
Wonder of this might help those of us dealing with chills and hot flashes due to our CLL. https://www.yahoo.com/news/experimental-pill-cut-hot-flashes-161925642.html
Discussion
Waldenstrom's, CLL or MGUS?
Hi--I was diagnosed with WM in the summer of 2023 by a hematologist. My PCP, however, thought it might be CLL. A second opinion (online)...
Discussion
Can CLL be hereditary?
Is it possible there is a genetic component to this disease? In my family history, my grandmother, my aunt and my mother — and oddly...
Discussion
CLL and immunization experience
I am wondering what experience, if any, people with CLL have had after receiving HepA/Hep B, Tdap, pneumococcal immunization, and Shingrix immunization. I appreciate any...
Discussion
Leptomeningeal Disease and CLL
My father (80 years old) has been diagnosed with leptomeningeal disease which has a very poor outcome. He has been taking Acalabrutinib successfully for the...
Discussion
Anyone diagnosed with atypical CLL?
DX of aCLL seems to have completely different symptoms than typical CLL. Just trying to find others who share the same atypical dx that my...
Discussion
CLL with lambda monoclonal gammopathy
I am so pleased to have found this group, have read so many posts. I am 81 years old and 1 year ago was dxed...
Comment
Hi @1retiredcboperator, Welcome to Mayo Connect. I’m from Wisconsin and can commiserate with you about the...
https://connect.mayoclinic.org/comment/1592601/
Comment
I hope you're being seen by a CLL specialist at Mayo Rochester. Oncologists treat many cancers...
Comment
Hi @sharina65 Welcome to Mayo Clinic Connect. I see you popped into the conversation about CLL...
Comment
@philipschuyler Lori has good advice. Also check out CLL Society website. Be sure you’re seeing a...
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