Great information. So appreciate your time.
Have you started on this medication yet.

When I had CLL for 10 months and my WBC count was 76,000 I requested medication. I had to learn about medication and CLL by joining groups and learning. I currently take Brukinsa. I know all medication may have possible strange ill affects but most of the time nothing happens? Last year I read that this medication can be effective for 10 to 20 years. This medication uses the "BTK inhibitor" to control (kill) those bad cells and it does not affect healthy organs or cells. I also read that eating healthy and exercise both had benefited my health. I am 74 and I visit the gym 3 times a week and I am active at my 5 acre property located in an oak tree forest. A few months ago I cut down a 50 feet tall pine tree with a 2 1/2 feet trunk for fire wood next winter. I plan to cut the wood into sections I can move then split the wood to use in my wood stove. I hope to start jogging again which I have not done in the past year (PETECHIA or exploding capillaries in the skin from over exertion.) I got a money grant from Leukemia Society for copay $4,000 and my insurance paid the balance so my cost was $0. My physical and mental health are both normal and better each day.My last blood test indicated every element in the test is 100% normal and my WBC count is 7,500. Celebrating Long Life (CLL)

The picture is sun rise at my property which has 85 trees on 5 acres. The grass in the summer dies from the hot dry heat to a golden color.

I requested medication after 10 months when my WBC count was 76,000. I did not have any lymph gland problems nor fatigue? I requested medication because it had the least ill affects. I know all medications or treatments can have possible ill affects. I think chemo has a very high ill affect. My medication is Brukinsa (this uses the BTK inhibitor) and I know this medication will be good for 10 to 20 years or until the bad cells mutate and a new medication is required. I think all medications are expensive and mine cost $15500 per month. I did get a money grant from Leukemia Society to pay the copayment ($4,000) so my medication did not cost me anything $0. I think you should learn about medication by doing research in the RESOURCES section that is here.