I've had CML for 20 years and want to encourage others

Hi @kaygrose, I’ve looked through several replies by members taking Imatinib but haven’t found comments on fatigue.
There is another discussion you may want to read through with members who have CML. Many discuss Imatinib and also Sprycel

~Does Anyone Have CML?
https://connect.mayoclinic.org/discussion/does-anyone-have-cml/

Have you mentioned the extreme fatigue to your oncologist?

I, too, have had CML for 20-plus years. They have made such great strides since I was diagnosed. I have been on Gleevec or Imanitib during most of that time and it has worked wonders. I do suffer from some fatigue but that's a small price to pay for what this wonderful drug does. Anyone diagnosed with CML, keep your head up. There is life with CML. God bless all of you.

Thank you for your reply. As I understand it, my brother has had treatment, though I'm not certain to what extent. The 'timeline' has motivated him to pursue something he has wanted for atleast 30 years, ... I know it probably bothers some that with the planned changes I am still referring to him in the male form. Hes been my little brother for almost 60 years, and I am not against it, it just takes getting used to and in the context of not being confusing i find it less confusing to not jump back and forth, but I will get used to it all. Anyway, with all else that has been explained as to what is being done, travel involved, and all, it's hard to determine what precisely has been done in regard to treatment though he did clarify that it can be and is being treated, but can not be cured. As far as other health issues he did have a heart attack and open heart surgery about a dozen years ago and is type 2 diabetic.

He was having every symptom.. not telling us about some of them . We thought he was stressed , graduation and a baby due ... He is home, waiting for second target treatment pill to be approved. He very nauseous and diarrhea at this time. He has to do summer school for one class, to graduate! I appreciate everyone here and the extra education

Oh gosh, you have a very stoic son. And I can certainly understand with all the stress on his shoulders that it was difficult to differentiate that from a potential illness developing.
I hope he gets his medication approved again so he can keep on with treatment. Patients shouldn’t have to beg for their meds…that is so frustrating. I had one of those targeted meds too. It was like jumping through hoops every month to get it approved one more time and when you’re not feeling well, that’s the last thing you want to do…acrobatics for health care!
I wish him all the best as he goes forward. One more class and he can get that diploma…but good luck studying with a new baby, huh? As his mom I can imagine you’d love to harken back to the days where you could cuddle him on your lap and let him know everything will be ok. He’s too big for your lap now, but he knows you’re looking out for him and will do what you can to help him and his new little family past this bump in the road.
Will you keep me updated with his journey?

Hi Martin, Welcome to Connect! And thank you for sharing such a positive story about your CML and the treatments you’ve been taking. Twenty years is a long time since your diagnosis and you’re right, so much has changed since then with available medications to help keep it under control. Your story and attitude are very inspirational.

So happy to have you here and I hope you’re a regular contributor to the discussion. Were you looking for anything in particular that led you to Connect?

CML Ph-negative BCR/ABL-positiveI am 65 and I have been diagnosed CML in Dec. 2023. Now I am taking HU 2x500 every day. I was told that TKI (Glevec or other) will not help me. I would like anybody with my case to share experience if had taken TKI with Ph-negative form of CML and if that helps them or not. Thank you.

Gavin start Bosutinib next week.. his white blood cells number are going down.. also watching his Uric acid levels and on a medication for Uric acid. He tired and hurts , we have home health coming in and a social worker..a change of life style and some education. Still waiting on the baby.. hopefully this weekend! Felt like a rollercoaster ride of emotions last 3 weeks. We all seem to be doing well. I am on FMLA but I been back at work.. lots of support and prayers

Welcome @dega. To help you connect with other CML members like @suzi71 @babyjakejake @anglis and many others I moved your question about tyrosine kinase inhibitors (TKIs) for your type of CML to this existing discussion:

- I've had CML for 20 years and want to encourage others
https://connect.mayoclinic.org/discussion/chronic-myelogenous-leukemia-cml/

You're right that Philadelphia (Ph) chromosome negative CML is usually treated with hydroxyurea (HU), low-dose cytarabine and interferon

I found this additional info https://cancer.ca/en/cancer-information/cancer-types/chronic-myeloid-leukemia-cml/prognosis-and-survival
"The European Treatment and Outcome Study (EUTOS) score is based on the percentage of basophils (a type of granulocyte) in the blood and the size of the spleen. It can be used to predict how likely it is that someone will have a complete cytogenetic response after treatment with a tyrosine kinase inhibitor (TKI) such as imatinib (Gleevec)."

Hi Kay: I have not been on here lately, but I was diagnosed in 1998 with CML, and I was only 52 at the time. I am now going on 77 this Nov. Imatinib is what got me through it all. I am now 6 years off of the Imatinib and holding a 0.000 undetectable status. I have to be checked constantly to be sure I am still TFR ( Treatment Free Remission). You or I should say I did get use to the fatigue. I had lots of bone pain in the beginning, and my doctor told me it was the Imatinib killing those cancer cells. There are various side effects, but the long range term of being treated is a good thing. CML is very treatable. Just take your pill everyday no matter how you feel. Rest if you need rest, and I learned to say NO to people who expected me to do more than I felt up to doing.