CLL leukemia: Just diagnosed, what can be done?
Husband 84 just diagnosed with CLL,
Is this common in older people and what things are done to stop from progressing?? We are new to this site and this diagnosis..
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Hello dear
Hope you Re doing well today
Thanks for god and for everything , and thanks for sharing this link it’s useful , it’s hard but I think we can make it easy if we didn’t fear , Lori as yesterday she listen to her doctor she known about cll is a disease he lives with it ,not like cancer , according to your opinion its ok to know about her Cll like this ?
Hi @sonia85, Anytime we or someone we love is diagnosed with a blood cancer, that’s just scary. So you’re only human to worry about your mom after finding out she has Chronic Lymphoid Leukemia. The good news is this one is usually slow to develop as you read in the article I gave you. It appears your mom is in the very early stage of the disease where there is no need to treat.
Your mom’s doctor is relying on her recent blood tests and her bone marrow biopsy to make that diagnosis. He plans to follow up every 3 months to monitor her blood work. That is plenty of time to make sure there are no changes in her blood cells and react if there are any changes.
Three months is the same schedule I’m on for monitoring my blood. My doctor is at ease with the 3 month span to be able to catch any potential issues early.
In your mom’s case, if this were me, I’d be comfortable with what her doctor said. She should get on with her life and enjoy every day. If she feels extra tired for an extended period of days or any serious changes in her health, she can simply call the doctor and get her blood tested earlier. I know people who have been on Watchful Waiting for years with no changes. It just doesn’t pay to worry about what ifs! Our imaginations are often worse than reality.
I sincerely encourage both you and your mom to exhale! I know you’ve been holding your breath. 🙂
Do you live near your mom? Do you often do things together? What brings your mom joy every day?
Thank you Lori, her doctor said she need morrow transplant SAP and we need to get a donor for her from her siblings, I can't donate to her because we are not match only from the family members can donate or the hospital will provide it but it will cost us more,
Did you go through all that during your time,
She's really suffering a lot, I'm going to be with her next week by God grace,, I'll talk to her to see if she can shave of her hair, thank you
Hi @majid12 I know you wife’s journey with AML and a transplant all too well. This type of leukemia requires some heavy artillery to win the war. But each battle is worth fighting. 🙂
She’ll begin her fight with at least 1 round of chemo for a week. The first one is called the Induction phase. It will be used to knock down the cancer cells in blood/marrow and hopefully get her into a temporary remission.
Then she’ll have a waiting period of about 28 days while her blood numbers rise again. After that, there will most likely be another round of chemo referred to as Consolidation. It helps to ensure most of the cancer cells are gone. Her type of AML is aggressive. So even though it looks like she’s in remission, it has a way of returning. That’s why the bone marrow transplant is necessary. Her old bone marrow failed to recognize the cancer cells. So they were allowed to proliferate. The hope is that the new immune system she’ll receive from her sibling will again recognize the cancer cells and destroy them. It’s really very fascinating.
If her transplant isn’t soon after that Consolidation, she may have another session of chemo again. It’s important to keep the body in remission so that most of the cancer is gone before going into transplant.
She may feel nauseated and lose her hair, like I mentioned. But for me, once I started chemo, I actually began to feel better because the cancer cells were dying off! My fever went away, I regained my strength and I started feeling human again! I was fit and ready for my transplant.
I don’t have many family members so I had to go through bone marrow registry for my donor. Transplant teams often look to siblings for the donors so you’re wife is fortunate to have some brothers and sisters. They’ll be asked for either swab samples from inside their mouth or blood samples to check for a match.
The transplant itself is basically a blood transfusion. But instead of blood, the bag is filled with stem cells and takes less than 1/2 hour to be infused through a port. It’s pretty anticlimactic considering all of the drama leading up to it!
Several days before the transplant can happen though, there will another session of chemo called Conditioning. This chemo prepares the bone marrow to receive the new stem cells from her donor. It’s necessary to clean out the old bone marrow so that the new, cancer free cells have a place to set up housekeeping. It takes a minimum of 10 days to reach engraftment and sometimes longer. That’s when the new cells start producing blood cells in their new environment.
Your wife will have a very compromised immune system while all of this is going on. So she will be taking a lot of medications to keep her healthy.
I know this all sounds complicated and intimidating. And it is… But her doctors and their teams of nurses will be guiding her through this journey one step at a time.
I’m so relieved that you’re able to be with her and I know she’s going to feel so much better having you home! She will be required to have a caregiver with her especially during the transplant and recovery period.
Has she begun her chemo yet?
CLL Diagnosis at 80 Stage 0 Discovered Incidentally
I have very brief lasting chills — so I just put something warmer on for a few minutes and they go away. This happens most days and several times a day. Not scary to me — anyone else have this happen? Just curious !
Dr. Diagnosed me in 2020, but said it appears my CLL began in 2019. I am now 82 and still at stage 0. I also have morning nausea which goes away after eating.
Welcome @alliefair. Thank goodness the CLL was discovered incidentally. I moved your message to this existing discussion:
– CLL leukemia: Just diagnosed, what can be done? https://connect.mayoclinic.org/discussion/cll-leukemia/
That way you can easily connect with fellow CLL-ers like @kegraves @pieter1961 @carl50 @mabfp3 @sandiegostu @annieg87 @teddytwo @shirlpat, who can share their experiences and if they get chills periodically throughout the day or nausea in the morning.
Alliefair, are you also under active surveillance and not taking any treatment specifically for CLL?
Yes. I have a hematologist oncologist in addition to my primary care physician. No treatments so far for CLL.
Hi Alliefair, I was diagnosed with CLL in March and had a lymph node removed. I’m not receiving treatment currently but am in the Wait and Watch period with review every 90 days. Like you, I have periodic chills and morning nausea. I’m glad you posted because I haven’t known anyone with those same symptoms. God bless you in your CLL journey.
Hello dimcdee, Thank you for your response. I don't find these symptoms alarming, but interested to know someone else has them as well. The fatigue I feel is common, I know, but the two I mentioned just seemed odd to me. Sending blessings to you as well.
@loribmt ,non matched maybe because they're her half brothers, no more relatives to turn to right now and we are yet to find donor immediately because her chemo is almost been completed ,we are still searching for donor, these really scare me now ,I don't want to lose her ,she's such a beautiful soul to lose, finding donor is really difficult,