My Bone Marrow Transplant (BMT/SCT) story: Will you share yours?

Hi @katgob…sending a hug. Day 3 for you! The next two weeks can be pretty challenging as your body starts feeling the after-effects of the preconditioning chemo and the transplant itself. As soon as those new cells engraft in your marrow, usually 14 to 20 days after infusion, you’ll start to feel much better again as the bone marrow starts producing new blood cells!

Just so you’re aware, fatigue will be your constant companion for a while. Don’t try to push yourself because it can’t be done. Just listen to your body when it tells you to rest. It’s not a failure on your part! So do your best to keep your spirits up during this period. It passes! Sending positive vibes for strength and courage. 💕

Lori,
My update. So far keeping nausea away. Today and tomorrow I have the 2 chemos for the research study. I must say I did not ask what the medicine was. Plus, due to the numbers of my 24 hr urine test weeks ago, I must have a catheter for hydration for two days.
As I have been doing, I am listening to my nurses and the doctor team that come by daily.
I will ask for compazine if the nausea increases. That will help me sleep as my urine is processed for me.
By the 14th my anti rejection meds start.
Thank you Lori. I am remaining positive and hearing the doctors say I am doing well.

Hi Kat…didn’t want to let another day go by without checking in! Day 8? That’s about the time things started to get a little dicey for me. How are you feeling?

I will update later. My whole post vanished as a Mayo Clinic survey popped! Guess Day 8 and my others days will come later.
As I knew by your timeline on your transplant, I am on target. Where I am supposed to be.
For sure my "not in oz" was day 3 realizing I had 2 chemos for the rejection coming.

Forty-four days ago, my husband and I went to see his primary care physician. My husband presented to his doctor that he needed a heart stint. His self-diagnosis was based on his shortness of breath and other people's heart stint stories. His primary care doctor didn't say much except, "Go to the emergency room now." So, we left the doctor's office drove past three other hospitals and went to Mayo Clinic's emergency room. Looking back, that was the best decision we made. Because, boy, that diagnosis wasn't even close! The ER doctor told us his heart was fine but something "weird" was going on with his blood.

I now know that Leukemia is not just one disease but an umbrella term for blood cancer. His official diagnosis is B-Cell Acute Lymphoblastic Leukemia with low hypodiploidy. He developed TLS (Tumor Lysis Syndrome) immediately after starting his first round of chemo. That was so much fun, not. The good news is he has reached MRD, his kidneys are recovering, and his immune system is good right now. The bad news is this is a rare B-ALL and the prognosis isn't good. So, Monday, he will start the second round of Chemo and the search is on for bone marrow donors so he can have a SCT.

I have begun my arduous research on HSCT and what to expect. It sounds like a tough road is ahead for both of us. I am not new to caregiving. I spent the last 4 years taking care of my sister who had ALS. I did everything for her. It was an exhausting journey. Her funeral was less than a month before my husband's diagnosis. I was just starting to take care of myself again. And now, here we go again.

If anyone has any advice or information that might help me get through this, please let me know. I am glad I found this message board because I do not want to put this out on my personal social media. It is nice to know that I am not alone.

@caregiverx2 Welcome to Mayo Clinic Connect! I’m so glad you found this site especially given your reluctance to use social media. I’ve posted 2 discussions for you to check out. One is for caregiver advice
https://connect.mayoclinic.org/discussion/transplant-caregiver-advice-got-tips-to-share/
And this one is about the journey. It was started by @loribmt who is a mentor for Mayo Connect. She is great at answering your questions!
https://connect.mayoclinic.org/discussion/my-bone-marrow-transplant-bmt-story-will-you-share-yours/
I hope this will be a good start for you. Please feel free to ask any questions you have! BTW, how did you find Mayo Connect?

Hi @caregiverx2 I’d like to add my welcome along with @becsbuddy. She tagged me in this conversation because I also had an Allogenic stem-cell transplant, along with several other members. We have a lively, ongoing discussion where you’ll be able to get a ton of information to help navigate you through this journey with your husband…everything from lodging, what to bring for a 3 month stay, how to stay healthy, etc…no subject to big or two small to answer! We have your back.

I’d going to ask our moderator to merge your discussion into this group, which Becky mentioned:
My Bone Marrow Transplant Story; Will you share yours?
https://connect.mayoclinic.org/discussion/my-bone-marrow-transplant-bmt-story-will-you-share-yours/

You’ll meet members, @alive @edb1123 @kt2013. jenmkr63 timt347
@jrwilli @katgob and others who have either had a transplant or are caregivers.
Will he be having this done in Mayo Rochester?

Lori,

Thank you for the welcome. This is all so scary. We are at Mayo Jacksonville Florida. We are fortunate to only live less than an hour from the hospital (if traffic is good).

Dear Caregiverx2, welcome to the “family”. I am an 11 year survivor of acute myelocytic leukemia (AML) and peripheral stem cell transplant from my sister. I was cared for by Mayo Clinic, so I think you are at the best medical center in the world.
Here are a few things I learned on my journey…
I also thought I needed to research and educate myself on all things about the disease and treatment. What I discovered was it was too overwhelming and I needed to trust that the Mayo team would provide me with the education I would need, based on my cancer and planned treatment. The internet wasn’t a good place for me to hang out, it made me worry more and it was exhausting to try and sort out what applied to me and what didn’t.
Another important lesson for me was to stay in the day. Again, as a world-class worrier, it tried to control what was not within my control. So, I learned to breath through the tough days, then lock them in a closet. And to celebrate every day, good or bad. Being a woman of faith, I leaned into that like never before. And in this, asking for strength and guidance to face each new challenge.
Mayo health care team members were with me every step and that made my path easier and the challenge manageable.
I hope my words will bring you comfort and know that I will keep you and your husband in thought and prayers.
Sending you a sunny day….

It’s great you live an hour away. I’m assuming the programs for Mayo Jacksonville is similar to Rochester. If so, your husband will most likely be required to be within 30 minutes of the clinic for about 100 days.
I know this all sounds so daunting and frightening. While I agree with you about wanting to learn as much about this process as you can, my suggestion is to limit your searches online. So much of the information may never even apply to your husband’s situation and it only serves to heighten the anxiety for both of you. It will be important to trust your husband’s transplant team for guidance as they will become his and your new family for years to come. I was told by my doctor and team repeatedly, that “we are married for life”. And they mean it.

I’m just coming up on my 5th rebirthday. While I joke that it’s ’no walk on the beach’ this life giving procedure is well worth the effort. I had AML, acute myeloid leukemia and had no other option for remission than to have this transplant. I was 65 at the time. Now 70 and feeling like nothing ever happened. I have unlimited energy, healthy and very active. My donor was 20 and I swear he gave me the fountain of youth. So, let’s get you and your husband through this too so you can get on with your lives!

When will he be having the transplant? Does he have a donor? What are your specific questions?