In 2019, 65-year-old @LoriBMT sat in a Mayo Clinic lab area awaiting her turn for blood work. She had been in the hospital for more than six weeks following a bone marrow transplant.
@LoriBMT is a positive person, but after weeks of feeling tired and week, she wasn't sure she would ever feel healthy again. When she looked in the mirror, she saw a bald head and pale, saggy skin.
Then a woman in the waiting room struck up a conversation and shared that she, too, had undergone a bone marrow transplant and was there for her two-year checkup.
"She was healthy. She had hair. She was a little bit tan. She looked like this font of energy," says @LoriBMT. "Then the guy next to her said: 'No kidding. I'm here for my five-year checkup.' I walked away from that conversation so inspired and encouraged — filled with hope. I can be this person. There is life after this."
The making of a mentor
@LoriBMT had been diagnosed with acute myeloid leukemia, also known as acute myelogenous leukemia, or AML. This cancer of the blood and bone progresses rapidly.
"I was perfectly healthy. And then within three weeks, had I not been rushed to the hospital for a blood transfusion, I wouldn't have made it to the next morning," she says. "AML can come on very quickly."
The first phase of @LoriBMT's treatment began near her home in Appleton, Wisconsin, with eight weeks of chemotherapy in the hospital to put her leukemia into remission. Because her leukemia-producing bone marrow cells had undergone chromosome changes, @LoriBMT needed a bone marrow transplant to replace them with leukemia-free cells that would regenerate healthy bone marrow. She decided to go to Mayo Clinic in Rochester, Minnesota, for her transplant. There, she received infusions of stem cells from a compatible donor, known as an allogeneic transplant. This was phase two — consolidation therapy — considered crucial to decrease the risk of relapse.
@LoriBMT's grueling treatment was successful, and her experience in the Mayo Clinic waiting room inspired her to help other people navigate leukemia and bone marrow transplant. While searching for ways to help, Lori discovered Mayo Clinic Connect, an online support community for patients and caregivers.
After a year giving informal support to other people with leukemia, Mayo Clinic Connect community moderators asked her to become a volunteer mentor. Connect volunteer mentors are active members in the community who have firsthand experience with a health condition. They welcome and support new members, check in on them and moderate discussions.
"If I can help, I do," says @LoriBMT. "I only hesitated a nanosecond when asked to be a mentor."
Same diagnosis, 46 years apart
Sky Toyne, a 19-year-old college student at Iowa State University in Ames, Iowa, had been experiencing odd symptoms for several weeks in fall 2021. When she finally found time to visit a health care professional, the care team took blood samples.
"Worried looks were exchanged, and bloodwork was drawn again," says Sky.
Sky's next stop was the Emergency Department at Mary Greeley Medical Center in Ames, where a hematologist asked her a series of questions:
- Had she felt more fatigued lately?
- Was she paler than usual?
- Did she bruise easily?
Sky's answers resulted in a trip to the oncology floor. She remembers needing to look up the meaning of the word "oncology."
A bone marrow biopsy confirmed a diagnosis of acute myeloid leukemia, and the prognosis was challenging. She would need a bone marrow transplant to give her the best chance of survival. She recalls her oncologist telling her, "You're going to have to put on your boxing gloves and fight."
"She had some molecular and chromosome changes that are considered high-risk," says William Hogan, M.B., B.Ch., a Mayo Clinic hematologist. "And even though she achieved a first remission, the risk of relapsing later is high. That was the rationale for considering transplant."
As an Asian American, Sky also had a lower chance of finding a bone marrow donor match in the national bone marrow donation registry. Fortunately, her brother was able to donate his bone marrow as a half match for Sky's allogeneic transplant. "Sibling match — that's our first choice," says Dr. Hogan. "There's a 1 in 4 chance that your brother or sister would be a full match. And there's a 50% chance that they would be a half-match."
Sky completed remission induction therapy at Mary Greeley Medical Center and went to Mayo Clinic for consolidation therapy, which included a bone marrow transplant in February.
Finding mentorship on Mayo Clinic Connect
Sky's oncologist at Mary Greeley Medical Center did his best to prepare Sky and her family for the intense therapy she would need.
"He said: 'You're starting a marathon. This is not going to be something where you're in the hospital and you're out and you're done.' He really set the tone for us. We understood that this was going to take all our energy and require all our focus," says Mari Toyne, Sky's mom.
Sky's parents worked together to learn as much as they could about acute myeloid leukemia and bone marrow transplant. Mari learned about Mayo Clinic Connect through patient materials she received from Mayo Clinic. She created an account and discovered a post from @LoriBMT about her leukemia experience. She took a chance and commented on one of @LoriBMT's posts.
"She reached out right away," says Mari. "It was so nice talking to someone on the other side. We talked to all the doctors, nurses and technicians. They can tell us clinically what was happening and what was going to happen. But talking to @LoriBMT — she was so inspiring. It was encouraging to talk to someone who had lived through it."
"We discussed a lot of potential issues that can happen," says @LoriBMT. "I said she's going to have some really bad days. Some days, I can move mountains, and other days I feel like I'm in a pit where there are bulldozers pushing gravel on me. Bone marrow transplant — it's not for the faint of heart."
Mari joined other groups online, including some specifically for parents of bone marrow transplant patients, but she says none have been as helpful as having @LoriBMT as a mentor.
"We can contact her and ask, 'Did you go through all this stuff?' and she explains her experience. From her symptoms to the mucositis, to the headaches to the bone pain — she covered all of that for us. So we knew what was normal and what we should expect. I can't express how incredibly helpful that was," says Mari.
Dr. Hogan agrees. "There is no substitute for talking to somebody who's gone through bone marrow transplant. Having a person you can relate to one on one — who can describe what it's like getting chemotherapy, radiation therapy or transplant, and going through some of the side effects — makes things a lot easier to understand and anticipate what will be involved. And seeing somebody who had a successful outcome provides real inspiration and hope during the difficult days," he says.
Meeting in person sparks true connection
Before Sky's transplant, @LoriBMT contacted Mari to check in and mentioned that she had an upcoming appointment at Mayo Clinic in Rochester. Sky and her family were going to be there at the same time, so @LoriBMT suggested meeting.
"At this point, we were kind of down. It was pretransplant, and we didn't know what to expect. It was kind of scary," says Mari.
They met in a patient lounge in the Charlton Building.
"I don't know what they were expecting," says @LoriBMT. "I'm 68, but I'm not old. I have all this energy. I introduced myself, and I just felt their sense of relief. We sat there for like an hour and a half just talking."
Sky and @LoriBMT had exchanged messages a few times, but meeting in person was especially meaningful.
"When you go through these experiences, it's very isolating," says Sky. "Being able to see someone walking and breathing that had already gone through everything I was about to go through with the transplant was really cool. I actually got to see someone who had experienced it all, and @LoriBMT is an awesome image of life after transplant because she's healthier than most people who haven't been through what we've gone through — and she's 68."
"Sky and I connected on a visceral level," says @LoriBMT. "I'd say: 'I bet you're at the point where you're really sick and tired of people telling you how brave you are. And every morning you go out and you're just trying to get through five minutes at a time.' And she'd say: 'Yeah! Oh, my gosh, I think you're in my head.'"
"@LoriBMT and I really latched on to each other because I think we are both very stubborn," says Sky. "One of the first things I told my parents was that I was not going to die from this. It's just not going to happen."
"Sky and I just bonded," says @LoriBMT. "I'm so amazed by the presence of this young woman. She has a very deep, abiding faith that she's going to make it through this."
The spirit of endurance
@LoriBMT and Sky continued to connect regularly after meeting in person. At one point, as Sky was recovering from her transplant, she asked @LoriBMT to share how she found her will to live.
@LoriBMT wrote Sky a letter explaining how she was able to endure her diagnosis and treatment.
"I changed it from 'will to live' to 'spirit of endurance,'" she says. "You never stop pushing yourself to keep going. That is the spirit of endurance. That plays a huge role in people. I never wanted to die, and I never gave up, but there were days when I asked, 'Oh, my God, how does a human being come back from this?' But if you don't like something, then you make a change. That's what keeps pushing me forward. I'm not going to let cancer take me down if I have an opportunity to go past it. The only two things we really have control over are our effort and our attitude."
Mari and Sky are grateful for @LoriBMT's mentorship and generosity. Mari encourages others to seek out patient mentors on Mayo Clinic Connect.
"I highly encourage people to at least check it out, even if they don't write anything," says Mari. "The information there is very, very helpful."
The people there are helpful, as well. Describing her commitment to her role as a connect mentor, @LoriBMT says, "I honestly feel like this is one of the reasons I was spared."
Learn more
This story first appeared on the Mayo Clinic Comprehensive Cancer Center Blog.
Learn more about Mayo Clinic Connect Volunteer Mentors.
Hello everyone, Loribmt is a true Angle, I had reached out to Lori for support and she jumped right in with both feet, calmed me down and gave me encourgement and best of all friendship.
She is a true hero and we are so grateful to have Loribmt as a mentor.
Thank you for all you do Lori we love you,
Teammayo#1
My husband was just diagnosed with Mylodesplasia and has as yet to undergo his first blood transfusion. He is 73 and I’m at the point between panicking and wanting to be as uplifting as possible for him. I’m trying to read as much as I can about what’s ahead, including bone marrow transplant. I’m wondering if his kids would be viable donors. I found this story to be very positive and I wish both women good luck and good health.
Hi @kathy115 I’m so sorry for the delay in responding to you! I was on the road this weekend and away from my computer.
Let me help you and your husband out with his new diagnosis. I know from experience something out of the blue like this clips you off at the knees and you want to know everything you can about the situation. I’m with you, knowledge is power. But there’s also a danger in looking too far ahead and worrying about what ifs. Your husband is at the very beginning of his journey myelodysplastic syndrome. There are several subtypes of this disorder which will dictate the treatment he’ll need.
I want to get you started with some informational reading from our Mayo Website. It explains a bit more of the disease, diagnosis and treatment. With your research you may have already come across this: https://www.mayoclinic.org/diseases-conditions/myelodysplastic-syndrome/symptoms-causes/syc-20366977
In our Connect forum there are some active discussions regarding MDS. I’ve posted a couple of them here for you. The conversations are listed in chronological order with the oldest first. There is a box in the discussion heading where you can reverse the order to newest to oldest.
I have been diagnosed and under treatment for MDS.
https://connect.mayoclinic.org/discussion/i-have-been-diagnosed-and-under-treatment-for-mds-whag-are-the/
MDS
https://connect.mayoclinic.org/discussion/myelodysplastic-syndrome-mds-1/
This is also a very good source of information with a little video from Dr Al-Kali, a specialist at Mayo in MDS. https://connect.mayoclinic.org/blog/hematology/newsfeed-post/myelodysplastic-syndromes-treatment-past-present-and-goals-for-the-future/
Regarding the potential for a bone marrow transplant: To find out if your husband’s kids are possible donors it’s a simple initial test of a mouth swab to see if they match.
https://bethematch.org/
Be The Match foundation has kits available but your husband hasn’t been tested for DNA for a transplant so I’m not sure the protocol for matching at this point. He can ask his hematologist. However, if he’ll require a transplant, all of that will be decided at the time. It’s fairly quickly discerned if his children will be potential donors or not.
Thank you for your positive thoughts on the story about Sky and myself. It’s been quite a journey for both of us, but it shows you that there is always hope! I want to help you find that too. ☺️
Do you have any specific questions for me?
Aw, @teammayo1, now you’re making me blush, gurl…
It’s been such a pleasure getting to know you and being able to help you out of trouble waters…🙃 But ya know, those conversations work in both directions with our mutual support, encouragement and that reward of friendship! So thank you, my friend. 🐝. Talk to you soon.
@loribmt WOW you are an inspiration!!!!! when I read my diagnosis last week on a piece of paper and still haven't talked to a doctor I was googling what CLL was and I got myself so upset I didn't eat or sleep for 3 days, my family doctor said STOP googling if you want information go to the Mayo Clinic website and get educated so it took almost 1 week before I did and although I still have not spoke to an oncologist this website gives me hope! I consider myself a super positive person but I have my moments! Thank you!
A diagnosis on a piece of paper with no explanation would rattle anyone. No matter how positive we try to be, we all have those moments where positive thoughts can be nudged aside with negative self talk. It’s tough to be human, huh. 😊
I’m really happy you found Mayo Connec and that I’ve been able to offer some help with your CLL journey in the ongoing conversations we’ve been having in the forum! It always helps to know other people are going through the same personal battle, doesn’t it? Hugs!
Am diagnosed of renal mass. Can somebody advice me on how to go about it,
The doctor said the only solution is nephractomy is the only solution.
What can i do please
@zenithi, you've been told that you have a renal mass. Were you told that this is kidney cancer?
For most kidney cancers, surgery is the initial treatment (nephrectomy or partial nephrectomy). You can see more information about treatment options for kidney cancer here: https://www.mayoclinic.org/diseases-conditions/kidney-cancer/diagnosis-treatment/drc-20352669
It sounds like you might need more information about this mass to feel comfortable with your treatment choices. Will you have another consult with your doctor? Have you considered a second opinion?
This is great, truly love it nothing like having someone to share their journey with the same diagnosis as you. I have rare leukemia called Blastic plasmacytoid dendritic cell neoplasm (previously known has killer cell leukemia) diagnosis July 11th 2021. If anyone have this diagnosis, can we connect with each other? I have had stem cell transplant this pass August. Have new computer tower no pictures at this time.
will be praying for your husband you and family.