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Shelley B

Shelley

I went from being in the best shape of my life to battling cancer in only a few short months.

Three years ago, I made the choice to change my lifestyle, and I lost 100 lbs., which I can honestly say has saved my life. Prior to my cancer diagnosis, I was sharing my weight loss journey online to help others make positive choices. Little did I know that I was about to fight the biggest battle of my life!

Light The Night event with white lantern and fireworks honoring blood cancer survivor

Alyssa

My story begins with a diagnosis of hypothyroidism but they noticed something unusual with my white blood cell count, which was elevated but I had no infection. Further tests revealed that it was lymphoma. My initial diagnosis was incorrect so I went for a second opinion at the University of Kansas Cancer Center. They performed extensive bloodwork and my official diagnosis was primary splenic marginal zone lymphoma (SMZL).

pre-B cell acute lymphoblastic leukemia (B-ALL)

Harper

In the late summer of 2021, 8-year-old Harper returned to in-person school for the first time since March 2020 for the start of third grade. Shortly after the beginning of the school year, Harper began to complain of headaches and bone pain and would fall deeply asleep each afternoon after school. Her pediatrician chalked it up to the rigors of in-person learning, wearing a mask all day, and indicated that a lot of children were experiencing similar symptoms.

Seth HL

Seth

It was in my sophomore year at the University of Colorado Colorado Springs right around March 2021 when I first discovered the lump in my neck. I was simply doing homework at my desk, and my hand unconsciously brushed against my neck. I stopped and started to feel the unusual lump in my neck.

Soon after that, the tests started.

Samanatha pre-B-cell acute lymphoblastic leukemia survivor

Samantha

Hi, I’m Samantha, and I am a pre-B-cell acute lymphoblastic leukemia survivor (B-ALL)! I was diagnosed in October 2018, the beginning of my junior year in high school. Before being diagnosed, I missed about a month of school due to being sick. I was misdiagnosed three times before they found out I had B-ALL. When I was diagnosed, the doctors told my parents and me that if it had been undiagnosed for a day or two more, I wouldn’t have woken up, and my parents would’ve found me. I’m so lucky it was found before it was too late.

Mario AML

Mario

I’m a very simple guy. I’ve worked in the financial industry for almost 10 years, however, my passion is cooking. In 2019, I had just lost 225 lbs. I was preparing to go back to culinary school.

There was a family incident in March of that year, and it put a lot of stress on us. I kept developing a strong workout routine to really help me get on the right track.

Pre B cell lymphoblastic lymphoma

Eliot

It was my senior year of high school, and I was thriving: MVP of the soccer team that went to the state finals; strong academics with an offer to study Natural Sciences at Durham University, one of England’s finest; fantastic friends who were to become even more important to me. My biggest challenge was getting a date for the prom! Things that were within my control were going really well. However, things outside of my control then flexed their powerful muscles, and that high school life ended and a new one began.

anthony

Anthony

December of 2017 was a difficult time for me. It is the month that is usually filled with happiness, excitement and Christmas cheer. For me, it was the month I found out that I had Hodgkin lymphoma. It’s crazy when you think about it – we see all of these facts and figures about people who are diagnosed with cancer and we never, really, truly believe it could happen to us.

Alison Ball & Keith Newman

Alison & Keith

This is a love story about two Team In Training honorees, Alison and Keith. Keith has been a recreational runner for many years and first learned of Team In Training (TNT) as a fundraising sponsor for a friend. Upon his diagnosis of follicular lymphoma in 2008, Keith says he knew right away that direct involvement with TNT was an obvious step; he became an honoree for the South Bay and Peninsula run teams during his initial chemotherapy treatments, and ran with the teams every few weeks in that first “honoree season.”

Doug

I have always been a builder. Professionally, I am an architect.  ​You could say that I’ve spent my life building spaces where people could grow. I never imagined, however, that I would someday have to rebuild my own. In February 2015, after experiencing months of excruciating and debilitating back pain that doctors mistakenly attributed to deteriorating lower lumbar discs, I had an MRI that revealed multiple vertebral compressed fractures.

Christopher

Christopher

In January 2013, I was diagnosed with PH+ acute lymphoblastic leukemia (ALL). I had just turned 19 and finished my first semester at the University of Florida. I missed the rest of my freshman year but after eight months in and out of the hospital, I achieved remission and my doctors allowed me to go back to school for the fall.

TS

Taylor

In February of 2019, I was diagnosed with stage 4 Hodgkin lymphoma (HL). What started with a simple cough quickly turned into the most challenging year of my life. When you hear the words “you have cancer,” the world stops spinning. There is no way to prepare for the cold, dark fear that takes over when there are so many unknowns. At this point, I didn't even know what lymphoma was. I was so lucky to have UCLA fighting with me and the incredible support of my entire family by my side. I owe it to all of them for pulling me through.

young, hispanic woman with glasses

Elizabeth

On November 8, 2021, I was diagnosed with stage III multiple myeloma (MM), an incurable cancer. Prior to being diagnosed, I thought I was a healthy young woman and was just living life with my children. I would have different pains throughout my body, but I didn't think much about it and would ignore them for the most part. The pains throughout my body were getting more and more frequent, so I went to the ER in October 2021 because I was in pain and could not eat, they said I was possibly having acid reflux and gave me a prescription for nausea.

hazy photo of middle-aged woman with blond hair gray eyeshadown pink lipstick and gold earrings and necklace in a black dress

Rebecca

My mother died of multiple myeloma (MM) in 2001, 10 months after her diagnosis. She lived in a small town where the only treatment they offered her was chemo infusions. She was on dialysis the whole time. She was brave but scared, nonetheless. She didn't have much time to process the whole experience. I was 51 at the time and still believed I was bullet-proof! Silly girl!

middle aged white woman wearing a colorful headscarf and white t-shirt with an orange ribbon on it sitting on a hospital bed

Amy

I was diagnosed with acute myeloid leukemia (AML) when I was 43 years old and at the height of my career as an RN. I took care of critically ill patients but did not realize when I was critically ill myself. My diagnosis came after days of having hip pain which became progressively worse until I was unable to walk without assistance. My husband and son took me to the emergency room for testing. The doctor sat on my bed to discuss the results, and at that point, I knew things must be bad, but I did not expect her to say I may have cancer.

young white woman in blue sweater holding coffee with young black man with beard and mustache wearing a knit cap and blue jacket holding a cup

Suesan

During caregiving for my partner, Dil, cancer has acted as a proctor of lessons we would have rather gone without. I have become more aware of accessibility issues because the chemotherapy and radiation treatment combined with overwhelming doses of steroids led to him having spinal fractures which impeded his mobility. Now when we go to a movie, are traveling, or generally getting around, I come armed with a pillow for his chair, he with his cane, an eye trained for impassable curbs or spaces that he can't comfortably navigate.

janiyah

Janiyah

Our beautiful Janiyah was diagnosed with acute lymphoblastic leukemia (ALL) at 14 months old.  Some will say by chance or luck, others say by the grace of God. Thirteen months earlier, Janiyah was diagnosed with hemoglobin C disease; simply defined as chronic anemia.

older white man headshot smiling wearing a brown suite white shirt and brown and blue tie

Gregg

The date was May 15, 2015, in the local office of the hematologist/oncologist and I was given this message after the results of my bone marrow biopsy taken a week earlier. 

Relapsed and Refractory

Refractory non-Hodgkin lymphoma (NHL) is NHL that has not responded to initial treatment. Refractory disease may be disease that is getting worse or staying the same.

Relapsed non-Hodgkin lymphoma (NHL) is NHL that responded to treatment but then returns. 

Treatment

Treatment for Hodgkin lymphoma is changing due to new drugs and research findings from clinical trials. Therefore, before treatment begins, it is important to consider getting a second opinion at a center with a Hodgkin lymphoma expert.

It's important that your doctor is experienced in treating patients with Hodgkin lymphoma or works in consultation with a Hodgkin lymphoma specialist. This type of specialist is called a hematologist-oncologist.

Supportive Care

Supportive care is given to improve the quality of life for patients with MF. The goal of supportive care is to prevent or treat the symptoms of MF.

Anemia

Anemia is observed in more than 50 percent of patients with MF at the time of diagnosis. Before considering treatment options, it is important for doctors to rule out and treat the most common causes of anemia such as bleeding, iron deficiency, vitamin B12 deficiency and folic acid deficiency.

Treatment

Physical Effects

Chemotherapy and Other Drug Therapies

Children treated with chemotherapy, drug therapy or other therapies may be at increased risk for the following side effects. Click here to read more about these side effects.

Getting a Second Opinion

Leukemia, lymphoma, myeloma and myelodysplastic syndromes are each different types of cancers. What's more, each disease has subtypes. This means that the signs of the disease, how it's diagnosed and treated and the expected outcomes vary. That's why it's essential to have the right diagnosis before you begin or continue with treatment.

Managing Sexual Side Effects

An important part of managing side effects that impact your sexual health is to determine what factors may be causing or contributing to the changes you are experiencing, so that you can address them. Sexual side effects during cancer treatment can include: