Search Results
Debra
In October 2011, while at work, I fell after attempting to sit on a chair, and I went to the emergency for x-rays. As soon as the technician began the process, he entered the room to ask if I had scoliosis. I replied, "no" and he proceeded with the exam.

Kennedy
Kennedy was diagnosed with mono at age 12. Within a week she developed swelling and had a hard time breathing when laying down. Our pediatrician advised us to go to the children’s hospital where they did CT scans, MRIs and discovered a soft-sized mass pressing against her airway. There we got the news you never want to hear, our girl had lymphoma. Before that day, she was a normal child, playing volleyball, singing in the choir, being a kid.

Carol
Meet carol. hodgkin survivor. indiana. Carol was diagnosed with Hodgkin lymphoma in 2010. After being a stay-at-home mom, she went back to school to get her teaching degree and found out she had a grapefruit size tumor in her chest when she was one week away from finishing her student teaching. She put off finding a teaching job for a year while going through six months of chemotherapy. She was able to work as a learning specialist while going through her treatments as she had a very supportive principal.

Kate
"You have cancer" is one of the scariest things you might ever hear. When Kate was diagnosed with non-Hodgkin lymphoma (NHL), she initially thought about how she wasn't strong enough and how she wasn't ready to die. Then she calmed down and told herself she didn't really have a choice.
"You have to do this; you have to be strong."
B-Cell Prolymphocytic Leukemia (B-PLL)
B-cell prolymphocytic leukemia (B-PLL) is a very rare and typically aggressive malignancy (cancer) characterized by the out of control growth of B-cells (B-lymphocytes). B-cells are a type of white blood cell that is part of the immune system. B-PLL usually affects older adults with a median age at diagnosis of 69 years, and it is slightly more common in men than women. Most of the time, B-PLL occurs as a transformation or evolution of a more slow-growing B-cell cancer, such as chronic lymphocytic leukemia. Rarely, this is a primary disorder.
Diagnosis
Diagnosing acute lymphoblastic leukemia (ALL) and the ALL subtype usually involves a series of tests. An accurate diagnosis of the subtype is important. The exact diagnosis helps the doctor
- Estimate how the disease will progress
- Determine the appropriate treatment
In children, a diagnosis of ALL generally requires a finding that 25 percent or more of the cells in the bone marrow are leukemic blasts of lymphoid origin (lymphoblasts).

Kendra
I first learned of The Leukemia & Lymphoma Society (LLS) when I participated in a Team in Training (TNT) event to walk a half marathon in San Francisco in October 2004. My friend in Michigan had lost her dad to lymphoma earlier that year, and she was training for the event from her home in Michigan. My training and participation were a way to support her during the loss of her dad. I never thought I could walk that far, and, through the support of the trainers and the motivation to support my friend, I had an awesome time completing that walk.

Caitlyn
My world started to turn upside down in January of 2019 after starting to exercise and trying to lose weight. At first, I thought I had pulled a muscle in my leg. The cramping continued to increase and turned into radiating bone pain. I went to get an x-ray to make sure nothing was broken. There were no broken bones or fractures, so they sent me on my way.

Scott
My experience with lymphoma began unexpectedly in August 2016. I began experiencing back pain with a large swollen band growing diagonally across my back. Thinking it was probably muscular, I went to see my physician who ordered an MRI. Cancer had never crossed my mind when he called me that same day and said I needed to be seen very soon by an oncologist. I was dumbfounded and left with no words. After scans, bloodwork, and a number of doctors collaborating on the findings, it was determined that I had stage 4B peripheral T-cell non-Hodgkin lymphoma (PTCL).
Treatment Outcomes
Treatment outcomes for people with CLL vary widely, and expected outcomes are influenced by the
- Stage of the disease
- Presence or lack of various factors associated with higher-risk disease
- Overall health of the patient
- Other considerations.
Current research suggests that newer treatment combinations and approaches may improve the length of survival. People with CLL should consult with their doctors to discuss individual potential outcomes. For survival statistics, click here.
Side Effects
Cancer therapy for juvenile myelomonocytic leukemia (JMML) can sometimes produce side effects. For most patients, treatment side effects are temporary and go away once therapy ends. For others, side effects can be more severe, sometimes requiring hospitalization. Some patients never have side effects.
Before your child undergoes treatment, talk with his or her doctor about potential side effects. Drugs and other therapies can prevent or manage many side effects.
Returning to School
Consider educating family members, friends, school personnel and healthcare providers about your child's possible long-term and late effects of treatment. In particular, talk with teachers about your child's needs before he or she returns to school, as they and other school personnel may not be aware of the potential for long-term and late effects of treatment.

Ernest
During my summer internship at General Motors in Flint, Michigan, I suddenly started feeling extremely restless. Soon after a lump the side of a golf ball appeared on my neck and I got an extreme sore throat. A doctor told me I just had a sinus infection and gave me Theraflu.

Michael
In 1995, Michael’s daughter Carley was diagnosed with acute myeloid leukemia (AML), M-7 – a rare form of blood cancer – at just two and a half years old. For the following year, Michael and his wife, Liz, practically lived at Rady Children’s Hospital in San Diego while Carley underwent heavy chemotherapy treatment.

Dani
My daughter was a professional dancer out on tour when she was diagnosed with acute lymphoblastic leukemia (ALL). She was 25 years old dancing in Detroit, Michigan, at the time, feeling short of breath and having night sweats. Being a dancer, you are in the best shape of your life, and you know when something is going on with your body. So as a mom not knowing what was wrong, I started to panic and told her to start at the urgent care. Two days later I was on a plane heading to Detroit where they told her they thought she had leukemia.

Todd
This cause is dear to me because my grandmother, Anne Zavorskas, passed away several years ago from Hodgkin’s disease--a form of leukemia. Also, many years ago, my mentor’s son, Ryan Hurley, had a recurrence of leukemia, which he was first diagnosed with at the age of three. He died at the age of 19. Unfortunately, leukemia at the time caused more deaths than any other cancer in children under the age of 20. These instances led me to my desire to donate time and money to this particular charity. I have volunteered my time and fundraising expertise ever since.

Joan
In October 2014, I was handing out candy to my neighborhood’s tiny ghouls and goblins, but the scariest thing that Halloween was a phone call from my doctor. My heart pounded as the doctor told me I had myelodysplastic syndrome (MDS), a rare blood disorder in which the bone marrow stops functioning properly. My current MDS diagnosis is refractory anemia with ringed sideroblasts. My treatment consists of red blood transfusions and Reblozyl® injections.

Steven
In 2017, I was 52 and in pretty good shape. I was at the gym working out, and after a certain lift, I could not get off the bench by myself. After being helped up, I somehow drove myself home. The next morning, I could not get out of bed without my wife lifting me up. We went straight to the doctor and got an MRI. Then we got the news “you have cancer,” and it is eating your vertebrate in your neck. I was sent to a spine and neck specialist and also to a cancer doctor to find out what kind of cancer. Multiple Myeloma (MM) was the diagnosis.

Myra
At age 2, Myra began having fevers and joint pain. Her parents took her to their pediatrician where she had bloodwork done. The results came back normal except it showed she was a little anemic.
“Myra never had any bruising or any issues other than the recurring fever,” according to her father.
Zainab
I'll never forget the call I received on April 17, 2017, when my then-three-year-old niece, Zainab, was diagnosed with leukemia. At the time, she was a bubble-blowing, pose-striking, diva princess. But for the next 2½ years, she became a tiny superhero whose mission was slaying the evil villain cancer. I've always felt a special connection to Zainab starting from the day she was born ― on my birthday, which I also happen to share with my younger sister Noura.

Marlana
My pawpaw, Archie, raised me my entire life. He was in the Air Force and stationed in Korea. He didn't have to, but he took me in as his own. And when I was 11, they got legal guardianship of me. My Dad was still in my life because he was raising my little brother, so I saw him often. but he just didn't raise me. Sometime around 2010, my Pawpaw was diagnosed with non-Hodgkin lymphoma (NHL). He went through treatment and chemo which caused him to go into remission.
Krista
Where do I begin? I am a 2x acute myeloid leukemia (AML) survivor with being diagnosed for the first time in 2008 at the age of 38. My family and I received amazing support through The Leukemia and Lymphoma Society (LLS) both emotionally and financially with the co-pay program, webinars, and information guides.

Greg
In 2017, our world turned upside down when my father, Greg, was diagnosed with acute myeloid leukemia (AML). The only chance to save his life was a bone marrow transplant. Both of my uncles were tested, but neither was a match. Praying for a match, my father was placed on the donor match list.

Allison
I was diagnosed with cancer at the age of 27 with non-Hodgkin lymphoma (NHL). I was a healthy 27-year-old who went to college playing golf and lacrosse. We found the tumor right by my heart, which was inoperable, so the chemo had to work. My husband and I moved back to Cincinnati to get treated at Cincinnati Children’s Hospital.

Mollie
Although I was a cancer patient many years ago, survivorship is a journey I take every day. Ever since my diagnosis, I’ve spent my free time engaging with the childhood cancer community and learning more about myself.