Search Results
Heather
My name is Heather and I was diagnosed with acute myeloid leukemia (AML) +FLT3/ITD on December 14th, 2017. That morning I noticed I was extremely pale and I had large bruises over my body. My doctor ran blood work STAT and within an hour I knew my platelets were below 20 and I needed to rush to the ER. I was pretty near death at that time. I was in Disseminated Intravascular Coagulation (DIC), which has a pretty high mortality rate.
Erica
By the time I was 32 years old, I was a 3-time cancer survivor. At 22 years old, I was diagnosed with MALT lymphoma, at a time (1999) when the doctors knew very little about it and believed it had only been found in men over the age of 80 in their stomach (mine was found in my neck).
Cayden
In April 2020, three-year-old Cayden began experiencing leg pain and developed an unusual limp that alarmed his mother, Courtney. Soon, the pain progressed to a stiff neck and loss of appetite. Just two weeks later, after multiple tests and doctor appointments, Courtney and her husband would hear the words that every parent fears, "your child has cancer". Cayden was diagnosed with a high-risk form of blood cancer, Philadelphia chromosome-positive acute lymphoblastic leukemia (ALL).
Jeff
A little over two years ago, I was diagnosed as having chronic lymphocytic leukemia (CLL). I was shocked and devastated by the news and immediately began seeing an oncologist. My team from the cancer center has been uplifting, positive, and supportive from the very beginning! They have been successfully treating my cancer and have taught me not to fear my disease.
Christa
I was diagnosed with acute lymphoblastic leukemia (ALL) at three years old. I experienced two and a half years of chemotherapy, lumbar punctures, blood transfusions, hair loss, and surgery. Since then, I have not wasted a single day. I live each day to the fullest, remembering a time when my future was unsure. I want to make the most of my second chance by striving to achieve what may seem like a challenge. My goal is to become a psychologist and specialize in the behavioral and cognitive development of children. I want to continue to be a part of The Leukemia & Lymphoma Society (LLS).
Henry
On April 6, 2021, we heard for the first time, “We think it's leukemia.” As I watched my boy jumping on the neighbor's bounce house enjoying the first warm spring afternoon, my mind went to one simple question, “Why him?” Up until that point, our then three-year-old, Henry, had been the happiest and healthiest toddler.
A. Timothy Lunsford-Stevens JD
In 1970, I was playing baseball in high school as a freshman, playing second base. A bully made a hit and ran from first to second base, tackling me. I got into a fight with him because of the pain I was feeling in my left hand. After the fight, I needed to go to the hospital. In setting my broken hand, they also did a blood test. The results showed why my hand was so fragile; I had acute myeloid leukemia (AML). I had chemotherapy but no radiation or other treatment. I lived in Georgia and went to MD Anderson in Houston for chemotherapy.
Dana
I was diagnosed with stage 4 non-Hodgkin lymphoma (NHL) in January 2018. I was lucky enough to get into City of Hope which is about 25 minutes from my house. I received all my treatment there. The first treatment was R-CHOP chemotherapy which required me to be in the hospital three to five days every three weeks for six months. I relapsed after six months and did an autologous bone marrow transplant in March of 2019. After about eight months, I relapsed again and prepared for an unrelated donor transplant.
CALEB
November 2017, my life changed forever when I was diagnosed with a fatal form of blood cancer called acute myeloid leukemia (AML). I had no idea what it meant. All I knew is that I woke up one day, like any other, and this time I woke up with a cancer that was going to kill me in a few months. The hardest part of that day was having to tell my Mother that her son has cancer. But after a lot of tears she said to me “Caleb, we’ve got this.” And I just remember that word “we” so vividly. I remember thinking I’m not in this alone. This is a WE thing!
Michele
The news came that I had been dreading after three days of being hospitalized. Finally, they would tell me my diagnosis. Why my blood counts were critically low. Why the pain in my right leg was excruciating. Why morphine didn’t touch that pain. Since arriving at the hospital, my inner dialogue was on repeat, “What’s wrong with me? Somebody please just tell me everything is going to be fine."
Kristy
On May 24, 2020, at 23 years old, I started getting dizzy out of nowhere. I thought maybe I needed to eat and sleep better, but it got worse. I went to the ER, and they said I was anemic and sent me home. I bought a bunch of food that’s supposed to help anemia, but I kept getting worse, to the point where I couldn’t get up to eat. I would throw up and get dizzy and almost pass out. I lost color, and my lips turned pale. I lost weight, and I pretty much looked like a zombie. Then one day I couldn’t get up, and I sat in the same spot for hours.
Addie
Charles Esten, an actor/musician who plays Deacon Claybourne on the TV show “Nashville,” is this year’s Light The Night Walk National Honorary Chair. Esten’s 15-year-old daughter, Addie, was diagnosed with leukemia at age 2 1/2 and, thanks to advances in treatment, is thriving today. Because of their personal connection to blood cancer, Charles, his wife Patty, and the entire Esten clan are strong supporters of LLS.
Lidia
I am still in treatment for leukemia, a diagnosis my mom was devastated to hear when I was just four years old.
My dream is to meet Roman Reigns and tell my story because his story makes me keep going.
I watch WWE and I even went to a WWE fight. I want to try to going to one next year!
I love seeing Roman and LLS fighting blood cancer!
Graham
In the fall of 2008 my wife and I got married. Shortly after returning from our honeymoon, I began developing pains and weakness in my joints. This continued through the holidays and I sought medical attention when the pain in my shoulders and hips became unbearable. After inconclusive X-rays and unsuccessful Cortisone shots, I began developing a pain in my abdomen around Christmas. The joint pains I wrote off as working out too hard and the abdomen pain I concluded was an ulcer.
Russ
(As told by Russ Parker’s wife Karen A. Parker) In the fall of 2004, Russ was looking forward to a surfing trip to Fiji with his son Rusty and a group of good friends. He was a real estate developer, surfer, soccer coach, swimmer and runner.
Judy
I was diagnosed with acute myelogenous leukemia (AML) on April 6, 1987, just four months after my 30th birthday.
My beautiful daughter had turned three in February. I loved being a mom, and a teacher. I was extremely active as many young parents are and was looking forward to spending more time outside "playing" as the weather improved in the great Canadian north. Life was good.
Renee
I was a senior in high school preparing to graduate. I had summer plans to work at my youth group camp and endless ideas for my future. That all came crashing down on May 27, 2002, when I was diagnosed with acute myeloid leukemia (AML). AML is a rare and rapidly growing cancer of the bone marrow that destroys the production of normal blood cells, red blood cells, and platelets. At the time of my diagnosis, my family was given devastating odds that only a miracle could fix. I was so dangerously sick that I needed multiple transfusions immediately, and that was just the beginning.
Leimomi
I was diagnosed with non-Hodgkin’s lymphoma in 1998 at the age of 38. My participation in a clinical trial included a stem cell transplant, five chemotherapy sessions, and full-body radiation treatments. I am an advocate for participation in clinical trials, which paves the way for new treatments or prevention methods. Although it was a rough experience, the responsibility of being a single mom kept me going. My inspiration for surviving was my son Brian who was 12 years old at the time. He was born with microcephaly (small brain) which made him totally dependent for all his needs.
Rachel
Rachel was diagnosed with stage 4B Hodgkin lymphoma in February 2015. She was 26 years old. The moment when her oncologist first spoke the words “you have cancer” were surreal to her. She looked to her parents who exchanged the same look of disbelief and shock, then quickly looked away before fear and sadness settled across their faces. Her mind started to race, “How am I stage 4? I don’t feel that sick. This has to be a mistake, where did this even come from? What happens now?”
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.
Kassandra
Exactly a month before my 24th birthday, I was diagnosed with acute lymphoblastic leukemia (ALL). As a young adult, hearing the words “you have cancer” come from a physician’s mouth was earth-shattering, to say the least.
Prior to my diagnosis, I had been working in clinical research and was enrolled in a Biomedical Science Master’s program with hopes of continuing to medical school and becoming a physician. However, my career aspirations were placed on hold when I received my diagnosis. Immediately, my dedicated student lifestyle turned into one of a full-time patient.
Jeffrey
My name is Jeff Kurowski and I am 35 years old. I have lived with chronic myeloid leukemia (CML) for two years and Crohn's disease (CD) for 20 years. I have had three feet of my intestines removed. I now depend on daily bowel suppression medication, monthly B12 shots, biologic therapy for a quality of life, and a daily targeted chemotherapy pill to stay alive.
Miranda
A little over a year ago, I finished a treatment that saved my life and gave me purpose. In October 2016, I was diagnosed with stage IV of Hodgkin lymphoma and was fortunate enough to receive medical care that allowed me to conquer my cancer journey.
Callie
In January 2016, I was diagnosed with stage II Hodgkin lymphoma. I was four months pregnant at the time, and it was decided to carry to term because this type of blood cancer is a slower spreading cancer.
In May 2016, I had a healthy boy and 10 days later began my first of many chemo treatments. The following October I had my last treatment and I was excited to get back to "normal" life.