Search Results
Landon
My cancer journey began on June 24, 2018. A month before that day, I'd experienced chest pains, night sweats, and shortness of breath. After scheduling a doctor's appointment, my primary physician determined that it was merely an upper respiratory infection. For a week, I took the medicine prescribed by my doctor, hoping that I would soon feel well again. With little to no signs of improvement, I scheduled another appointment for Monday, June 25th. We didn't make it to that appointment, because on June 24th, I lost oxygen and passed out.
Alyssa
From December 2021-January 2022, I had just come off orientation for my new job as a registered nurse. I was working the night shift and just thought I was experiencing the "usual" night shift symptoms. I was ALWAYS tired, had terrible back pain, and had such a shift in my appetite. I went for a physical just to be sure. My bloodwork was normal (slightly elevated WBC but told it could have been from stress at work), and my doctor sent me for physical therapy for my back pain. After going to physical therapy for weeks with no improvement, I noticed a lump on my neck.
Kerry
I’m a 26-year-old woman who never expected my life to change so dramatically. I was living what felt like an ordinary life — working at a school, spending time with friends, and keeping up with my daily routines. But things took an unexpected turn when I started experiencing night sweats. At first, I dismissed it as a cold or something minor, especially since I worked around kids who were always bringing home new germs. However, when the night sweats continued, I became frustrated. I began researching the cause and read that swollen lymph nodes could be a sign of something serious.
Lauren
To be healed by the miracles of modern medicine and prayer was the most profound experience of my life. It is difficult to articulate the gratitude my family and I feel in our hearts for the people who made it so. There is no scenario where I would be here today, writing this account, without the research made possible by The Leukemia & Lymphoma Society (LLS).
Maggie
My son, Benjamin, was diagnosed with acute lymphoblastic leukemia in February 2019 at the age of four. Due to the unique nature of his presentation, he was placed in the VHR (very high risk) category and underwent three and a half years of treatment. My background is in theatre and education, but having just moved to New York, I was not working when Benjamin was diagnosed and was lucky enough to be able to devote 100% of my time to him. I spent his treatment years learning as much as I could about the disease and how I could best care for him.
Henry Jr
I was the longest leukemia patient on G111 at the Cleveland Clinic. I spent 135 days on the floor fighting every day. I was there so long that when they could not find a way to get my numbers back up, we would call it Ground Hog Day. Every day for about a month, nothing would change. Finally they said that they can keep me alive like this for only nine months, and I have used five of them already. It was time for a bone marrow transplant.
Joy
On December 29, 2011, I heard those numbing words “you have cancer.” I was 23 years old, about to turn 24 and my whole world came to a screeching halt. After months of feeling “off,” multiple visits to all kinds of doctors, repeat blood work, scans and biopsies, it was finally determined that I had non-Hodgkin’s lymphoma.
Shelley
Twenty years ago I was diagnosed with acute lymphoblastic leukemia (ALL). My husband, Remi and I were married and just moved to Virginia, where Remi was stationed in the Navy. In the short six weeks we lived there, I never felt 100% and I was at the doctor four times in six weeks. At my last appointment, I requested that they draw my blood. They told me I had mono, my counts were so low, they took me by ambulance to the nearest hospital.
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.
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.
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.
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.
Fely
Hello, my name is Fely Agustin, I am 38 years old and a mother to two teenagers. One is going to be a freshman in college and another a freshman in high school. I am married to a wonderful husband of almost 17 years. I was diagnosed on May 6, 2015 with Waldenstrom Macroglobulinemia (WM).
Greysun
Hi! My name is Greysun! I was diagnosed with acute myeloid leukemia (AML) on March 23, 2011. I was fortunate to get outstanding medical treatment at UNC Children's Hospital and the cancer center. I have been through many rounds of chemo followed by up to six weeks of hospitalization after each one. I have had radiation to my brain followed up by my first bone marrow transplant.
Lisa
I lost my big brother Vincent J. Di Cristo to two forms of cancer on February 14, 2014. He apparently had both high grade B-cell non-Hodgkin lymphoma as well as Burkitt lymphoma. I’m very confused as to how he could have had two different types of cancer because as far as I know, he was always in good health.
Dulcy
I was 18 and had just moved away to go to nursing school, when I was diagnosed with chronic myelogenous leukemia (CML). In 1997, the only treatment option for CML was a stem cell transplant, a far cry from the oral treatment options available today.
Miguel
In 2017, I found out I had non-Hodgkin lymphoma (NHL). I was always a healthy person who exercised almost daily at the time, so this came as a complete shock. I immediately wanted to start treatment; the sooner the better. My wife did all the research and investigating into where I could find the best treatment as quickly as possible. We were emotionally devastated by the entire ordeal.
Nicole
My name is Nicole, and I am a 21-year-old cancer survivor! Last year, on February 1st, I started to go for chemotherapy after being misdiagnosed for TWO years! For those two years, I was told that the softball-sized lymph nodes in my neck were all because of allergies… I knew something was wrong when it became the size it did, and being vain was going around it. I went to Astera Cancer Center in East Brunswick, NJ, for my 6 months of chemo. Even though I only went there to get chemicals pumped, I loved everyone around me. They didn’t just treat me as a number.
Paul
I was first diagnosed with acute lymphoblastic leukemia (ALL) at age 25 and since then I've had two bone marrow transplants and CAR-T. For the past 8 years I have been on and off "healthy" and undergoing or actively recovering from treatment. I talked about some of the things I did during those treatments to help my motivation and morale, but there is a lot about the treatments themselves that were unique to someone like me, a mixed race, young adult with blood cancer.
Loxley
In early September of 2020, my son started to complain of back pain. I took him to the pediatrician, where he was assessed and a multiview x-ray was ordered. It was normal. I agreed to keep a log of his back pain complaints.
Ira
In August 2014, at age 48, I was literally in the best shape of my life. I was an avid cyclist, averaging more than 150 miles per week, leading groups of riders for my cycling club, and completing multiple 100-mile century rides in a single season. Over the course of just a few days, while cycling, I noticed a sudden setback in my performance. Virtually overnight I lost stamina, speed, and endurance. Roads or hills I had ridden countless times before instantly became unmanageable. Thinking I was battling the flu or a virus, I visited my doctor. Blood tests revealed an abnormality.
Hannah
My name is Hannah Gallant. I am an 11 years old from Quispamsis, New Brunswick Canada. In August 2016, after several trips to the doctor and the hospital because I wasn’t feeling well, my parents brought me to the hospital for blood work. I wasn't worried, because I thought it was just growing pains. We got the results that same day, my parents found out it was a form of leukemia called acute lymphoblastic leukemia (AML). They didn’t tell me until the final diagnosis took place at the IWK. I was very worried, and even though I didn't know what leukemia was.
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.
Avi
My journey began a few months into 2020. I was making plans to celebrate my birthday by going to some amusement parks I hadn't been to in many years. Unfortunately, that's when the pandemic hit, and going to the parks was no longer an option. A few months later, I started to get sick. Fever, night sweats, little to no appetite, weight loss. We didn't know if it was COVID-19 or not. I went to urgent care, and they didn't help (sent me home with Tylenol), and I was still not feeling it. I went to get bloodwork as something was off and I was starting to show signs of jaundice.
Kate
On May 17, 2018, our family was thrown into the world of blood cancer. Our family's patriarch, our bonus dad, and our beloved "Candy Boy," as he was affectionately nicknamed by his youngest daughter, found out that he was in the aggressive stages of acute myeloid leukemia (AML).