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Hardee
In April 2020, I was diagnosed with Stage 2 Hodgkin lymphoma (HL). My life was turned upside down after this diagnosis, and I was in extreme denial even months into my treatment. I was forced to go through six months of chemotherapy and two surgeries to treat it. Being diagnosed with cancer at the age of 20 in the midst of a pandemic taught me many things. One of the biggest things I learned is to never take anything for granted. One day I was a normal 20-year-old hanging out with my friends, and the next I was shaving off all my hair because of treatment.
Taylor
Hello! I am Taylor, and most people know me for being a human biology premed student at the University of California San Diego. However, what most people don’t know is I was diagnosed with a rare blood cancer in March of this year. I have systemic mastocytosis (SM) which leads to lots of anaphylactic reactions and hospital visits. I spend lots of time getting tests because my cancer is rare and infusions at the cancer center. I have had several types of chemotherapy drugs and many biopsies.
Da’Ni
Thirteen-year-old Da’Ni was diagnosed with acute lymphoblastic leukemia (ALL) in July 2018. She endured eight months of intense treatment before starting maintenance therapy. Da’Ni is currently six months in to maintenance and back in school. She’s an 8th grader and a straight A student. Da’Ni plans to go to medical school and become an oncologist to help children like herself one day.
Shayne
Shayne was diagnosed with T-cell Acute Lymphocytic Leukemia in May 2005 when he was just 18 months old. He endured 42 months of chemotherapy, multiple blood transfusions and several surgeries before achieving remission. Today, Shayne is 10 years old, in the fourth grade and a honor roll student. He is doing great and remains in remission. Shayne loves school and plays basketball and baseball. He also participates in track and field, where he throws both the shot put and javelin.
John
I've been a cancer survivor since my bone marrow transplant at Seattle Cancer Care Alliance in 2004. I have minimal side effects and continue doing what I love -- spending time with family and friends, cycling, and teaching high school photography and video production. One year after my transplant I did my first Team In Training event, a century ride in Lake Tahoe. I continued to do four more events. My high school video students put on a film festival every year to support the Northwest Chapter of The Leukemia and Lymphoma Society.
Matilda
In March 2024, during my first year of college as an international student in America, I was diagnosed with lymphoma. The diagnosis came unexpectedly during a compulsory admissions check-up where they discovered a tumor in my chest that had grown extensively within just two months.
Bethaney
My name is Bethaney Jones and I am a Hodgkin's lymphoma survivor. I was diagnosed in April 2018 after a routine check up for a cough that lasted for months.
After my diagnosis, I was unable to complete the school year with my awesome third graders. I endured six months of chemotherapy and I was able to ring the bell on October 12, one day after my 28th birthday.
Madison
Hello! My name is Madison, but that's not what you need to remember. The name you need to remember is Brodie. You see, I am joining the 2023 Student Visionaries of the Year campaign in honor of my childhood friend, Brodie. In November 2018, Brodie was diagnosed with acute myeloid leukemia (AML) while only in the 6th grade. With a short fight of a long, five months, Brodie gained his wings on April 9, 2019. But today the war wages, on and we are battling this together. Our war is against leukemia, and I have no doubt we are going to win.
Jaden
My name is Jaden, and I am an 18-year-old Political Science student at Penn State University. I have been deeply involved with The Leukemia & Lymphoma Society (LLS) since I was 10 years old, a journey that began with a profound personal experience.
Jack
On October 19, 2018, after complaining about excruciating pain in his back, we took our 16-year-old son Jack to see the pediatrician. The doctor checked him out and told us to immediately get him to the Children's Hospital of Colorado and go to the 7th floor to see Dr. Maloney. Not paying attention and thinking nothing was wrong, we didn't notice that the 7th floor was the Center for Cancer and Blood Disorders. We met with doctors, had a blood test done, and they came back with the dreaded words, "Your child has cancer." Specifically, he had acute lymphoblastic leukemia (ALL).
Monica
As a First Connection® volunteer with The Leukemia & Lymphoma Society (LLS) for almost two years, I have had the opportunity to connect with patients and survivors to share their stories and experiences while battling this deadly illness. Every day I come across so many touching and courageous stories that inspire me to do more and more to support this cause.
“People Just Didn’t Get It”: Treating Young Adults with Cancer
Think of spring break: warm sunny skies, a refreshing drink, and hopefully, a feeling of freedom.
The History of Leukemia
Table of contents
Hannah
As a busy college student, Hannah is focused on attending her business and art classes - a very different world than the cancer one she was a part of just a few short years ago. At 13 years old, Hannah was diagnosed with Burkitt lymphoma and went on to battle it successfully a second time.
Jane
In October 2015, I was diagnosed with Hodgkin lymphoma (HL). After growing up never getting sick, I had cancer. It was incredibly difficult to comprehend at the age of 13 that I was about to endure something most people won’t experience in a lifetime. I went through four rounds of chemotherapy and was in remission in January of 2016. Once you’re in remission, you believe that that’s the end. You’ll have a few check-ups here and there, but in your head, you envision no more cancer.
Chloe
At the age of 13, I became the youngest stem cell donor at Johns Hopkins Hospital. At 15, I am a Student Visionary of the Year in the 2024 Leukemia and Lymphoma Society (LLS) campaign. LLS has become an integral part of my life over the past two years. In the spring of 2022, the peaceful life of our family was shattered by my mom’s diagnosis of acute myeloid leukemia (AML). Learning that a stem cell transplant was the only cure, I volunteered to donate my bone marrow to her.
Cooper
I am Cooper, and I am a leukemia survivor. I am 26 and creating businesses around the creativity space. I am a healer and author of multiple books. I was diagnosed with leukemia at the age of seven. I did treatment for 2½ years with chemotherapy. I have been in remission for 16 years. I am grateful to be here. I have donated around $100,000 to The Leukemia & Lymphoma Society (LLS). I have done Pennies for Patients (PFP), Student Of The Year (SOY), and been an Honored Hero for multiple events. My high school raised $10,000 in one week for PFP.
David
My dad, David, was diagnosed with acute lymphoblastic leukemia (ALL) on March 1, 1993, after looking at his blood under a microscope in college class. He started three years of intense chemotherapy on March 8, 1993, and finished it on January 26, 1996, while a third-year medical student. He was told that there was a 50% survival at five years and 30% survival at 10 years and that he would likely not be able to have children. During that time, he got married. Two years after finishing chemo, my oldest brother was born. I have three older brothers and an older sister.
Jason
From an early age, Jason Wexler showed an interest in curing cancer and would even make "potions," according to his mother, Sherri. An extrovert like his father, Kevin, Jason has always liked making a difference for others and has great ideas to share.
When he turned sixteen, the sophomore at The Grauer School in Encinitas knew he wanted to do something to help give back. Jason learned about the "Students of the Year" program for The Leukemia & Lymphoma Society (LLS) and knew he had to get involved.
Asha
Hi! My name is Asha. I was diagnosed with stage 2 Hodgkin’s lymphoma when I was 18 years old in December 2018 during my freshman year of college. I noticed a bump on my neck that I thought may have been an insect bite until another one appeared next to the first one. When I saw that the bumps were connecting to each other that is when I told my parents.
Krista
Prior to my diagnosis, I was a much-loved daughter to my parents, a dedicated dog mama to my Golden Retriever, a loyal friend, and an enthusiastic high school history teacher. After my diagnosis and seven-year battle with refractory Hodgkin lymphoma (HL), I was still all of those things and somehow so much more.
Yarnall Family
To be of service to others comes naturally to the Yarnalls. Bob is a 25-year Marine Corps veteran and a teacher. Kim is a chiropractor for over 22 years.
Robert
In 1990, I was diagnosed with M3 acute myeloid leukemia (AML) - now known as acute promyelocytic cancer (APL) - when I was a twenty-year-old college student studying abroad in Northern England.
I had ignored obvious symptoms for about a week leading up to my diagnosis, and it took another full week just to coordinate my departure from the UK to the University of Washington Medical Center in Seattle, not far from where I grew up. A host of complications followed during my first round of induction chemotherapy including massive amounts of internal bleeding.
Justin
My husband, Justin, was diagnosed with T-cell acute lymphoblastic leukemia (ALL) in June 2021. At the time, he was a healthy, energetic, 33-year-old dad of three. He just completed all treatment in January 2024. We received some funds from The Leukemia & Lymphoma Society (LLS) as well as information and inspiration. Throughout treatment, my husband fought so hard and had very difficult moments. He went into septic shock from a blood infection, had an ICU stay, and had to get both his hips replaced because of an infection that led to bone on bone. He couldn’t walk for months.