Search Results
James
I have leukemia/lymphoma and have been fighting this illness for seven years. I became ill in 2011 but made somewhat of a recovery until 2015 when I got really sick (upper respiratory issues) that took the medical system in Las Vegas more than a year to diagnose as leukemia. By the time I was hospitalized the first time, my white cell count was over 38,000. It took three hospitalizations before my illness was diagnosed. By the time I was diagnosed with lymphoma, my lungs had severe, unrecoverable damage, leaving me on oxygen most of the time, even during sleep.
Varad
I graduated in 2021 with an engineering degree and landed a full-time analyst position at a promising startup. My future was brimming with plans, and by 2022, I was gearing up to leave India for the United States — a dream I had nurtured for years.
Bryana
Hello everyone! My name is Bryana and in September 2022, at 23 years old, I was rushed to the hospital unable to breathe. I recently went on a trip to Las Vegas and had gotten sick while there, but never expected what was coming for me next. I was initially diagnosed with pneumonia but when I had a CAT scan done, the radiologist noticed an abnormal 5cm mass in my chest pushing on my bronchial tubes. My oxygen levels were low and my CBC came back abnormal, I had a severely low amount of WBC which brought up suspicion.
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. Thinking I was battling a flu or virus I visited my doctor. Blood tests revealed an abnormality.
Jason
I’m a father of 4, a first responder, and a military reservist. I was diagnosed with stage 4 diffuse B cell lymphoma. After losing my cousin to leukemia and 2 months later receiving my diagnosis, my whole world was turned upside down.
Richard
It was Monday morning in January 2021. I gave my results to my wife at the kitchen table. She asked if I had read them, and I said no. I had been struggling with a chronic cough, fatigue, and shortness of breath for two to three months, so a CT scan was done to evaluate my lungs. I was simply too tired to read them. My wife scanned the papers and immediately started crying. There was a large 16 cm. tumor in my chest that was creating the symptoms and pressing on my lungs.
Mya
It was the end of my senior year in high school, and I was thrilled to be admitted into NYU’s Tisch School of the Arts to achieve my double bachelor's. I worked hard. Despite the many restrictions of the pandemic, I volunteered, performed virtually, and worked two jobs all in preparation for a bigger life.
Thomas/TJ
This picture is of my brother and my son. Both fought valiantly from acute lymphoblastic leukemia (ALL) and Hodgkin's lymphoma respectively.
It started in 2009 when my son, Thomas came home from his freshman year in college. He was diagnosed with Hodgkin's lymphoma and was treated right away. He went through the regular protocol which lead to the next level and then trial drugs, radiation, and autonomous stem cell transplant.
Christy
I fell in love with distance running in 2010 while training for my first marathon as a member of Team In Training, raising money for The Leukemia & Lymphoma Society. Since then, I have completed five full marathons and one ultra-marathon (49K). I started getting into mountain running in 2016, and aspire to run some mountain races here in Alaska, including Mount Marathon in Seward!
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.
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.
Carlos
In 2019, I was diagnosed with stage 4 mantle cell lymphoma (MCL), a life-altering moment that set me on a challenging path. I endured rigorous chemotherapy treatments, followed by a life-saving transplant in 2020. Afterward, I underwent 18 additional rounds of maintenance therapy. Today, I am proud to say I've been in remission for nearly five years.
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.
Sherri
I lost my dad to leukemia 20 years ago, fundraising all year in his honor for the year he knew about his diagnosis but didn’t tell anyone. We also lost his mom (grandma) to leukemia in 2002 and my mother-in-law in 2007 to leukemia. I proudly support The Leukemia & Lymphoma Society (LLS) and try to donate every year, but this year, I hope to donate a big chunk to help current patients and their families.
Zoraa
Being a cancer survivor was never on my bucket list.
Suzanne
My mother was diagnosed with multiple myeloma (MM) in February 1987. She passed away in December 1997. I was diagnosed with MM in February 2017. My diagnosis was not only a surprise but daunting because I was my mother’s caregiver and experienced what she faced battling this disease. I’m currently undergoing treatment with the bispecific drug Teclistamab with success. The Leukemia & Lymphoma Society (LLS) has provided me with educational and financial assistance, so I greatly appreciate this organization.
Jamaal
Jamaal Simmons had non-Hodgkins lymphoma (NHL). He was such a brave person. He worked at Publix supermarket and he went to Clark Atlanta University. He was about to graduate from college when he passed away.
It is now 14 years since he's been gone. But I still donate and collect donations and I've been doing this for many years. I will keep on doing it to help fight this blood cancer.
- Jamaal's mom, Sharon Williams.
Rhonda
This is my second time participating in the Light The Night as a cancer survivor. I have had blood cancer twice.
In 2012 I was diagnosed with Non-Hodgkin Lymphoma. After being in remission for almost 7 years on December 17, 2018 I was diagnosed with Acute Myeloid Leukemia. I had a bone marrow transplant in March and I am in remission.
I must say I’m grateful that team NCA (National Christian Academy’s school cheerleaders) would do Light The Night in my honor.
Diana
My introduction to The Leukemia & Lymphoma Society (LLS) began in the early 2000s. I joined a Light The Night Team to support research and programs for cancer patients. I then discovered Team In Training and ran my first marathon and my second as a Team Mentor. At the time, I knew cancer was a terrible disease, but it wasn’t until 2012 that cancer became more personal. In May 2012, my cousin Richard, who was like an older brother to me, passed away from pancreatic cancer. Just two years later, my mother was diagnosed with breast cancer.
Bruce
I was diagnosed with stage III mantle cell lymphoma (MCL) in October 2004 following a routine physical exam. I wasn’t feeling ill, but since I quit smoking many years ago, as a precaution, my primary care physician recommended having a computed tomography (CT) scan of my lungs to see if I had any residual damage.
David
I walked into urgent care with a cough, they took an X-ray and discovered a mass in my chest that was 18x14x13 cm. I was hospitalized that same day and then was officially diagnosed with stage 3 mediastinal B-cell lymphoma (PMBCL). This occurred in 2018 just days after my 23rd birthday and only seven months after I moved to New York City.
I decided to run the NYC marathon this year with Team In Training (TNT) because 2023 marks five years of being cancer-free!
Dr. Adams
Jerry M. Adams, Ph.D., leads an LLS Specialized Center of Research grant.
His team is investigating apoptosis, the nature process of cell death. When apoptosis goes wrong it can lead to proliferation of cancer cells. It cells fail to die when they are supposed to they can develop into leukemia, lymphoma or multiple myeloma, and become more resistant to treatment. To improve treatment, the team is studying new drugs, used either alone or in combination with other therapies, to flip on the cell death switch.
Mona
I was 13 years old when I was diagnosed with stage 4 Hodgkin lymphoma (HL). That was in 1997, and I can now proudly say I’ve been cancer-free for 21 years! But being a 21-year cancer survivor comes with a lifelong diagnosis and long-term effects. But no matter the fight, I’m thankful each day for the opportunity to say I’m a “survivor.” And I do my absolute best to thrive each day and continue the fight for those who have left us too soon.