Search Results
Joe
My son Joe was 5 years old when he was diagnosed with T-cell leukemia just three days after the birth of his brother Cole – Joe was admitted to the ICU, and on Sunday, the next day, they did a spinal tap and a bone marrow biopsy. At midnight that night, he started his chemotherapy treatments.
In the first 30 days, his bone marrow had cleared to zero, and he was technically designated as a “low risk rapid responder.” All things being equal, he has done a phenomenal job through this.
He is in long-term maintenance and he finished his treatment on December 13, 2014.
Nandini
Everything was picture perfect in my life. A beautiful family with two beautiful daughters and husband. And then, in March 2009, I was diagnosed with acute myeloid leukemia (AML).
I had been recovering from aplastic anemia since 2002. However, AA progressed into AML. A transplant was the best cure available and a kind unrelated donor was found who gave a new lease to my life. After a painful bone marrow transplant recovery, I am now in remission. My older daughter just went to college and my younger daughter is in fourth grade.
Myra
Over the course of Myra’s career in oncology nursing, she’s seen the hurdles that families face and heard from patients about the daily struggles to access the care they need to stay alive. Unfortunately, she is too familiar with patients who are forced to choose between life-saving treatment and going against a doctor’s recommended treatment plan simply because the cost is too high.
Dean
In October 2015, after a trip to the ER with pain in my abdomen, I was diagnosed with stage 3, large B cell, multiple location, non-Hodgkin lymphoma.
My oncologist originally told me that the treatment plan would include 10 chemotherapy rounds, followed with radiation. I was out of work for eight weeks until my doctor decided I was in good enough health to return work.
Cancer affects everyone in your life that loves you — emotionally and financially. When you are sick, the bills do not stop coming, and in some cases, cancer can ruin people financially.
Cary
Cary was diagnosed with Acute Lymphoblastic Leukemia in the fall of 2012. After spending more than 100 days in the hospital, undergoing intense chemo treatments, and blood transfusions Cary is now in remission. You can only imagine the struggle and heartache a cancer diagnoses was at only 33 years of age with a wife, 3 small boys, and a career.
Lorelai
I was diagnosed with acute myeloid leukemia (AML) when I was 11. Throughout my entire cancer journey, I had a lot of people in my corner. But what I found most helpful was following The Leukemia & Lymphoma Society’s (LLS) social media platforms and reading the articles on their website. Through LLS, I felt like someone actually understood what I was going through. Recently, I have been one of the very lucky students chosen to receive the LLS Scholarship for Blood Cancer Survivors which will be the reason I am able to continue attending college.
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.
Janel
Throughout my childhood, my grandmother instilled in me the importance of helping those in need and gave generously to various charities and organizations. Her unwavering dedication to serving others inspired me to continue her legacy and give back to my community.
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.
Clinical Trials
Taking part in a clinical trial may be the best treatment choice for some myeloma patients. Clinical trials are under way to develop treatments that increase the remission rate of myeloma or cure the disease. Today's standard treatments for cancer are based on earlier clinical trials. The Leukemia & Lymphoma Society (LLS) continues to invest funds in myeloma research.
James
I was diagnosed with stage 3 follicular lymphoma (FL), a type of non-Hodgkin lymphoma (NHL), at the end of 2017, and our world was turned upside down. I lived a pretty healthy lifestyle, stayed active, and ate well. I never thought I would be diagnosed with cancer until I received the phone call from my hematologist/oncologist late on a Friday night. My body went numb as I listened to the diagnosis and the aggressive treatment plan around the corner.
Erika
I am a 36-year-old cancer survivor. In February 2014, I found a suspect lump and had become unusually tired. I was a career-driven single mother of a very active 10-year-old boy, so when I say unusually tired it was time to call the doctor. Within days I was thrown into the crazy and often times confusing world of hospital appointments and insurance company battles for various procedures and surgical biopsies. We became pros at the waiting game.
Lisa
It was 2009. Obama had just been sworn in as president, captain Sully successfully landed United Airlines flight 1549 on the Hudson River during an aircraft malfunction, and all souls on board survived.
Autologous Stem Cell Transplantation
In autologous stem cell transplantation, the procedure uses the patient’s own stem cells for the transplant. The stem cells are collected from the patient in advance and are frozen. After the patient undergoes high doses of chemotherapy, either with or without radiation therapy, the stem cells are then returned to the body. This type of transplant is often used to treat blood cancers such as Hodgkin lymphoma, non-Hodgkin lymphoma and myeloma.
Natasha & Cindy
My first day of treatment was on July 18, 2018 at UCLA Medical. That's where I met Natasha. I was a bit nervous going in not knowing what to expect so the nurses connected both of us. That same day Natasha found out she was in remission and I couldn't be happier for her. We both were diagnosed with Hodgkin lymphoma, going through the same treatment, and had the same doctor.
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.
Matthew
In 2014, I was diagnosed with Burkitt’s lymphoma, one of the most aggressive of all blood cancers and without quick action I would have had only 90 days to live. That was three years ago.
Rommy Omarys
My younger sister was diagnosed with lymphoma in 2022. She is the youngest of four siblings. I am the oldest, and for me, she has always been my baby sister. We all go through different difficulties ― family, personal, economic life, etc. ― but when a disease affects your body to the degree of being between life and death, the perspective is different. With the greatest sadness in the world and the possibility of not seeing my sister again in this physical plane, I never lost hope. The light in the dark was always strong and bright.
Katie
I was diagnosed with Leukemia when I was 20 months old. I endured treatment for a little over 2 years until I was declared cancer free. Since I was diagnosed so young, I do not remember the treatment. However, I do remember the support from The Leukemia and Lymphoma Society (LLS) as my family participated in the LLS’s Light The Night walk every year for the past 18 years!
William
The Leukemia and Lymphoma Society (LLS) holds a special place in my heart. I lost my mother to therapy associated with acute myeloid leukemia (AML) in July 2021. AML is a type of blood cancer that affects the bone marrow and blood. It can be very aggressive and progress rapidly without treatment. There are still certain forms of AML that do not have effective treatments, like the one my mother had. LLS was a resource I knew about from my work in solid tumor cancer research. It helped provide me with patient and caregiver resources that I needed at an extremely difficult time in my life.
Matthew
In the summer of 2020, I was diagnosed with stage 2 Hodgkin lymphoma (HL) after finding a lump in my chest. I had just finished track and field in my sophomore year of high school and thought that the lump in my chest was a popped rib or something with an easy fix. It wasn't.
Reginé
I thought it was 'just another torn meniscus' back in the fall of 2019. The symptoms and signs all seemed too familiar and I just knew I'd have to get my meniscus repaired again, but this time in my left knee. After following through similar protocol in preparation to meet with the orthopedic doctor, upon my doctor's visit I was told my knee could not be further evaluated until deeper investigation by another physician: a musculoskeletal oncologist.
Art
I was living in San Jose and had gone walking with a friend in a local park that followed the stream. It was December 15, 2006. Tom noticed that I had difficulty climbing up the five-foot stream embankment that the path went through. I myself didn’t recall this. Ten days later while visiting my wife’s children in Fairfax, the children and I went on a trail as we always did on Christmas morning. I found myself badly winded and returned to their home while they continued the hike. Then I noticed that I was not attracted to the Christmas feast.
Allison
During the start of the pandemic, my boyfriend began working out from home with all the gyms being closed. While working out, he discovered a lump under his arm. We both waved it off as nothing to worry about, but he still asked his doctor about it just in case. His doctor wanted him to get it biopsied. I dropped him off for surgery, still naive that anything would actually be wrong. He wasn't showing symptoms, he was active and healthy, plus he was young. “We” were young. We were in love, talking about getting engaged, and just moved in together. What could go wrong?