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Sydney

My grandfather, Michael, passed away from leukemia in 1991. While I never had the pleasure of meeting him, I have always considered him to be my guardian angel. My grandmother and best friend, Patrice, has been a loyal advocate, supporter, and donor to The Leukemia & Lymphoma Society (LLS) ever since his passing. Additionally, she served as vice president for two years and president of LLS for four years. We love how committed LLS is to the research and care of those with blood cancer.

Anna

As many of you know, in 2015 our daughter Anna was diagnosed with acute lymphoblastic leukemia (ALL). She had a very successful treatment, and God answered my wife and my prayers. As of March 2023, Anna has been cancer-free for five years making her a cancer survivor. On October 21, Aimie, Anna, and I will participate in the Light The Night (LTN) walk for The Leukemia & Lymphoma Society (LLS). Funds raised through LTN allow LLS to fund treatments for patients who have blood cancer. As you can imagine, this cause is very special to Aimie and me.

Elizabeth

I was diagnosed with lymphoma in October 2017 after three months of dithering doctors even though I live in New York City and had good health insurance. After three months of dithering and a diagnosis, I was told the next appointment at the treatment department was in two months. I had the good fortune to have heard about Dr. Morton Colemen because he had treated a friend's mother 15 years before. He became my doctor that day, and I revere him.

Jeff & Melanie

My wife, Melanie and I had always been pretty healthy. We exercised, tried to eat right and discovered the value of meditation. But things changed in 2018.

Melanie had developed a cough that just wouldn't go away. She had it for months. And then she discovered a lump near her collarbone. Tests revealed on Sept. 6, 2018, that the lump was Hodgkin lymphoma and it was present in several other lymph nodes. She began a months-long treatment regimen of chemotherapy and radiation. It wasn't easy.

James

I am a cancer survivor and my story starts in the summer of 1999. On June 9, an MRI revealed a tumor the size of a golf ball in my brain. A biopsy showed it to be a primary central nervous system non-Hodgkin lymphoma. I remember this date vividly because it was my wife’s birthday and she had to break the news to me. This marked the beginning of our journey.

Lisa

As a new graduate with a master’s degree in psychology, I, among many others, am applying to jobs out in the 'real world.' Recently, one of the job applications asked me to describe myself in three words. My answer consisted of adjectives such as determined, capable and diligent. The one word that best describes me though is one I did not say, and that is survivor.

Alison

My story began in the summer of 2012.  My cancer-fighting hero, who happens to be my father in law, Dave Warner, was diagnosed that July.  Not only is he my father in law, but I call him Dad, because that is exactly what he is. In June 2012, Dad started to notice a large lymph node that was swollen in his groin.  My immediate reaction was “Go to the doctor and get antibiotics. I'm sure it's just an infected lymph node that amoxicillin can clear up!  Right??” Wrong. Never did I expect the next step to be a biopsy to see if it was cance

Emad

After six weeks of experiencing excruciating pain, I was diagnosed with enlarged B-cell stage 4 gastric lymphoma in July 2016. My oncologist in Tarzana, CA was connected to a lead doctor in City of Hope and that COH doctor advised her to send my biopsy for further testing to see if it was double mutated. The test results came positive and my cancer cells had double mutated. This meant that my body would’ve not responded to regular chemotherapy of one day every three weeks.

Cathy

I had blood cancer and for that, I’m lucky. I’m not being facetious, I really believe I’m lucky. The doctors told me that Stage 2 Hodgkin lymphoma (HL) is highly treatable and this is the cancer to have if you’re going to get cancer. But that’s not the only reason why I’m lucky. The very first philanthropic effort that I did with my BFF was when we were 17 years old and allowed to donate blood. This is one of the first times I realized I was lucky. By giving blood I could give the gift of life. It’s something I also had in common with my husband who is an avid blood donor.

Janet

My caregiver journey began in 2005, when my husband found a lump on his neck and was diagnosed with a rare form of non-Hodgkin lymphoma. After being admitted to the hospital for nine rounds of chemotherapy, he went into remission.

Cristina

My story begins in October of 2018. I had recently graduated from college, moved away from home for the first time, settled into my own apartment, and started a full-time job. I felt like I was on the verge of greatness with all of these new and exciting beginnings in my life. I didn't know that I was about to have another massive beginning... the beginning of my battle with Hodgkin's Lymphoma. I was sitting at a cancer fundraiser dinner, anxiously twirling the spaghetti on my plate. I had a gut wrenching feeling in my chest that something was wrong.

Jill

My world changed forever in April 2021. Life was going so well . . . I was 35 years old, my kids Henry (9), Olivia (7), and Ruby (5) were getting excited about summer break (and all the trips we had planned), my insurance business was in full swing, and all my plants and flowers were in bloom. I was doing what I loved most, working in the yard, when I noticed my right pinky finger was going numb, and I began having trouble walking. We immediately went to the ER. The doctors initially thought it was a stroke, but luckily a fantastic neurosurgeon was on call and saw the MRI.

Randall

I am a 36-year survivor of non-Hodgkin lymphoma (NHL). In 1987, I went through six months of chemo, had one month off, then went through 25 straight days of radiation. It is an amazing story, one which I may write about when I retire in about 12-16 months.

My son wasn't even two yet when I started treatments. Today he is 38 and has the two cutest, little girls a “Poppop” could ask for. After the chemo, they told me there was a 70% chance I'd be sterile from the treatment. We found out my wife was pregnant in December 1989. My daughter was born in August 1990.

Russell

In the tapestry of life, there are moments that test the strength of the human spirit, moments that challenge our resolve and redefine our sense of purpose. For Russell, a Filipino-American music artist and entrepreneur, such a moment arrived six months after marrying the love of his life ― a moment that would alter the course of his life forever.

Debra

I was diagnosed with non-Hodgkin lymphoma in 1995, just several months after my husband was required to go on dialysis for polycystic kidneys. We had three very young children then and my only chance of survival was to have an allogeneic bone marrow transplant, which at the time was considered experimental. I left my home and children for three months, which was so difficult, and went to Pittsburgh for my transplant.

Nanci

I was diagnosed with chronic myelogenous leukemia (CML) in January 2009. My doctor said the average life span was three years if not for the newer drug called Gleevec, a drug that The Leukemia & Lymphoma Society (LLS) had been involved in the research of it. I started on Gleevec in February, but after a week I was taken off it to bring my immune system back up. Back on Gleevec, I reached remission in July 2009. I now have been in remission for 12½ years. I now take the generic brand due to the cost.

Tony

I was diagnosed in 2016 with multiple myeloma (MM) and was able to get a bone marrow transplant in 2017. After I recovered, I was cancer-free for five years. Then two years ago, my cancer came back, and I am now going through with two types of therapies to keep things at bay and doing well. Besides the ups and downs of working full-time and cancer coming back, my oncologist who saw me through retired last December, and I got a new one. However I was not happy and started seeing one of his associates and really liked her, but she is now leaving the practice in two weeks.

Izabella

When I was twelve years old, I was diagnosed with a very rare type of leukemia found in children. I was life-flighted, had various treatments and procedures, and even had four blood transfusions. As incredibly shocking and terrifying as it all was, I pulled through in only a week of treatment. My type of leukemia is called chronic myeloid leukemia (CML). This leukemia is something that will be a part of me forever. Even still, I take a daily oral chemotherapy pill. Despite all of this, I maintain my path in life and will not let anything stop me.

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.

Story

Story was diagnosed with biphenotypic leukemia (BAL) in July 2010. She was four years old at the time. She was treated with two rounds of “high-risk protocol” chemo. She was in complete remission after 60 days. However, because of her particular diagnosis, we were advised that she needed a bone marrow transplant to have the best chance of long-term remission. Her older sister, Lyric, who was just six at the time, was a perfect match. 

Clinical Trials

Taking part in a clinical trial may be the best treatment choice for some acute myeloid leukemia (AML) patients. Clinical trials are under way for patients at every treatment stage and for patients in remission. Today's standard treatments for cancer are based on earlier clinical trials. The Leukemia & Lymphoma Society continues to invest funds in AML research.

Click here to read more about clinical trials.

George

My awareness of The Leukemia & Lymphoma Society (LLS) began years ago when a close family member was diagnosed with leukemia. In the wake of such devastating news, I felt compelled to lend a hand.  I am honored to join the LLS family in their fight to cure blood cancers.

Reid

We just wanted to reach out and say how much The Leukemia & Lymphoma Society (LLS) has helped us. From attending Light The Night (LNT), to getting a blanket in the mail, to receiving funds when I couldn't work to keep Reid safe from the pandemic. Anytime I have needed assistance or reached out, the staff I have chatted with are so amazing and make you feel like you're so included and important. You have made us feel loved and gave us hope and inspiration. Reid was diagnosed at 2 years old, and he is almost done with B-cell acute lymphoblastic leukemia (B-cell ALL) treatment.

Jaden

After having swollen lymph nodes for some time, my nine-year-old son, Jaden was diagnosed with lymphoma in May 2016. This little guy took the news like a champ.

He was admitted as an inpatient for eight days, and is now receiving outpatient chemotherapy. He is fighting cancer better than most adults and teaching everyone around us what it really means to be hopeful, faithful, brave, courageous and grateful.

Kaidyn

Kaidyn was only six months old when he was diagnosed with acute myeloid leukemia (AML). About two months later, he received a bone marrow aspiration and was started on chemotherapy. Over the next ten months, Kaidyn was in and out of Children's Hospital of Oakland. It was there that he took his first steps, said his first words, and even flirted with every nurse in the oncology unit! Kaidyn is now a healthy three-year-old boy with an ear-to-ear grin who participates in his local Light The Night Walk each fall.