Search Results
Louis
Louis had been on a journey to achieve greater health. For 10 months, he had been on a healthy diet and exercise program and had lost 80 pounds. His doctors were pleased and he was able to stop taking most medications he was on. However when he went for an annual physical he was diagnosed with chronic myelogenous leukemia (CML) at only the age of 33.
Elissa
Ten years ago, my mother-in-law was diagnosed with stage 4 non-Hodgkin lymphoma (NHL). She has since been deemed cured and has had no recurrence since her successful treatment. Some of her medicines were funded by The Leukemia & Lymphoma Society (LLS). We spent years racing for Team In Training (TNT) to fundraise for LLS.
Vickie
I was diagnosed in 1974 at the age of 24 with Hodgkin lymphoma (HL). I had never even heard of it. The doctors did not know if I would survive as it was very aggressive. I had exploratory surgery (CAT scans and MRIs did not exist then as far as I know) and five weeks of radiation (I still glow in the dark, saves on night lights!!). Other than a couple of "unusual lymph nodes" over the years, I have been cancer-free. I went on to have two more great careers and was happily married for the first time at 49.
Alexis
My grandma has been close to me for as long as I can remember. Holidays, birthdays, and summers — I always remember being with her and my grandpa. We took trips on cruises, visited Hawaii, and I had amazing chances to get closer to them. When my grandma was diagnosed with leukemia, my family and I knew we wanted to do something bigger. We joined The Leukemia & Lymphoma Society’s (LLS) Team In Training (TNT) to run the Walt Disney Marathon Weekend Dopey Challenge, and it was an amazing experience.
Watch and Wait
Watch and wait (also called active surveillance) involves closely monitoring a patient's condition without giving any treatment until symptoms appear or change. Some people can manage their blood cancer — depending on the disease — with their doctors for years using a watch-and-wait approach. It is usually recommended for patients in early stages of indolent (slow-growing) or chronic forms of blood cancers.
Michael
In 1995, Michael’s daughter Carley was diagnosed with acute myeloid leukemia (AML), M-7 – a rare form of blood cancer – at just two and a half years old. For the following year, Michael and his wife, Liz, practically lived at Rady Children’s Hospital in San Diego while Carley underwent heavy chemotherapy treatment.
Dan
When cancer hangs your cleats up for good
At my first appointment, the physical therapist asked me why. Why did I want to run a marathon? And I didn't have an answer, partly because when you meet someone, you don't want to blurt out all sorts of emotional baggage, and that's the sort of question that can trigger a lot of baggage.
Matt
On February 2nd, 2019 my youngest daughter, Harper, was diagnosed with leukemia. Three and a half years later as I'm writing this I have a lump in my throat and tears in my eyes. Harper and our family are fortunate. She has great insurance, access to world class care, treatment options that are highly effective, and an amazing support network. That said she, and all cancer patients, must fight for their lives. I'll never forget spending the evening before her birthday in the emergency room with severe bone pain (a common side effect from her treatment).
Abby
In 2015, our identical twin daughters, Kenedi and Kendal, were diagnosed with acute myeloid leukemia at three months old. After a brutal six months of living in isolation with them in one room at the hospital, the twins were released off treatment and in remission. We enjoyed 12 months of at home as a family of five, we were devastated to learn Kendal relapsed. She underwent two more rounds of intense chemo as well as a bone marrow transplant that ultimately failed, Kendal died in our arms in September 2017. One week later, Kenedi celebrated two years in remission.
Christian
In March 2017, I was diagnosed with Hodgkin's Lymphoma.
This came as a huge shock. I immediately starting thinking about how this might impact my wife and our two young daughters' lives.
I had 2.5 cycles of ABVD and ISRT radiotherapy and have been in remission since August 2017. I couldn't have down it without the support of my family, friends, LLS.org support groups and even the ice hockey team I had to stop playing with, who sported violet stick and shin guard colored tape when playing the rest of the season.
Helping Blood Cancer Patients and Families When It's Needed Most
In honor of Blood Cancer Awareness Month, Dr. Gwen Nichols reflects on our vital work to support blood cancer patients and their families.
Nicole
I first became involved in Team In Training (TNT) and The Leukemia & Lymphoma Society (LLS) in March of 2020 because I was very interested in running the New York City Marathon. I knew that I wanted to run for a charity that meant something to me, so I knew I had to be a part of this team.
Luz
My name is Luz, and my story begins in a magical town in Mexico where I spent a wonderful childhood surrounded by my family. As the youngest of nine siblings, I learned the value of support and connection, values which continue to guide me today as a happily married mother of three beautiful daughters. For over twenty years, Chicago has been my home.
Liz
In December 2010, my fiancé, Darla, was diagnosed with stage 4 small B-cell lymphoma (NHL). Her doctors developed a plan to start her on chemotherapy as soon as possible. She became very sick over the next couple of weeks. When she went to her first treatment three weeks after diagnosis, they could not administer the chemotherapy due to her being so ill. They put it off for a day and began Rituxan® treatment the next morning. She began having an allergic reaction to the drug. They stopped the treatment and tried to stabilize her, but later that evening, she passed away.
Rob
My blood cancer story started in 1987 when I was diagnosed and treated for testicular cancer with surgery and chemotherapy. As I progressed to the end of the chemo regimen, my blood counts would not return to normal. A bone marrow biopsy showed that I had developed treatment-related acute myeloid leukemia (AML) as a result of the chemotherapy for the testicular cancer.
Gary
In 1999 I had a lump on my neck, and after strong urging from my wife and my mother, I finally went to my family doctor. My white blood cell counts were really high, and antibiotics didn't help. Eventually, a biopsy indicated chronic lymphocytic leukemia (CLL).
Donna
I would first and foremost like to introduce you to a most special lady. My Nana.
Bishoy
Born in Egypt, at the age of three, me and my family immigrated to the U.S. when I was diagnosed with acute lymphoblastic leukemia (ALL). I grew up in Long Island, New York, where I received treatment for 10 years. On my 13th birthday, I underwent brain surgery and remains cancer-free.
Elijah
Diagnosed with ALL in 5th grade, my hopes for a normal and healthy childhood were quickly shattered. The impact on my family began as devastation but has since metamorphosed into restoration, healing, and a closeness beyond this world (bonus, my brother and I have never fought since the day I received the news of my disease).
Sophia
My wife and I would have never heard of The Leukemia and Lymphoma Society (LLS) if it were not for losing our 12-year-old daughter on March 12, 2013 to undiagnosed leukemia. If you've heard me speak of my daughter Sophia, you've heard this word: perfect. Her laugh, her eyes, her beautiful smile were all perfect. Sophia was a loving, kind and compassionate child. She loved her friends, her dogs (Katie & Daisy), and her family. Perfect. Sophia's story is very different from others.
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.
J.J.
The first time I remember hearing of The Leukemia & Lymphoma Society (LLS) was through Team In Training (TNT), specifically from a brochure I picked up at a bike shop that invited one to train for a 109-mile bike ride with TNT. It was 2007, and I thought it sounded like a blast. I convinced my girlfriend at the time, Stacey, to join me. We used the occasion to buy some fancy new bikes. With some fundraising and committed training dates, we would be able to say we had done a Century Bike Ride! Cool!
Lila
It’s January 11th, 2017, well past midnight, probably around 3 am. I am on the side of a mountain in Africa, 1000 miles away from home, in pitch black out, -20º with the winds, and I can barely feel my fingers. All I can see is the headlamp spot of light shining on the trail.
I think to myself, “Well, Lila, maybe this was not your best idea!” I look up and call my teammate in front of me, my best friend Dawn, and say, “Dawn, I am sorry I talked you into this.” She just looks at me, gives a knowing smile, then turns back to the path in front of us!