Search Results

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!

Alexandra

My dad was diagnosed with leukemia this past fall. Our family was left in utter shock as my dad was the epitome of health his whole life. From our yearly ski trips, hiking and biking excursions, and running four marathons (motivating me to run my first with him), there was nothing he couldn’t do. He still continues to be the strongest man I know five months into his battle. He continues to face every day with a smile on his face and his head held high.

Stephanie

Ever since I saw my dad run the New York City Marathon in 2019, I knew it was something that I wanted to strive toward. When the pandemic hit in 2020, I put that dream on pause to start a full-time job as a clinical research coordinator for bone marrow transplants. 

Melissa

I want to tell you about my hero, my wife, Melissa. She is service-focused from the time she gets out of bed until the time she returns. She's been a part of Team In Training for the past three years and has raised well into five figures to help others. That's what made her Hodgkins lymphoma diagnosis all the more ironic.

Champions in myeloma research, Part 2: A conversation with Suzanne Lentzsch, M.D., Ph.D.

To commemorate both Myeloma Awareness Month and Women’s History Month during March, I’ve been talking with LLS-funded women scientists who are driving discovery for myeloma patients. As we close out the month and my two-part series on myeloma researchers, I’m excited to share my recent conversation with Suzanne Lentzsch, M.D., Ph.D., Professor of Medicine and the Director of the Multiple Myeloma and Amyloidosis Program at Columbia University. 

Jacqueline

After a year of misdiagnoses, I was diagnosed with stage 3 Hodgkin lymphoma (HL) on Valentine's Day 2007 when I was 22 years old. I had to take medical leave from my senior year of college to move home with my parents to undergo treatment in Albany, New York. After seven months of chemo, I was in remission and have been since!

Virginia

Last August I was diagnosed with stage 2A Hodgkin lymphoma (HL). I was going into my senior year, but instead of going to my first day of school, I had to go to my first day of chemotherapy. In October, after two full cycles of chemo, I got to ring my cancer-free bell and begin my recovery process. Today, I am in the process of growing back all my red hair and training to play Division One soccer at George Mason University in the fall.

Christine

Christine Attia knows first-hand how overwhelming and terrifying a blood cancer diagnosis can be. She lost her 27-year-old fiancé three years ago after a courageous six-month battle with acute myeloid leukemia (AML), a blood cancer which has seen few improvements in treatments in more than 40 years.

Integrative Medicine and Complementary Therapies

Integrative medicine (IM) is a form of medical therapy that combines practices and treatments from complementary medicine (yoga, acupuncture and massage) with conventional medicine (surgery, chemotherapy, radiation treatment and immunotherapy). Many cancer patients are using integrative medicine (IM) to help ease their cancer symptoms and reduce the side effects of cancer treatment. By integrating complementary therapies into conventional treatment plans, healthcare providers are better able to address the physical, emotional and spiritual needs of their patients.

BRIDGE (Blood cancer Research Initiative Developing Greater Engagement) with community patients

The Weill Cornell Medicine (WCM) Meyer Cancer Center (MCC) has an internationally recognized, clinical/translational blood cancer research program focused at its Manhattan campus. Elsewhere in New York City, the borough of Queens has 2.3 million and the borough of Brooklyn has 2.5 million residents. Both are among the most ethnically diverse urban areas in the world, and each separately ranks just behind Los Angeles and Chicago in population. Over 50% of patients diagnosed with blood cancers in New York City live in Brooklyn or Queens, and half of those are non-white.

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.

Moving Forward: 4 Young Blood Cancer Survivors Look Ahead

Blood cancer survivors have a unique path ahead of them—and that can feel challenging.  

Questions come up: Does treatment mean I have to pause everything? Do I tell my friends or coworkers (and how)? With my medical bills, how can I afford the education I want?  

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.

Gina

I was diagnosed with CML on May 25, 2010. Up until December 16, 2013 my disease was managed by oral chemo, then unexpectedly, I went into a blast crisis and progressed to acute lymphoblastic leukemia (ALL). I was told that I may not live to the end of the year unless an aggressive regimen of in-patient chemo, administered at the University of Pennsylvania hospital, was able to slow the proliferation of blast cells. Thankfully, the chemo worked and I began the preparation for a stem cell transplant. I had the stem cell transplant on May 1, 2014.