Search Results
Gwendolyn
Gwendolyn describes herself as a wanderlust who never likes to let the grass grow under her feet. After college, she moved from her hometown in Florida to Houston and spent the next few years moving around Texas for work. She started her new life in Texas where her son, Sterling, was born and raised. She loves traveling, but following a trip to Belize, she started to notice white spots on her skin and other strange issues happening with her health. After doing some research on her own and going to the doctors, she was told she likely had lupus.
Tina
As a lymphoma survivor, I want to take a moment to share my personal journey, as well as tell you all how The Leukemia and Lymphoma Society (LLS) was with me every step of the way.
It all started in March 2018. We had been living in the UK with our two young daughters, and life was good! I had been feeling tired and had this hollow sound behind my ear. I saw doctors in both the UK and the U.S. who assured me it was most likely just my body trying to get over a sinus infection.
Katharine
My mother, Nancy, was diagnosed with acute myeloid leukemia (AML) with a FLT3 mutation in March 2022. Over the next year and a half, she went through multiple rounds and regimens of inpatient and outpatient chemotherapy. At every step along the way, every member of my mom's care team kept mentioning how the outlook for patients like my mom was so much better now than it had been even 10 years ago thanks to advances in medicine.
Betsy
My dad, my best friend, lost his short 15-day battle with acute myeloid leukemia (AML) on January 23, 2008. Dad was 72, but not just any 72-year-old man. He had so much life in him. He was very active in his community and loved his wife (they were married for 44 years), his daughters (my sister and I), and especially his three grandchildren! He lived every moment to the fullest and you knew he enjoyed life just by listening to his infectious laugh! He always had a smile on his face, a story to share, and those always needed words of wisdom to share.
Austin
Four were spoken that day. Four crushing, breathtaking words, “Your son has cancer.” My world, my life, and my dreams for my son’s future suddenly halted while the rest of the world kept going on around us on May 14, 2011. Only days before, I was deciding what theme to have for his third birthday party and what outfit he would wear for his pictures. Days later, my husband and I were signing consents for the specific protocol of poison that would be pumped into Austin and having to digest the laundry list of possible side effects.
Chloe
At the age of 13, I became the youngest stem cell donor at Johns Hopkins Hospital. At 15, I am a Student Visionary of the Year in the 2024 Leukemia and Lymphoma Society (LLS) campaign. LLS has become an integral part of my life over the past two years. In the spring of 2022, the peaceful life of our family was shattered by my mom’s diagnosis of acute myeloid leukemia (AML). Learning that a stem cell transplant was the only cure, I volunteered to donate my bone marrow to her.
Larry
Larry Loose, a great big bear of a man with a penchant for classic cars, off road racing, dirt bikes and living large. This man, my husband of twenty five years, had worked 12-hour days for decades in hopes of being able to retire early, move to the desert and spend our later years as snowbirds in beautiful Arizona.
Heather
The Leukemia & Lymphoma Society’s Light The Night Walk serves as an inspiring, empowering and comforting event, made possible by those who share, remember, and advocate for the fight against cancer. Each year, we here at LLS are graced with countless stories that demonstrate and display the spirit of this event. Heather Lee’s story is one of them.
Judith
In 2016, my Mom/daughter's grandma, Baba (Judith W), was diagnosed with acute myeloid leukemia (AML). After her first round of chemo, she was discharged from a one-month hospital stay on my daughter's third birthday. Best birthday present ever. She continued fighting the disease with more chemo and ultimately received a stem cell transplant from an amazing donor. Amid the uncertainties of her recovery, we hosted our first lemonade stand fundraiser on Mother's Day weekend the following year in hopes of helping.
Kate
On May 17, 2018, our family was thrown into the world of blood cancer. Our family's patriarch, our bonus dad, and our beloved "Candy Boy," as he was affectionately nicknamed by his youngest daughter, found out that he was in the aggressive stages of acute myeloid leukemia (AML).
Donna
I was shockingly diagnosed with a monoclonal spike in November 2019 (six months after the unexpected death of my mom). Treatment was started in June 2020. I went to Mt. Sinai NYC where they have a team that just deals with multiple myeloma (MM). I am grateful that a couple of people recommended I go there. They treated me with four drugs, one of which wasn’t available at my local oncologist. The regimen was Velcade, Revlimid®, daratumumab, and dexamethasone. I had this induction therapy until my stem cell transplant in March 2021.
Mara
I was in my second to last year of nursing school and just over one year into my marriage when the headaches became too much to bear. I was 21. I was tired all of the time, but I was working in a busy ER and going to class when I wasn't at work. I had lost some weight, but I had been exercising more and getting a lot while working in the ER. I had a cough, but they tell you that you'll be sick a lot when you're in nursing school. Unfortunately, I happened to touch my neck one day while studying with classmates for a big exam. There was a lump there that I had never felt before.
Matt
I’ve lived a mostly normal 27 years on this earth. A life filled with wonderful academics, Division 1 athletics (pole vault), financial internships, and fantastic sales roles at companies I really enjoyed.
However, my life changed drastically on February 28th, 2023.
In the middle of the night on that Tuesday, I was woken up by a call from an unknown number. I let it ring through… maybe it was spam? Then they called again.
Caitlyn
My world started to turn upside down in January of 2019 after starting to exercise and trying to lose weight. At first, I thought I had pulled a muscle in my leg. The cramping continued to increase and turned into radiating bone pain. I went to get an x-ray to make sure nothing was broken. There were no broken bones or fractures, so they sent me on my way.
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.
Reese
Before we knew the world of childhood leukemia, and long before bone marrow transplant was a part of our vocabulary, we had sweet little identical twin girls, named Reese and Quinn. The twins were born in Chicago on April 10, 2014. Reese and Quinn were healthy babies who grew into healthy toddlers and then their little sister Claire joined our world in 2016. These sisters are the best of friends and the greatest supporters of each other.
