Skip to main content

Search Results

callie

Callie

In January 2016, I was diagnosed with stage II Hodgkin lymphoma. I was four months pregnant at the time, and it was decided to carry to term because this type of blood cancer is a slower spreading cancer.

In May 2016, I had a healthy boy and 10 days later began my first of many chemo treatments. The following October I had my last treatment and I was excited to get back to "normal" life.

graysen

Graysen

Graysen was born in March 2017. She was born the day before my birthday and we often say that she was the greatest birthday present ever. She was such an easy-going baby - happy, curious, and sweet with a magnetic personality. She was seemingly healthy, happy and 21 months old when we shockingly learned she had leukemia in November 2018. It was a diagnosis we never saw coming and one we were forced to simultaneously digest, navigate and hit head on.

stage 4 diffuse large B-cell non-Hodgkin lymphoma (DLBCL)

Zoraa

Being a cancer survivor was never on my bucket list.

Jamaal

Jamaal Simmons had non-Hodgkins lymphoma (NHL). He was such a brave person. He worked at Publix supermarket and he went to Clark Atlanta University. He was about to graduate from college when he passed away.

It is now 14 years since he's been gone. But I still donate and collect donations and I've been doing this for many years. I will keep on doing it to help fight this blood cancer.

- Jamaal's mom, Sharon Williams.

drew

Drew

One thought that never crossed my mind as a parent was the fear of a cancer diagnosis for my five year old son.

A few months shy of his 6th Birthday, Drew had very typical cold symptoms, but they were persistent and he was extremely fatigued.  After a two visits to his primary care physician, come over the counter medicines and finally a trip to Urgent care, we had a lot of questions but no answers.  My husband took him to his primary care Dr on Monday and we insisted on a blood test. 

ariel

Ariel

I was diagnosed with acute promyelocytic leukemia (APL) on January 24, 2019. I hadn’t been feeling well for a while. I was having very odd symptoms. For example, I was having joint pains, I kept hearing this whooshing noise, my gums were bleeding, and the biggest symptom was I would get out of breath so easily. Walking up the steps of my apartment building felt like running a marathon. I went to an urgent care clinic and described these symptoms, and the doctor gave me an antibiotic and sent me home. I’ll never forget his face before he discharged me. I could see he was unsure.

Man in blue shirt and mask in a hospital bed with a medical worker holding a bag of stem cells

Peter

My story starts a year and a half before diagnosis when a serious body surfing accident led to blood tests showing significantly low red and platelet counts. My primary care physician (PCP) retested several times in a short period, and when the counts came back closer to normal, she chose to stop her inquiry without scheduling further tests or redoing the same test, say, six months later to see if the lower values were actually correct. There was no discussion of what it would have meant if the lower counts were, in fact, an accurate representation of my blood health.

SH

Steven

I have a rare blood cancer. It is Waldenstrom macroglobulinemia (WM), a type of non-Hodgkin lymphoma (NHL), but some doctors say it has the same characteristics as POEMS syndrome.

I have very painful neuropathy, and it affects my legs and feet to the point that some days I cannot walk.

I have a spinal cord stimulator with the battery implanted in my back.

I am thankful to The Leukemia & Lymphoma Society (LLS) for my grants and all the other assistance, especially through this COVID pandemic.

Kevin

Kevin

In 2011, I was given two months to live after I was diagnosed with acute myeloid leukemia (AML).

I had to stay at the Bone Marrow Transplant Center at the Salt Lake City Hospital for a very long time and undergo a very hard fight.

My aortic valve failed this year from the chemo, but I had open heart surgery in May 2017 and I am grateful to be alive!

I live in honor to all that passed in our family and those who are still fighting blood cancer. 

JE

Jacqueline

It’s been five years since my daughter was diagnosed with stage ¾ Hodgkin lymphoma (HL). She had just graduated college, and she had a lump on her right clavicle area. We went to the doctor, and then it all started, from CT scans to biopsy to telling us that it would be six months of chemo, and that’s it.

Maria

Maria

By the end of November 2008, I started feeling an overwhelming fatigue. I developed a fever and my physician sent me urgently to the emergency room. There I was found to be depleted of blood and needed a transfusion. It seemed so unreal.

After a couple of days and a bone marrow biopsy, I was diagnosed with acute myeloid leukemia (AML). I learned that if I had not sought help in the ER, I could had died.

acute myeloid leukemia (AML)

Ryan

At 22 years old, I was diagnosed with acute myeloid leukemia (AML). My first hospitalization was a month long which was followed by four more hospital stays for my chemotherapy treatments. In between each of those hospitalizations were home nursing visits, blood transfusions, doctor’s appointments, and even more hospitalizations to treat potentially life-threatening infections. I lost a total of 40 pounds throughout those months. Despite the many struggles I encountered during those months, I was able to successfully complete my treatments.

Hodgkin lymphoma (HL)

Yaneiry

Certain things come into your life to show you how strong you are. Life is so fragile, and we don’t know if we will be here on this earth in the future. This process shows me that the most important thing in life is having health and making beautiful memories with loved ones. 

chronic myeloid leukemia (CML)

Tim

It was December 2006. I was 28 years old, and I discovered some purple bruises on my leg. I had never seen anything like these on my body before, so I went to my primary care physician. He took some bloodwork, then called me to say I needed to go to the hospital at once. My parents’ friend drove me and my parents to the hospital, and I ended up staying at the hospital for four days.

Lyndi

In March 2019 I began feeling off...I didn't know what it was. I thought perhaps it was a loss of relationship that broke me to my core, or that fact that an old friend had asked me to be kidney donor for someone I had never know. I agreed to be tested to see if I was a possible match. Fast forward to October when I was tested a possible blood clot that had formed from all of this. I was having continual pain in my right shoulder blade.

Lorelai_acute_myeloid_leukemia

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.

Shelley B

Shelley

I went from being in the best shape of my life to battling cancer in only a few short months.

Three years ago, I made the choice to change my lifestyle, and I lost 100 lbs., which I can honestly say has saved my life. Prior to my cancer diagnosis, I was sharing my weight loss journey online to help others make positive choices. Little did I know that I was about to fight the biggest battle of my life!

Zeena A

Zeena

As an oblivious 14-year-old, I never imagined that I would soon go through the most difficult journey of my life. While on summer vacation with my family, we quickly realized I was not my energetic, joyous self. My favorite activities seemed like energy-draining tasks, and my large appetite had suddenly disappeared. The once quick trip up the stairs turned into a painful trek up a mountain and a walk down the street to a treacherous marathon with no end.

Dylan

Dylan

I was diagnosed with acute lymphoblastic leukemia (ALL) the summer of 2017, right before the start of my junior year in high school. Due to slow immune recovery after chemotherapy, I experienced many delays in treatment. By spring of the following year, I had a CNS and marrow relapse, requiring me to have a life-saving bone marrow transplant in June of 2018. Following the transplant, my body struggled to produce enough T-cells, which put me in medical isolation for the entirety of my senior year in high school.

Mia

Mia

As Mia started her third grade year at elementary school she began complaining of pain in her legs. At first, her mom just thought it was normal growing pains. But then Mia started sleeping a lot more, lost her appetite and just didn’t have her normal level of energy. Mia’s parents, Alma and Ernesto, decided it was time to take her to the doctor.

Amanda

Amanda

"He was selfless, unbelievably selfless," said Amanda about her father, Andrew. "He did everything for everybody. He worried enough for our family plus more. And never showed it. He worked extremely hard to provide us with everything we could possibly need." 

myrrah

Myrrah

Acute lymphoblastic leukemia survivor travels from India to receive LLS-funded treatment

When Myrrah was just six years old, she was diagnosed with acute lymphoblastic leukemia. Her family lived in India at the time, where she received a year of intense treatment. When her blood work showed no signs of cancer, her family celebrated with a vacation to Europe. Then, during a routine checkup they learned that Myrrah’s cancer had returned and the doctors said there was nothing more they could do.

Cindy

Cindy

Our church choir had put on a big Easter program in 2002, lots of practices and multiple performances. After the fact, several, including me, came down with an upper respiratory infection. All my friends got better, but I didn’t. Then I started having low energy to the point that I couldn’t do my daily workouts. Next came the appearance of big, ugly bruises on my legs. At that point, I thought I was anemic. When I called to get a doctor’s appointment, the only opening was with his nurse practitioner.

Pilar

Pilar

My name is Pilar, and I am 34 years old. I used to work for the workforce board of Philadelphia, working with youth, until I was diagnosed with acute myeloid leukemia (AML) back in October 2020. It has been a hard battle, but I am positive and blessed to have the support of my family and friends. Additionally, I was very fortunate my sister, Marcela, was a match to be my donor.