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B-cell acute lymphocytic leukemia

Sofia

Sofia’s story starts in November 2022. Actually, it starts on March 17, 2019, when she was born. She has been my fierce, independent, strong-willed little girl from the get-go. Once she started walking, she was an unstoppable force. Contrary to her cautious, older brother, Sofia seemed fearless. She loved to climb to the top of the playground structure meant for kids twice her age. She loved gymnastics and took after Mommy with her love of the bars, anything she could hang or climb on. 

AML

Sophia

I was diagnosed with acute myeloid leukemia (AML) one month before finishing my freshman year of high school. It was shocking and devastating to me and my whole family. I had to leave school, be hospitalized, and begin intense chemotherapy immediately.

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." 

Big Climb honored hero

Tristan

I live in Colorado but grew up in Massachusetts and am an elite rock climber. I've traveled worldwide to climb and was the 2015 collegiate national champion. In April 2022, I was bouldering by myself and hit my shoulder on a rock behind me. Falls happen as frequently as a baseball player may swing a bat while climbing. This fall was nothing out of the ordinary except my shoulder was bruised far worse than I would expect from how hard I hit it, growing to the size of my hand by the next day. I remember looking at it initially and thinking, "Geez, I hope that's not leukemia."

Stem Cell Transplantation

The goal of stem cell transplantation is to cure the patient’s cancer by destroying the cancer cells in the bone marrow with high doses of chemotherapy and then replacing them with new, healthy blood-forming stem cells. The healthy blood stem cells will grow and multiply forming new bone marrow and blood cells. There are two main types of stem cell transplantation. They are

Helping Siblings Cope

When a child is diagnosed with cancer, everyone in his or her family is affected by the experience, including the child's brothers and sisters. Siblings can feel angry, anxious, lonely or sad. They may even feel guilty for being healthy or for resenting the attention their sibling is getting. You can help your children cope with a sibling’s diagnosis in some of the following ways:

grace

Grace

Volunteering for an organization was part of my senior capstone in the Spring of 2021. I wanted to volunteer for an organization that was for the long term and meaningful to me. One of my best friends, who is also my cousin, was diagnosed with acute myeloid leukemia (AML) in 2020. I felt so helpless and also didn't know anything about AML, so I turned to LLS to educate myself. LLS is an integral factor and I wanted to do my part. I became a story volunteer, where I had the opportunity to interview and speak with other volunteers and supporters.

Janel

Janel

Throughout my childhood, my grandmother instilled in me the importance of helping those in need and gave generously to various charities and organizations. Her unwavering dedication to serving others inspired me to continue her legacy and give back to my community.

miguel_nonHodgkin_lymphoma

Marie and Miguel

Miguel was diagnosed with non-Hodgkin lymphoma (NHL) in early 2017. He was an active, healthy man his entire life, so this diagnosis came as a total shock. Both he and his wife didn't know what to expect or what the outcome would be and were both beyond devastated. After surgery, chemotherapy, numerous procedures, and hospital stays, Miguel and his wife were thrilled to hear the doctors say he had no evidence of disease as of late 2017.

Auden Emery

Auden

Eight-year-old Auden was diagnosed with T-cell acute lymphoblastic leukemia (ALL) in May 2015 – one month after him and his twin sister, Emery, celebrated their third birthday.

Immediately, Auden underwent aggressive treatment causing him to have blood stream infections, anaphylactic reactions, kidney stones and broken bones, just to name a few. But he kept a positive attitude through it all and Emery has been by his side, cheering him on at every stage of his cancer journey.

Auden’s treatment continued until August 2018, and today, he is proud to say he is cancer-free!

molly

Molly

Molly was just 2 years old when diagnosed with acute lymphoblastic leukemia (ALL).  We noticed a few petechiae on her back and went to see her pediatrician.  Two days later she was having surgery to have a mediport placed and starting chemotherapy.

The first few months were horrible.  She lost the ability to walk or even sit up due to the steroids she took daily.  She was a zombie and didn't talk or smile.  It was so sad to watch her so lifeless.  Often times we cried and cried and felt helpless. 

rhonda

Rhonda

In 2012, I was diagnosed with stage 4 non-Hodgkin lymphoma. I had 10 rounds of radiation and six treatments of chemotherapy (R-Chop). It was a very rough journey, however, by the grace of God, the love of family, and of course, the wonderful doctors and advances in cancer treatments I persevered through.

peter

Peter

I do not aspire to be a hero, I just want other patients to realize that any one of us can have a long life after receiving such a horrible diagnosis. Times may be difficult but anything is possible.

On September 5, 2015, I celebrated the 25th anniversary of my autologous bone marrow transplant for non-Hodgkin lymphoma that took place at the Dana-Farber Cancer Institute in Boston.  I want to thank my wife, children, and the many doctors, nurses, and technicians who treated me and continue to look after me in my senior citizen years.

courtney

Courtney

In 2007, I was diagnosed with acute lymphoblastic leukemia. After a long and painful 2 year and 3 month treatment full of chemotherapy, a coma, IV's. etc., I finally finished treatment. Around 2008, I began working with LLS to share my story and since then, I have continued to share my story through different programs held by LLS. Throughout the last 11 years I have been with LLS, they not only helped countless people, but they have also treated me like family and have always asked me about my life and they truly care.

Myra

Over the course of Myra’s career in oncology nursing, she’s seen the hurdles that families face and heard from patients about the daily struggles to access the care they need to stay alive. Unfortunately, she is too familiar with patients who are forced to choose between life-saving treatment and going against a doctor’s recommended treatment plan simply because the cost is too high.

Ryan

Ryan

I am a cancer and bone marrow transplant survivor. In June 2013, at the end of my eighth grade, I was diagnosed with acute myeloid leukemia (AML). On top of that, it was the worst subtype of AML and my outlook was considered very grim.

jeremiah

Jeremiah

In February 2018, my youngest twin (by three minutes), Jeremiah was diagnosed with acute lymphoblastic leukemia (ALL). Our world and lives were turned upside down, to say the least.

As a single mother, I never felt or experienced pain like this in my entire life. It felt like everything was crashing around me. Jeremiah began treatment with chemotherapy at the Children’s Hospital.

chronic myeloid leukemia (CML)

Tom

I was diagnosed with chronic myeloid leukemia (CML) in January 2023. I am very thankful for all the research that has led up to medications and treatments that I am able to benefit from today. God has a plan, and I feel a large aspect of that plan is bringing together those with needs and those with resources to help. It is so overwhelming to me to understand that there are those who support this wonderful research even though they don't have a name or face to tie it to. Through their generosity, people like me can continue living.

white family with New Year's Eve hats on including bald girl with a pink shirt on

Adelaide

I was first diagnosed with acute lymphoblastic leukemia (ALL) in September 2014 when I was six years old. I relapsed three additional times between 2014 and 2021. I had a bone marrow transplant in 2020 during COVID-19 and relapsed again six months after the transplant. In July 2021, I received huCART-meso cells at the Children's Hospital of Philadelphia (CHOP). Since that time, I have remained in remission. 

Louisiana's Junior Leadership Board

Jaden

When I was nominated to be a Student Visionary of the Year, I had no idea how it would impact my life. I was allowed to join a groundbreaking philanthropic leadership development program for high school students. Throughout my courageous seven-week journey, I had a goal of creating a world without blood cancers. It was bigger than winning; it was about making a real impact on the world around me. I learned business marketing skills, used effective communication tools, and met with fellow change-makers in my local area. By the end of the campaign, I felt like a new person.

Signs and Symptoms

Some patients initially have no symptoms of MDS, and abnormal results from routine blood tests may be the earliest signs of the disease. For patients with symptoms, it is common not to feel well because of the lack of normal, healthy blood cells.

Anemia is a decrease in the number of healthy red blood cells. Red blood cells carry oxygen throughout the body. Anemia may cause symptoms such as:

Cathy

Cathy

I decided to call my cancer the “little c” rather than the “Big C.” I wasn't giving it that much power over 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.

Matt Corely

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).