Search Results
Nevaeh
Nevaeh was diagnosed with acute myeloid leukemia (AML+MLLr)+CNS chloromas on February 2, 2022, at 12 months old. Nevaeh first showed symptoms of high fevers, no appetite, and little to no energy. After a trip to the ER, a few tests, and x-rays, I was told Nevaeh had COVID and pneumonia. She was discharged with instructions to go back if her symptoms worsened. The following morning, Nevaeh’s health was declining. I called 911, and she was rushed to the ER and admitted to the pediatric unit.
Emily
One night in August 2017, I had sudden and extreme back pain. My husband took me to the hospital where they told me I was fine and sent me home. Three other hospitals later, they finally did blood work and diagnosed me with Acute Myeloid Leukemia. I was only 26 years old at the time and otherwise very healthy.
I did not fully understand the severity of the situation and asked the doctor if I would be back to work the following week. I started my first round of chemo within 24 hours of diagnosis. However, my leukemia was resistant to the induction therapy.
Amber
On November 22, 2013, I was diagnosed with Chronic Myelogenous Leukemia (CML). There was no sign that anything was wrong until I went in for routine blood work. My platelet count, which should have been in the 150,000 to 400,000 mcL range, was over a million. After a bone marrow biopsy, my oncologist discovered that I had Philadelphia chromosome–positive CML.
My diagnosis opened my eyes to just how much has been accomplished in the fight against cancer.
Emily
I was diagnosed with B-cell acute lymphoblastic leukemia (B-ALL) when I was 28 weeks pregnant. I came into the ER with a high fever from the flu, and one routine CBC test later, had me rushed for more tests and a bone marrow biopsy to confirm leukemia.
I was transferred from an already very large and experienced hospital to another due to being pregnant. Thankfully a doctor wanted to take my case . . . two hours away.
Nanci
I was diagnosed with chronic myelogenous leukemia (CML) in January 2009. My doctor said the average life span was three years if not for the newer drug called Gleevec, a drug that The Leukemia & Lymphoma Society (LLS) had been involved in the research of it. I started on Gleevec in February, but after a week I was taken off it to bring my immune system back up. Back on Gleevec, I reached remission in July 2009. I now have been in remission for 12½ years. I now take the generic brand due to the cost.
Deana
In May 2008 at nine years-old, I was diagnosed with acute lymphoblastic leukemia (ALL). I went from being told I had a 10 day stomach virus to being told I had leukemia. The doctors said told I didn't come in when I did, I could of lost my life.
A year went by, and I was stuck in the hospital missing out on family and important events. I even had my tenth birthday in the hospital, but I was too sick to enjoy it.
Rose
My brother Hopoate is a leukemia survivor. At the young age of 2, he was diagnosed with acute lymphocytic leukemia (ALL) and finished his chemotherapy when he was 4-1/2 years old. He has been cancer-free for about 17 years now. He is now 21 and thriving.
Jeff
A little over two years ago, I was diagnosed as having chronic lymphocytic leukemia (CLL). I was shocked and devastated by the news and immediately began seeing an oncologist. My team from the cancer center has been uplifting, positive, and supportive from the very beginning! They have been successfully treating my cancer and have taught me not to fear my disease.
Rick
Rick Ostroff and his family have a legacy of philanthropy with a heartfelt connection to a disease he never had. During the first three years of his life, he spent time on the leukemia floor of Children’s Hospital in Boston but eventually was found to have the critical illness of gamma globulin anemia rather than then-fatal leukemia.
George
My awareness of The Leukemia & Lymphoma Society (LLS) began years ago when a close family member was diagnosed with leukemia. In the wake of such devastating news, I felt compelled to lend a hand. I am honored to join the LLS family in their fight to cure blood cancers.
Reid
We just wanted to reach out and say how much The Leukemia & Lymphoma Society (LLS) has helped us. From attending Light The Night (LNT), to getting a blanket in the mail, to receiving funds when I couldn't work to keep Reid safe from the pandemic. Anytime I have needed assistance or reached out, the staff I have chatted with are so amazing and make you feel like you're so included and important. You have made us feel loved and gave us hope and inspiration. Reid was diagnosed at 2 years old, and he is almost done with B-cell acute lymphoblastic leukemia (B-cell ALL) treatment.
Kaidyn
Kaidyn was only six months old when he was diagnosed with acute myeloid leukemia (AML). About two months later, he received a bone marrow aspiration and was started on chemotherapy. Over the next ten months, Kaidyn was in and out of Children's Hospital of Oakland. It was there that he took his first steps, said his first words, and even flirted with every nurse in the oncology unit! Kaidyn is now a healthy three-year-old boy with an ear-to-ear grin who participates in his local Light The Night Walk each fall.
Martin
I have a unique story. In 1978 after being married for three weeks, my wife was diagnosed with acute lymphoblastic leukemia (ALL). Seven months later she passed away.
Tracey
I was diagnosed with chronic lymphocytic leukemia (CLL) in 2021 after a routine physical after my 50th birthday. It was a complete shock, and I was scared and unsure of what my future would look like. With the help of my doctors and The Leukemia & Lymphoma Society (LLS), I feel prepared to make informed decisions about my future. I participate in medical research studies and intend to join a clinical trial (that a clinical nurse at LLS told me about) when I need treatment.
Megan
At 31, I was diagnosed with acute myeloid leukemia (AML). It all started with what I thought was a cold or maybe COVID. I kept working, brushing off the symptoms as something minor. But things got worse. I had a persistent cough and unexplained bruises, and I felt constantly out of breath. When I lost part of the vision in my right eye, I knew something was seriously wrong, but without insurance, I hesitated to seek help.
Kelly
In 2001, I was diagnosed with T-cell acute lymphoblastic leukemia (T-ALL) at age three and survived thanks to three and a half years of intense treatment at the City of Hope Los Angeles. I am now 25 years old, a college graduate, and working for The Leukemia & Lymphoma Society (LLS), hoping to give back to those who helped save my life. I have volunteered with LLS since 2009 after being chosen as their "Girl of the Year" to inspire candidates to raise money for blood cancer research. In 2017, I became a candidate for the Student of the Year campaign raising over $60,000 in seven weeks.
Lana
Lana's journey with The Leukemia & Lymphoma Society (LLS) began in 1991 when she was diagnosed with acute lymphoblastic leukemia (ALL). Overcoming numerous physical and cognitive challenges associated with her illness, Lana emerged as a dedicated advocate for cancer awareness and support. She became an integral part of the Orange County LLS community, participating in various programs such as Honored Hero, Light The Night, and So Cal Cancer Connection, among others.
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.
Avery
I am writing as a parent of a cancer survivor. My daughter, Avery Smith, who is now 8 years old, was diagnosed at age 3½ with leukemia. In 2016, our then 3-year-old daughter Avery was complaining of muscle aches, backaches, and for a solid week was running a pretty high fever. We took her to the doctor, and after a few visits, they weren’t really sure what was going on. After some bloodwork, our pediatrician called us and said Avery had some very concerning numbers.
Julian
On October 9, 2017 eight-year-old Julian suddenly became ill with a fever and headache. We gave him some over the counter medicine and made an appointment with his pediatrician. By the time he was in the doctor’s office the next morning, Julian had worsened and his doctor immediately ordered labs.
Shelley
Twenty years ago I was diagnosed with acute lymphoblastic leukemia (ALL). My husband, Remi and I were married and just moved to Virginia, where Remi was stationed in the Navy. In the short six weeks we lived there, I never felt 100% and I was at the doctor four times in six weeks. At my last appointment, I requested that they draw my blood. They told me I had mono, my counts were so low, they took me by ambulance to the nearest hospital.
Catherine
In March 2014, I woke up at my normal time to get ready for work. I could barely move - I was so ill and every part of my body hurt. I didn't’t think anything of being sick since I had started to feel ill on Sunday and it was just getting worse. I figured that I would stay home sick and be back to work the next day.
Jason
I’m a father of 4, a first responder, and a military reservist. I was diagnosed with stage 4 diffuse B cell lymphoma. After losing my cousin to leukemia and 2 months later receiving my diagnosis, my whole world was turned upside down.
David
My beloved husband, David served the community of Arlington, Texas, through the fire department for 38 years. Throughout his career, he served the city and trained and mentored other up-and-coming firefighters. He retired in 2017, and just nine months later, he was diagnosed with acute myeloid leukemia (AML), a very aggressive blood cancer. His oncologists believe it had simmered in David's marrow for a couple of years before it went acute. It came on with similar symptoms to the common flu.