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 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.
In November 2014, my daughter Valerie was born. Shortly after, I was diagnosed with an upper respiratory infection by my doctor and received 3 rounds of antibiotics because it just wasn’t going away. Life was hectic as I learned to care for my newborn and I was getting into a new routine. Some of my lymph nodes became swollen. I was having night sweats. I developed a rash and high fevers.
I'm officially nine months in remission and just celebrated my first birthday (27!) since finishing chemotherapy treatment.
I would like to introduce everyone to my little warrior, Hunter. When he was just four years old, he had an enlarged stomach that just kept getting bigger and bigger with no answers as to why.
Hello, my name is Nikolas. I am 16 years old, almost 17, and have been battling acute lymphoblastic leukemia (ALL) for eight years.
In November of 2021, I found a lump on my neck that lead me to my primary care doctor's walk-in clinic due to the amount of growth I had seen over a few weeks. I believed it to be related to thyroid or my previous diagnosis of lupus of the skin, which I later found out I did not actually have.
The Leukemia and Lymphoma Society (LLS) holds a special place in my heart.
Where do I begin? I am a 2x acute myeloid leukemia (AML) survivor with being diagnosed for the first time in 2008 at the age of 38. My family and I received amazing support through The Leukemia and Lymphoma Society (LLS) both emotionally and financially with the co-pay program, webinars, and information guides.