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Joaquin middle aged hispanic man wearing navy beanie and ski jacket with two hispanic girls one in a pink jacket and one in a purple jacket holding a snowball in front of snow covered trees

Sophia

When I was in middle school, my dad was diagnosed with acute lymphoblastic leukemia (ALL). During this time, The Leukemia and Lymphoma Society deeply supported our family. Sadly, my dad passed in 2021, but my loved ones and I continue to honor his spirit by making the most out of our lives. I became a volunteer because I strive for a future where cancer has a cure. All donations are deeply appreciated and will go to cancer research! 

CLL

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.

Leukemia Survivor

Nikki

If you were to sit down with Nikki Henshaw, you'd find out she has a full and blessed life. She has a supportive husband, two beautiful children, and just started her own part-time business so she can be a stay-at-home mom. But in 1994 she found out that she had acute lymphoblastic leukemia (ALL), a diagnosis no 14-year-old wants to hear. While she did go into remission only a month later, she still had to undergo intense treatments for the next three years. As a result of her treatment, she had many challenging side effects.

Little girl with red headband and shirt holding medical instrument next to a woman with glasses

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.

Little girl with leukemia on a scooter with a purple ribbon headband

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.

young woman with blond hair and long eyelashes lying in hospital bed wearing a black sleeveless top showing a port and a tattoo

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.

AML Subtypes

Doctors classify acute myeloid leukemia (AML) into subtypes by using various tests. It's important to know your AML subtype because it plays a large part in determining the type of treatment you'll receive.

acute myeloid leukemia (AML)

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. 

Amber

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

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.

young white woman sitting in a car wearing a head scarf, wire rim glasses, a floral sundress witha nose ring

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.

Heather

Heather

The world works in mysterious ways, it truly does! When I first volunteered with The Leukemia & Lymphoma Society's (LLS) Team In Training (TNT) program in 2015, I never in a million years thought I would be fundraising in honor of my husband Dave. I started out fundraising for my step-grandmother Margaret and his grandmother Pearl. Eventually, the list of people I ran and fundraised in honor or memory of grew to way over 20! All that time it turns out I was fundraising for Dave, too, we just didn't know it yet!

acute lymphoblastic leukemia (ALL)

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.

campbell

Campbell

Hi!  My name is Campbell Brandt.  I am 9 years old and a student at Spring Run Elementary School in Chesterfield County, Virginia.  I love to dance, play softball, ride my scooter, sing karaoke, listen to music and watch the Disney channel.  I like to dance and sing to Katy Perry, Taylor Swift and Carrie Underwood.  I am a pretty typical 9-year-old girl, except that I have fought cancer.

jeffrey

Jeffrey

My name is Jeff Kurowski and I am 35 years old.  I have lived with chronic myeloid leukemia (CML) for two years and Crohn's disease (CD) for 20 years.  I have had three feet of my intestines removed.  I now depend on daily bowel suppression medication, monthly B12 shots, biologic therapy for a quality of life, and a daily targeted chemotherapy pill to stay alive.

betsy

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.

Jude

Jude

From 2013 to 2014, after he was diagnosed with acute lymphoblastic leukemia (ALL), Jude endured four cycles of intense chemotherapy, lengthy hospitalizations, difficult side effects, and months of home isolation. Jude's younger brother, Finn, was born in May 2014 in the middle of Jude's chemotherapy cycle. In August 2014, his family finally celebrated as Jude finished the more difficult part of treatment.

Chemotherapy and Drug Therapy

About Chemotherapy

Chemotherapy drugs kill fast-growing cells throughout the body, including both cancer cells and normal, healthy cells.

Chemotherapy is typically given in cycles. Each cycle is made up of a certain number of days of treatment, followed by a certain number of days of rest. The rest days allow the body time to recover before the next treatment cycle begins.

AS

Allison

My story is not all that different from many others. It began with two-year-old me not feeling well and my mom taking me to the pediatrician on a Monday. They diagnosed me with an ear infection and gave me antibiotics. On Friday, still not better, my mom asked my dad if they should let the doctor take another look at me. In my mom’s words, “Something’s not right with my little girl.” Fortunately, the doctor ran a platelet test. My results were so off the charts that she also ran the test on herself to make sure the machine was not broken.

CML Phases and Prognostic Factors

CML has three phases. The phase of your chronic myeloid leukemia (CML) plays a large part in determining the type of treatment you'll receive. Doctors use diagnostic tests to determine the phase of CML. Determining the CML phase is based primarily on the number of immature white blood cells (blasts) in the patient’s blood and bone marrow. 

Phases of CML

Chronic Phase. Most patients are diagnosed with CML in the with chronic phase of the disease.

​People with chronic phase CML:

Treatment

Parents are advised to

  • Seek treatment from a hematologist/oncologist who is experienced in treating JMML, or from a hematologist/oncologist who is in consultation with a cancer center.
  • Speak with their child’s doctor about the most appropriate treatment. 

Without treatment, JMML progresses rapidly. There are two widely used JMML treatment protocols: stem cell transplantation and drug therapy.

Ph-Positive ALL Therapy

About 25 percent of adults with ALL have a subtype called “Ph-positive ALL” (also known as “Ph+ ALL” or “Philadelphia chromosome-positive ALL”). The leukemia cells of these patients have the Philadelphia chromosome, which is formed by a translocation between parts of chromosomes 9 and 22. A piece of chromosome 9 breaks off and attaches to chromosome 22, and a piece of chromosome 22 similarly breaks off and attaches to chromosome 9. The abnormal chromosome 22 is known as the Philadelphia chromosome. This chromosomal alteration creates a fusion gene called BCR-ABL1.

Relapsed and Refractory

Some chronic myeloid leukemia (CML) patients still have leukemia cells in their bone marrow after initial treatment with a tyrosine kinase inhibitor (TKI). "Refractory" is the term used to refer to a disease that has not responded to the initial treatment. Relapse is the term used to refer to the return of a disease after a period of improvement. 

TKIs used for "initial" or first-line treatment for chronic phase CML include:

Clinical Trials

Taking part in a clinical trial may be the best treatment choice for some Hodgkin lymphoma (HL) patients. Clinical trials are under way to develop treatments that increase the remission rate or cure the disease. Today's standard treatments for cancer are based on earlier clinical trials. The Leukemia & Lymphoma Society continues to invest funds in HL research.

Click here to read more about clinical trials.

AML Subtype

Determining the AML subtype is an important factor in treatment planning for your child. This determination is made based on certain features of the leukemia cells identified with the diagnostic tests. The doctor will speak with you about the drugs and “treatment protocols” (detailed plans of treatments and procedures) that are indicated based on your child’s AML subtype.