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greysun

Greysun

Hi! My name is Greysun! I was diagnosed with acute myeloid leukemia (AML) on March 23, 2011. I was fortunate to get outstanding medical treatment at UNC Children's Hospital and the cancer center. I have been through many rounds of chemo followed by up to six weeks of hospitalization after each one. I have had radiation to my brain followed up by my first bone marrow transplant.

Allie AML

Allie

On July 18, 2020, I rang a bell in the lobby of the Cincinnati Children's Hospital that signified the end of my chemotherapy treatments and the beginning of my remission. At age 15, I was diagnosed with acute myeloid leukemia (AML). I entered the hospital on December 1, 2019, with dangerously low red blood cell and platelet counts.

Philadelphia positive B-cell acute lymphoblastic leukemia (Ph-positive ALL)

Krisha

I started noticing some things were "off" with my body. In early August 2022, my daughters noticed several large, unexplained bruises on my legs. I just brushed them off as being clumsy or running into something. Then, while lying in bed reading to one of my daughters, my lower jaw and lip went numb, like when you have Novocaine. I got up and moved around, and it got better. This started to be a daily occurrence, and about a week or so later, I woke up and could not open my mouth. I thought I had TMJ, so I called my dentist. He had me come in and looked at my mouth/jaw.

middle aged white man in a ball cap with a scruffy beard and mustached wearing a black t-shirt lying in a hospital bed giving a thumbs up

Nicholas

It started with a stiff neck. Then came fatigue and a sore throat. I started feeling full after only a few bites of food. Workouts were getting more difficult to complete. My heart rate was consistently north of 100 just lying in bed. Rationalized. It's maybe strep. Could be mono. I prescribed myself antibiotics and popped ibuprofen. Nothing was working. Reluctantly went to an urgent care after weeks of feeling like this. Bloodwork was done.

Sarah and daughter

Sarah

In August of 2014, after a routine medical procedure, doctors suspected that Sarah may have a lymphoma type cancer. Soon thereafter, with her husband by her side, doctors confirmed that Sarah indeed had cancer, stage 2 Hodgkin lymphoma.

Gwen

Gwendolyn

Gwendolyn describes herself as a wanderlust who never likes to let the grass grow under her feet. After college, she moved from her hometown in Florida to Houston and spent the next few years moving around Texas for work. She started her new life in Texas where her son, Sterling, was born and raised. She loves traveling, but following a trip to Belize, she started to notice white spots on her skin and other strange issues happening with her health. After doing some research on her own and going to the doctors, she was told she likely had lupus.

Virginia

Virginia

I have been living with chronic myelogenous leukemia (CML) since August 6, 1997. The way I see it, I’m alive today because of The Leukemia & Lymphoma Society (LLS). The pill I take each day that keeps my leukemia in remission exists today much because of research grants awarded to Brian Druker, M.D., PhD., of Oregon Health & Science University.

Side Effects

Most ALL treatment side effects are temporary and subside once the body adjusts to therapy or after the therapy is completed. If side effects become severe, children may need to be hospitalized.

Side effects common to ALL and its treatment include:

lori

Lori

Our daughter Britta Wolfarth was 19 when she was diagnosed with AML. We were shocked because we thought it was a blood disorder due to her lupus. The same day for the guy diagnosed she started treatment at West Penn in Pittsburgh right away.

Britta underwent months of chemo and radiation. Britta had to have a bone marrow transplant. Her first owner fell through but the transplant team at West Penn never gave up and found us another donor 2 months later from the National Registry.

Marie

Marie

In early 2017 we found out my husband Miguel had non-Hodgkin's lymphoma diffuse large B-cell. It was the most frightening and overwhelming time of our lives. To this day I am amazed at how we got through it.

Layla

"Our LLS chapter has been there for us, with support and information that has helped immensely. We've formed a friends and family Ttam for the Light The Night Walk and it feels so rewarding to raise funds to help others who, like Layla, are bravely battling blood cancers." Alecia | Layla's mom

young white woman in a hospital bed with short hair wearing a gray hoodie and holding an orange sign about fifth round of chemo

Ashlyn

My name is Ashlyn, and I am a leukemia survivor. At the age of 17, during my senior year of high school, I was diagnosed with acute myeloid leukemia (AML). AML is a rare cancer that affects your bone marrow and blood. My life changed on March 21, 2023, when I got this news. How could this be possible? Why me? Will I survive? These were some of the first few questions that entered my mind. I went through five rounds of chemotherapy and nine grueling months of being inpatient in the hospital. I wasn't able to go on my senior class trip to Disney World or attend senior prom.

Julian

Julian

I was a 10-year-old kid when I was diagnosed with leukemia. I was a happy, energetic kid who loved being outside and was a straight-A student. However, my whole childhood was put on hold indefinitely once I had cancer. Rather than having sleepovers at my friend’s houses, I was sleeping over at the hospital. It was hard to lose my energy, smile, confidence, and hair as treatment took over my life. It was really hard to understand as I was just a kid getting injections, procedures, chemotherapy, and surgery without truly understanding why.

volunteer in black top with big smiles wearing necklace

Julie

My name is Julie. I’m a loving mother of three outstanding kids, a successful businesswoman, wife, breast cancer survivor, and now mother of a true cancer warrior. Ellis, my now 9-year-old son (age 4 at diagnosis), was diagnosed on March 21, 2020 with leukemia. This diagnosis was mere days after the world spiraled into shutdown from COVID-19.Our life, as my family and I knew it, was forever changed the week of March 15, 2020.

Polycythemia Vera

Polycythemia Vera (PV)    
  • Is one of a related group of blood cancers known as “myeloproliferative neoplasms” (MPNs). Too many red blood cells are made in the bone marrow and, in many cases, the numbers of white blood cells and platelets are also elevated.
  • With careful medical supervision, PV can usually be managed effectively for many years.

Follow-Up Care and Survivorship

Survivorship Workbook

Use this Survivorship Workbook to collect all the important information you need throughout diagnosis, treatment, follow-up care and long-term management of a blood cancer.

Diagnosis

Diagnosing acute lymphoblastic leukemia (ALL) and the ALL subtype usually involves a series of tests. An accurate diagnosis of the subtype is important. The exact diagnosis helps the doctor

  • Estimate how the disease will progress
  • Determine the appropriate treatment

In children, a diagnosis of ALL generally requires a finding that 25 percent or more of the cells in the bone marrow are leukemic blasts of lymphoid origin (lymphoblasts).

Michael and Ashlee black and white photo of Mom with three earrings in right ear and teenage son with stylish hair in a hospital room

Michael and Ashlee

Michael and Ashlee have a unique mother-son relationship. They share a podcast about their cancer journey. They have a website and a YouTube channel, and, yes, they even do rap songs about their hospital experiences together.

Signs and Symptoms

It is common for children with AML to feel a loss of well-being because of the underproduction of normal bone marrow cells.

Symptoms of a low red blood cell count (called “anemia”) include the following:

  • Fatigue
  • Weakness
  • Shortness of breath during normal physical activities
  • Lightheadedness, dizziness or faintness
  • Headaches
  • Pale complexion

Symptoms of a low white blood cell count (called “neutropenia”) include the following:

LLS volunteer Light The Night

Allie

When I was in fourth grade, back in 2015, my older brother Nate (a freshman in high school at the time) was rushed down by ambulance to the U of M Masonic Children’s Hospital. His spleen was holding 10x the normal amount of red blood cells. This led to the discovery of his cancer. He was later diagnosed with chronic myeloid leukemia (CML).

Armaan

Armaan

In January 2014, Armaan celebrated his 5th birthday.  He was tested for anemia a few days later at the urging of his pediatrician as he looked a little pale.  Our world was rocked several hours later when the pediatrician called to notify us that Armaan had leukemia.

Armaan was immediately admitted into Lucile Packard Children's Hospital in Stanford where he had a PICC line inserted into his arm and started his first round of chemotherapy.  He is now in remission although he faces two more years of treatment to help ensure he doesn't relapse.

Janet

Janet

I support LLS because leukemia and lymphoma has impacted my family. On Mother’s Day in 2006, my cousin's six year-old daughter, Sydney was diagnosed with acute myeloid leukemia (AML). After a year of fighting so hard, Sydney passed away.

The doctors at the New York Hospital were amazed and acknowledge that because Sydney did not give up and she fought such a painful battle, she had done so much for the advancement of research in leukemia.

Fertility

“Fertility” describes the ability to conceive a biological child. Human reproduction requires three elements: mature sperm, mature eggs and a person with a uterus to carry the pregnancy and give birth. Some cancers and some cancer treatments affect fertility.

Shameel acute lymphoblastic leukemia (ALL)

Shameel

Telling a child that they have cancer and explaining what that means is one of the most difficult conversations you can have with your child.

Shameel was diagnosed with acute lymphoblastic leukemia (ALL) at age 7. As a mother, I couldn't imagine my young, courageous boy, who appeared happy and healthy, not being able to do stuff like tennis, ice skating, piano, and swimming, which he enjoyed and had mastered. It was very shocking to me, and I was in denial for almost a month as cancer does not run in our family.

YolandaBeaton

Yolanda

As many people were afraid to go to the doctor I was propelled to have a colonoscopy due to the death of Chadwick Bozeman. That decision changed my life. In December 2020, I was diagnosed with Stage 4 Mantle cell lymphoma (MCL) is a type of non-Hodgkin lymphoma at age 44. Here I was amid a pandemic, just celebrating Christmas and ringing in the New Year as a newly diagnosed cancer patient. Like many people diagnosed with cancer, my first thought was, “I’m going to die.” I thought I’d die before seeing my daughter grow up.