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Nik ALL

Nik

Hello, my name is Nikolas. I am 16 years old, almost 17, and have been battling acute lymphoblastic leukemia (ALL) for eight years.

Jaziel acute lymphoblastic leukemia

Jaziel

Hello, my name is Jaziel, and I am a three-time leukemia survivor. My story began in 2008 when I was initially diagnosed with acute lymphoblastic leukemia (ALL). I was treated for a few years and became cancer-free (remission) in 2011. During my first battle with cancer, The Leukemia & Lymphoma Society (LLS) helped me and my family immensely by assisting us with rent, gas, and sometimes simply sharing the stories of other survivors, encouraging me to keep fighting.

Young woman, long brown hair, white tank top Hodgkin lymphoma (HL)

Lynn

In 2013, I heard the words that no one wants to hear, "You have cancer." I was 37 years old, healthy, and an active mom of two. After being sick and misdiagnosed for six months, I finally got some answers: stage 4 Hodgkin lymphoma (HL), and I started chemo immediately.

Your mind goes to places that you are never prepared for. Two young children that depended on you . . . all the what ifs, what will happen ifs . . .

Hodgkin lymphoma (HL)

Celeste

Celeste is my daughter; she was 10 years old when she was diagnosed with Hodgkin lymphoma (HL). She had a cough for about two months that just would not go away, and we thought it was her seasonal asthma coming back, so we made an appointment with her pulmonologist. At the appointment, her doctor paid careful attention to everything we were saying and ordered a chest X-ray that showed a large mass in her chest.

We went straight to Boston Children's Hospital and then on to treatment at The Jimmy Fund.

Smiling black teen girl with lymphoma in black jacket and pants holding mylar balloons and a gift bag

Izarhea

First of all, I want to thank God for keeping me sane as he forced me to grow this year. On June 25, 2023, I was diagnosed with Hodgkin lymphoma (HL), and to be honest, I wasn't tripping at first because I had no idea what that meant. Then my mom explained to me that I had cancer. I went from ending my junior year to celebrating my 17th birthday to getting my port installed and starting chemo all in the same month. I remember telling my dad how scared I was for my whole life to change, but I eventually saw how necessary that was.

Blood Cancer and Treatment Options

Treatment Options

After your child is diagnosed with a blood cancer, you will work with members of the healthcare team to determine the best treatment plan. Treatment options vary depending on the patient's diagnosis, age, overall health, and other factors. Your child’s treatment plan might include

Treatment Outcomes

All patients are advised to discuss survival information with their hematologist-oncologists. Keep in mind that outcome data can only show how other people with CMML responded to treatment, and cannot predict how any one person will respond.

Unfortunately, lasting remissions are not common. The expected survival time ranges from a few months to a few years after the initiation of treatment, depending on a variety of risk factors including the percentage of blasts in the blood and marrow, the white blood cell count, and the presence of certain gene mutations.

Choosing a Blood Cancer Specialist or a Treatment Center

Taking an active role in making decisions regarding your treatment can have a positive effect on your health and quality of life. One of your first choices as an active participant in your care is to either select a specialist to manage your treatment or to choose a treatment center.

You may be seeking a blood cancer specialist or a treatment center because you:

Printable Question Guides

 

 To download or order copies of the Communicating With Your Healthcare Team series, click here.

Before you visit your doctor and other healthcare providers, it's a good idea to write down your questions or concerns. For a list of suggested questions to ask about certain topics, download and print any of the following guides:

Cancer Drug Therapy and Nutrition

Some drugs used to treat cancer can interact with food in ways that your treatment team will inform you about. When you begin a new treatment or start using a new drug, tell your doctor about any food allergies you have and ask:

JJ

J.J.

The first time I remember hearing of The Leukemia & Lymphoma Society (LLS) was through Team In Training (TNT), specifically from a brochure I picked up at a bike shop that invited one to train for a 109-mile bike ride with TNT. It was 2007, and I thought it sounded like a blast. I convinced my girlfriend at the time, Stacey, to join me. We used the occasion to buy some fancy new bikes. With some fundraising and committed training dates, we would be able to say we had done a Century Bike Ride! Cool!

David

On June 17, 2014, 12-year-old David Stim visited his pediatrician's office to have a routine school physical. During the exam, the nurse practitioner noticed an enlarged lymph node on the right side of his neck and surmised that it probably due to a reaction to something, as is almost always the case in pediatrics. Since David had been treated for strep throat the month before, there was not much cause for concern.

jaime WM

Jaime

My name is Jaime. I am married to my best friend, Brad, and we have three children, two daughters and a son. We also have a daughter and son in-law plus five beautiful grandchildren. I am very fortunate and count my blessings every day.

My cancer story started in April 2009.

Chemotherapy and Drug Therapy

Chemotherapy is generally used only in patients with blast-phase CML as a way to get the CML back into chronic phase. Very high-dose chemotherapy is used to prepares patients for an allogeneic stem cell transplantation.

Signs and Symptoms

Many people are diagnosed with CLL even though they do not have any symptoms. The disease may be suspected because of abnormal results from blood tests that were ordered either as part of an annual physical or a medical examination for an unrelated condition. An unexplained elevated white blood cell (lymphocyte) count is the most common finding that leads a doctor to consider a CLL diagnosis.

Generally, CLL symptoms develop over time. As the disease progresses, a person may experience

Splenectomy

A splenectomy is the procedure done to remove the spleen. Before effective drugs became available for hairy cell leukemia, splenectomy was the first-line treatment for the disease.

Making Treatment Decisions

Adults living with blood cancer must make decisions about treatment, family, work or school and finances. If your child has been diagnosed, you must make similar decisions for your son or daughter.

Gathering Information and Support

You'll need to choose:

Side Effects

Therapy for acute lymphoblastic leukemia (ALL) can produce side effects. For most patients, treatment side effects are temporary and go away once therapy ends. For other patients, side effects can be severe, sometimes requiring hospitalization.

Before you start treatment, talk with your doctor about potential side effects. Drugs and other therapies can prevent or manage many side effects. Many treatment side effects go away or become less noticeable over time.

Common Side Effects

The side effects you may experience depend on:

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.

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:

ARB

Alayna

September 8, 2021: I didn’t know it at the time, but the mass I found in my neck the night before I started my senior year of high school would forever change my life.

Casey

It was in May, 2014 that 24-year-old Casey Moore began experiencing her first symptoms of chronic myeloid leukemia (CML). For a week straight, Casey had been vomiting every day and was losing a significant amount of weight. This was unusual, as prior to her symptoms, she considered herself a happy, healthy woman focused on her relationship and career. At the time, she was living with her boyfriend and working full time in a chiropractic office -- with no apparent signs of an illness.

Ethar

Refugee Family Gives Back to LLS after Daughter Survives Leukemia

Sixteen-year-old Ethar and her family moved to the United States from Iraq in 2015. Just one year later, she was diagnosed with T-cell acute lymphoblastic leukemia.

“It all started when my lymph nodes began to swell and the pain became very intense,” said Ethar. “It was at this point, that I went to the emergency room with my father so we could try to make sense of what was happening to me.”