Search Results
Nora
Nora was diagnosed with acute lymphoblastic leukemia (ALL) on August 20, 2018. This is the day our lives were turned upside down and forever changed. Nora was about three weeks away from her second birthday, and we were in utter shock that she would now be fighting an unfathomable battle. After all, this was Nora, our go-hard, go-fast, ray of sunshine. Never did we imagine anything could get her down. But yet, here we were.
Cassie
In April 2023, I started to notice that I was having trouble breathing. I was a perfectly healthy 34-year-old woman who did kickboxing three times a week and was very physically active. I ended up going to a doctor who, for three months, misdiagnosed me with asthma and acid reflux. After about three visits to his office, I was crying to him, begging to be referred to a specialist. I really felt that there was something wrong with me that wasn't asthma.
Isabel
I never expected to have my whole adult life colored by cancer. In the fall of my freshman year of college, I was diagnosed with chronic myelogenous leukemia (CML). I was freshly 18 and didn’t have much of a vision for my future, but what vision I had definitely didn’t include chronic leukemia. It was a difficult and shocking time, trying to make new college friends while in and out of the hospital, navigating emotional terrain most of my fellow students were very far away from.Today I am 30, and a CML survivor of over 12 years.
Treatment
It's important that your doctor is experienced in treating patients with acute leukemia or has access to an acute lymphoblastic leukemia (ALL) specialist.
Types of ALL TreatmentDoctors use several types of approaches and treatment combinations for ALL:
Treatment of Acute Promyelocytic Leukemia
Acute promyelocytic leukemia (APL) is a unique subtype of acute myeloid leukemia (AML). APL cells have a very specific abnormality that involves chromosomes 15 and 17, leading to the formation of an abnormal fusion gene called PML/RARα. This mutated gene causes many of the features of the disease. APL accounts for about 10-15 percent of all adult AML cases diagnosed each year.
Jonathan
I’ll start from the beginning.
In 2012, I was diagnosed with testicular cancer. I had surgery to remove the mixed germ cell tumor and then was on the road to recovery. My lymph nodes were larger than they should have been, so I opted to err on the side of caution and had a lymph node dissection to have them removed. That was an invasive surgery that kept me out of work and from doing any physical activity for over six months. Once I healed up, I went back to work as a full-time police officer in Worcester, MA.
Tim
I knew multiple myeloma (MM) was a blood cancer. After all, my mom was diagnosed with myeloma at 62 years old in 2005. It’s extremely rare that I should also be diagnosed in 2021, but it happened. There’s no strong data that shows that it’s hereditary at this point. But more doctors are seeing family members being diagnosed. It's also becoming one of the most diagnosed cancers among African Americans.
Harjeet
In May 2018, I moved to Edmonton from India with my husband hoping for a new career, a new life, and to start a family. Things were all right at first. Everything was going smoothly; I was living my normal life, but life had different plans.
In May 2019, I began experiencing high fevers with no other symptoms. Weeks passed, and I found myself in the emergency room numerous times. I was told that it was just a normal viral fever and took Tylenol to relieve it.
Paul
Thank you on behalf of the Freeman Wilner Family for this Honored Hero Award in memory of my father, Dr. Freeman Wilner, he was a hero to many.
Addison
Florida is my happy place. It's where I've vacationed for over three decades. And when my husband and I had kids, it became our family's happy place too. Schedules are forbidden on vacation. We tell time by the sun as we sit on the beach with our feet in the sand, watching the tide roll in and out. While on vacation, we celebrate birthdays ― and they're done up big ― because that's the only way that we know how to celebrate birthdays ― BIG.
Laura
When you hear the words, “Your child has cancer,” your whole world stops, without permission, as you and your child are thrust onto the rollercoaster ride of pediatric cancer, desperate to get off with your sanity and your child’s life intact. Those months, or as was the case for us, years in treatment, are relentless, fraught with confusion and uncertainty as you desperately and constantly search for answers. For direction. For hope.
Disease Complications
Myeloma and treatment of myeloma can lead to mild to serious health complications and side effects. Some of these symptoms can be managed with ongoing supportive (palliative) care. Others may be medical emergencies requiring immediate attention. Always tell your healthcare team if you experience new or worsening symptoms.
PainPain related to myeloma or myeloma treatment can include
Pain Treatment
Pain can be managed effectively in a number of ways, depending on the cause and type of your pain. Treatments may include:
Options for Egg Preservation
You may be able to take certain steps and precautions to preserve fertility before, during and after treatment.
The Affordable Care Act (ACA)
The Affordable Care Act’s Patient ProtectionsThe Affordable Care Act requires health insurance plans sold through www.healthcare.gov and its state-based marketplaces to comply with a number of requirements. Many of these – including the ones described below – are meant to ensure that patients have access to meaningful health insurance coverage. It’s important to be aware that some health plans, available today through non-governmental sites, may not include these patient protections.
Related Diseases
Myeloma shares some similar features and symptoms with other blood disorders, including:
Mike
My personal story with blood cancer started in 2020 but nobody really knew how long it was brewing. A day came when back spasms started raging and my Primary Care Physician (PCP) sent me to physical therapy (PT). It didn’t take more than 1 visit to PT to know that was a bust and finally my PCP sent me to the Hematologist. This is where my blood cancer story becomes reality, in no more than 5 minutes, the Hematologist sent me directly to the Huntsman Cancer Institute.
Samuel
On June 21, 2019, my sweet, goofy, little boy, Samuel, turned 3 years old, and we had a big celebration. We threw Samuel a beautiful birthday party surrounded by family and friends at a local farm. The kids played, fed the farm animals, went on pony and tractor rides, and ate pizza and cake. It was a day Samuel still remembers and talks about. He has always been so bright, even as a baby, saying words like “tickle” at 10 months old.
Gregg
The date was May 15, 2015, in the local office of the hematologist/oncologist and I was given this message after the results of my bone marrow biopsy taken a week earlier.
Graft-Versus-Host Disease
Graft-versus-host disease (GVHD) is a potentially serious complication of allogeneic stem cell transplantation and reduced-intensity allogeneic stem cell transplantation. In this treatment, a patient’s own damaged or diseased blood-forming stem cells are destroyed. Then they are replaced with healthy stem cells from a donor.
Our History
The Leukemia & Lymphoma Society (LLS) was born out of a family's grief following the death of their teenage son. Robert "Robbie" Roesler de Villiers, son of a well-to-do New York family, was only 16 when he quickly succumbed to leukemia in 1944. Five years later, frustrated by the lack of effective treatments for what was then considered a hopeless disease, parents Rudolph and Antoinette de Villiers started a fundraising and education organization in their son's name.
Fundraise for LLS
Fundraise for LLS
Make an impact in the fight to cure cancer.
The Leukemia & Lymphoma Society® (LLS) is a global leader in the fight against cancer. LLS does more to advance science and support patients than any other cancer organization.
Join the fight against cancer by participating in one of our fundraising events: Light The Night, Team In Training, Big Climb, Visionaries of The Year, Student Visionaries of The Year, Ski, Scenic Shore, USA BMX, and more.
Diagnosis
While certain signs and symptoms may indicate that a person has MF, a series of tests are needed to confirm the diagnosis. It is important to have an accurate diagnosis, as it helps the doctor to:
- Estimate how the disease will progress
- Determine the appropriate treatment
Some of these tests may be repeated both during and after treatment to evaluate the effectiveness of treatment.