Search Results
Dean
In October 2015, after a trip to the ER with pain in my abdomen, I was diagnosed with stage 3, large B cell, multiple location, non-Hodgkin lymphoma.
My oncologist originally told me that the treatment plan would include 10 chemotherapy rounds, followed with radiation. I was out of work for eight weeks until my doctor decided I was in good enough health to return work.
Cancer affects everyone in your life that loves you — emotionally and financially. When you are sick, the bills do not stop coming, and in some cases, cancer can ruin people financially.
Blood Cancer Survivors Find Special Meaning and Connection as Employee Champions of LLS Light the Night Events
The Leukemia & Lymphoma Society (LLS) is proud of our continuing partnership with Gilead and Kite Oncology as the National Presenting Sponsor of Celebration and Community at Light The Night events across the U.S. helping bring people together and raise critical funds to support patients and their families.
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 SupportYou'll need to choose:
Blood cancers that cause high monocytes: Understanding the connection
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Childhood and Young Adult Resources
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Resources for Children, Young Adults and ParentsOne-on-One Support
Brittany
Brittany, a 37-year-old mother, is currently fighting leukemia for the second time. Known for her generosity and support for others, Brittany enjoys traveling, spending time with family, and above all, loving her son. Unfortunately, on August 6, 2022, Brittany received an unexpected diagnosis of acute myeloid leukemia (AML) when she was 35 weeks pregnant. This news shattered her perfect pregnancy plans and forced her into a battle against cancer.
Kay and David LaFrance
As an 18-year breast cancer survivor, Kay was just starting to enjoy retirement in 2018 when she was diagnosed with mantle cell lymphoma. Even though she had fought cancer before, she was stricken with despair and disbelief and felt terrified of the road ahead of her. She had to travel to a different city to receive her specialized treatment, which was outside of her insurance network, so much of the costs came out of her own pocket. After a long, hard fight, she is now in remission, but lives with the everyday fear of her cancer coming back.
Joshua
My name is Joshua. I was born and raised in South Florida and moved to Oregon after high school 8 years ago. I can’t say that I had a difficult childhood growing up just difficult circumstances that were challenges to overcome. I am what most people would consider an introverted type of personality, and while I was raised in a home with very caring parents and sisters, I’ve just always found it difficult to fit in, especially once I got to high school. I’m tall, at almost 6 feet, and very smart, always in advanced placement classes.
Towards Equity in Specialized Cancer Care for Adolescents and Young Adults with Newly Diagnosed Acute Lymphoblastic Leukemia
Our study is designed to directly inform the pathways through which health insurance influences access to care at an SCC for individuals with AYA ALL using a combination of cancer registry, survey, and cost-benefit analyses.
Kelly
In January 2020, I was a 21-year-old full-time pre-medical student diagnosed with Stage 2E Nodular Sclerosis Classical Hodgkin lymphoma, about three weeks after getting engaged to the love of my life and primary caregiver, Alex. We put our entire lives on hold to begin this battle, but we had a huge support network that cheered us on with the slogan, "Let's Get Excited." I was treated for my cancer at Mercy Hospital in Springfield, Missouri, where Dr. Jessica Snider & Dr. Kimberly Creach successfully cured my cancer.
Suzanne
My mother was diagnosed with multiple myeloma (MM) in February 1987. She passed away in December 1997. I was diagnosed with MM in February 2017. My diagnosis was not only a surprise but daunting because I was my mother’s caregiver and experienced what she faced battling this disease. I’m currently undergoing treatment with the bispecific drug Teclistamab with success. The Leukemia & Lymphoma Society (LLS) has provided me with educational and financial assistance, so I greatly appreciate this organization.
Exercise for blood cancer patients
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Susanne
I am a four-time diffuse large B-cell lymphoma (DLBCL) survivor and a recent stem cell transplant (SCT) survivor. DLBCL is a type of non-Hodgkin lymphoma (NHL). My first diagnosis was in 2007, then 2012, 2013, and 2023. I received invaluable support financially from The Leukemia & Lymphoma Society (LLS). People often ask how I am so positive after all I've been through. I think we need to take whatever we are dealt and make the best of it each day. The key is a positive attitude, gratitude, and a strong support system.
Carlos
I was diagnosed with acute myeloid leukemia (AML) in June 2021 in Puerto Rico. I was introduced by a hospital social worker to The Leukemia & Lymphoma Society (LLS) for educational resources for patients and caregivers. My stem cell transplant was performed at Auxilio Mutuo Hospital in 2022. After applying for financial help from the LLS, I received help from several programs. LLS provided valuable educational materials that helped me to understand the condition and to make informed decisions. I am now 19 months post-transplant and in remission.
Every Year Counts: Celebrating My Healing from Hodgkin Lymphoma
Many blood cancer survivors remember the day they were diagnosed, and they never forget it. For Racheli Alkobey Peltier—Director of Diversity, Equity, and Inclusion at The Leukemia & Lymphoma Society (LLS)— when that date comes around, it’s a chance to mark her progress.
Each year, Racheli marks important milestones in her experience with blood cancer—taking time to reflect, feel gratitude, and look ahead. These dates are her “cancerversaries.”
Tony
I was diagnosed in 2016 with multiple myeloma (MM) and was able to get a bone marrow transplant in 2017. After I recovered, I was cancer-free for five years. Then two years ago, my cancer came back, and I am now going through with two types of therapies to keep things at bay and doing well. Besides the ups and downs of working full-time and cancer coming back, my oncologist who saw me through retired last December, and I got a new one. However I was not happy and started seeing one of his associates and really liked her, but she is now leaving the practice in two weeks.
Resources for Survivors
Survivorship WorkbookUse 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.
Fertility and Pregnancy
In addition to our programs and services for blood cancer patients, families and caregivers, The Leukemia & Lymphoma Society (LLS) is pleased to offer an extensive directory of national and international resources. These organizations can help with cancer-related issues like financial assistance, support and counseling, assistance with transportation, and summer camps.
Manual
Since being diagnosed with myeloma, I've been glad to have the assistance of LLS. For one thing, research they helped fund resulted in Velcade®, one of the drugs I'm being treated with. For another, their financial assistance program has come in very handy during my illness. Thank goodness for LLS. Manual Tapia | Multiple Myeloma Survivor You can tell just by looking at him that Manuel has a positive outlook. It has served him well since his diagnosis with multiple myeloma.
Funeral Planning
A funeral or memorial service can help you cope after the loss of a loved one. In the early days of grief, navigating the practical issues that arise after death may feel overwhelming. Your loved one may have left instructions for you, or the decisions may be up to you or another family member. Many people may not be aware of the cost of funeral planning or the options available to families. Even if you do not plan to hold a traditional funeral, certain decisions still need to be made.
Is Leukemia Genetic?
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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.