Search Results
Jeff & Melanie
My wife, Melanie and I had always been pretty healthy. We exercised, tried to eat right and discovered the value of meditation. But things changed in 2018.
Melanie had developed a cough that just wouldn't go away. She had it for months. And then she discovered a lump near her collarbone. Tests revealed on Sept. 6, 2018, that the lump was Hodgkin lymphoma and it was present in several other lymph nodes. She began a months-long treatment regimen of chemotherapy and radiation. It wasn't easy.
Oya
My three kids are my precious jewels, the reason I get up every morning. As a single parent, providing a good life for them is what fuels my drive to succeed. Little did I know that need to care for them would end up saving my life.
Laraine
November 21st is Family Volunteer Day. The Leukemia & Lymphoma Society (LLS) encourages you to volunteer as a family today. Whatever you choose to do, do it together. Some ideas include: take a few minutes to call a friend, neighbor or colleague; cook a meal together and drop it at the doorstep of someone in need; rake a neighbor’s yard or put a book in a neighborhood lending library.
To honor this day, we are sharing the story about a family faced with a cancer diagnosis, who banded together when the future seemed so unclear.
Disease- and Treatment-Related Pain
People with cancer can have pain caused by the cancer itself, its treatment, or both. They may also have pain caused by other health problems that are unrelated to cancer (like arthritis or diabetes).
Increased pain does not mean that the cancer is getting worse, but you should always tell your healthcare team if you have increased pain.
It’s important to remember that no matter what the cause, pain can be treated.
Melissa
We really want to be someone else’s story of hope.
My husband, Thomas, was diagnosed in February 2022 with blood cancer, specifically, multiple myeloma (MM). He was in the hospital in Mallorca, Spain, where we live, for 16 days, getting dialysis and chemotherapy. After that initial stay, he was discharged but continued to go to the hospital three days a week for four months until his kidneys started working on their own again.
Debra
In October 2011, while at work, I fell after attempting to sit on a chair, and I went to the emergency for x-rays. As soon as the technician began the process, he entered the room to ask if I had scoliosis. I replied, "no" and he proceeded with the exam.
Jeffrey
My story starts with being diagnosed with multiple myeloma (MM) in 2022. It is a terminal cancer that right now does not have a cure, but it is treatable. Life can and will take unexplained twists and turns, like without warning, your back hurts, and for me, that was from a compression fracture in my L4 – L5 vertebrae from lesions due to the MM, and that leads to learning that you have cancer. Like a lot of us, when you first hear those words, you are at a loss to explain how this came to be.
Steven
In 2017, I was 52 and in pretty good shape. I was at the gym working out, and after a certain lift, I could not get off the bench by myself. After being helped up, I somehow drove myself home. The next morning, I could not get out of bed without my wife lifting me up. We went straight to the doctor and got an MRI. Then we got the news “you have cancer,” and it is eating your vertebrate in your neck. I was sent to a spine and neck specialist and also to a cancer doctor to find out what kind of cancer. Multiple Myeloma (MM) was the diagnosis.
Cheryl
When I first found out that I had multiple myeloma (MM) 4½ years ago, I was shocked. I was in the hospital for a broken leg. I had twisted my leg, and it was badly broken. While I was waiting for surgery, a doctor came into my room and began to talk to me. She explained to me that my leg had broken because I had cancerous bone lesions. As I listened to her, I felt my heart sinking, I had a broken leg, not cancer. It didn't seem possible. Cancer was the last thing I would have imagined. I went through radiation, chemo, and cell replacement therapy.
Kenya
I was diagnosed with two blood cancers — multiple myeloma (MM) and chronic myelomonocytic leukemia (CMML).
Cancer entered my life at five years old when I lost my father to pancreatic cancer. Then again, when my oldest sister was diagnosed with breast cancer, she is now nine years cancer-free. Then again, when my mother was diagnosed with breast cancer. Sadly, we lost my mother in May 2019 to breast cancer
Getting a Second Opinion
Leukemia, lymphoma, myeloma and myelodysplastic syndromes are each different types of cancers. What's more, each disease has subtypes. This means that the signs of the disease, how it's diagnosed and treated and the expected outcomes vary. That's why it's essential to have the right diagnosis before you begin or continue with treatment.
Elizabeth
On November 8, 2021, I was diagnosed with stage III multiple myeloma (MM), an incurable cancer. Prior to being diagnosed, I thought I was a healthy young woman and was just living life with my children. I would have different pains throughout my body, but I didn't think much about it and would ignore them for the most part. The pains throughout my body were getting more and more frequent, so I went to the ER in October 2021 because I was in pain and could not eat, they said I was possibly having acid reflux and gave me a prescription for nausea.
Paul & Lynn
In 2017, after 44 years of working in the railroad industry, Paul Sauter was just starting to enjoy his retirement, when his health started to decline out of nowhere. Typically, he was in extremely good shape and enjoyed long hikes with his wife, Lynn. One day, while on a mountain climb trip in Arizona, Lynn was concerned when she noticed Paul was not his usual athletic self. When he was unable to get out of bed because of severe back pain, she knew something wasn’t right.
Al
I am a four-time cancer "survivor" (not totally comfortable with the term), just grateful to be alive. I was first diagnosed with testicular cancer in 1997. I had surgery to remove a testicle and radiation as a follow-up.
Thomas
Before I was diagnosed with multiple myeloma (MM) at age 34, my life looked very different from what it is today. I was a husband and a father. I had a full-time job at the Federal Bureau of Prisons, and I worked out a lot. And now? Well, I still work out a lot; that’s never changed, and I’ll always be a father. But the rest of it? It’s all gone away. And I couldn’t be any more at peace with it than I am now.
Kristen
In the fall of 2012, Kristen Comer noticed her energy level wasn't as high as it had been, but she thought nothing of it. It wasn’t until the fall of 2013 when she had unidentifiable bruises on her body and no change in her energy levels, that her general practitioner drew labs to determine a diagnosis. After three panels of blood work, Kristen was diagnosed with chronic myeloid leukemia (CML) on December 31, 2013.
Paul
I have been very active with The Leukemia & Lymphoma Society (LLS) for over 20 years including serving on the Wisconsin Chapter Board and Leadership Development Committee, fundraising for virtually all of the campaigns, patient mentoring, and advocacy leadership. When sharing my story and motives for involvement in “the early years,” I always qualified it by stating that I was motivated not to help myself but to pay it forward and hopefully contribute to improving the quality and quantity of life for future patients and families.
Ron
Ron was a private man. He didn’t seek the company of many. But the friends he had were close, and more than anything, he cherished his time the most with his loving wife and best friend, Paulette. The two of them shared a love for fishing and traveling. They traveled all across the western United States searching for the best fishing spots. They even had a place in Baja California where they spent most of their time fishing together. Ron was unapologetically himself, and he never once cared about what others thought of him.
Alice
In March 2023, while visiting my daughter and son-in-law in San Francisco, I saw the Climb2Cure trip to Patagonia listed on The Leukemia & Lymphoma Society's (LLS) website. They have always talked about their backpacking trip to Patagonia in Argentina and Chile as their favorite hiking trip ever. This event would be my 16th LLS fundraising adventure since going into remission from multiple myeloma (MM) in 1999.
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.
Rebecca
My mother died of multiple myeloma (MM) in 2001, 10 months after her diagnosis. She lived in a small town where the only treatment they offered her was chemo infusions. She was on dialysis the whole time. She was brave but scared, nonetheless. She didn't have much time to process the whole experience. I was 51 at the time and still believed I was bullet-proof! Silly girl!
Donna
I was shockingly diagnosed with a monoclonal spike in November 2019 (six months after the unexpected death of my mom). Treatment was started in June 2020. I went to Mt. Sinai NYC where they have a team that just deals with multiple myeloma (MM). I am grateful that a couple of people recommended I go there. They treated me with four drugs, one of which wasn’t available at my local oncologist. The regimen was Velcade, Revlimid®, daratumumab, and dexamethasone. I had this induction therapy until my stem cell transplant in March 2021.
Imaging Tests
Imaging or radiology tests pass different forms of energy (x-rays, sound waves, radioactive particles or magnetic fields) through your body, creating pictures of the chest, abdomen, head, neck and other parts of the body.