Search Results
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!
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.
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.
Trisha
On November 15, 2019 at 29 years old, my world changed forever. I was diagnosed with Plasma Cell Leukemia. It is basically a hybrid of Multiple Myeloma and statistically only shows in men over 60. I wanted to be special but not like this! At my 6 week postpartum appointment with my second babe, my stomach had not been shrinking like it should but I assumed it was because it was my second baby or the diastasis recti. My OB did a ultrasound and saw a lot of ascites and that my liver was massive so she instructed I go to the ER as that was not normal.
Merton
On November 3, 2014, I drove to work and, upon arrival, knew that something was seriously wrong with me. I called my love, Holly, and informed her that I could not drive myself home as I was afraid of hurting someone else. She came to my work to pick me up and told me we were going to go to my primary care physician to demand a complete blood panel workup. At this point, I was told by my primary care physician that I was suffering from systemic gout. I was prescribed multiple rounds of steroids and a pill that was supposed to break up the shards that were affecting my joints.
John Patrick
During the summers of 2020 and 2021, I remember feeling really tired, I figured it was because of the summer heat, so I didn't pay much attention to it. Every year dating back to about 2008, about twice a year, I also have had back issues where the pain was so bad that it was hard for me to straighten up, and I would walk hunched over during that time. It would last for about two weeks at a time. I also noticed that it felt like my ribs would pop in and out of place.
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.
Studies on clonal hematopoiesis in the 911 WTC first responders
The terrorist attacks on the World Trade Center (WTC) created an unprecedented environmental exposure to WTC aerosolized dust and gases that contained known and suspected carcinogens including polycyclic aromatic hydrocarbons, polychlorinated biphenyls, polychlorinated furans, dioxins and asbestos. Studies from Dr.
Rick
Rick Ostroff and his family have a legacy of philanthropy with a heartfelt connection to a disease he never had. During the first three years of his life, he spent time on the leukemia floor of Children’s Hospital in Boston but eventually was found to have the critical illness of gamma globulin anemia rather than then-fatal leukemia.
Brianna
"He was the king of positivity" is what Dr. McCarthy at Roswell Park said to me the day after my Dad passed away from complications of GVHD or graft-versus-host disease. My Dad was a leader, someone who was always willing to help others, and always had a smile on his face. Not only was I his co-caregiver throughout his cancer journey, but he was also my caregiver during mine.
Glenis
The body is ultimately wise. Through this most recent medical ordeal, I learned to listen to what my body was telling me. In 2018, I felt symptoms above and beyond the fibromyalgia ailments that I had been plagued with for 25 years. I had unusual inflammation despite eating healthy and walking on a regular basis. I developed an unrelenting throb of pain in my lower back. My internal medicine doctor at the time dismissed my complaints.
Nicolasa
The first time I heard of Team In Training (TNT) and raising money for The Leukemia & Lymphoma Society (LLS) was when my friend and I wanted to run the Nike Women's Half in D.C. We filled out the application and got accepted and started raising money, not having a clue about where this path was going to lead us. It was at that time that I began to realize the impact leukemia and lymphoma have had on my family and friends, whether they or a loved one had gone through treatment. I wrote all of their names on my singlet and carried them with me along that course.
Tawilhua
My name is Tee, and I am a survivor of multiple myeloma (MM), a rare blood cancer. Before my diagnosis, I was an active principal at the school where I worked, was involved in my community, and lived a life of purpose. And then I was diagnosed with the “Big C.”
Today, I still have a purpose-filled life, it simply looks different than before. Telling my cancer story is a part of living a fulfilled life after a cancer diagnosis. So here is Tee’s story.
