Search Results
Latasha
After a family vacation with her four kids and husband of 20 years, Latasha couldn't eat or hold her head up. After being in bed for almost a month, she thought she had the flu when her doctor broke the news that she had been diagnosed with acute myeloid leukemia (AML) and anemia.
Sal
Meet Sal. Chronic Myeloid Leukemia Survivor. Florida. Sal was diagnosed with chronic myeloid leukemia (CML) before his daughter Olivia celebrated her first birthday. After multiple courses of treatment proved unsuccessful, he underwent a bone marrow transplant in September 2011. Now, almost three years later, Olivia is almost 5 and her Daddy is celebrating his "three-year post-transplant birthday"! Sal is healthy and strong - and has the energy to play and laugh with her. Most beautiful of all, he can now dream of being at her side for all kinds of birthdays to come.
Dylan and Conner
When Dylan was a senior in high school, at the age of 17, he was diagnosed with stage 4 Hodgkin lymphoma (HL). He was getting ready for his last semester of high school and ready to pursue his dreams of playing college volleyball when life confronted him with a massive health battle. He spent the next six months putting up a constant fight and underwent 12 chemotherapy treatments. Although every day was a battle, Dylan ultimately came out on top and was declared cancer-free in the summer of 2021. He is now set to graduate from Miami University next fall and plans to become an educator.
Justin
My husband, Justin, was diagnosed with T-cell acute lymphoblastic leukemia (ALL) in June 2021. At the time, he was a healthy, energetic, 33-year-old dad of three. He just completed all treatment in January 2024. We received some funds from The Leukemia & Lymphoma Society (LLS) as well as information and inspiration. Throughout treatment, my husband fought so hard and had very difficult moments. He went into septic shock from a blood infection, had an ICU stay, and had to get both his hips replaced because of an infection that led to bone on bone. He couldn’t walk for months.
Carol
I have been told that my story is rare, so I would like to see if there is anyone who has had the same experience. I was diagnosed with multiple myeloma (MM) in February 2023. I started chemo treatment in March 2023 and continued through May 2024. In February 2024, I noticed some changes happening to my body. I was losing weight, losing hair, had extremely dry skin, and had less and less energy. When I went for my PET scan in May 2024 to see if I had lesions in my spine from the MM, I was told they were completely gone, and I was most likely in remission.
Joseph
I came down with chronic lymphocytic leukemia (CLL) in 2006 which transformed into an aggressive form of non-Hodgkin B-cell lymphoma (NHL) in 2013. In 2015, I received an umbilical cord transplant at Penn Medicine Hospital in Philadelphia which was successful. This month, I celebrate nine years post-transplant.
Kate
When I went for my annual physical in 2013, my doctor called me to tell me that my bloodwork looked strange. He asked me to get it tested again to be sure of the result. I did not have any symptoms at all. Within a week, I was diagnosed with chronic myeloid leukemia (CML), something I'd never heard of. I had no idea what this would mean. It took me a while to find the right oncology team, but once I did, they were amazing. After lots of tests (including a bone marrow biopsy), I was started on medication, at a low dose, because I'm a pretty small person.
Carlos
I was diagnosed in September 2017 with myelodysplastic syndromes (MDS), and by May 2019, I was told of the need for a bone marrow transplant (BMT). And even though they told me about a "new life after transplant," my life has completely changed. I could not go back to work because of graft vs. host disease (GVHD) and multiple infections during and post-transplant. I’m still on immunosuppressants and chemo-brain with cognitive issues. It has been very hard not to return to practicing Family Medicine since my patients could literally kill me.
Shanna
Everything was going great in life. I had just quit my job to pursue my dreams of starting a business, moved closer to family, bought our first house, and got a puppy. Then, a small lump on my neck changed my life forever.
I, a 25-year-old half marathoner with no health issues, was diagnosed with stage 2a Hodgkin lymphoma (HL). The chemo (ABVD) about killed me. I went from living an active life to needing help with the simplest of tasks. But I made it through, and boy, did we celebrate.
Robert
I’m 37 years old, and I was recently diagnosed with stage 4 high-grade diffuse large B-cell lymphoma (DLBCL). Life was going well. I got promoted at my job and was doing great when all of a sudden, my life changed forever. It started with severe leg and back pain. I went to the hospital and had some basic tests done, and they sent me home. Two days later, I was back in the hospital because the pain was so intense I could barely get out of bed or walk without assistance.
Signs and Symptoms
People who have chronic myeloid leukemia (CML) may not have any symptoms at first. Often, patients learn they have CML after a routine physical exam or a blood test. CML signs and symptoms tend to develop gradually. Those with symptoms often report experiencing:
Signs and Symptoms
Signs and symptoms vary from patient to patient and depend on the type of CMML. Click here to learn more about subtypes of CMML.
Those with a myelodysplastic subtype (MD-CMML) tend to present with low blood cell counts. Signs and symptoms may include:
Signs and Symptoms
Some patients initially have no symptoms of MDS, and abnormal results from routine blood tests may be the earliest signs of the disease. For patients with symptoms, it is common not to feel well because of the lack of normal, healthy blood cells.
Anemia is a decrease in the number of healthy red blood cells. Red blood cells carry oxygen throughout the body. Anemia may cause symptoms such as:
Watch-and-Wait
Some people with MDS who do not have very low blood cell counts or other symptoms may not need to start treatment immediately. Some people can manage their MDS with their doctors for years or even decades using a watch-and-wait (observation) approach. By using the watch-and-wait method, your MDS specialist can monitor your condition with regular physical exams and blood tests. The watch-and-wait approach lets you avoid therapy's side effects until you need treatment. Treating MDS during this early stage has not proved helpful.
Ph-Positive ALL Therapy
Tyrosine Kinase Inhibitors (TKIs)In addition to chemotherapy combinations, children with Philadelphia chromosomepositive (Ph+) ALL and Philadelphia chromosome-like (Ph-like) ALL are also given a tyrosine kinase inhibitor (TKI) medication.
Tyrosine kinases are enzymes that are a part of many cell functions including cell signaling, growth and division. These enzymes may become too active in patients with an ALL subtype called Philadelphia chromosome-positive ALL (Ph+ ALL).
Thomas
My name is Thomas, and I was diagnosed with stage 2 Hodgkin lymphoma (HL) two weeks after my 30th birthday. Nobody wants to hear the words, "You have cancer," and even though my wife had some suspicions due to my recent weight loss and lower energy levels, it still came as a shock to both of us. The news hit hard, especially since all other aspects of my life were going extremely well. My wife and I had just moved to a new state earlier in the year, I received a promotion at work, we had just returned from a business trip out of state, and overall, things seemed to be going our way.
Zach
It was 2020, and besides the obvious chaos in the world, at that time my life was going great. My business was thriving, I had just gotten engaged, and my fiancée and I were beginning to talk about starting a family. I was at what felt like the peak of my life. Everything was going my way, or so I thought.
Heidi
My story starts a year before I was officially diagnosed. For months, I had been having GI issues, severe stomach pain, unexplained weight loss, and unexplained anemia. I was seeing the nurse practitioner (NP) at my primary care provider’s (PCP) office who kept prescribing antacids and attributed my symptoms to anxiety. It wasn't until a full year after my symptoms began that I went to a different NP at that office for swelling in my neck that had originally been dismissed as a muscle strain. She didn't like what she saw and immediately sent me for a CT scan.
Steve
I was diagnosed with non-Hodgkin lymphoma (NHL) after moving from New Orleans to San Antonio, Texas. What started as a routine visit to an allergist for swelling in my cheeks, eyes, and neck turned into a life-changing moment when a CT scan revealed the unthinkable. In that devastating instant when my doctor delivered the news, I discovered that sometimes life's darkest moments can lead you to exactly where you need to be. The people of San Antonio didn't just welcome me ― they embraced me, making their city my sanctuary.
Yarnall Family
To be of service to others comes naturally to the Yarnalls. Bob is a 25-year Marine Corps veteran and a teacher. Kim is a chiropractor for over 22 years.
Jonathan
Life is such a blessing. Sometimes we think that there’s no way out, we limit ourselves, or we simply think to give up. Truth is, like we say in my family, “Solo hay que estar vivo para ver cosa,” or “You only have to be alive to witness things.”
My parents are first-generation immigrants from the Dominican Republic. I am a cancer survivor.
Kori
This may be the most vulnerable thing I’ve ever shared. I tend to not like to share too much of my personal life on social media. I am a businesswoman, so a few pictures of my kids, family, or vacations are usually the extent of what I put out there. But if what I’m about to say here about my story helps even one person listen to their gut or body, then I am proud to have helped. Please take a few minutes to read this.
Treatment Outcomes
Parents of JMML patients are advised to discuss survival information with their child’s hematologist-oncologist. Keep in mind that outcome data can show how other children with JMML responded to treatment, but it cannot predict how any one child will respond.
Signs and Symptoms
MF usually develops slowly. MF often does not cause early symptoms and may be found during a routine blood test. When fibrosis develops in the bone marrow, the bone marrow is unable to produce enough normal blood cells. The lack of blood cells causes many of the signs and symptoms of MF. These include: