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Lawrence Paul "LP"

In July of 2017, our world was turned upside down. Our son, Larry Paul (LP), was experiencing back pain and was extremely tired. After multiple trips to doctors and ER visits over seven days, he was taken down to UMMC in Baltimore and diagnosed with T-cell acute lymphoblastic leukemia (T-ALL). After a 28-day battle of fighting ferociously, he passed away. When he was sent home from the hospital after 24 days, the doctors were convinced that he was going to beat this. The toxic chemo created a massive pulmonary embolism that went undetected.

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.

Sofia

Sofia’s story starts in November 2022. Actually, it starts on March 17, 2019, when she was born. She has been my fierce, independent, strong-willed little girl from the get-go. Once she started walking, she was an unstoppable force. Contrary to her cautious, older brother, Sofia seemed fearless. She loved to climb to the top of the playground structure meant for kids twice her age. She loved gymnastics and took after Mommy with her love of the bars, anything she could hang or climb on. 

Aryan

Hello, my name is Aryan. I am 13 years old. I was almost five years old when I first got diagnosed with cancer. It started as a normal summer like always, and we were planning to go somewhere. My dad was always traveling because of work, so it was just me and my mom. I would mostly spend time at my grandparents’ house because I could play games with them. One day my dad saw a bump on the back of my head, and our pediatrician told us that it was a lymph node. My pediatric doctor told my parents that it's normal, part of recovery from a fever or cough and to monitor it.

Santino

I know the pain of being told that you have cancer twice, but I also know the joy of being told that you have beaten cancer twice. I write this message to bring encouragement and to instill a fight in people who have had a relapse of cancer. Being told once that you have this disease is already heartbreaking, but to be told that it came back and you will need chemo again is soul-crushing.

Amy

I am a stage IV non-Hodgkin lymphoma survivor (NHL). The diagnosis came as a complete shock since I was a relatively healthy, active young adult working and enjoying life with family and friends. With a family history of breast cancer, I was advised to start having screening mammograms in my 20s. After a few clear screenings, I approached my 2018 screening and annual health visit to my primary care doctor's office with optimism. Within 48 hours, I received the dreaded call many women fear ― abnormal results.

Lilly

Treatment

It's important that your doctor is experienced in treating patients with acute myeloid leukemia (AML) or has access to an AML specialist.

Doctors use several types of treatment for adults with AML, some at different stages. Click on the links below to read more about each type of treatment.

Chancez

Hey, my name is Chancez (ironically, I was blessed with many chances last year). I became a part of The Leukemia & Lymphoma Society (LLS) community last year and was provided financial support. I was also presented with love, care, and daily reminders of all the support that was available to me to get me through such a rough period in my life. A friend of mine suggested that I share my story to help others in our community, especially young adults who are in the same predicament I was once in.

Jonathan

I was diagnosed with B-cell acute lymphoblastic leukemia (ALL) on July 26, 2019, and even without the involvement of a pandemic, I imagine that’s reason enough to believe that to me 2018 seems like a lifetime ago. Still, I can remember it well enough: A wide-eyed younger version of me arrived at college orientation, somehow simultaneously thrilled to begin a new chapter of his life and paralyzingly terrified of the imminent unknown.

Elisa

I was diagnosed with stage IV Hodgkin lymphoma (HL) in April 2022 at 27 years old. After months of debilitating symptoms and a week-long hospital stay, I finally had an answer as to what was going on with my body. I was relieved to have an answer, but "cancer" was the last thing I expected. Ironically, after my diagnosis and first chemotherapy infusion, I felt better than I had in months. I didn't feel like I had cancer; the only reminders were a few enlarged lymph nodes and the mediport protruding from the right side of my chest. 

Rylie

My name is Rylie York, I am 20 years old and I'm currently a sophomore at Baylor University. I'm originally from Round Rock, Texas and I am a patient at Texas Children's Hospital in Houston, Texas. I was diagnosed with stage 4 Hodgkin’s lymphoma at 18 in the middle of my senior year of high school. I have relapsed twice since then and completed my bone marrow transplant this past August and September.

Will

I am a cancer mom. I WAS a cancer mom. My youngest son, Will, was diagnosed with Hodgkin lymphoma (HL) at age 19 in April of 2019. He, his dad, and I were beyond shocked when we heard the news that the swollen lymph nodes that came up out of the blue one March morning were indeed HL. We didn't really know anybody personally that had it. We didn't know what exactly all the words meant at that moment in time, but we knew it wasn't what we had planned for our youngest son.

Mike

Jeannine

I got started with The Leukemia and Lymphoma Society (LLS) when our good friend, Tim Mauro, ran for Man of the Year and my husband, Larry, was his “campaign manager.” Tim’s father-in law, Bob, was battling non Hodgkin lymphoma. Watching them battle with him and seeing everything they did to help was such an inspiration, and seeing how many people were bonded together, raising money to find a cure, was amazing.

Madeline

My daughter is Madeline Conley.  On January 7, 2014, three days after her 15th birthday,  she was diagnosed with leukemia (AML/MDS).  She was a high school cheerleader and cheer coach who was basically ripped out of her normal active life and immediately admitted to the hospital, where she spent the next five months. It was the scariest thing we've ever been through.

Rohan

I am an acute myeloid leukemia (AML) survivor. I am now 10 months post-transplant and feeling stronger every day.I was born and raised in the Bay Area to South African Indian parents. I hold degrees from UC Berkeley and USC. I have built my career around advocating for equity in tech and marketing services that uplift underrepresented communities.

Doug

I have always been a builder. Professionally, I am an architect.  ​You could say that I’ve spent my life building spaces where people could grow. I never imagined, however, that I would someday have to rebuild my own. In February 2015, after experiencing months of excruciating and debilitating back pain that doctors mistakenly attributed to deteriorating lower lumbar discs, I had an MRI that revealed multiple vertebral compressed fractures.

Edmund

U.S. veterans’ sacrifices can occur on the battlefield … or much later.

Houseboys sprayed Agent Orange on weeds around the Quonset huts of Edmund Montefusco and his fellow soldiers in Korea in the early 70s, but it was decades before Edmund’s rare, slow-growing hairy cell leukemia made itself known.

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.

Louise

During the last week of July 2019, Louise, then-two-and-a-half-year-old, developed unusual red dots on her chest and some gnarly, yet explainable, bruises all over her body. We chalked the rash up to wearing an unwashed shirt and the bruises to being an extremely active two-year-old. Then, after her gums bled one afternoon, we hopped on Google and became increasingly concerned with the search results. However, Louise wasn’t acting “sick,” so her parents ignored Dr. Google’s diagnosis.

Dating, Sexuality & Intimacy

As a young adult you may be dating, in a relationship, or married. Cancer can make navigating romantic relationships complicated.

Dating can be intimidating no matter your situation. Remember, every date before your diagnosis probably did not go perfectly. You may have bad dates after your diagnosis as well. You may also meet incredible, new people.

Amanda

I am now a two-time acute myeloid leukemia (AML) survivor. When I was diagnosed with AML, it was an absolute complete shock. At the time of my diagnosis, I was a stay-at-home mom to my then three-year-old son. In a matter of a few hours and three words, “You have cancer,” my life completely turned upside down.

Treatment Outcomes

The cure rates and survival outcomes for patients with ALL have improved over the past few decades. Today, nearly 90 percent of adults diagnosed with ALL achieve a complete remission, which means that leukemia cells can no longer be seen in the bone marrow with a microscope. Still, despite high remission rates, relapses still commonly occur in adults and survival rates for adult patients remain at approximately 20 to 40 percent. However, these rates can vary significantly, depending on the patient’s ALL subtype and other prognostic factors.

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.

You'll need to choose: