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bone marrow saves lives

Liz

I've been affiliated with The Leukemia & Lymphoma Society (LLS) for many years through the volunteer/fundraising opportunities available to my kids. Little did I know I'd be visiting your website for my own needs once my mom was diagnosed with acute myeloid leukemia (AML) in January 2023. I'm overwhelmed with the advances made by LLS and find your organization to be a tremendous resource filled with hope. I always click on your stories and decide I want to share mine because I feel like my story and that of my mom's offers just that, HOPE!

Hodgkin lymphoma, man, black, ringing bell

Benedict

I was diagnosed with stage 4 Hodgkin lymphoma (HL) in June 2023. This was after months of testing, worrying, praying, and worrying some more. Honestly, the testing period was so stressful that it was almost a relief to know exactly what was going on when I was diagnosed. This is because while I was testing, I was taking official visits to prospective universities every weekend. I am a football player, and at the time, I was trying to decide which scholarship offer I was going to accept ― which university I was going to pin my hopes and dreams on. It was a stressful time.

young Asian-American male in purple t-shirt

EJ

I was diagnosed with large B-cell non-Hodgkin lymphoma (NHL) on May 2, 2023. It was such a shock to me, but months prior to the diagnosis, I already wasn’t feeling well. I was dealing with body aches every day, and nothing would help take the pain away. It wasn’t until I had a bad case of food poisoning that I ended up in the ER. After multiple scans, doctors were concerned about a suspicious mass on my chest. After more tests and biopsies, I started my journey fighting NHL. 

Young blond woman in a cap and gown, green stole and platform shoes

Rachel

I want to share my story about the day I was told the dreaded three words, "You have cancer," and how my life changed forever. I was diagnosed with stage 4 non-Hodgkin lymphoma (NHL) during my freshman year of college three years ago. I had started noticing symptoms including chest pain and fatigue, and I was constantly sick. I was continually going to the hospital with various infections and illnesses.

young ethnic girl sitting in a hospital chair wearing a yellow ball cap and a black sleevelss tshirt holding a pink phone with a blanket on her lap

Danya

I've been waiting for that moment for six months, since the day the doctors told me I had to do chemo to treat my Hodgkin lymphoma (HL) in February 2023. From constant ER visits, going through multiple thoracentesis, concerning symptoms, and a biopsy on the neck due to a visible lump, I finally got the answer to what had been (at the time) weighing so heavily on my shoulders. I had cancer. I was in a state of shock. This was all very new to me, and to be honest, it took me a while to process and accept the new change I had to endure.

older white woman with short white hair wearing silver hoop earrings and a black and white polka dot blouse

Laura

My mom was diagnosed with non-Hodgkin lymphoma (NHL) in August 2022. Over the course of a year, she underwent chemotherapy, caught COVID-19, underwent CAR-T therapy, and fought through many respiratory infections. My mom was a fighter. She wasn’t going to let a cancer diagnosis slow her down. She wanted to live. Between me and my sisters, we all took turns taking my mom to all her appointments.

Cottle

Joshua

Just three days after Christmas, my world was turned upside down. I was admitted to the hospital because I was unable to keep any food down and felt terrible overall. Upon admission, I had a multitude of issues, just a few being extremely high uric acid levels, severe dehydration, pancreatitis, and nephrosis. They also discovered that I had lost 20 lbs.! Later in the hospital, I would lose 20 more.

Jane_Hodgkin_lymphoma

Jane

In October 2015, I was diagnosed with Hodgkin lymphoma (HL). After growing up never getting sick, I had cancer. It was incredibly difficult to comprehend at the age of 13 that I was about to endure something most people won’t experience in a lifetime. I went through four rounds of chemotherapy and was in remission in January of 2016. Once you’re in remission, you believe that that’s the end. You’ll have a few check-ups here and there, but in your head, you envision no more cancer.

HL

Thomas

I had bariatric surgery on May 11, 2022. At the time, I weighed just under 600 pounds, and I understood that there was a higher possibility for complications. My three-hour procedure turned into a six-hour procedure, and my overnight stay in the hospital turned into a week. During surgery, they discovered my spleen was significantly larger than normal, and in the days following my surgery, I kept losing blood. After two exploratory surgeries, four units of blood, and a trip to the ICU later, I was finally released from the hospital with no confirmed cause of bleeding.

Caregiver sister

Erin & Meghan

I always loved fall. It is such a special time. My birthday is the first day of fall. I love unpacking my favorite boots, lighting pumpkin spice candles, and making warm soups. Fall always signified that special holidays and quality time with family were quickly approaching. These were events to get excited about! But in the last few years, fall has taken on a new meaning for me.

mike

Mike

It started with a cough that would not go away. A cough so bad that it would stop him in his tracks and he'd have to rest afterwards for a few minutes just to catch his breath and regain strength. This was in March 2016. My husband, Mike, was like any other 31 year old "healthy" person. He figured the cough was allergies or a stubborn cold. He finally agreed to go to urgent care because of course he didn't have a primary doctor. The doctors had the same thoughts: allergies or a stubborn cold. They treated him for these things and none of them helped.

Tricia

Tricia

My story is truly about the little family that could. In 2002, I felt I had it all: a loving partner, a new job offer, and plans to start a family. Upon my return from a business trip in May, that feeling shifted as a large lump appeared on the side of my neck. Several doctor visits, tests, and sleepless nights later, I received a phone call on the way to a meeting from a doctor. He asked me to pull the car over. He told me I had cancer. Everything stopped.

Joshua

Joshua

Just three days after Christmas, my world was turned upside down. I was admitted to the hospital because I was unable to keep any food down and felt terrible overall. Upon admission, I had a multitude of issues, just a few being extremely high uric acid levels, severe dehydration, pancreatitis, and nephrosis. They also discovered that I had lost 20 lbs.! Later in the hospital, I would lose 20 more. I remained in excruciating pain for three weeks while multiple branches of the hospital were trying to find out what was wrong with me.

stage 4 Hodgkin lymphoma (HL)

Kathryn

My symptoms became pretty intense in December 2017. I was 21 at the time and living a healthy and active lifestyle, but my symptoms were starting to interfere with my quality of life. I was experiencing a cough, fatigue, unexplained weight loss, and pretty intense back pain, along with several swollen lymph nodes primarily on the left side of my collarbone.

Avery

Avery

When I was a senior in high school, my life changed forever. In my senior year, playing my last season of basketball and gearing up to play college softball that next fall, everything was looking up. I had great friends, and great family, not to mention that I had the best-looking curly hair there ever was. Back in September 2019, I noticed a knot in my right armpit. At the time, I was playing high school softball and was just moved to a new position. I thought the reason for my underarm pain had been from soreness, so I put it off until the season was over.

Side Effects

The main goal of treatment for myeloma is to get rid of myeloma cells. The term side effect is used to describe how treatment affects healthy cells. Patients react to treatments in different ways. Sometimes there are very mild side effects. Other side effects may be serious and last a long time.

Myeloma patients should talk with their doctors about side effects before they begin any type of treatment. There are drugs and other therapies can prevent or manage many side effects.

Procarbazine

Generic name Procarbazine Pronunciation  proh-KAR-ba-zeen Brand name(s), other common name(s) Matulane® Drug type   DNA-damaging agent How the drug is given By mouth Indications and Usage

Procarbazine is FDA approved with other anticancer drugs for the treatment of stage III and IV Hodgkin lymphoma. Procarbazine is used as part of the MOPP (mechlorethamine, Oncovin® [vincristine], procarbazine, prednisone) regimen.

Dan Klotz

Dan

When cancer hangs your cleats up for good

At my first appointment, the physical therapist asked me why. Why did I want to run a marathon? And I didn't have an answer, partly because when you meet someone, you don't want to blurt out all sorts of emotional baggage, and that's the sort of question that can trigger a lot of baggage.

jane

Jane

In 2008, I retired from teaching art, mostly because I was feeling tired all the time and didn’t want the program I was running to suffer because I couldn’t keep up. I figured it was old age. I was enjoying my first full year of retirement when I woke up with a backache. After two months of tests, in July 2010, I was diagnosed with multiple myeloma, a treatable but not yet curable blood cancer in the plasma cells of the bone marrow. 

Matthew

Matthew

Our Matthew was first diagnosed with acute lymphoblastic leukemia (ALL) in August 2015 at the age of 12. He relapsed with ALL in December 2016 and underwent his first bone marrow transplant in February 2017 with marrow from an anonymous male donor from New Jersey.

In January 2019, he was diagnosed with mixed phenotype acute leukemia (MPAL). He underwent his second bone marrow transplant in February 2019 with marrow from his first donor's twin brother. Our two families have become very close since we were able to meet after the first transplant.

Nicole_tnt_teammate

Nicole

I first became involved in Team In Training (TNT) and The Leukemia & Lymphoma Society (LLS) in March of 2020 because I was very interested in running the New York City Marathon. I knew that I wanted to run for a charity that meant something to me, so I knew I had to be a part of this team.

Penny Man LLS

Penny Man (Jonathan)

My name is Jonathan, but I really like to be called "The Penny Man.” I have been collecting pennies for over 15 years and then donating them to The Leukemia & Lymphoma Society (LLS). I first started collecting in high school in 2006 when a classmate of mine passed away from leukemia. My teacher, Mrs. Jean Cassetta, started a schoolwide campaign in partnership with LLS in memory of our friend Andrew, and I never stopped saving pennies since.

Zachary acute myeloid leukemia

Zachary

Two months after we were married, my husband was diagnosed with acute myeloid leukemia (AML) in July 2021. I was 33 weeks pregnant with our first baby when he was admitted to St. Louis University Hospital for the next month of induction treatment. Prior to diagnosis, Zach had been experiencing fatigue and palpitations and would become winded just walking up our flight of stairs. We thought he was having residual effects from some prior illnesses that he was hospitalized for in April and May. We know now that those instances were the beginning of his immune system starting to fail.

volunteer and healthcare professional for patients with blood cancer and their families

Luz

My name is Luz, and my story begins in a magical town in Mexico where I spent a wonderful childhood surrounded by my family. As the youngest of nine siblings, I learned the value of support and connection, values which continue to guide me today as a happily married mother of three beautiful daughters. For over twenty years, Chicago has been my home.

family impacted by blood cancer leukemia standing on the beach

Maggie

My son, Benjamin, was diagnosed with acute lymphoblastic leukemia in February 2019 at the age of four. Due to the unique nature of his presentation, he was placed in the VHR (very high risk) category and underwent three and a half years of treatment. My background is in theatre and education, but having just moved to New York, I was not working when Benjamin was diagnosed and was lucky enough to be able to devote 100% of my time to him. I spent his treatment years learning as much as I could about the disease and how I could best care for him.