Lymphoma

By the time I was 32 years old, I was a 3-time cancer survivor. At 22 years old, I was diagnosed with MALT lymphoma, at a time (1999) when the doctors knew very little about it and believed it had only been found in men over the age of 80 in their stomach (mine was found in my neck).

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.

My introduction to The Leukemia & Lymphoma Society (LLS) began in the early 2000s. I joined a Light The Night Team to support research and programs for cancer patients. I then discovered Team In Training and ran my first marathon and my second as a Team Mentor. At the time, I knew cancer was a terrible disease, but it wasn’t until 2012 that cancer became more personal.

I am a physician-scientist with a primary focus on treating and understanding blood cancers like MDS and AML. It's a job I love and one that has given a lot back to me over the years. However, it was also a very unlikely outcome for me. I was born in Montevideo, Uruguay where I lived until I was 5 years old.

In April 2020, I was diagnosed with Stage 2 Hodgkin lymphoma (HL). My life was turned upside down after this diagnosis, and I was in extreme denial even months into my treatment. I was forced to go through six months of chemotherapy and two surgeries to treat it. Being diagnosed with cancer at the age of 20 in the midst of a pandemic taught me many things.

As a First Connection volunteer with The Leukemia & Lymphoma Society (LLS) for almost two years, I have had the opportunity to connect with patients and survivors to share their stories and experiences while battling this deadly illness. Every day I come across so many touching and courageous stories that inspire me to do more and more to support this cause.

My name is Jaime Fernandez and I am a Clinical Social Worker with UCI Health. I have the pleasure and honor of working with individuals diagnosed with blood cancers. Supporting my patients and their loved ones as they navigate these diagnoses has become my driving force.

Life is unpredictable! I started becoming sick from February of 2020. My condition was ruining day by day with no symptoms besides a very bad cough that lasted for a month. I was 23 and 3 months into my marriage when I was diagnosed with Hodgkins lymphoma (HL) in October of 2020. I am from a country where the healthcare system is broken.

Michele Synder decided she wanted to volunteer with The Leukemia and Lymphoma Society (LLS) because she herself and millions of others have been impacted by cancer. Both of Michele’s parents passed away from cancer and during that time, a lot of people were there for them. She knows how important that was for her and her family. That support provided them with so much comfort and healing.