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Megan is
Blood Cancer United

Young girl smiling with white hate and white shirt that says Cancer picked the wrong diva

Seven years ago I was 18 years old and a freshman in college. I could not have been more proud of myself. I had a 3.7 GPA, I joined the cheerleading team (first time I ever cheered before), became a member of a sorority and was involved in a local organization related to my major.

I went home for Thanksgiving dinner and my family noticed I didn't look well. I knew something was wrong, but I had an "excuse" for all my symptoms. The next thing I knew, I was scheduled for surgery to have a lymph node removed under my arm. The surgery took place a few days later, and I was disappointed that I had already missed two days of class. All I wanted to do was go back to school and let this all be over. Therefore, I convinced myself that I would have this lymph node removed and be back at school in no time. Little did I know that was not the case.

A week after surgery I went for a check-up and was then brought into the doctor’s office. It all happened so fast, and I'll never forget the conversation that took place next. I was diagnosed with Hodgkin's disease and met with an oncologist that day! I was told that I could not go back to school and had to start treatment immediately. I was unable to return back to school to finish my finals for the current semester, and I was forced to take the spring semester off. I was devastated.

I'm not sure if I ever truly processed what was happening. I just remember staying focused on getting through chemotherapy and determined to go back to school. Six months later, I finished all 12 rounds of chemo and I not only returned to school for the following semester, I doubled up on my classes and graduated with my class! It’s seven years later and I'm in the midst of planning my wedding. I would have never had the chance to be here if it wasn't for my support team, researchers, oncologist, societies such as LLS and many more. I want to dedicate this to current patients and their caregivers affected by LLS and remind them to stay strong and positive. Most importantly, have a goal. Give yourself something to look forward to because you deserve it!

Megan

Lymphoma Survivor

We are Blood Cancer United.

Everyone affected by blood cancer—patients, survivors, caregivers, researchers, advocates, fundraisers, everyone—has a story. Share yours.
Man wearing gray shirt, running a race

Coy

Hodgkin lymphoma (HL)

Lisa and a man standing in a football stadium holding white, yellow and red Light The Night lanterns

Lisa

Lymphoma survivor

Katie, primary mediastinal large B-cell lymphoma (PMBCL) patient

Katie

primary mediastinal large B-cell lymphoma (PMBCL)

Ellise

stage IV Hodgkin lymphoma (HL)

Holly

subcutaneous panniculitis-like T-cell lymphoma (SPTCL)

Jacqueline

Hodgkin lymphoma (HL)

Lori

follicular lymphoma (FL)

Michael and Ashlee

hepatosplenic T-cell lymphoma (HSTCL)

Kerry

Hodgkin lymphoma (HL)

Crystal

Hodgkin lymphoma (HL)

Eva

Hodgkin lymphoma (HL)

Brescia

Hodgkin lymphoma (HL)

We are Blood Cancer United.

Everyone affected by blood cancer—patients, survivors, caregivers, researchers, advocates, fundraisers, everyone—has a story. Share yours.
Man wearing gray shirt, running a race

Coy

Hodgkin lymphoma (HL)

Lisa and a man standing in a football stadium holding white, yellow and red Light The Night lanterns

Lisa

Lymphoma survivor

Katie, primary mediastinal large B-cell lymphoma (PMBCL) patient

Katie

primary mediastinal large B-cell lymphoma (PMBCL)

Ellise

stage IV Hodgkin lymphoma (HL)

Holly

subcutaneous panniculitis-like T-cell lymphoma (SPTCL)

Jacqueline

Hodgkin lymphoma (HL)

Lori

follicular lymphoma (FL)

Michael and Ashlee

hepatosplenic T-cell lymphoma (HSTCL)

Kerry

Hodgkin lymphoma (HL)

Crystal

Hodgkin lymphoma (HL)

Eva

Hodgkin lymphoma (HL)

Brescia

Hodgkin lymphoma (HL)

The Leukemia & Lymphoma Society (LLS) is now Blood Cancer United. Learn more.