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Jonathan is
Blood Cancer United

Smiling young boy in a small room with a breathing apparatus

I was diagnosed with diffused large B-cell lymphoma (DLBCL) with concentrations in the brain and lungs. Lymphoma itself is a cancer that starts in the cells that are part of your body’s immune system, with DLBCL being the most common type of non-Hodgkin lymphoma (NHL). While it is so common, it is also extremely aggressive as it attacks your white blood cells which are responsible for fighting infections. The silver lining in the middle of all of this was that my doctors felt that I had a high chance of survival because of my age.

Every two weeks for six months, my parents took me to the hospital to receive chemotherapy. Although I felt weaker and weaker with each round, I kept my chin up and continued fighting. In addition to chemo, I also needed to receive a stem cell transplant. This was the most nerve-wracking part because of the fatal possibility of my body attacking the cells administered to me. How was I, at 23, supposed to accept that the thing that was supposed to help me the most could also quite literally have more dire consequences for me?

A friend I met at the hospital lost his battle as I was going through mine. At that time, all I had was prayer, family, friends, and groups of people I didn’t even know who were praying for my health. Despite these moments being very stressful, there was always an internal peace I felt throughout the process. It was like I knew nothing was going to happen to me. I used to joke around and laugh in conversations with doctors/surgeons right before major surgeries. I particularly remember speaking to them about how I missed eating rice, beans, and chicken.

I am a firm believer that the attitude you assume when facing any difficulty will dictate your outcome. In the upcoming weeks, my oncologist spoke to my family and me to state that I was cancer-free.

It was a miracle.

I began rehab shortly after. I remember getting up after my last brain surgery. For three days I wasn’t able to lift my head off the pillow. The big day came, the day I would get on my feet again. I got up and took my first steps. I felt a bit frustrated because in my head I knew how to do this, I’d done this before. But I couldn’t walk without assistance. You could see the joy and tears of happiness on every person’s face in that room. From that day on, I worked day by day to restore my health.

In 2017, I was cleared to resume my studies, and I chose St. John’s University. The SJU community has welcomed me with open arms during these two years. I’ve been blessed to join organizations that promote the common good such as the Catholic Community for Animals (CCA), the Latin American Student Organization (LASO), and the Caribbean Student Association (CSA).

St. John’s University prepared me mentally and spiritually to become the best professional/citizen possible. I interned at New York Presbyterian (Queens) and met healthcare professionals who I admire just as much as those patients who remain strong throughout their hospital stay. At the lowest point in my life, I was not able to speak, eat, or walk. I was like a newborn who had to learn everything. All I had was hope, prayer, and the support of my family and friends.

I want to say to you all today, do not give up no matter what struggles you may have. God’s time is perfect. My goal in life is to serve as a beacon of hope for all those who are fighting, admiring the survivors, and honoring the taken. Faith kept me alive, and today I am thankful for opening my eyes, hearing, and being able to stand on my feet because many people are not able to.

In closing, I would like to thank the amazing medical staff who treated me, from the housekeepers to the surgeons, my mother who never left my side, my father who always advocated for me when I was unable to, my family and friends who until this day have been supporting me, and finally, my partner in life at the time because she never gave up on me. I love all of you.

I want to share a quote that inspires me every day: “Courage is not having the strength to go on; it is going on when you don’t have the strength.” --Theodore Roosevelt

Love yourself, love each other, love the planet.

Jonathan

Diffuse large B-cell lymphoma (DLBCL)

We are Blood Cancer United.

Everyone affected by blood cancer—patients, survivors, caregivers, researchers, advocates, fundraisers, everyone—has a story. Share yours.
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James

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Janie

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Katie

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Nicole

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Smiling young boy in a small room with a breathing apparatus

Jonathan

Diffuse large B-cell lymphoma (DLBCL)

Liv, smiling, standing in a room with a bookcase and balloons

Liv

NHL survivor

We are Blood Cancer United.

Everyone affected by blood cancer—patients, survivors, caregivers, researchers, advocates, fundraisers, everyone—has a story. Share yours.
Headshot of Amrita wearing a black dress, a cancer survivor

Amrita

diffuse large B-cell lymphoma (DLBCL)

Snapshot of Dave Warner and family, a cancer survivor

Alison

Volunteer

Tina

Diffuse large b-cell non-Hodgkin lymphoma (DLBCL)

James, volunteer and survivor, pictured with group of friends

James

Volunteer and survivor

Photo of Janice, diffuse large B-cell lymphoma (DLBCL) patient

Janie

diffuse large B-cell lymphoma (DLBCL)

Katie, NHL patient, holding infant

Katie

Diffuse large B-cell non-Hodgkin lymphoma (NHL)

Headshot of Kenneth, wearing a suit and wire frame glasses, smiling

Kenneth

Diffuse large B-cell non-Hodgkin lymphoma (DLBCL)

Back of man wearing red satin Survivor Light The Night/LLS jacket

Jorel

Lymphoma Survivor

Smiling man, holding IV pole, doing a selfie

Dane

Stage 3 diffuse large B-cell lymphoma (DLBCL)

Nicole smiling at Light the Night Walk, holding white lantern, in green shirt reading "Nicole Cares"

Nicole

Non-Hodgkin lymphoma (NHL) survivor

Smiling young boy in a small room with a breathing apparatus

Jonathan

Diffuse large B-cell lymphoma (DLBCL)

Liv, smiling, standing in a room with a bookcase and balloons

Liv

NHL survivor

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