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Keisha is
Blood Cancer United

Close up of Keisha in a white t-shirt, with long hair and tortoiseshell glasses, looking determined

In 2017, I was diagnosed with a rare and chronic form of non-Hodgkin lymphoma (NHL). I was beyond devastated as I knew there was no cure for my condition, and I also knew my life would be altered in many ways. I was also finishing my last semester in graduate school and almost gave up my dream of graduating. But with the support of my family, school, physicians, and The Leukemia & Lymphoma Society (LLS), I persisted and received my Master of Education in 2018.

Quarantining through the pandemic affected my treatment. Offices were closed, so I was unable to go to the hospital for treatment, which left me without any way to manage my NHL. As my condition worsened, I became vigilant in my advocacy of patients’ rights and started a website which gave me a space to blog about my experience during quarantine. In 2021, my love of writing helped me self-publish my first book. My book discusses living with a chronic condition during quarantine, as well as other events that took place during that time. I also discuss my childhood and how it shaped me into who I am today.

I am currently an Educational Leadership Doctoral Candidate, an Adjunct Professor, a Doctoral Fellow, and an Education and Social Justice consultant. I try to share my experiences because, despite obstacles, our stories can become testimonies to help or encourage others. I hope my students and my children see that despite challenges, we can still make a difference and be the change we want to see.

Throughout my journey, LLS has been supportive in many ways. I have a Light The Night (LTN) team, “Keisha’s Crusaders,” and my former students participated in the LLS Hero Squad program. LLS has provided a space for me to learn about my condition, allowed me to join support groups, and to find assistance. I truly appreciate everything that LLS does for patients and families. Sometimes blood cancer patients are forgotten because people cannot always visibly see our condition, but blood cancer impacts our lives tremendously. I appreciate LLS for providing a space to educate, lead, and encourage support to end blood cancers.

Keisha

Non-Hodgkin lymphoma (NHL)

We are Blood Cancer United.

Everyone affected by blood cancer—patients, survivors, caregivers, researchers, advocates, fundraisers, everyone—has a story. Share yours.
Lisa and a man standing in a football stadium holding white, yellow and red Light The Night lanterns

Lisa

Lymphoma survivor

James, volunteer and survivor, pictured with group of friends

James

Volunteer and survivor

A blood cancer patient stands with friends at an outdoor Blood Cancer United event, wearing colorful leis and holding heart-shaped signs while posing together in front of a branded backdrop, creating a celebratory and supportive atmosphere.

Carlos

non-Hodgkin lymphoma (NHL)

Portrait of a blood cancer survivor wearing glasses and a checkered button-down shirt while seated indoors against a neutral background. The image highlights resilience, advocacy, and the experiences of individuals living with or recovering from blood cancer.

Robert

non-Hodgkin lymphoma (NHL)

Alec standing in front of LightThe Night signage in a park at a Light The Night event. Alec is wearing a blue shirt with the words, "Survivor, Light The Night" printed on it and holding a white Light The Night survivor lantern.

Alec

Primary mediastinal large B-cell lymphoma (PMBCL)

Side-by-side portraits showing a blood cancer survivor and Team In Training participant in 2012 and 2022. In the first image, the individual wears a Team In Training shirt and points to the program logo. In the second image, the same individual stands wearing multiple race medals earned through endurance fundraising events. The photo illustrates a decade of resilience, survivorship, and advocacy in the blood cancer community, highlighting the impact of fundraising, patient support, and blood cancer research.

Max

non-Hodgkin lymphoma (NHL)

Black-and-white close-up portrait of a family gathered together at home, with a young child in the center and two adults nearby. The image highlights the importance of family support, connection, and resilience during a blood cancer diagnosis, reflecting the experiences of patients, caregivers, and loved ones navigating blood cancer treatment and survivorship together.

Maria

Hodgkin lymphoma (HL)

Person wearing a light pink blazer and event credential stands in front of a step-and-repeat backdrop featuring The Remission Film Festival logo, with an IV pole displayed beside them. The image highlights advocacy, storytelling, and awareness within the blood cancer community, showcasing a film festival event focused on sharing blood cancer survivor and patient experiences through film and media.

Edward

non-Hodgkin lymphoma (NHL)

Emily smiling in a photo with her husband and her three young children in an urban setting

Emily

non-Hodgkin lymphoma (NHL)

A young hispanic mom in a gray tshirt with her bald son wearing bright green boxing gloves and an I Am a Warrior tshirt

Peyton

non-Hodgkin lymphoma (NHL)

Photo of Jan, Lymphoma survivor

Jan

Lymphoma

Copilot said: Close-up selfie of an older adult wearing glasses and a navy shirt with an “I Voted” sticker, seated in a car, highlighting everyday resilience and community engagement within the blood cancer community and survivorship journey.

Fred

non-Hodgkin lymphoma (NHL) and chronic lymphocytic leukemia (CLL)

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