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Debra is
Blood Cancer United

Professional headshot of Debra, with a long ponytail, smiling at the camera

In October 2011, while at work, I fell after attempting to sit on a chair, and I went to the emergency department for x-rays. As soon as the technician began the process, he entered the room to ask if I had scoliosis. I replied, "no," and he proceeded with the exam.

As the year progressed, so did the pain in my back. For the next two years, I continued to suffer with unexplainable, excruciating back pain, which none of my attending physicians could find a cause for or give a name to. One physician, in particular, told me that I needed to have my head examined, because there was nothing wrong with my back. In September 2013, at the age of 52, I was diagnosed with multiple myeloma.

Unbeknownst to me, I was suffering with several bone fractures in my back. At the time of my diagnosis, 85% of my blood cells were contaminated. After a two-week stay in the hospital, I began biweekly doses of chemotherapy, along with daily servings of herbal tea and a change in my diet. By January 2014, only 15% of my blood cells were contaminated. In February 2014, I underwent an autologous bone marrow transplant.

Today, I celebrate three years of REMISSION. I would like to thank my loving family and close circle of friends for supporting me during this most trying time of my life. Moreover, I would like to thank The Leukemia & Lymphoma Society for three years of support.

Since I could not walk without sending waves of pain throughout my body, I was forced into early retirement. One of my greatest fears was having to go without health insurance and being denied medical treatment. Hats off to LLS for awarding me a yearly grant which has afforded me the grand opportunity of retaining my health insurance. Mere words are not enough to show my deep and sincere appreciation. May God Bless You All.

Debra

Multiple myeloma survivor

We are Blood Cancer United.

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

Merton

multiple myeloma (MM)

OLYMPUS DIGITAL CAMERA

Melissa

Caregiver

Paul

multiple myeloma (MM) and myelodysplastic syndrome (MDS)

Ron

multiple myeloma (MM)

Babette

multiple myeloma (MM)

Ilse smiling in a nicely landscaped setting

Ilse

Myeloma Survivor

Shandra holding balloons with letter 40, Multiple Myeloma survivor

Shandra

Multiple myeloma (MM)

Lynn, and three others in white and black shirts smiling

Paul & Lynn

Myeloma survivor

Professional headshot of Debra, with a long ponytail, smiling at the camera

Debra

Multiple myeloma survivor

Roy, myeloma survivor wearing black framed glasses and a blue zip up shirt

Roy

Myeloma Survivor

Deidra

Myeloma Survivor

Paul, a cyclist wearing a jersey standing by a road bike in a field

Paul

Multiple myeloma (MM)

We are Blood Cancer United.

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

Merton

multiple myeloma (MM)

OLYMPUS DIGITAL CAMERA

Melissa

Caregiver

Paul

multiple myeloma (MM) and myelodysplastic syndrome (MDS)

Ron

multiple myeloma (MM)

Babette

multiple myeloma (MM)

Ilse smiling in a nicely landscaped setting

Ilse

Myeloma Survivor

Shandra holding balloons with letter 40, Multiple Myeloma survivor

Shandra

Multiple myeloma (MM)

Lynn, and three others in white and black shirts smiling

Paul & Lynn

Myeloma survivor

Professional headshot of Debra, with a long ponytail, smiling at the camera

Debra

Multiple myeloma survivor

Roy, myeloma survivor wearing black framed glasses and a blue zip up shirt

Roy

Myeloma Survivor

Deidra

Myeloma Survivor

Paul, a cyclist wearing a jersey standing by a road bike in a field

Paul

Multiple myeloma (MM)

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