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Myeloma Stories

Paul G. – Darien, GA

I was diagnosed with multiple myeloma in 2007 and received a stem cell transplant at The Winship Cancer Center later that year.

The story of cancer is seldom about the patient. The story is about providers, researchers and families; particularly families. It can be confusing and frightening. It is difficult enough for adults, but it is much more difficult for children. My story is best told by one of my grandchildren as a school project for Veteran’s Day.

Jackson Kiser Veteran’s Day Essay October 15, 2013
Mello/5th Grade

I have several members of my family who have served in the military. I choose to write this essay about my grandfather, Paul Griffin. We call him Ahpa.

He served in the Navy from 1963 until 1990. During this 27 year career, he served in Vietnam. He has lived in many different places, such as Florida, Texas and Hawaii.

While in the Navy, my Ahpa learned some valuable lessons. He developed skills that he still uses today, including discipline, bravery and strength. Unfortunately, he is fighting a different battle today: Cancer.

Throughout his struggle, my Ahpa has taught me the importance of these principles. I am so proud of him. When he feels sick, he is still there to help me with my math homework. Even when he is exhausted from the medicine, he still plays baseball with my brother Sam. And even though his body hurts, he takes my youngest brother, Griffin, to the pool to play for hours.

He is my hero!! If you ask him about his years in the military, he will tell you he feels honored to have been a member of the United States Navy. After a long career, he retired a Captain.

Categories
Myeloma Stories

Sara C. – Johns Creek, GA

In October of 2010, I was figure skating and as I entered a spin I felt extreme pain in my lower back. After over the counter drugs didn’t seem to help, I went to a doctor who x-rayed my back and proclaimed I had a lot of arthritis (due to many falls taken figure skating). He told me no more jumping or impact sports and recommended yoga. He also gave me prescription pain meds. I tried yoga and even sports massage, but the pain never got better, so I scheduled an appointment with an orthopedist. In late December, a few days before the orthopedist appointment, the pain was so severe I couldn’t get out of bed. My husband called an ambulance. It took 3 firefighters and 2 paramedics to put me on the stretcher to take me to the hospital.

After x-rays and a CT scan, the emergency room doctor told me the pain was caused by a collapsed L2 vertebrae and I had lesions on some of my other vertebrae which were all caused by a cancer called Multiple Myeloma. They admitted me to the hospital. Here’s what went through my mind: Cancer? At age 47? But, I’m in great physical shape, or was! Am I gonna die? Will life ever be normal again? Will I ever walk, skate, or even lead an active life again?

After 4 days in the hospital and numerous tests, multiple myeloma was confirmed, my pain was under control, I was fitted with a body brace and sent home. A few days later, January, 2011, my oncologist told me “we’ve got this” and eventually, I’d be fine. He did an MRI and skeletal survey and determined that, in addition to the lesions on my spine, I had lesions on my thigh, hip and arm bones. The collapsed vertebrae was repaired with a vertebroplasty. I was treated for 4 months with velcade, dexamethasone and revlimid and achieved a complete remission.

During that time, I began to do yoga and was able to do a little figure skating. Next, I had an autologous stem cell transplant which resulted in a stringent complete remission. After the transplant I had monthly infusions of Zometa for 2 years and took Revlimid for 3 years. Now, almost 4 years later, I am happy to say that I am still in stringent complete remission.

2 months after the transplant I returned to figure skating and, 6 months after the transplant, I returned to teaching figure skating classes. I can jump and spin again and still take some falls. I have passed 2 United States Figure Skating tests (one being the adult gold test- the highest adult level) and competed again last year, skating a 2 minute 40 second program.

My recovery has been remarkable and I am stronger and more active than ever. Every day I am thankful for modern medicine and the prayers and positive thoughts of my family and friends. My life is relatively normal – except for the annual testing at the transplant clinic and visits to the oncologist every few months. Also, I have met some truly exceptional people through mentoring myeloma patients.

– Sara

Categories
Myeloma Stories

Doris M. – Atlanta GA

On April 2004, I went to my doctor for my routine physical exam, never suspecting that this visit but would be anything but routine. My doctor voiced her concern about the excessive protein appearing in my urine. I immediately asked why she was especially concerned. Her response was a scheduled appointment with an oncologist for further test.

I followed up with my doctor to receive a definite prognosis. The oncology results confirmed my doctors’ suspicious that I had a form of cancer called Multiple Myeloma, a disease I had never heard of.

After getting over the initial shock of my diagnosis, I was set on a course of being thoroughly educated about the disease, its impact, and the several options I had to address its management as I was told there is no known cure.

Initially, I decided to do nothing, since there was no cure, thinking that I would just let nature take its course, especially since I was given three to five years life expectancy with this disease. It wasn’t until I underwent a barrage of test to establish a baseline to make a treatment recommendation, and after I prayed intensely about my diagnosis, that I told my family about my cancer.

— Doris M.