Honored Kid

Abigail O.

Age 16
Abigail O. Kid Photo


Shakopee, MN, US


Acute myeloid leukemia (AML)

Date of Diagnosis

September 2012


Cancer free

Treated At

Children's Hospitals and Clinics of Minnesota Mayo Clinic Rochester

Change your kid's logo

My Story

Abby’s Story www.caringbridge.org/visit/abbyolson On Facebook: AbbyvsAML It all started with a bump on her head that had popped up in late July early August 2012. At first we didn’t think much of it, because kids get bumps and scrapes all the time. When it didn’t go away and became more painful Mom, (Tricia) made an appointment to go see the doctor. On Friday September 21st, 2012 Abby had the lump removed at the Allina clinic in Shakopee. When the doctor removed it she was not concerned. A biopsy was sent in and we still had no idea of how that lump would change our lives. Abby is a very active girl. When she isn’t running around with the neighborhood kids playing, she’s active with football, baseball, boating, camping, sledding, and many other activities. She enjoys playing Barbie’s, cooking, reading, watching movies, snuggling with her four dogs or throwing a dance party. She is a very thoughtful girl and always thinks of others needs before her own. She is also a very funny girl and after spending some time with her you can’t help but smile and laugh. On September 26th, 2012 Tricia got a call from the clinic saying they needed to see us immediately, this is never a good call. Marty (Dad), Tricia and Lorin (Step Dad) all met up at the clinic for the news. Abby was diagnosed with Acute Myeloid Leukemia (AML). AML is a type of leukemia that is usually found in adults and it is rare for people under 40. AML is a cancer of the blood and bone marrow-the spongy tissue inside bones where blood cells are made. Acute means that it is a rapidly progressing cancer. The next day we were off to Children’s Hospital in Minneapolis to get further testing and to begin treatment. Abby went through four rounds of treatment. Each round consisted of chemotherapy followed by three to four weeks of recovery. Between rounds we were able to go home for seven to ten days. The treatment presented different challenges, including a blood clot in her right atrium and a very serious infection. Abby was brave during every step. She had a central line in her chest for administering the drugs, receiving blood or platelets and for drawing blood for tests. She had a G-tube placed in her stomach to administer medications or food when she wouldn’t eat. Abby faced this with a fighting attitude is excited to have her normal life again. She missed her family, friends, school and her dogs while going through this treatment. Abby completed treatment in January and developed an Alpha Hemolytic Strep infection (something she got from her own body). She was in the PICU on a ventilator for two weeks and on kidney dialysis for two weeks. Abby had to learn to walk again. We were released from the hospital on February 26th, 2013. We were given the “all-clear, no more cancer” on March 25th, 2013. She had her Hickman and G Tube removed on March 27th, 2013. Her recovery from her fourth round was difficult with lots of physical therapy and clinic visits. We lived for 8 months in remission! She is surrounded by her parents, grandparents, aunts, uncles, cousins and friends with constant support. Her community brought her gifts, treats and helped the families out; this support is very much appreciated by Tricia & Lorin, her sister Jill and her biological father, Marty. We encourage Abby (and ourselves) to celebrate every day. We live each day for the little things, for the moments that matter most. Abby is looking forward to being a kid again. She can't wait to go back to school. For her future she is currently hoping to be a chef, to make movies, to learn to drive, to get married and have kids and to be a mom. Abby relapsed in September 2013. She endured three more rounds of chemotherapy from October 2013 until January 2014 at Children's Hospital in Minneapolis.We moved to Rochester on February 10th and began pre-transplant chemotherapy. Abby was isolated in the transplant unit at the Mayo Clinic Hospital, St. Mary’s. Her chemo was more intense than during her rounds previous. She was very ill and required tube feedings well past hospitalization. Abby received her transplant on February 19th, 2014. Shortly afterward she developed early signs of Veno-Occlusive Disease, her liver was failing. She was put on a study as a compassionate use patient. Abby was moved to the PICU and was put on dialysis. She had a catheter placed in her neck and a PICC line placed in her arm. She recovered and was moved back to the transplant unit. We checked out of the hospital and into a place we rented in Rochester on March 23, 2014. We were able to move home to Shakopee on April 2, 2014. Abby had a weekly appointment at the Mayo Clinic and a weekly appointment with Children’s in Minneapolis. We continued to monitor her for fevers and signs of infection. If she spiked a fever of 100.4F or higher we had to immediately go to the Children’s ER for antibiotics and possible admission. Abby went home on tube feedings and meds several times a day, including an IV medication.
After a significant improvement in her health in July 2014 she started to decline in health in August 2014. She had to have a PICC line placed in her arm, was on IV fluids and had several appointments a week both at Children’s in Minneapolis and at the Mayo Clinic. Her liver and kidney functions were concerning, she had significant GI problems and she began to show signs of graft vs. host disease of her skin. Abby was on oral steroids and topical steroids to control the rash on her skin. She was on multiple medicines to protect her from infection. She was unable to return to school because of the medications she is on. Abby’s skin began improving in January 2015 and she is now considered CURED!
Abby is doing very well considering all she has been through. If you were to ask her how she was, even on the darkest day she always said “good” or “fine.”
She is surrounded by her parents, her sister, grandparents, aunts, uncles, cousins and friends and even people we don’t know with constant support.
We encourage Abby (and ourselves) to celebrate every day. We live each day for the little things, for the moments that matter most. For her future she is currently hoping to be a chef, to make movies, to learn to drive, to get married and have kids and to be a mom.
By sharing the gifts of your time, talent and money with the St. Baldrick’s Foundation, you're supporting research to give all kids with cancer a better chance for a cure.

The Childhood Cancer Ripple Effect

Who's Honoring Me

Help kids take childhood back from cancer — support lifesaving cancer research today.

Children who are fighting or have fought cancer inspire others to be part of the Foundation's mission — to support the most promising research to find cures for childhood cancers and give survivors long and healthy lives.

Photo submission policy

Please read the photo submission policy and accept below.

By submitting a photograph of yourself on www.StBaldricks.org, you agree to the following terms and conditions for submission of your photograph:

We strongly encourage all users to submit a before and after photo, so that donors and fellow participants can easily recognize and relate to one another.

Any photo containing cartoons, comics, celebrities, nudity, pornography, sexually explicit images or any copyrighted image (unless you own the copyright) is not permitted. This is because photos of celebrities and cartoon or comic images are generally copyrighted by the owner.

Uploading images of other people without their permission is also prohibited.

This photo submission policy applies to StBaldricks.org users. The St. Baldrick’s Foundation reserves the right to review all photos and to remove any photo for any reason at our sole discretion. If you see a photo on StBaldricks.org that you believe does not conform to this policy, email to WebQuestions@StBaldricks.org