Honored Kid

Scarlett M.

Age 14
Scarlett M. Kid Photo


Middle River, MD, US


Acute myeloid leukemia (AML)

Date of Diagnosis

July 2011


In remission

Treated At

Johns Hopkins Children's Center

Change your kid's logo

My Story

Scarlett is a beautiful, bright blue-eyed, girlie-girl filled with a spunk and passion for life far beyond her 13 years of age. During routine bloodwork at her 2-year checkup, abnormal cells were found which led us immediately to Johns Hopkins for further examination. Within 4 days of that pediatrician visit, the normalcy and innocence of Scarlett's childhood came to an abrupt halt. She was immediately admitted to the JH Childrens Center to begin numerous invasive surgeries, pokes/prods, scans, tests, feeding tubes, chemotherapy drugs and medicines of every color. She was no stranger to life-threatening infections and we lived on edge more days than we could count. We were blessed that after the 1st month of chemotherapy, her Leukemia was 'undetectable' and they would be able to proceed with chemotherapy treatments alone. At this point, she was going to be able to avoid going through a bone marrow transplant which could significantly decrease her chances of survival. If the cancer cells returned at any point during treatment (or even today), she would have to then endure the transplant. Through her 5 month stay at JHH battling AML M7, she persevered through intense chemotherapy treatments and monstrous side effects, but she never failed to win the hearts of the nurses, doctors, families that surrounded her with her silly, comedic antics and mature, quick wit. She loved playing nurse and on days when she felt well enough she would spend hours on end in the nurses' station entertaining the staff and brightening their day. She quickly became known as the JH Pediatric Oncology 'mascot'. We had more scary, heart-stopping moments than we care to remember, but she continued to amaze us with her will to fight and her infectious spirit. She showed us what the true meaning of courage and strength really is and forever changed our lives and the lives of countless others along the way. Just days before Christmas of 2011, Scarlett finished her treatments and was able to move back home to celebrate with her family, including big brother, Gavin (now 15). She is currently in remission and now just has annual outpatient clinic visits for precautionary blood draws and assessments. As parents, it is very hard not to live in constant fear that she will relapse and need to endure a bone marrow transplant, but we are working hard every day to not let that fear overshadow the 2nd chance at life that God so graciously bestowed upon her/us. There have been a few scares over the years when we thought relapse could be lurking...aches in her legs/feet, unexplainable bruising on her back, loss of pigmentation in her skin which could mean a drop in a certain blood count, terrible migraines...however, she is, fortunately, being carried by our prayers to Our Heavenly Father and He has kept her healthy. 

She is currently loving 8th grade and just got into the Women in Medicine program in the HS she applied to so she could begin to study and intern in her career passion...pediatric nursing.  These last 8 years of being home and in remission has made us happy beyond comprehension. She dotes on her 6 yr old baby brother, Brayden, and her 2 furry siblings, Tye & Snowflake. Our lives are full and happy and we could not imagine it any other way. She excels and LOVES being in school and with her friends. It is still so exciting to see her healthy appetite return after those endless months of only being able to eat through a feeding tube. Pizza is still the favorite, so even chemo couldn't kill her love for that! She enjoys summer, boating, swimming and playing in the warm sunshine more than ever. We make sure that we never squander a moment, always remembering how it felt to be trapped in hospital walls that whole fateful summer. Sharing the magic of the Christmas season together is even more exciting than ever too. We all continue to look forward to the upcoming months/years and no matter how hectic they will be (it's a given!), we never lose sight that each day we are given with Scarlett and each other is a blessing never to be taken for granted. God Bless His Children...

The Childhood Cancer Ripple Effect

Help Give Kids a Lifetime

Infants, children, teens and young adults are depending on us to find cures for childhood cancers — and to give survivors long and healthy lives.

Support lifesaving childhood cancer research today.

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