Through My Eyes is a series in which those affected by childhood cancer share a behind-the-scenes look into what it’s like to be in their shoes. Read every perspective. Become aware and donate to help create solutions for kids fighting rare pediatric cancer.
- Perspective: Cancer Dad
- Name: Aaron Plummer
- Spouse: Kayla Plummer
- Daughter: Merritt Plummer
- Cancer: Stage 1 Rhabdomyosarcoma, group 3
- Diagnosed: 03.04.19
- Treated at: Levine Children’s Hospital
- Feels: Thankful
Aaron was featured on our social channels (Instagram & Facebook) on 9/5/19 to share what it’s like to be a daddy, husband, and provider while helping his daughter fight for no more cancer. It’s real and it’s raw… just like childhood cancer.
My Daughter Has Cancer…
“In February the babysitter went to change Merritt’s diaper and discovered what looked like small grapes coming out of Merritt’s vagina. After a visit to Merritt’s pediatrician she determined that it had prolapsed and sent us to a urologist at their other office to determine why. That urologist did a quick ultrasound and discovered a tumor in Merritt’s abdomen. After seeing the pediatric urologist at Atrium Main, we were immediately admitted to Levine Children’s Hospital where Merritt had a biopsy surgery, CT scan, and bone scan the following day.”
03.04.19 At 17 months old Merritt was diagnosed with Stage 1 Rhabdomy
The New Normal…
“It’s so frustrating that Merritt has to see this as her “normal” life because it is far from normal for any child at her age. I have for years heard people refer to children of Merritt’s age being in their “terrible twos”. I disagree with this term because it is not terrible twos, it is a child that is trying to figure out life itself, their emotions, and why things happen the way they do without knowing how to express themselves. Now take that and throw the “cancer life” on top of that. Try having an almost
And then the new normals as a parent… No parent should have to turn a deaf ear when their child wakes up screaming and crying for 30 minutes wanting milk, but can’t because she isn’t allowed to eat and drink this morning due to scans. No parent should have to be thankful that their child’s white blood cell count is good enough to go to a fundraiser to benefit them. No parent should have to sit in the waiting area at the hospital just scrolling through their phone, hoping to make the minutes of waiting not seem like hours…..even though they still do. No parent should have to sit in a post-op area just thankful to have their child back in their arms as they wake up from anesthesia, even though they are fussy with a scratchy throat because they had to have a breathing tube during their MRI. No parent should have to be extremely thankful that they don’t have to ride on the CT scan table with their child this time. No parent should have to pray endlessly for the best possible results from scans that determine future surgery and radiation, but they will not get results until Thursday. No parent should have to be so thankful for their child returning back to their “crazy” toddler self just hours after all of this.
No parent should have to ever do any of this, but this is what has become our new normals. No parent should have to we know that there are others out there that haven’t had days as good as ours along their journey.”
The Necessary Evils of Childhood Cancer…
“The toll chemo drugs
On average Merritt has had a fairly smooth treatment process with little sickness. This day during Chemo week 20 brought vomit and many tears over port access. Imagine physically holding your child down screaming & crying “Daddy Move” while nurses are trying to access the port for chemo. Many parents can explain to you about the heart breaking moments involved in getting their child to comply with their cancer team. The memories of pinning them down will never fade.
The Juggling Act
“Family, work, life and cancer… juggling everything is exhausting. I am lucky enough to be able to have a work place that is willing to work with me and allows me to be with Merritt at every single treatment and any specific day that is affected by her treatment. But it is hard to go to work on days that are not affected by it because no matter what… Merritt is always in the forefront of my mind no matter what I am doing.
We are good about going with the flow and taking things as they come but not having control of your life and a lot of what you are able to do is hard. Your entire life revolves around numbers like hemoglobin and ANC and things like constant sickness for weeks at a time. So just having to see that controlling Merritt’s life and what she can and cannot do would have to be the hardest part.
Chemo days are the days that the average person doesn’t realize that even when the chemo Merritt receives only lasts for 1 hour that day… it still makes it a 6 hour day round trip from the time we leave the house until the time we get home…and some days the chemo itself lasts for 7-8 hours when we get to clinic at 8 am and are leaving around 4. Non Chemo days I work usually 10 hour days. I luckily work local, 12 minutes from our house, so if I were needed for anything I could be there fairly quickly. I usually get off work around 3:30 or 4:00. When I get home I first spend a little time with Merritt before taking care of things around the house like mowing the yard, changing the oil in a vehicle, or a long list of other things needing to be done. I then come in and fix dinner. I like to do this because I know even though I have worked all day, taking care of Merritt can be just as much if not more tiring for my wife. We then eat dinner and then usually play outside with Merritt before going to bed.”
“When you turn on the news, open the newspaper, or read through your social media you see a lot of negative in the world today… but there are still A LOT of good people in the world. The number of people that we don’t even know that recognize what Merritt is going through and they do what they can do or what they are led to do to show their support for her and us. Whether its an encouraging word or letting us know they are praying for us or anonymously paying our bill at a restaurant. Even just now, 175 miles away from home sitting in a restaurant eating breakfast and the waitress comes up and tells us that someone has taken care of our bill. It is very humbling to know that there are so many good and caring people out there that just want to help in any way that they can. I am so thankful not for the fact that my daughter has cancer but for the fact that we do have Merritt here with us. We are able to fight with her to beat this because we know there is a reason for everything and we are seeing this make differences in the lives of others.”
Dear Merritt… aka Fuzzy,
I love you more than anything and everything on this Earth. I will never forget that first time that I laid eyes on you and got to hold you in my arms. That was the best feeling ever. It was at that point on that Friday afternoon on September 8,
Love always and forever,
If you are a dad reading this and your child has cancer, we applaud you. It is so hard to do what you do to stay strong for your family. Thank you to Merritt’s dad for giving us a glimpse into being a daddy, husband, and provider while helping his daughter fight for no more cancer. This is childhood cancer. Are you aware now?
Photos courtesy of Aaron Plummer. You can follow Merrit’s journey with
*** THROUGH MY EYES: THIS IS CHILDHOOD CANCER