Ava’s Story

Site created on May 3, 2019

Added 5/24/19: Many have asked how they can help support Ava through this process, please go to https://www.gofundme.com/acwzn8-cancer-sucks if you would like to make a donation as donations through CaringBridge do not go to the family.

Greetings friends and family, we want to start by expressing our gratitude for the outpouring of love and support we have received in the wake of Ava's diagnosis. Your well wishes, prayers, words of encouragement, good vibes, etc. have been greatly appreciated.

We have decided to use CaringBridge as our platform to keep everyone updated in one place. Please feel free to share this page with others that are wanting to be kept informed of Ava's progress.

Here is a summary of what has transpired thus far and as we learn more and move forward we will post updates.

In early March Ava began expressing that her left leg hurt. The pain started in her lower leg so we would rub it and she would fall asleep. Initially it appeared to be a typical ache that could be experienced during a growth spurt (aka "growing pains"). However, by early March the pain moved to Ava's knee, the pain started to wake her up at night and she began to limp. We made an appointment to get it checked out and on 4.19.19 she received an x-ray which showed inflammation. Due to finding so much inflammation it was recommended for blood work to be done and from those results it was decided to do an MRI. On 4.23.19 we had an MRI done and that is when they found a bone tumor above her left knee and referred us to the U of M for a biopsy and to Children's Hospital to work with a team of specialists.

On 4.24.19 we headed to the cities, Ava was a total trooper as we drove her around to various clinics for multiple appointments. We headed back again on 4.25.19 for the biopsy which was nerve racking as they had to give her anesthesia and then literally drill into her leg. After the biopsy she needed to lay low for several days and she is supposed to be minimally weight-bearing, using crutches, for 6-8 weeks in order to let her leg heal from the procedure.

On 5.2.19 we were informed that Ava has osteosarcoma, a rare bone cancer. They have not staged the cancer yet and we do not know if it has metastasized. Next week we go in for more tests and to begin treatment. Here is the treatment plan as of now:
-There will be an outpatient surgery to place a port in her chest in order to administer chemotherapy
-She will likely have 4-6 chemotherapy treatments in order to reduce the size of the tumor
-They will then do a surgery to remove the tumor and will use bone graft and/or prosthesis to rebuild any bone/tendons/etc. that had to be removed as well
-She will then have additional chemotherapy treatments

At this point we are trying to maintain as much normalcy as possible so that Ava is not fearful of the future. Ava knows that she has cancer but does not understand what all is to come and therefore we are going to take it one day, and one side effect, at a time. Right now we are working on managing pain while still playing, laughing and enjoying our time together!

Once again, from the bottom of our hearts, thank you for your support of our family and your interest in following this journey we have embarked on.

Much love,
The Pattschull Family

Newest Update

Journal entry by Amber Pattschull

I know many of you have been wondering how Ava is doing. 


First of all, I want to apologize that it’s taken me this long to post, you see I’m normally a positive person doing my best to change my perspective in bad situations. However, until recently I have always viewed 2019 as a negative time in our lives. It’s been hard for me think, talk let alone look at photos during that time without becoming a puddle of tears. It wasn’t until yesterday sitting with my sister, opening up about my feelings regarding that time of our lives that we don’t talk about, I received a text from a dear friend about how her mom donated money in Ava’s honor, even though she herself is going through her own challenges. It’s like the universe was talking to me. My sister made me realize how Ava’s story actually inspires people. It’s crazy how one can go through something so tragic, battle the shit out of it, WIN and touch so many lives, even those she has never met. 


So It’s time shift my perspective, our perspective! Ava did it! She beat Cancer 💛 she is a survivor and not everyone’s cancer journey ends the way Ava’s did. Ava is still writing her story. 


Since my last post; Ava has had Many doc visits. They were every three months, then moved to every four months. Hopefully this year we can space them out even further.  Her scans continue to be clear of cancer, thank the lord. All her other tests keep coming back with no changes, except for hear hearing. Her high pitch earring loss continues to decline little by little, this is the side effect from the chemo but it’s nothing significant to be alarmed with. Plus, she has also graduated from physical therapy, meaning no longer needs to go. 


In the fall; Ava did end up getting surgery to remove her growth plates. As she continues to grow with uneven leg length; this surgery removed two growth plates in her right leg and one good growth plate in her left leg. By having the surgery it should stop the abnormal growth in her leg and the hope is that with the growth plates she has left, this will reduce the difference she has now. It takes about a year to even know if the surgery was a success as you have to wait for growth spurts. For now she wears a heel lift to help with the difference in length to reduce any hip and back pain. 


Other than that; Ava is a normal 11 year old, in 5th grade, loving school, always hanging out in her room, listening to music, making up dances to her favorite songs, and talking on the phone forever with her friends. She’s growing up so fast it’s almost like she’s a teenager without being a teenager, yet. She continues to be this bright shining light that doesn’t let anything get her down, always looking at the good in people and the love for everyone and everything around her just pours out of her. 


From the bottom of my heart thank you all for the support that you’ve gave my family during, after and your continued support. 


Much love ❤️ 

The Pattschull’s 

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