Max was born with wonky feet that curled into one another. At the time, we thought they would naturally correct themselves as the baby scrunch started to disappear. And in some ways, they did. I look at pictures of the first year, and they don’t look too bad.
When he was two and half, he was fitted for his first set of
SMOs to provide him with additional stability.
We quickly upgraded to AFOs that went up to his knees. Although they seemed to help him with standing,
he always seemed to be fighting us to both put them on and to wear them. (Yes, he looks happy in the pictures - I rarely take pictures of my children angrily screaming at me)
During this time, he also started to lose his hearing (leading to the dreadful cochlear implant surgery)….and he constantly struggled with feeding issues (leading to us transition to a labor-intensive blended diet)….and he started to suffer from adrenal failure and you get the point – somewhere along the way, the braces were deprioritized. We still would put them on and try and work on standing and taking steps, but honestly we were fighting battles on a LOT of fronts and his feet just didn’t get the attention they probably deserved.
Then, the seizures started and it was clear that the
neurological issues were causing damage throughout his body, particularly in
causing his feet to become even more pointed and stiff, so much so that his
AFOs eventually no longer fit and the physical therapist advised that it was no
longer safe for him to be weight bearing even with a sizable wedge to support
his feet.
During the summer of 2022, we went to the GFPD conference where we had a
conversation with a physical therapist.
I was complaining about lifting him and she laid out what the next few
years would look like if we weren’t able to use his feet for a load bearing transfer
i.e. if we had to fully lift him every time we wanted to move him. He is only getting bigger and soon our house
would need to be a series of lifts and transfer systems. It was clear – we needed to prioritize getting him back to
weight-bearing on his feet.
Our first step was to meet with his physiatrist at Lurie’s Childrens Hospital in Chicago who proposed a series of casting in which he would get fitted for a new cast every 2 weeks. These casts would move and adjust his feet with each iteration and hopefully slowly get Max's feet back to a typical 90°/0° angle.
Because the casts are permanent, Max would no longer be able to take baths or go swimming (his faves). They also discussed surgery in which they would need to remove a portion of the bone in his foot – and then more casting. Because his feet were so severely impacted, there was a good chance that the casts would not be as stable and could shift on his legs/feet. If that were to happen, we would have to go to the emergency room immediately to have the casts sawed off.
“Don’t worry” they told me, if the process doesn’t work, they will just “amputate his feet.” ("and that made me want to diiiieeeee..." sung in the voice of Taylor Swift). Needless to say, the whole process was extremely anxiety inducing. I would just lay awake at night wondering how we would get through it and blaming myself for letting it come to this (would it be my fault if Max had to have his feet removed?!?)
While we waited for our turn (the waitlist for the casting program
was intense), we went and saw his neurologist.
As I laid out my hesitations, she advised us to visit with Dr. Pavone at
Marianjoy Rehabilitation Hospital for a 2nd opinion.
When we met with Dr. Pavone, she suggested that perhaps we
could do removable casts. Same process as at Lurie's, but we would be able to remove the casts for baths,
swimming, and even if Max was just having a bad day. Todd and I figured it was worth a try – if it
didn’t work, we could always try the more intensive program at Lurie’s. Plus, she had never mentioned amputating Max’s
feet, which I greatly appreciated.
We started the process in September and we are currently on our 6th set of casts and I can’t believe the results. We’ve gone from -45° to -20° on the right foot and -60° to -28° on the left foot, plus the curvature in the feet has also been partially corrected. In fact, the results have been so incredible that Max is now once again able to stand in a stander with the assistance of the braces and a wedge for the first time in 3 years. His teachers couldn’t believe how tall he’s gotten! We plan to continue the process as long as we’re still seeing results.
It feels truly like a Christmas miracle and we are so
continuously grateful for the knowledge and kindness of the staff of Marianjoy,
Dr. Pavone, and his physical therapist, Trinette .
Personally, I’m equally grateful for my husband who has handled
the majority of the process from the appointment scheduling, to making sure the
braces are on correctly each and every day, to doing a few of the appointments
solo due to my work commitments. He has
been an absolute champ and truly deserves all the credit!
As a final fun note, the results have been so strong that
Dr. Pavone is planning to feature Max in her upcoming publication about the process
and program!
Cheers to progress and 2nd opinions! We hope 2024 brings each of you joy, happiness, and hope in the new year!
No comments:
Post a Comment