Today was Leah's big 1-year appointment. This was the big one, where she would have the full brain-spine MRI and kidney/bladder studies and go to SB clinic to see all her doctors. Unfortunately she has a little cough and runny nose, so we had to cancel the MRI but we did everything else. We canceled the MRI because she would have to be put under general anesthesia, since it is a 2-hour procedure and it's virtually impossible to expect a 1-year old to lay still for that long. We'll go back in about a month for the MRI.
This morning we started out in Radiology for an ultrasound first and then a test to check the overall health of her kidneys. We did a kidney and bladder ultrasound to make sure they still look healthy. Then she had another test where the technician inserted a catheter, filled her bladder, and checked to see if there was any reflux back into her kidneys. They also wanted to see how much of that liquid she was able to void on her own. After those 2 tests, we had a bit of a break before we needed to go to clinic, so we grabbed some lunch in the hospital cafeteria. As we were finishing our lunch, we saw a little girl, about 2 years old, roll by us in her little wheelchair. She also had braces on her legs, so we decided to stop by and chat with her mom. As it turns, out she does have SB too and they were also there for clinic. The mom (who I "know" from the SB parents' facebook page) told us about the wheelchair and how they started the process to get her daughter into it. It was really nice meeting yet another family!
After lunch we headed to SB clinic where we were to meet with our nephrologist (kidney doctor, SB doctor and rehab doctor. First, the nephrologist came in and gave us the good news that Leah's kidneys are perfect. Yay! We are so fortunate that we still don't need to cath her, and that she's able to go on her own. Once we're ready for her to get out of diapers, we'll need to figure out a bathroom management program, but it's very nice not having to think about that right now.
Then Dr. Marker, our SB doctor, came in. He hadn't seen us since Leah's shunt revision last month and he was really happy with how she looked. We talked about how mobile she's becoming - lots of crawling and rolling in her zip-zac. He was fiddling around with her feet and asking us whether she's in any kind of standing equipment, which she is not. So he told us that it's about time for her to get into braces and get a stander. And that she could get fitted for them today! We were really excited!! Our SB clinic shares the office space with an orthotics company, so someone came in and took casts of her feet to custom-make her Ankle-Foot-Orthotics (AFO's), which will be ready in a few weeks. She'll also get us the stander. Since she does not have feeling or movement in her legs, it is very important for her to start bearing weight on her legs and feet. She needs that to get used to standing if she wants to walk, but more importantly getting up on her legs is necessary for growth and development of her bones and muscles.
The final doctor to come in was the rehab doctor, who confirmed that she does need to have orthotics and supported the AFO's and stander. She also recommended us to Sister Kenny, a rehabilitation center connected to Children's and Abbott, for "wheelchair school." Basically we go there to get information on all the different wheelchair options we have for her and they can help us decide what's right for Leah now and as she grows. This is a good option, as they are independent of any wheelchair vendors who have a vested interest in us buying their product. The process to get a chair can be very lengthy so it's good to start now. She will grow out of her zip-zac before we know it and we want her to keep up with kids her age, both in mobility and getting up a little higher to be more at eye level with her peers. The family we saw today in the cafeteria waited 6 months to get their chair, so it's not something that just happens overnight.
So that was our very exciting day! I cannot believe she's going to get braces soon and that she'll be starting the process for standing and walking. Just in the last 2 weeks she's gotten so much more mobile. She is army crawling all over and is even starting to get to things we don't want her to touch, like outlets and the fireplace. Ty and I keep looking at each other and saying how amazing it is that she's learning how to get where she wants to go. Leah amazes us constantly.