Today we had a routine checkup for Joshua with his Doctor at the Hospital.
Before every appointment, he gets weighed and measured by the nurses.
Today, for the first time, his height was done standing up instead of laying down using the device that babies get measured with :) That is because today is the first time he could stand up well enough! He was 87cm tall, which is just over the 20th Percentile, and he weighed about 11.8kg, which is just below the 15th Percentile. Which is great.
Today, we had a student doctor along with our normal doctor, and we got to start the appointment with the student doctor. The Student Doctor was actually a trained physiotherapist, so she did know stuff about stuff (Ha!) and have experience with children with Cerebral Palsy. She did a full check up on him, checking his chest and ears and throat and all the rest, and she also took his head circumference. She got 43.3cm. I think at last measure, I got about 44.4cm. I know my fellow Mum's of children with Microcephaly will be laughing at that, because we have it down to a fine art when it comes to positioning the tape measure to get the true maximum head circumference (Which is how it is supposed to be done) but health professionals often just slap it on and get a reading without particular care for trying to get the biggest possible measurement... and hey... every millimetre for our kids counts!! LOL So yes, either way, his head is still small.
So the particularly great thing about this appointment was that Joshua was able to debut his solo walking to his Doctor. His Doctor was of course, thrilled to see it. He has told me many times that Joshua is doing so much better than expected and he said it again today. That for the severity of the insult to his brain that Joshua suffered as a baby, he would never have imagined that he would be seeing him like this. I told him "well there you go, when you see babies like that, don't doubt them!" Hah! He says he although he doesn't see a lot of children like Joshua, Joshua is the first one he has ever seen "get better" over time, that every other child he has seen has either gotten worse or just stayed stable. He asked me if there was anything in particular that we have done over the last 6 months or so that has contributed to Joshua's great gains and I said No, honestly, it is just him and the fact that he wants to do things. That is the truth. I know it would sound great to say it was due to a lot of hard work on my part, or that we'd found a magical therapy that has amazing results, but we haven't. We've only ever done conventional therapies like Physiotherapy and Occupational Therapy and compared to a lot of parents, I think my focus on "therapy" is a lot less, this is all Joshua. He woke up one day and decided he wanted to walk. He walked with his walker for 6 months and then took his first independent steps when he felt like it. He is doing great with his walking. He still falls a lot, and still crawls as well, but he is doing a lot of walking around the house and I don't take his walker to day care anymore either. We have been taking a break from day time AFOs since he started walking independently but I think we need to get back into using them, at least on the right foot, as it does do a lot of silly things still. The left leg is not too bad.
So they still think that Joshua is a Level 3 on the Gross Motor Function Classification System (GMFCS). I am not sure how much I have talked about that in the past, it is basically a grading system that grades the severity of the impact of a person's Cerebral Palsy. 1 being Mild and 5 being Severe. So they are still grading Joshua as Moderate. I said now that he is starting to walk on his own do you think he is moving more towards a level 2, but she wouldn't say that, but she did say that it is not fixed. Honestly, there is not really any doubt in my mind that he will end up a lesser level. I think he will end up at most a 2. This is the levels for 2-4 year olds: