Mike and Ian hanging out on the
Tuesday, August 26, 2008
Camping on the Olympic Peninsula
Mike and Ian hanging out on the
Thursday, August 21, 2008
Will's day with the doctors.
We started the day with two neuromuscular specialists. I have never seen anyone examine William like these doctors. We were there for an hour and a half! At the end of the visit they didn't have much new information, but did order some blood work. As far as I know we are looking at William's thyroid and for a couple of disorders that cause muscle degeneration. I don't think that anyone feels like these are likely problems, just more of the "ruling it out" tests.
From there we saw an occupational therapist who watched Will eat his lunch. She felt great about Will's eating. He is doing a really good job of feeding himself and isn't showing any food aversions (which originally they were a bit concerned about). She does not need to see Will again.
Then to the nutritionist. Will gained a lot of weight! He still isn't on the chart, but the trajectory of his weight gain shows catch-up weight gain which is what we want to see. If he continues at this pace we will be on the chart very soon. This was by far the best news of the day. The nutritionist also said she didn't need to see Will again.
Our last appointment was with the developmental PA. She mostly just followed up with all of our other appointments. She was also pleased with William's progress and thought that his pulling up was quite an accomplishment. We finished with a blood draw (harder on me than William) and that finished out a very long day.
William will be visiting the geneticist in September and we are also scheduled to have a swallow study done (he is choking/gagging more than normal when he eats) and an appointment with the audiologist to check his hearing. We've been having some ear infection issues since about March which is common with kids that have hypotonia. We just want to make sure that it isn't affecting his hearing.
So, that was Will's very long day. This is how he coped...
Wednesday, August 20, 2008
Boys at play (in a messy house)
For anyone who is keeping count, I TRY to take pictures of Ian, but he usually insists on trying to see the picture before I've finished taking the picture. As a result I mostly have blurry shots of him running for the camera -- these digital age kids! :)



I thought that Will was ready to transition to one nap a day, but apparently not. He fell asleep in the exersaucer while I was fixing his lunch. We're back to two naps...
Saturday, August 9, 2008
Tacoma Tall Ships Festival
Ian and I also built a boat with glue and and felt and a paper sail. It was pretty popular all the way home and now the surviving pieces are residing in our garage. Oh well, it was fun while it lasted.
Of course the best part was the fair food. You have to love anything that comes on a stick. I think this might have marked when William decided that he did like food. Perhaps it was the chocolate crepe? We had a pretty good day seeing Tacoma and the ships. The highlight for Ian was the trains accross the street from the festival. In fact, as we crossed over the bridge an Amtrak train went right under us and the engineer waved at Ian. That pretty much made everyone's day.
Thursday, August 7, 2008
Brotherly Love

I just love this picture. During the chaos of moving it was as if the boys were saying "hey, we got each other at least." Now we're back to an SUV where they can't reach each other which most days is a good thing. Yesterday the most meaningful interaction between the two of them was Ian hitting William in the head with a toy vacuum. I'm sure it was an accident...I think.
Our current news on William. He has learned to sit up by himself! This is a big, big step that I'm sorry our therapist back in Wayne missed. And, as we speak he is getting on his hands and knees...hopefully we'll see some four point crawling soon. Despite his delays, he is getting all over the house in an army crawl and is a busy, busy little guy. We are finally getting him enrolled in the Kindering Center here where he will get his therapy. He did great during his evaluation and it seems that all of his delays are still just gross motor. The special educator and speech therapist said he was still in the normal range for everything else. We are so happy with this news since we have spent lots of time worrying that perhaps he might have other delays as well. Now we're just trying to get him to EAT and hopefully walk and maybe someday we'll put all this behind us. After so much testing and worrying, I'm starting to feel like perhaps there is a light at the end of the tunnel.
Ian is doing well. He keeps us on our toes, but seems to be settling into his new house. I think before the furniture arrived he thought this was some sort of weird vacation. He kept asking to go home! I guess now that his toys and bed are here he has it figured out. Now if we can just get the hang of this potty training thing...
Wednesday, August 6, 2008
Fun at the Oregon Coast...
Here we go...
We hope that now our friends and family will have an easy way to keep up with us now that we've ventured to the other coast. We'll try to keep this current with pictures of the boys and updates on what we're all up to. Enjoy...