Friday, February 26, 2010

TGIF!!!!

This week we....



  • Had 2 Speech therapy sessions
  • Had 1 Occupational therapy session
  • Had our first official school session
  • Learned that Olivia and Peter can crawl onto the kitchen table by themselves
  • Stayed up too late watching the Olympics
  • Finished and filled our 2009 Tax Return
  • Interviewed 2 babysitters
  • Had 2 Physical therapy sessions
  • Sold some old stuff on Craigslist
  • Ruined the netbook by dumping coffee on it
  • Went to cheer on Mike as he participated in an wrestling tournament
  • Spent 2 hours on hold with the insurance company
  • Did NOT have to drive to Duke on Wednesday
  • Cleaned the house too many times to count!
  • Had some great phone conversations with good friends that I don't talk to nearly enough

I'm so glad this week is over. We don't have big plans for the weekend but I'm ready for a break!

Thursday, February 25, 2010

Wednesday WITHOUT Clinic

Yesterday marked the first Wednesday since September that we did not have to go to clinic. We had a pretty great time just hanging around the house. The kids both slept in until after 9am (that in and of itself is a miracle). We made cupcakes, I did laundry. Peter gathered the remote controls and phones from all over the house and put them in the tub in the master bathroom and then turned the water on. I got there just in time and we were able to rescue them all from a watery death. The netbook was not so lucky. I dumped my cup of coffee on it and it's dead. It turns out that Wednesday afternoons are pretty nice, Mike gets off early on Wednesdays and he got home before 5pm! We're not due in clinic until next Wednesday and I'm realy hoping that this is the beginning of a transition to clinic every other week instead of every week.

Wednesday, February 24, 2010

Visiting Daddy at Work

Last week we got to stop by Mike's office and have lunch with him. The kids loved seeing his office. Both Olivia and Peter were excited to see so many people in uniform. When we got out of the car Olivia ran straight toward the legs of a complete stranger for a hug. I guess she saw the uniform and was sure it was Daddy before she saw the face. Fortunately I got there just in time. Once we got into Mike's office I was not quick enough to stop Peter from walking right over to another soldier in uniform and trying to climb into his lap. Fortunately he had kids of his own and he was completely happy to let Peter sit on his lap for a bit. I think that is one of the bittersweet aspects of military life. When Mike is deployed I hate seeing all the other guys around in uniform, it is a constant visual reminder that my husband was gone. Now that my kids are old enough to recognize that familiar uniform I have a different perspective. That uniform symbolizes Daddy and it brings them comfort even if it's worn by someone else's Daddy.


Monday, February 22, 2010

Emotional Upload

I've been so emotional the last couple of days. I hope that today's post will give me a chance to unload a bit.

Peter has reached that sweet spot where everything starts to click together in his little head. All of a sudden he seems like such a big boy. He is so coordinated. He is gaining new skills overnight. He's still not talking much but he is making more animal noises. I'm happy for him. However watching him make these developmental milestones is heart wrenching. I had heard from doctors/therapists/other parents that one day there would come a point in time where kids just start putting everything together. That moment never came with Olivia, but we're living in it right now with Peter. I'm watching Olivia struggle to regain the same skills that Peter is just magically able to do. It's painful.

Olivia seems to be feeling a lot better physically but I have no idea where she is cognitively. Now that she's moving around and feeling better she's spending more time wondering around getting into stuff. I'm noticing how short her attention span is. She's not playing with her toys appropriately anymore. She really seemed to be able to focus on an activity more when she wasn't feeling well. In the hospital she loved to color, paint, and do puzzles and she hasn't been interested in any of that stuff for months. Over the last week she has become obsessed with chewing things. Often kids with Sanfilippo syndrome have a compulsive need to chew. Up until this point we hadn't really noticed that with Olivia but this last week has been awful. She's putting everything in her mouth, and if she can't find something else to put in her mouth she will stick a finger or two in her mouth. It's awful. She has moments of brilliance followed by moments that are not so brilliant.

Of course Peter's going through his intellectual growth spurt as Olivia is having a rough week. I had a great conversation with Olivia's occupational therapist today. She noticed the difference in Olivia's chewing right away and asked about it. At the end of Olivia's therapy session we had a conversation about how God has a plan for each child. We were both in tears but it was a good conversation. I don't know what God's plan is for Olivia but it is comforting to know that one exists.

It was a really long day here, one of many over the last week. I need to find a babysitter that can provide some respite care but I've not been able to find one yet. I've tried care.com and sittercity, I'd love any suggestions!

At least the day ended well. Mike and I were talking in the kitchen when Olivia walked between us and said "poo poo" and then proceeded to pull down her pants and pop a squat on the floor right between us. Mike jumped quickly into action and she got to the potty in time to make a successful deposit. I know this might not normally be cause for celebration but I'm so glad that she is able to get her pants and pull-up off by herself now, not to mention the verbalization of her need to potty.