
Olivia is doing really well. She loves school and giggles as soon as we turn around the corner to onto the street of her school. One of the kids in Olivia's class moved up to the elementary school class so now there are a total of 4 kids in her class. They have a great teacher and a fantastic aide. Olivia is making progress towards her IEP goals.

Here are some of the notes from her latest quarterly IEP report: "Olivia is using signs and PECS to express when she is hungry and thursty during meal times; more comfortable moving around the classroom and playground; she can point and match well and her receptive understanding of directions is improving".
I was able to help with one of their recent fieldrips and we had a blast! The class had an installation on display at the New Orleans Museum of Art so the whole school took a field trip to the art museum and then had a picnic lunch and some play time at the park. It was such a great experience to hang out with such amazing kids and teachers. All the kids in Olivia's school have some sort of special or unique challenge so we were a pretty unique group. I am so glad that I was able to go! At the museum Olivia showed off some of he stair climbing skills. We've definately worked hard on this so it was really exciting to see her doing so well in such a new environment. We have also decided to resume ABA therapy and finally found an ABA therapist and completed all the paperwork and initial evalations and Olivia will begin ABA therapy next week.
Showing off her stair-climbing-skills:

We are continuing to love the civilian healthcare system! It still seems like such a luxury to be able to call the doctor's office, speak to a real person and schedule a same day appointment in less than 5 minutes! Olivia has had a case of pink eye and a sinus infection but other than that she's been pretty healthy since the move. Olivia also saw a pulminologist earlier this month.

This was the very first time she's ever seen an actual pulminologist. Olivia has been on pulmicort and xopenex for about 2 1/2 years. We raised some cocerns about this with her doctor at Ft. Bragg about a year ago but those concerns were dismissed. The pulminologist has decided that we should stop the brathing treatments and see if we notice a difference. It still feels very strange to not have the 20 minute nebulizer treatments as a part of our morning and evening routine. We have had to use Olivia's inhaler a couple of times and we're looking forward to our next appointment with the pulmonologist next month.
Olivia is playing with toys more and interacting with Peter more. We're seeing new apects of her personality emerege. We've learned that Olivia loves the tuna fish at Subway. She recently started paying attention to tv and movies, Olivia will sit an watch about 10 minutes of a favorite movie or Micky Mouse Clubhouse episode. In the mornings Olivia wakes up when she hears me making coffee but I'll bring her milk and she'll continue to stay cuddled in her bed with her toys until it's time to get dressed. Olivia has started to say a few words again. She says "mamma" pretty consistantly and has added "dadda" over the last couple of weeks. She will also say and sign "eat" and will imitate words more often. She definately likes vocalazing and is quick to let us know when there is something she wants or needs.
Olivia also loves to jump! For christmas my parents gave Olivia a trampoline and jumping on her trampoline has become one of her favorite activities!












