Hi all! Well, we took a day trip to Lynchburg, VA with our Robug. We went to see Dr. Mumper at the Rimand Center, (www.rimlandcenter.com) where we were hoping to get lots of encouragement and hope for treating Rowan and helping him come out of his fog. We were not disappointed! Here's a summary of the day:
We got up at 6, ate breakfast, and got on the road. Thanks Deb and Ed for letting us borrow your car, it was such a blessing! A very smoothe drive. It took us 3.5 hours to get there, but there was a suprising amount of grace on the trip. Rowan barely whined at all and we only had to use the DVD player for less than half the trip. Joel and I had some excellent conversation and quality time. I love car trips but only for that reason. Most of the time, travelling with young children doesn't feel worth it unless there's some good conversation!
We got there around 10:30 and had to wait 40 minutes to get in, but that was fine, because they have a little pond and a playground out back that we enjoyed until it was our turn. When we met with Dr. Mumper, she got to spend some time with Ro and see what she thought we might need to do next. She then ordered some tests to be done to specifically tailor his treatment plan to his particular needs. That was so great to hear! She doesn't want to just do general treatments that 'most kids on the spectrum respond to' but rather find out exactly how his body is working, what vitamins he needs, etc, and then work on that so that we are sure to see results. So coming up, we'll be doing urine, stool, and blood tests, and hopefully sometime next month we'll find out the results. Our prayers right now are that the tests would clearly point out what we need to fix and that it will be obvious and quick and easy.
Very exciting! It was well worth the 8 hours in the car. My friend Danni watched Bella all day and Ashton, my sweet housemate, watched Asher until we got home, which was around 5. All in all, a great trip that renewed our hope again that Rowan can come out of this.
That evening, we had a family dinner at Ben and Bek's house, with the added bonus of Deb and Ed being there to enjoy italien sausage that they brought from Oswego. So good! After that, we all hung out here at our house for ice cream and good talks, until Joel and I crashed around 9:30 and had to go to bed. Man, i remember the days when i could stay up until 1:30 AM and still get up early and not be dead the next day. Those days are just memories now. :-)
On another note, last week Rowan had his screening with the school district to see if he qualified for special needs pre-school services. Good news! he does! Rowan will be starting pre-school next month for 3 hours a day, 4 days a week, about 1/2 mile from our home! What a blessing. I'm excited for him to be with other kids his age.
I love the Lord! I love that He is going to heal my son, and even though most days I dont want to admit it, I am glad that He is working on my heart, even if it feels like He's killing me.
:-)
Love to all,
Jenn
5 comments:
so proud of you Jenn! You get more amazing every day!
Excellent news about the dr. visit, and the preschool program. Is that at Springfield, or the new Sugar Creek school? D has thrived in Spec. ed class @ Springfield.
lauren: thanks! Love you
robert: I wondered which school daniel went to! (it's daniel, right?) I think the one Ro is going to go to is Sugar Creek. If the class sizes are smaller at Springfield I may ask to switch. we shall see!
The same principal that has been at Springfield the past 3 yrs is the new principal at Sugar Creek - Scott Frateroli. Great guy. I'm sure he's assembling an excellent Spec. Ed dept. there. Daniel's special ed teacher for the past 3 yrs is staying at Springfield - thus his remaining there. We've worked hard to get an IEP that gives the resources he needs. As long as they do the IEP, either school would be fine. You have a nice, short commute w/ Rowan next year!
http://www.youtube.com/watch?v=KSwhpF9iJSs
This sounds really promising Jenn. You should check it out.
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