She was able to use it a little earlier today and was more open to using it when some friends stopped by. She'll have speech therapy on Monday and we'll be able to personalize it even more. We'll be able to put in pages and words that are specific to her. Very exciting!
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So we're sending it back to get the silver color she wanted. I was tempted for a couple minutes to just keep the pink one. But one more week of waiting is probably better than looking at really ugly pink for years and years on end.
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Rachel is now vaccinated against H1N1. Whew!
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Blue Cross approved her Dynavox but MA denied it. Now that we have the denial we can go ahead with everything and finally have it sent! It should be about a week but at the longest it could be a couple more.
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Rachel was approved for her Dynavox! She should have it within a month. We've been working on this for at least two years, it's so great that it's finally happening. Rachel regaining the ability to express herself is going to be incredible.
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Rachel turns 6 today! Happy Birthday Rach!
(We should also be finding out if she's approved for her Eyemax system anywhere from now up until another 4 weeks.)
Update: Luke's been trying to ask Rachel what she wants for her birthday. After blinking "No" for everything he jokingly asked her if she wanted a rock. She blinked "Yes".
"Do you want me to paint it?" he asked.
"No" she blinked.
"So you want a dirty old rock out of the garden for your birthday."
"Yes" she blinked.
Sigh.
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Rachel's completely free for the summer. She has a break from therapy and school for a few months. For the first time in four years Rachel is without schedule.
She still seems to be fighting some illness. Once her antibiotics started working with the last illness she was doing great but now she seems to have just a cold but she's been adding a fever to the mix every once in a while just to confuse us.
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Rachel's been having a harder time with her seizures the last two days. She's on a new med that's making her liver worked harder so she processed her dilatin too fast and her levels were way too low. They drew up a lot of blood work yesterday and we should find out the results and med changes today.
I'm also not sure if it's allergies but she's extremely gunky and sneezy even with her allergy med. Last night she spiked a really high temp and barely slept a wink. Not sure what's going on if it's just a bunch of little things all together or if there's something bigger going on but keep her in your prayers today. Thanks!
On a better note, the paperwork for her Dynavox is going to be submitted this week and we'll find out in 6-8 weeks if she gets one.
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Today Rachel was amazing with her Dynavox!!! She has one for a 30 day trial. When she first got to school she went through each of her eight friends and said "Hi" to each of them, using their names that Wendy had put into the computer the night before. Then one of the students said, "Hey! Rachel's talking!" and so they all ran over to her. She went through the screens and said, "Mine, back off" So all of the kids backed up. Then she said, "Look, don't touch." Later Wendy had turned away and she heard Rachel say, "Hi Jordan" and when she turned back around Jordan was the only one standing there. There aren't any pictures of the kids on the screen so that means she was able to read his name and could tell the difference between his name and the names of the other students.
Then they had circle time and her teacher asked for words that started with an H. Rachel started flipping through through the screens quickly and then found 'helicopter'. Later when she had a seizure she said, "That stinks." We're so excited she's finally able to express herself!
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A couple of weeks ago Rachel lost her two front teeth. We also have added a new seizure med to try for four months and if she reacts ok then we'll slowly wean her off of her dilatin. If she's able to be off of dilatin then she won't have to put up with some of the side effects such as larger gums. With the addition of the new med we've been noticing stronger seizures but it might be following her trend of having fewer and fewer seizures but the couple that she does have are stronger. That's just with the addition of the new med and we haven't started reducing the dilatin at all yet. So we'll see how it goes and hopefully it works.
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Rachel's feeling much better but she's a little crabby now. I think she wants to go back to school. Although we did send her to therapy we're letting her recover even more before we send her back to school.
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Her fevers are definitely gone and she's not working so hard to breathe. It's now more like a really, really bad cold. Luke asked her yesterday if she could breathe better and she blinked yes. Thanks for your prayers everyone, she's still not doing great but at least we can see that she's slowly getting better.
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Rachel's been sleeping for almost the entire last 24 hours. We have antibiotics in case it is bacterial and neb treatments to help her get the gunk out of her lungs. So now we have everything at home that the hospital would have done for her and we're feeling a lot better about it now that a Dr. has checked in on her quite a few times. Please keep praying, she seems happier to be home but still has to work hard each time she exhales.
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Rachel's in the hospital with something repiratory and viral. Could just be a really bad cold but with Rachel it's that much harder for her.
We're still all trying to decide if she can go home or not because she still has to work so hard when she's breathing. I'll try to update soon but so far it looks as if we'll stay another night. Keep her in your prayers. Thanks!
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Not sure how it got past the filters but a bunch of spam started building up in the comments. Rachel seems to be doing a little better.
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