Showing posts with label medical. Show all posts
Showing posts with label medical. Show all posts

November 5, 2008

Ophthalmology today

We had a 4+ hour visit with Hannah's new ophthalmologist today. I like Dr. Carothers, and so did Hannah. He was very thorough, as was his assistant. The good news is that her cataracts are stable and have not grown! There were some concerns as to whether Hannah was showing some latent amblyopia, but he was able to rule it out, so that was good as well. She just has plain old low muscle tone in her eyes.

(click on the picture get get a better view of the questionable eye)

Hannah has latent nystagmus (shifty eyes! I bet you can't trust a kid with shifty eyes-they probably sneak Halloween candy into their rooms!), which is not a big problem. She does have some significant hyperopia; she's quite farsighted. Her new prescription will have bifocals. I am quite pleased because I have been thinking about bifocals for her for quite a while, and Dr. Carothers brought it up without my input. (See, sometimes I do keep my mouth shut in a doctor's office. Who'd believe that??)

We'll probably make the journey down to Newport News where I know they carry the new Specs4Us frames. It is very important for Hannah's frames to fit correctly, without any sliding down the nose, so she can have optimal use of the bifocals. Wendy just had Carley fitted with Specs4Us and loved the fit. Kids with Down syndrome tend to have flatter profiles than typical children, and the bridge of the nose is usually close to non-existent. Add in low-set, small ears, and it's difficult to make mainstream frames fit. It takes someone who really understands the nuances of the Ds bone structure to adjust frames to fit well.

I am hoping that the bifocals will help her be more comfortable with smaller fonts in chapter books. Right now she limits her pleasure reading to picture books (Level 3 or 4) because the fonts are larger. She does read easy chapter books (Flat Stanley, Magic Tree House, etc), but it is considerably more work for both her eyes and her reading skills, so we do that during school time when I can encourage her.

We had to scurry after the appointment because the dentist was awaiting at 2:00 today as well! This was a new-to-Hannah dentist. Our first try with the "recommended" dentist for Hannah left a sour taste in my mouth. So now, for the first time, she is going to our regular family dentist. She LOVES going to the dentist. I think they are going to offer her a paid position when she's old enough--she was such an ambassador in the waiting room! You'd think that her complimentary toothbrush was gold-plated--she treasures it so! "Oh! Thank you so much! I like this new toothbrush. Mom? Can I use it tonight? It's so nice!" (Or, maybe she thought a "complimentary" toothbrush meant she was supposed to use compliments???)

Her teeth are terrific. She has just four deciduous teeth left to lose, then she can get braces. "Just like my friend Amelia."

Tomorrow we are off on a field trip to hear the Richmond Symphony with the Girls' Group+brothers. Maybe I can pay Amelia to convince Hannah braces are fun?

October 15, 2008

Housekeeping Blogkeeping

To answer a few questions from commenters:

Hannah had persistent pulmonary hypertension when she was born. It took her nearly a month to be able to breathe room air. This was not related her to congenital heart defects. She had heart surgery at age 2.5 to repair 2 ASDs, a VSD, PDA and a clefted mitral valve. She had to wait until her hypertension was resolved before she could be considered for surgery.

We have had terrific support and inclusion within the local homeschooling community (we moved here less than a year ago). I also belong to one of the several yahoo groups that focuses on homeschooling special needs. The homeschooling community in Newport News was not as organized as it is here in the Richmond area, so we pretty much did our own thing. That said, we have always been very independent homeschoolers; after 15 years of homeschooling I don't feel that I need that much "support". I do spend a fair amount of time encouraging new homeschooling families, especially families with children with special needs. This helps me remember WHY we homeschool--when I have to explain it to new families I remind myself what motivated us to start on this path.

Hannah currently takes three different homeschool classes, all of her classmates are typically developing (as far as I can tell!). She takes Ballet (and she is CLUMSY), Art, and Theater. Theater is her favorite. One nice thing about homeschool classes is that they generally have a wide age range for groups of children. Hannah, at age 10, does best socially and academically with children who are in the 7-9 age range. If she had the short stature that is typically found with Ds, she'd be able to fit in perfectly in this age group. However, she is about the size of an average 12 year old, so she does stand out a bit more. Homeschoolers are pretty used to kids being different in lots of ways, and we've found that Hannah is accepted easily by teachers and children alike.

Hannah did attend a preschool when she was 3-4 years old. It was the same school her siblings attended--a granola/creative/exploratory learning school housed in a Unitarian Church. All three kids had fabulous experiences there. We did have the public school provide therapy services in our home during those years. We didn't want them interrupting her "regular kid" time.

Hannah has not had any formal therapies since we moved from North Carolina when she was six.
Well, that's not exactly true. She has had no meaningful therapies since we moved...we had one wimpy SLP for a time being, but I can't honestly call it "therapy". We continue to work on oral motor at home, and work on vocabulary, pragmatics and syntax daily as well.

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Now, a little fun.


I've been playing.....but I don't know how to screen capture (without downloading a program, and my 'puter is very naughty when it comes to anything that involves my video graphics card. It must be sent back to hp to get fixed before the warranty expires in December.) So that's why I have to send you to Wordle.