Wednesday, March 30, 2011

Conductive Education in Phoenix

Five of us local moms have raised just about enough money ($15,000)  to have the Conductive Education summer program in Phoenix!  We are still short $5,000 of the 20k needed - but we think we can raise the rest in order to have the summer camp here!

Click here to find out more about the program that is based in Tucson.  If donating, please specify it is for the Phoenix location/Amy:   http://www.swgaitway.org/default.asp


Thanks to all of you who have supported this cause!

Amy

Thursday, March 17, 2011

Big Girl Bed

I'm sure many of you can relate to the horror of putting your child in the crib, hearing a ruckus a few minutes later, and then finding her standing (OUTSIDE OF THE CRIB!) at her toy box playing with the cd player. Oh yes, the closet door was wide open, the lamp and side table knocked over...  bring back any memories for anyone?  This was our night recently, and although we knew it would happen someday, it wasn't supposed to happen the night before Paul and I left for Vegas!  Which  just happened to be our first outing together, without Katie in tow, in several years.

Katie is now in the "toddler bed" version of her crib which basically means the front of the crib is taken off.  We were excited that we finally had some baby-proofing to do for our 5-year-old, Woo Hoo!  About time!  (Yes, Katie just had a birthday)  We had to take everything out of her room, duct tape the light switches (because the first night she kept turning them on), put those things on the door handles, put up some high shelves, etc... So here we are a few weeks later and it is going pretty good, this whole "big girl bed" thing.

Wednesday, February 23, 2011

moving forward

I can't believe it has been almost a month since my last post.  We have all been suffering from this coughing, sinus, sore throat thing that is going around, me for 3 weeks!  UGH!

Katie's newest thing is that she will scoot over to me and grab my hand, pull herself up, and we will walk to wherever it is she wants to go.  Usually to the playroom, or the kitchen is popular when she spots some cookies on the counter.  It's nice that she can have a say on where she wants to be, usually near the sweets!

She also understands at horse therapy - if she pats the horse, it will go.  She loves being on the horse and last week she was hugging it most of the time.

Two small steps for Katie, one giant leap towards her potential!  


Oh, and the tongue thing is over with, for now anyway.




Tuesday, January 25, 2011

Another tongue episode

 It took me days to find this Campbell's Soup logo!  But look at the resemblance - totally worth the wait!  Except for the uncombed hair and lack of bow - bows just don't happen in this household.
Oh I've tried....
Katie has been doing this with her tongue for four days, and it is pretty consistent. I think it just means that since the tongue is a muscle, (and didn't I read somewhere, "the strongest muscle"?!) and the fact that she has low muscle tone, maybe her tongue is finally strong enough to be able to do this.

If you read my blog on 9/30/10 you'll remember Katie's other tongue phase, where it hung out of her mouth for about three weeks. It drove me crazy.  Well, all I can say is at least this phase is a cute one, and  unlike the last one, I am not worried about walking through the mall with other mothers giving my child a pitiful look - that was horrible.  At that time I just wanted to scream, "No, no! Her tongue doesn't usually hang out of her mouth!  It's just a phase - she really is model material!"

If anyone out there is an expert and knows anything about the whole tongue thing, please let me know.  Because, I am assuming it means her mouth and tongue are getting stronger, and that she will be leading a Toastmasters meeting someday.

Friday, January 7, 2011

Glasses

I took Katie to have her eyes checked because lately she keeps throwing off her glasses - I figured she needed a new prescription.  And the fact that they are pretty scratched, it was time for a new pair anyway. Imagine my surprise when the doctor told me that Katie did not need her glasses anymore!  Her vision has corrected itself, and she is glassses-free!  He said that this happens about 50% of the time in young kids who are far-sighted. So, I don't know if the stem cells had anything to do with this, but for me it is one less hassle, and that is huge!  Now to tackle the hair combing dilemma - I wonder if the crewcut will ever become a new fad for 4 year-old girls?  Isn't Shiloh Jolie Pitt headed that direction?

Monday, December 27, 2010

Christmas

We had a terrific Christmas! This was the first year that Katie would see a present and know that it needed to be opened, tearing at the wrapping paper! It was great to see the cognitive strides in "understanding what a present is" that we have not seen in the past.

Thursday, December 16, 2010

Sure is loud around here!

For about the last two weeks, Katie has been REALLY loud! Loud in a good way though, shrieking for the fun of it is my guess. We were at Swan Rehab last week where they see a lot of stroke victims and where Katie gets her treadmill therapy.  They see mostly older people and not too many 4 year-olds, at least not when we are there.  It's one big room that is divided in areas, but I could hear Katie all the way in the lobby - having a good time and letting everyone know - shrieking in delight!  I heard someone say to her, "Let's use your inside voice." 

So, I had a conference with Katie's teachers and therapists about her goals and I asked them if she seems to have been louder at school in the past few weeks, which they confirmed.  One of the therapists said that it means her core is getting stronger, that kids can't get that loud until their core is strong enough.  I think she also said something about her vocal cords maturing and her mouth muscles becoming stronger - maybe that was the school psychologist - but anyway, I guess what it comes down to is - all of this screaming is a really good sign!  Paul and I may be wearing ear plugs soon, but it's all good!

Friday, December 3, 2010

A note today from Katie's school Speech Therapist

"At circle time, Katie raised her hand when Miss Rhoda asked, "whose name starts with "K"? ( sign of K was given as only other cue) OMG!!!!  Katie also participated in response by stomping her feet when another child asked for the whole class to stomp for that child as applause. No help was needed for Katie- she knew what to do."

Things Katie does like this simply amaze me!  Guess it's time to start going over the alphabet more consistently at home!

Tuesday, November 30, 2010

A few updates


 Katie's tongue is not sticking out anymore.  Her continous "tongue sticking out" phase lasted about two or three weeks, then went away. Then came back when she knocked out her two front teeth (for a few days) and now is gone, I think for good. Whew!



Katie the pirate! Note her tongue was sticking out - this was right after she knocked out her two front teeth.






















Katie was in a wedding this past weekend! See if you can spot her in this video!


Katie is walking better - in this video she has on her braces and the SPIO (pants) underneath her regular pants - they give her extra support and help her balance. 





Tuesday, November 16, 2010

SPIO

I ordered a "SPIO" (Stabilizing Pressure Input Orthosis) for Katie.  This is an undergarment that is similar to SPANX (for women, to hold in our cellulite!), or a girdle - if you can't visualize a SPANX.  Katie's is a spandex type of material, and for her I got the pants only - which is worn under her regular pants.  It is intentionally tight on her so that she receives input, and it should help her to know where her body is in space.

So I put it on her today for the first time, sent her to school, and I get a note home from her teacher that she took 5 or 6 steps today, that's a lot for this girl! This SPIO just may be worth the $100 that it cost!  We'll see how it goes tomorrow at treadmil therapy - that should be a good test.

*The SPIO seems to be helping her - She walked to me at treadmill therapy and it was the most balanced I have ever seen her - about 6 steps!  Then, I went to the school for a conference, and Katie's teacher showed me how far she had walked the day before, and I would guess it would have to be at least 10 steps!  Her teacher said she pushed her walker aside, and walked over to where all the other kids were calling for her. (This SPIO is also really good for kids with autism - and a 90 day refund policy!)  I think I made a good investment!