GOOD NEWS!!!!!

Skyla got to see Shelly for some much need PT. Shelly also measured Sky's dorsiflexion, and found that with her knee bent Sky has FULL RANGE!!! Yep that's right she is doing that good. With her knees straight she still has about 5-8 degrees to go but is getting there at a amazing rate.

Shelly also said Sky no longer needs her leg braces!!! She now has these plastic shoe insoles that slip in to her shoes. It makes it really hard for her to go on her toes and if she breaks them then we know she was walking on her toes again.

Walking on her toes is still a big habit we are trying to break. If she is in tie shoes she walks flat but on , bare feet or flip flops she pops up on her toes. Luckily she isn't doing it to often that its causing problems.

Not out of the woods yet but at least the end is finally in site. I knew it would take about 6 months and now that we are heading in to our 7th month its nice to get some good news. Sky gets to go back to PT with Shelly in 2 weeks and we are just really going to work her out. She is one step closer to those Twinkle Toes shoes :)

I know "about time"

Sorry I know it has been a long time, but no news is good news right?

Miss Skyla is doing wonderfully. She still walks on her toes but its only when she is in socks, flip flops or bare foot. If she has tie shoes on we are good. She has lots of rang and its fun to see her try things she could do before. One was the walking heel toe in her tap dance. This was something 6 months ago she could not do and now is a pro and so excited she was able to do it by her big recital because "it made the dance look so good" according to her hehehe.

One fun dilemma we got to deal with is our insurance. Children's Hospital is the ONLY children's hospital in our area. They have any and all child specialist and a grate emergency room. The big head honchos at our insurance company decided that they didn't want to renew a contract with Children's hospital and dropped them as a provider. When I got the letter I was so mad. Sky had a apt with her Ortho Doc Dr. Skinner and her Physical therapy Shelly, but our insurance was no longer excepted and we would have to pay out of pocket. I called Shelly and told her what was going on and she had a fix for our problem.

Shelly's hubby manages a ortho office and Shelly is also an employee over there as well. So Sky's ortho doc filled out a prescription for more PT for sky but over at this new office that is a provider with our insurance!!! Shelly will give Dr. Skinner the updates on Sky and we will just take it from there. Since sky is doing so well and out growing her leg braces she only needs to be seen once a month for a few months.

Luckily with enough phone calls by me and others flipping out about our insurance dropping Children's, our insurance just sent out a letter saying they finally made a deal and Children is now a provider again. We are going to continue to go to this other place just because its a bit closer but I'm so glad we have Children's again!

Like I said before everyone at Children is AMAZING. Not only have they made this whole thing easy to deal with they have truly bent over backwards to help us and to make sure Sky is getting all the attention and care she needs. We go back for our monthly visit on the 28th with Shelly. I'll post some updated pic then.

O I almost forgot...... Sky got her Twinkle Toe shoes!!! They are a size to big but are sitting on her dresser in the box for encouragement. Hopefully by the time we are done she will be in them. There not the ones she originally wanted but are way cute and blink. Ill take some pic of them too. :)

Update

Sorry its been so long since I gave a update on Skyla, its just been really un-eventful. Sky is still wearing her leg braces and her range of motion has improved like crazy. There is so much she can do that she couldn't do before. There just little things but little things we all take for granted, and I never even really though about till i found out she couldn't do them. We are still fighting to break the habit of the toe walking. She has the range to walk flat, but is still used to walking on her toes and when the braces are not on we have to remind her constantly. Its a bit frustrating!

She is also not going to Physical therapy any more. Well she has not been in about a month. She goes on the 13th just to see how she is, then we see the Ortho Doc a month from that in Sept. He will then check her out and let us know how long she needs to wear the braces and if we need to continue physical therapy once a month. So progress is happening it just been a bit slow but it is moving forward.

Sky's new style

From my last post I'm sure everyone could tell how upset I was that we had to wait for Sky's leg braces even longer. Well when I was on the phone with Tony he could tell as well and apparently made a call right after he got off the phone with me. Tony called the company that was re-making the braces and told them how upset I was, and how we have all ready waited 2 month for these things. Well "ask and ye shall receive" they made her braces in 2 days shipped them over night and Tony called me Monday afternoon to tell me he had them in his hands!!! We set up a appointment to see Tony the next day and I'm so happy we finally have them and Sky is wearing them.

They are a perfect fit! She is not being irritated anywhere by them and is adjusting really well to them. The first day she got them she had them on for 2 hours before she started complaining that her legs hurt. Today only 2 days later she had them on for 3 1/2 hours we took them off and gave her legs a 30min rest and then we put them back on and that was about a hour ago.

Here are some pics of what they look like.....


This is from the side you can see how it goes a little past her toes and almost up to her knee.

She got to pick the colors and the cute heart ribbon that goes across the middle strap.

They slide right in to her shoes and she runs and climbs like normal all ready in them.

This was a pic she asked me to take. We have to get her some new shoes that are big enough to fit her braces. This is her first pair, she picked them out and thinks they are so cool. We had to go one whole shoe size bigger then what she normally wears, which isn't bad at least they don't look huge on her. She cant wait till next week when we go shopping for a few more pairs (she LOVES shoe shopping)

So have I mentioned she has adjusted really well to them all ready? She was watching a movie and it was really nice to see her in her normal spot, in her movie watching pose hehe. Seeing her do so well in them has really made all my fears I had about them go away. She is a trooper, and a really good girl about all of it. She knows how important this all is and how everything we have her do or wear is to help her walk better. Its nice when your kids just do what you ask, and don't fight you on it.

2 MORE weeks, you have got to be kidding me!

So I got a call today, a call Sky and I have been waiting for...... Her leg braces were finally here (were being the key word in that statement).

We got told last Fri that the braces should be in Tue or Wed of this week. They came right on time, Sweet now we can get Sky fitted in them and adjusted and let the real work begin to get my toe walker on flat feet! Yeah like I said before I'm not that lucky.

The place that made the braces put a joint on that Tony asked for, it has a stopper that would make it imposable for Sky to go up on her toes. Well guess what... they put the joint on back words and didn't even put in the stopper. So needless to say they didn't work the way we wanted and are now waiting for the new braces to be sent out.

Lucky the place keeps the mold till they know we are satisfied so it was a easy fix, we just now have to wait another 2 weeks to get them. Its so frustrating these mold where done in April its been almost 2 whole months and we still have no braces. Physical therapy is great and working wonders but it would be so much more worth it if we had those braces. Sky has to wear them for about 6 months and its things like this that are just prolonging the time.

I am very grateful though for Tony and catching the problem and reacting to it so fast. Its very reassuring that every one involved really wants to make sure we have the right tools for Skyla to help her walk normal as soon as possible. We have a amazing team!

O and Sky was also a little sad she doesn't have them yet, she is very excited about getting them. Who wants to make bets on how fast that excitement will fly out the door once they are on her legs? hehehehe :)

More PT

So I just wanted to update you all a little bit. Sky has now had 3 PT appointment's with Shelly and is doing an amazing job. She remembers to do her stretches everyday, and works really hard to try and do the things Shelly challenges her too.

When Sky went for her evaluation in May they measured her feet to see how far away from 90' she was. Her left foot was at a -5 and now is at a -3, her Right was at a -10 and is now at a -5 (we want her at a +10 at the least, by the end of all this). She still has a long way to go but has made a huge improvement all ready. She can walk flat for a wile now (as long as she is thinking about it) and she is even getting better at standing flat and bending her knees. She cant go down very far but at least she can do it a bit now. She is learning a whole new range of movement and its so rewarding to see her do it. I never really knew how simple movement I take for grated, where so physically hard for her to do and to now see her trying and getting better it so rewarding.

Sky emotionally is doing great. She gets so proud of herself when she does something new, and at 4 years old she understands pretty well why learning to walk the right way is so important. She doesn't fight me with stretches and most of the time will do them through out the day on her own. Her leg braces should be here next Tue or Wed so that will be a whole new thing once we get those but she is excited for them too because she knows they will help more.

I'm so proud of her and all the hard work she is doing, I'm so grateful for all the wonderful people we get to work with that are just as passionate about her walking on flat feet and having full range of motion as we are.

Sky + Shelly + Physical therapy = Tons of fun!

Ever since Sky's evaluation visit last month with her physical therapist, she has been looking forward to going back and seeing and playing with Shelly again. She really liked Shelly, and Shelly did a amazing job of getting sky's attention and winning her over.

We finally got to go back on Thur June 3rd, and Sky got a good 1 hour work out with Shelly.

This was her excited waiting face....



When Shelly came out Sky ran and gave her a huge hug and told her how excited she was to play with her. Shelly then asked how we have been doing at home with the stretches she gave us to do, and if I have been making sure to stretch Sky when she is warmed up. I told her how we have been stretching everyday since our last visit and I always make sure its after she has been running around playing.

Shelly told us she was pleased then told Sky "I have a great Idea on how to warm up your legs before we stretch" Sky got excited and hand and hand they walked to a room filled with different bikes. Shelly then strapped a helmet on Sky and gave her a cool bike that she got to ride around the hospital on. Sky thought it was so cool she got to ride a bike, and the whole time Shelly walked with her and the 2 just talked away.


After Sky's 5 laps around the 2nd floor, Shelly had Sky show her one of the stretches we have been doing at home....
I'm Happy to report the stretches have ALL READY been working and Sky is showing improvement. A month ago when Sky did this stretch her arch would flatten to the ground, it is now staring to arch up like it should, which means her whole foot can and is hitting the ground more and her whole foot, not just the balls of her feet, are supporting her body weight like they should. She still has a good way to go before walking flat will be comfortable and a normal way of walking but we are on the right track and she is doing great.

After some fun stretching games Shelly then worked on Sky getting her heals down more as she walked. Sky had fun on the balance beam walking forward and backwards. Yep that narrow beam Sky is on, she was walking backwards on it. Walking backwards made her have to put her heals down to keep her balance, who knew.
After the beam Sky got strapped in to this cool looking contraption (I had pics but they got deleted, stupid computer) Its a machine they use for kids who cant stand on their own, it helps to develop the muscles for standing. it looks like a chair with wheel chair feet holders. You place your feet on the platforms and strap in your feet. You then adjust the height of the platforms your feet are at 90', and your knees are bent and in line with your hips. Then this big padded cushion comes in and goes right in front of your knees. Once your all strapped in the seat then gets tilted till you are standing. The seat is big and helps to support your back, and the pad at your knees supports you from your thigh to your calf to support your knees and to stop you from bending your knees. Sky stood with both feet flat and at 90' for 10 whole minutes, that's the longest she has ever stood flat in her walking life. To pass the time Shelly and her played a few games of memory. After the 10 min Sky started to complain her legs hurt and she wanted out. We happily complied cause our time was just about up anyways.

The bad news is her leg braces are going to basically do the same thing the machine did, and she will have to keep those on for longer then 10 min (bring on the whining I can handle it!). Speaking of her leg braces, they were finally ordered on the 19th of may (after changing the order a few times) and should be here any-day (it takes about 2 weeks). As soon as they come in we go down and see Tony, and he will fit and adjust them to Sky's legs if need.

It feels good to all ready see some changes just from doing a few stretches at home. It has made me even more excited about getting her leg braces on and continuing PT with Shelly. O and since Sky is doing so well Shelly said she more then likely wont have to sleep with them on (woohooo not a battle I wanted to fight). We are now going to PT 2x's a week right now its every Monday and Thur. Sky is all ready asking if Monday is here yet....Shelly I hope you know how much your loved all ready :)