Monday, January 23, 2012

Dora, I good girl, yah!



Tell me this kid isnt in there and doesn't need to communicate! Oh no I'm sorry wouldn't be able to communicate

Monday, January 16, 2012

Scoliosis, Rett Syndrome and my Abby






Last year I told you all how Rett Syndrome Sucks. I told of our journey with Scoliosis and Rett Syndrome along with pictures of xrays. On these xrays you could see that Abby's curve had doubled in just a few months time. Despite the facts that we had enrolled her in Hippotherapy and upped her PT time outside of school her curve still doubled.

It took us several months to find a Chiropractor and Massage Practice that would take Abby on. With a huge discount and help from our church we were able to come up with a plan of treatment. Once again Thank You Fountain of Life and Nashua Baptist!

You can view the video of her progress here.

Never the less...it was not enough. Although we do intend to keep her in all her therapies we had to make the decision to brace Abby. It was not an easy one to make and almost everyone said the same thing..."Bracing doesn't work with Rettgirls. They don't tolerate it."

Here are some pics from Abby's brace fitting...that she is tolerating beautifully



When they first put it on. I was so upset but I knew if I cried she would too and she was being so good.
Here we go..she can sit up
Look at her Cheesing at the technician
On the way out. Sitting up as straight as can be....and yes..her legs really are that long!

Thursday, January 5, 2012

Christmas 2011

This Christmas we did things a little differently and just loved it...for the most part. We invited a family friend and had a peaceful all about us and the Lord kind of Holiday.

Sunday morning Abby was pretty interested and confused with other people's gifts

And one posed smile from Bubba
Yeah. What she get...what she get?
What? I'm being good
What did ya get Aunt Pam????
Look at my pretty outfit!
Check out all the bows in her hair! I think those and this lighted aquarium were her favorite!

See ya soon!

Wednesday, January 4, 2012

Rett Spell

Isn't she pretty? Pretty evil I tell ya!

Nah I shouldn't say that.

Anyone living with Rett Syndrome can tell you that we call it..it being Rett Syndrome the invisible monster. We never know how or when it will tighten it's grasp on our children but when it does...all other life shuts down.

As far as Rett Syndrome goes Abby is a pretty happy kid. I once even has a Neurologist tell me she was the least afflicted case he had ever seen. Now she is not the least afflicted case I have ever seen but more often than not Rett Syndrome is worse for other kiddos than my Abby.

Most days, at first glance Abby appears to be normal. As long a she's quiet. Then you will notice the odd, rhythmic movement of her hands. Maybe another sideways glance and you see that this very tall 7 year old is drooling and licking her hands. By this time you are intrigued..you can't help yourself. She is so pretty...what could be (wrong) with her?

She catches your eye and locks you there. It's like a Jedi mind trick. You can't look away. She then looks at you and dead serious says," Ah mag ackah likea boggah noo?"

You find yourself looking away in shock then back at her. You might reposition yourself in the room/store/church. What is it? My God what has a hold of that beautiful little girl?

Rett Syndrome. A horrible cage like monster that has control over everything she does. Rett Syndrome comes in stages.....Stages we don't like to talk about or even think about which one our girl is in. Not after stage 1 anyway. I think we may be entering another stage or phase in our Rett Syndrome journey. Abby is different...difficult..hard to deal with.

She relies on me or others for everything. EVERYTHING. She cannot eat, drink, dress,clean herself or even pick up a simple...a simple...anything. She must be carried to her room and to the bath. She is getting quite heavy...Tiny girl that she is.

I really don't know if she is becoming more aware of how trapped she is. If she is just down right pissed? I don't know if there is something hurting her. Maybe a little of all of the above?

I know she stopped sleeping there for a little bit. Yes stopped. Easy thing to do with Rett Syndrome for some of the kids. Melatonin had been a God send for us for many years and it just stopped working. Her Neuro put her on a different med and hallelujah it's working. She had us cut it in half last night because it is an adult strength medicine and she was up to almost 1am.

With the no sleep came these epsiodes or fits. I can no longer take Abby...almost anywhere. Not by myself and not without someone to help me. Even then it is usually too much for her. Unless I can hold her tight, give her my full attention and an ipod too with music or videos for her to concentrate on s.he freaks out. I mean FREAKS OUT. She screams in terror, claws at me. Bites. Her eyes always pleading for me to help her...get her out of there. Doesn't matter where it is. You get her back in the car or back home and she's fine. Happy as a clam in fact I don't know if this is a stage, or a phase or anxiety...I know it's at least anxiety I just don't know what to do to help her.

So that is where we have been and what we have been doing. Trust me..it's exhausting.

Christmas pics and a great surprise to fill you all in on soon.