Apraxia Awareness Day 2014 and Better Speech and Hearing Month

http://flipagram.com/f/A4GdsUmryU

Mark your calendars. Apraxia Awareness Day will be May 14th.

We will be meeting with Rep. Amy Alexander Carter to receive the 2nd (ever) resolution of the state of Georgia's Apraxia Awareness Day.  

The resolution will be given to Luke at 'more than words' Pediatric RiteCare Clinic on May 4th. 

Last year was the 1st day of its' kind and we were so blessed to have played a tiny part in bringing it to our state.

http://maggieandluke.blogspot.com/2013_05_01_archive.html?m=0

http://maggieandluke.blogspot.com/2013/05/celebrating-luke-on-apraxia-awareness.html?m=0

http://maggieandluke.blogspot.com/2013/05/childhood-apraxia-of-speech-awareness.html?m=0

Please join us at the Better Speech and Hearing event and by wearing blue and white on May 14th. 

I made the little flipagram video at the top of this page to celebrate our Luke and all of his MAJOR accomplishments. 

Please take a minute to watch it. 

Luke most definitely ROARS. 

And we are ever so grateful.

To God be the Glory!!!

Valdosta State University Speech and Hearing Clinic

Wordless Wednesday....not because we are wordless. 

Quite the contrary.

I just haven't blogged in a while. 

Haven't felt like it.

And then someone messages me about my blog and how much it has meant to them or how much hope it has given them.

And I know that I have to share something.

So here are some pics.

I never quit taking pictures. Never.

Enjoy!

And the Greatest of These Is Love

The Nativity

Luke wanted to be a giraffe or a gorilla in the church nativity last year.

I was just thrilled that he had an opinion and a voice to express it with. 

And I seriously considered getting him his own special costume. 

But instead, I just posted his wants on Facebook and basked in his progress. 

We then had a long heart to heart about the difference between The Nativity and Noah's Ark and finally compromised on being a donkey.

Fast forward to this year, 2013. 

Luke's preschool has a Christmas Program where it is tradition for the 4 year old class to act out The Nativity Story. 

Luke came home at the beginning of the month and told us that he tried out for a play. 

We made a big deal out of it. High fives and lots of hooting and hollering.

Maggie asked what part he auditioned for. 

He came back with "you know that guy that is with Mary and Baby Jesus, I gonna be him. What's his name? Moses?"

And I giggled inside. 

"Close, Luke. That guy's name is Joseph."

"Oh yeah, Joseph. I gonna be Joseph in the play at my school."

(Later he came clean with the fact that "they pulled my name from a hat" but still we couldn't be prouder of our Joseph.)

Although he didn't have any lines, they did sing 2 songs. 

Away In A Manger has never been sung as sweetly.

http://m.youtube.com/watch?v=pX1xQXzV5Bw

And as the program drew to a close, he bowed. The only kid that bowed. (Wonder where he got that from?!?) ;)

Blown away by our little miracle and God's blessings.

Unexpected Staycation

When your AC goes out unexpectedly on Labor Day weekend and you live in the south, you try to sweat it out. But reality sets in quickly.

Luke got his "wish". He has been wanting to "live" and swim at this new hotel and that is what we did for the weekend. 

Hot tubbing

Dimples and Shirley Temples

Sweet dreams.

Fine Motor Practice through ABC's

Aa is for Aquadoodle

Cc is for Crayola Color Wonder

Hh is for handwriting homework 

Nn is for name

Pp is for practice 

Rr is for ride

Definitely enjoying the "ride" with my precious babies. 

It's in Black and White

This post has been a long time coming. Luke has flourished this year (socially, emotionally, and physically). His speech is understood by almost everyone.

Gone are the days that I have to repeat what he said to others and play translator. He is a verbal communicator and we couldn't be prouder.

Many of you know that I left teaching to devote my time to his care and ended up homeschooling Maggie in the process. While it was the most rewarding year of my life; it was also one of the most difficult. 

There were days that I didn't know if I had....enough.

Days when I wanted to call in sick and cancel therapy.

Days when Luke said I want to quit "peach". (which I responded without missing a beat...when you fix that sentence and say "speech" correctly, we will discuss it). 

Sounds harsh, but this apraxia thing can't be taken lightly.

We talk tough.

We love hard. 

And we work hard.

It takes work. A lot of it. And work, we did.

I basically scripted, prompted, cued and corrected all day long.

The good news is....after 7 speech therapies per week (4 privately and 3 via public school) from Sept.- May; Luke will only need to have 2 x 30 minutes of private speech therapy starting Aug 5th. (school therapy is also decreasing to 2 x 30 min. (1:3)

I write this not to pat myself on the back, but to stress that it isn't easy and it isn't always fun. 

But we persevered, made adjustments and pressed on. 

And because of Luke's hard work, our phenomenal team's efforts and God's grace....we made it. 

It's in black and white, too.

Luke's diagnosis has been downgraded to residual apraxia of speech and an expressive language delay. 

Yep. 

You read it correctly. 

We are beating apraxia. Although CAS sometimes shows up in motor planning; Luke is now testing above his age group in speech. 

Praise be to God. 

For without Him, none of this would have been possible.

Reaching New Heights

Never did I think that I would attend the CASANA conference.  (For those of you reading who don't know what that is...its the mecca for information about Childhood Apraxia and it happens once a year)

I had secretly hoped that one day, after we were done with intensives and the many therapies that I would go.

With help from the Georgia Council for Disabilities, this secret little dream of mine became a reality. I attended the CASANA Conference 2013 that was held in Denver, Colorado.

I was able to learn from the best of the best about apraxia; the latest research, the cutting edge therapy techniques, the genetic pieces of the puzzle, and much, much more. 

Thinking Outside the App with the AZ Speech Guy aka Jeremy Legaspi, M.S., CC-SLP

Phonological Awareness with Dr. Amy Skinder-Meredith 

Play and Social Thinking with Nancy Tarshis, MA, MS, CC-SLP

But most importantly I met other mothers and families that have experienced apraxia firsthand.  We shared stories during our breaks, met over food, and even bonded by painting.

I had my copy of Anything but Silent autographed by Kate Hennessy and I finished reading it in about 2 hours ;)

Smiling with Brooke about finally meeting in real life

Mary Squared: Mary Mahon (an iMum) and Mommy Square

Our group's table at Canvas' and Cocktails

Nancy Kaufman and I with our finished masterpieces

At the luncheon, they announced that the 10th annual CASANA conference will be in Nashville, Tennessee! Yee-haw!!!

And then there was my chance meeting with this mama. She is the epitome of the word warrior and is just as crazy as I am about winning the war on apraxia. The similarities between us are so close that it is almost scary. I am positive that God knew we needed to meet.

My spirit is renewed and I returned home to spread and share the information gained with others.