Saturday, July 2, 2011

First week of summer school = SUCCESS!

"Any rough times are behind you"
How poignant is THAT fortune?! hahahaha....

Well - the first week of summer school is OVER! :)

Ashton had a pretty good week, with only one real meltdown in the computer lab. NOT BAD!

He went on to have a good day on Thursday.. so he got to go see Cars 2 as his reward!!! It was a really cute movie and Ashton said "I want to see it again!" and Holden said "it was better than the first!"; to which I laughed because when I took them to see the original Cars at the movie theater, Holden fell asleep. He was only 4years old at the time and the movie is nearly 2hours long; he just couldn't quite make it through. Hahaha...

But yes - summer school is going pretty well! He was supposed to of seen his ESY OT at school on Thursday; I need to get ahold of her to see how it went. ESY teacher should be starting this week and well, who knows about ESY speech. Still haven't heard anything so I'm guessing one hasn't been found. Guess that means we'll be looking at compensatory services near the end of summer.

Have a Happy & Safe 4th of July weekend everybody!

Thursday, June 30, 2011

I happened upon this blog post yesterday

It was titled Dear School Personnel, Community Members and Neighbors. I happened upon it from a friend's Facebook page who had linked to it. I have copied it in it's entirity here as it was written by Marianne, from The Life Unexpected: Raising a Special Needs Child. I plan to send this to my son's last year school teacher and will send it to his teacher in the fall as well as to any of the administrators that will deal with him on a day to day basis. It very poignantly describes what every person who knows a special needs child, or will come in contact with a special needs child should know. If you choose to copy this letter or blog post, please give credit to the ORIGINAL WRITER, as I have done above. Thank you!

To Whom it May Concern,
I am the parent of a special needs child.  I was overwhelmed, confused, heart broken and struggling to unravel the complexities before me.
Please do not pass judgement of me without knowing why I did not attend the school PTA breakfasts or community picnics.  Please take a few minutes to understand why I did not take you up on your offer to have lunch or grab a cup of coffee.  Although we see each other in the supermarket or at school functions, I don’t think you really ever knew me, actually, I can guarantee that you did not know me because just as my child was different, so was I.
I was in survival mode to keep my family in tact and to give my child the best quality of life possible.
I was presented with parental decisions that have torn me apart and kept me up more nights than I can possibly remember.
I had spent most days of the week at therapy and doctors appointments and most nights up researching treatments and medication options.
I was forced into isolation at times due to the stigma and misconceptions that are epidemic in our society.
I became proficient at prioritizing my life and learning to let the little things go, to look at others with compassion instead of tabloid material and to turn a blind eye to the stares or ignorant comments.
I did the best I could.
I survived.
I am one of the lucky ones, my child has blossomed and has exceeded all our expectations.
I have now become strong, I have become confident and I have become a fierce advocate for parents of special needs children.  The growth did not come without much pain and many tears but it came.
So I ask you, please
The next time you see a parent struggling with a raging child, a child terrified to go into school, a child making odd movements or sounds, a child that seems to be in a world of their own… .Be kind.  Give a smile of recognition for what that parent is going through.  Ask if there is anything you can do to help, give them a pat on the hand or offer for them to go ahead of you on line.
The next time you have a birthday party for your child remember that their child has a hard time with a lot of sensory issues and social situations.  Please send their child that invitation and know that more times than not they will not be able to attend but appreciate being included.  Understand that in order for their child to go to the party they may need to stay for a little while and please make them feel welcome.  When they let you know that their child cannot make the party consider inviting that child for a one on one playdate or an outing at the park.
The next time you are grading homework papers please understand that their child struggles, some with learning disabilities others with the exhaustion of  their disorders or the obsession with perfectionism.  The Perfectionism is not necessarily to have the answers right but to have it “feel” right for them.  They have spent hours doing what most can do in ten minutes. A paper returned with red circles and comments only hurts a child’s self esteem and causes school anxiety. Please understand that when they see the school come up on their caller ID their hearts sink, remember to tell them about all the gains their children are making as well as their deficits.  Take a minute before that call and know that they appreciate all you do and want  a collaborative  relationship in their child’s education.
The next time you are in the teachers lounge, please do not discuss their child.  Please do not make negative comments about their parenting or their child’s behavior, it gets back to them and it gets back to other parents in their community.
The next time you pass the cafeteria and see their child sitting alone please consider inviting that child to eat lunch in your classroom and be your helper that period.  Consider working with  guidance counselor to set up a lunch buddy group in a different area.
The next time they are at the CSE meeting planning their chid’s IEP know that they are educated, informed and confident knowing special education law.  Know that they have found the courage to stand up to conformity and will explore every option to give their child the differentiated educated that will show their gifts and not just their disabilities.  Understand that educating a child with special needs is one of the most difficult tasks a parent can face,  know that the last thing they want is an adversarial relationship.  Please show them the same respect they show you.
The next time you are creating an educational plan please take into consideration that their child may have specific interests or obsessions.  Foster those interests, instead of taking away that art class for a resource class consider adding an art class instead. Think outside the box, these parents do.
The next time you see that child in a wheelchair unable to speak or control their movements, don’t stare, don’t look away, say hello.  Do not assume that because this child is nonverbal that they are not intelligent or do not understand the awkwardness that you feel.  Take a moment out of your day to show kindness, support a parent enduring incredible pain and just give them a smile.
The next time your child comes home telling you how Johnny or Susie is so weird, take the time to teach about differences.  Take the time to talk  about compassion, acceptance and special needs. Please remember that your child learns from you.  Be a role model, mirror respect and discourage gossip.
The next time you hear a comment about how out of style these kids are, educate about tactile sensitivities and the fact that these kids cannot tolerate many textures and fits.  Imagine what it would feel like to have sandpaper in your stilettos or tight elastic holding on your tie.
The next time you see an out of control child do not assume it is bad parenting.  Understand that many of these disorders have an organic basis, are biological and are real illnesses. When you hear the word mental illness, take out the “mental” and remember  ”illness”.
Know that it is this generation that can stomp the stigma and create a world of acceptance.
The next time other parents are talking about “Those Kids” be our heroes, stand up for us.
The next time you see a special needs child know they are not just special in their needs but in their brilliance as well.
Take the time to meet our children.  Take the time to know us.


Have a nice day!

Monday, June 27, 2011

Mini Va Beach surf event & pics!

Ashton got the privilege to participate in a mini surf camp yesterday, and had a blast doing it! He has absolutely no fear of the water and I think he thinks he knows how to swim (but he doesn't, LOL!) He had a blast though and it was a great day to spend at the beach with family! Enjoy the pictures!!!

Mom, the sun is WAY too bright for a picture... LOL

Uncle Kevin took Ashton into the water as soon as we arrived

Ashton, nearly knocking himself over from a wave

Looking for Mom :)

Mom, do you HAVE to take my picture?!

Ashton had quite a crew helping him get on the board and in the water

Hey Mom! Did ya see me?!?

Waiting on a wave!

Trying to help Ashton stand!

He did actually STAND UP at one point but that pic was blurry :(

look at dem eyelashes!

Holden caught a sand flea

Ashton on the board again riding a wave in

totally lovin' the waves

whoa! hold on, i'm gonna fall! lol



that was fun! Let's do it again in August!

Have a nice day!

Friday, June 24, 2011

Vote for Surfers Healing in the Vivint Gives Back Project

As many who have been here before may know, I absolutely adore the people of Surfers Healing. They gave my son a chance to experience something he's never had the chance to do before, and that was to surf out on the ocean's water, with a professional surfer. 

Ashton in Aug '10 @ the Va Beach Surfers Healing event

It was one of the best, and most unique experiences of Ashton's life. He went out with no trepidation, whatsoever, and had an absolute blast! The picture taken above (by me), shows the absolutely amazing look of excitement and wonder on his face. I was awe-struck by how this tough-looking surfer dude was able to connect with my son, and help him enjoy this wonderful and unique experience. There was a pod of dolphins out in the water behind the surfers at one point, and Ashton just laid on the board, totally soaking up the experience. He loves animals, especially sea creatures, so this was an especially amazing moment for him.

I just got "unofficial" word yesterday, that he's gotten accepted into the 2011 Surfers Healing VA Beach surf event, YAHOO!! As a matter of fact, Ashton is also going to be participating in a mini-surf event this weekend, which is set up by the volunteers from the Surfers Healing VB team. What an amazing way to start and end the summer!!!

Vivint is giving away $1.25 Million to charities. Help us win!

Vivint (home security alarm company) is giving back to their communities by giving away $1.25million dollars to be given out to various winning charitable organizations. Surfers Healing is definitely deserving and could help SO MANY more children with autism if they just had more funds.

Please help me, help them by voting today and doing so each and every day! They are quite a distance away from being in a top spot, but I know we can help them win!

Thank you!!! :)

Have a nice day!

Thursday, June 23, 2011

Summer School starts MONDAY!

Well, this has been a nice week off, but it's nearly time to get back to the grindstone for Ashton. Summer school starts this coming Monday. School is from 8am-12:45pm, Mon-Thurs. I don't know yet what his bus-ride will be like, but presumably, it'll be a fairly long ride since the school is some distance from our house. We'll see.

I hope and pray that Ashton makes up for lost time and lost ground over this summer school session. He had come so far in previous years at school and he really, really backslid this past school year. He's going to end up missing one week of the 4 weeks session due to camp, but I'm not too worried about that.

We're also still waiting to hear about his ESY Occupational therapy and ESY Speech therapy services. The start date was 6/20, this past Monday. When I called yesterday, they haven't found a speech therapist or occupational therapist for him yet. :( I was hoping to get some of the hours covered during summer school but since that starts next week, I'm guessing we won't start until the following week unless they get on the ball and find someone today or tomorrow. He's got 6hrs of OT and 4hrs of ST coming to him. We have heard from his ESY academic instructor and I've sent her his schedule for the summer, so we can figure out how best to get him his 12hrs in.

So here's to xx FINGERS CROSSED xx that Ashton excels with this summer school program and does really well and makes up for lost time. That, combined with 4 weeks of camp (social programs), should make up for what he didn't get this past school year.

Have a nice day!

Saturday, April 16, 2011

Happy 9th Birthday to my little man!!!!


Holden Christopher
3:02 AM on 4/16/02
6lbs 1oz, 18 1/2in long

Yes, I'm seriously not kidding, the boys' birthdays indeed are only two days apart. It's hard to imagine that ^that^ tiny little newborn, is my now, 9yo handsome young man. Holden was very planned and very much wanted. We wanted to have two children, approx 2-3years apart. We however, didn't realize it would have been so close to our plan of 2-3years apart.


Literally, exactly 9 years ago at this moment (1:00am EST), we were on the phone calling our families because my water had just broke around 12:30am. We figured that David's parents would leave (we lived in Northern VA at the time) once we got to the hospital and checked in. Well, what we didn't plan on, was for me to go and have Holden 2.5hours after my water broke. The next phone call any of the family got, was after Holden had already been born, 3.5weeks early no less! He's been like that ever since.... fast and never stops moving!!! >:)


First smile caught on camera - 3weeks
He's been a handful ever since! ;) Mischievious and a bundle full of energy who never stops talking (seriously, he started talking in sentences in 18months). He picked up on things very quickly and knew his ABCs (sight and sounds for both upper and lowercase), shapes, colors and could count to 20 by the time he was 2years old.

18months old
Halloween '03 (2.5yrs)
When he turned 3, he was reciting his address, phone number, date of birth and could say the "Pledge of Allegiance" and could sing the "Star Spangled Banner"! (remember, I SAID he was a handful! hehe) He started preschool the fall after his 3rd birthday and learned so much. He was a reverse-mainstreamed student in a special ed preschool program. Because of having an older brother with Autism, he was a perfect role model as he was smart, out-going, verbally precocious and well, he was very sweet with the special needs kids in his classroom. He greatly enjoyed preschool but wanted more!

Holden with friends Andrew & Tori (age 3.5yrs)
When Holden was in kindergarten, it became apparent there might be some issues going on. However, we didn't get a diagnosis until half-way through his 1st grade year, ADHD. He was starting to struggle in school and his self-esteem was quickly eroding. Plus, he had become this quiet little boy, except for when he couldn't contain himself and his impulses. However, with meds he started to do better!

Halloween '06 (4.5yrs old)

Norfolk Zoo - Aug '07 (5.5yrs old)

April '08 - Birthday Party (6yrs old)

April '09 (7yrs old)

Camping Trip July '10 (8yrs old)

SPRING 2011 - 9 Years Old
He's now in 3rd grade and is doing exceptionally well. His most recent report card was A, A-, B+ and another B+! AWESOME JOB Dude!! We're SO proud of him!! He enjoys playing soccer, wrestling and loves to run. He also loves to read, but I would dare say, his favorite things to do is play video games! Pokemon ones in particular. :) He's just recently wrapped up his 2nd full year of wrestling and has moved onto soccer for the spring. He's very active and loves being outside and playing baseball and soccer. He also recently participate in the local Shamrock Marathon Final Mile race and finished with a time of 8:32! :) He placed in the top 3rd of the 3300+ runners and had a better time than any of his friends that ran the race with him from his school.


We're very proud of Holden and how he's dealt with having a special needs older brother. Like Ashton, Holden tolerates from Ashton what he will tolerate from no one else. It's an incredible relationship that they share. :)

Thank you for letting me share my littlest birthday boy with you!! Later today is their birthday party, so hopefully I'll have lots of birthday pics to share  tomorrow!! Happy Birthday little man - we LOVE LOVE LOVE YOU LOTS!! XOXOXOX! Mommy!
Ciao!

Thursday, April 14, 2011

Happy 12th Birthday, big boy!!!!

Happy 12th Birthday Ashton!!!!
(posted in red since it's Ashton's favorite color)


Ashton - 2 days old

Ashton & Mommy '01

Proud Big Brother - 3yrs old
Christmas brothers - '03
Ashton - halloween '04

Ashton - halloween in '06
Kiss the camel! - June '07
Mommy & Ashton at VA Beach - Spring '07

Feb 2008
Spring 2010

To my sweet, sweet baby boy.... who is no longer, well, a baby but is quickly becoming a young man. You are almost a teenager my sweet boy! A TEENAGER!

You were our "planned" surprise... meaning, we'd planned to have kids, just not quite as soon as we found ourselves becoming parents. You were a gorgeous newborn, absolutely perfect in every way. A head-full of dark hair that was so soft and was probably the cause of all that heartburn I had when I was pregnant with you. (old wives tale..... if you have lots of heartburn when pregnant, than your baby will have lots of hair.... YOU did). You were much smaller than we'd anticipated; you were supposed to be 8+lbs and 22in long.... you came in at a tiny 5lbs 14oz, 17.5in long. You were always so alert and your eyes were the purest windows into your sweet little soul..

As you grew, you were always smiling, always. Such a happy and friendly baby and toddler. You loved to eat, despite the nasty reflux that plagued you for the first two years of your life. Around 18months we began to notice a change; you were no longer that social and happy-go-lucky baby. You would often stare up at ceiling fans for an extremely long time and well, you had to have everything lined up, just so.

At 2 and a half years old we received your official diagnosis; Autism. I was also pregnant at the time and your world was about to be rocked upside down and all the way around. Luckily, you adjusted to your preschool pretty well and the adjustment to becoming a big brother? Well, it went as well as anyone could have expected. I think you thought you had a new toy to play with!

Your little brother was probably the single-best thing we did for you. You had a built-in playmate and he (by nature of his personality) forced you more and more into "OUR" world so that you couldn't retreat into your world as much. Your love for him is so obvious; your joy when he's gone and you see him again "Holden, I'm so glad you're back!" which is followed by hugs, is evidence of your love for him. He's the one person who can push you around and you don't fight it. He is your very best friend and you tolerate from him, what you tolerate from no one else.

Your interests have changed vastly.... whereas you once enjoyed all things dinosaurs, animals and ABCs, you've moved on to bigger and better things! Super heros, comics, and spelling things out takes up your time now (I guess your obsession with the ABCs paid off since it helped you spell). However, two things have never changed.... your love of movies and books! Wow! You could sit and watch movies all day with books in hand, ALL DAY LONG! As a matter of fact, I think you have on a few occasions!

You are now a big huge, 6th grader! You're just an inch shorter than me (though, being that I'm not quite 5foot tall, that doesn't say much), and well, you know how to throw your weight around! Strong, but sweet. Handsome, funny, smart as a whip! While you still have many years ahead of you for learning how to adjust to the world around you, I've got glimpses of who you will be. You will be caring, always happy, quick friend to others, and always, ALWAYS smiling. You adjust to new situations and new people better than any other kid I know; in fact, you thrive on the challenging and new.

We were blessed when we first found out I was pregnant with you, but I don't think we ever imagined just how much. You show us every day, in the face of adversity, just how awesome you are. We love you...... VERY VERY MUCH and I hope you have the very best of birthdays today!!!

Happy Birthday baby boy!

Ciao!


Wednesday, April 13, 2011

It's a matter of perspective......


Life happens.....


Things happen......


even more importantly.....
things happen in life for a reason ......


I know I've moaned and groaned and complained about this school year. It may seem, that nothing positive has happened, and that would be very wrong to say, because lots of positive things *have* happened.

1. Ashton got to experience a (mostly) once in a lifetime opportunity last August; the joy, magic and healing of Surfers Healing. Ashton has always thoroughly enjoyed the water and has never really been afraid of it, and he took to surfing, well, like a fish! Thanks to Kalani, one of the Surfers Healing surfers, and Surfers Healing for allowing Ashton to have such a wonderful experience.
Ashton & Kalani
Catchin' a wave!

2. Ashton got to experience the fun of snow! Yes, it's snowed here before; nearly almost every year that we've lived down here. But Ashton just never seemed to take much interest in it. However, this year he had a ball (pun intended) throwing snowballs at his brother. Take a look at this winning smile!
BIG SMILE Ashton!
See, snowball in hand! ;)

3. Ok... so while having a trip to the Emergency Room is not necessarily a positive thing, the care Ashton received and how well he did with a totally unexpected trip and new situation/surroundings, was amazing! He had, what the ped. neurologist said was a basilar migraine or a complex paralytic migraine.
Sleeping in the ER
See, he even had to have an IV :( and pulse oximeter and he did awesome!

4. and while school has been the thorn in my side since nearly the beginning..... the fact that we've made it to middle school is amazing! I look at how far he's come since fall of '01 when we got his Autism diagnosis and wow. amazing changes.
First Day of school this year

I remember this day, 12 years ago like it was yesterday.... having been told that because my blood pressure was rising and the fact that we were expecting a largish baby (8+lbs and 22in) that we should induce two weeks early to ensure a healthy delivery for all.......... After having been on bedrest from 29weeks until 37weeks for pre-term labor, we were in for a ride of a lifetime!


The story continues tomorrow.....


Ciao!