Showing posts with label special needs. Show all posts
Showing posts with label special needs. Show all posts

Friday, February 24, 2012

Kindergarten progress

Since we have reached winter break of the 2011-2012 school year, I wanted to include an update on how Diego is doing in school.
  
A big help for us are the new daily charts that are sent home with his communication notebook.  The staff staples a sheet in the book that details for us what he ate, his bathroom use (doing great!), which class or therapy he had that day, and at least one or two highlights of the day.  It is exactly the type of update I like to see since he is not able to relay all that info to us.  I think back to when I was young and my Dad asked us how school was every day and just saying “good” was not enough.  He wanted details and now I do too.

Diego is actually doing some basic addition and subtraction, writing numbers more clearly and had his first oral presentation just a few weeks ago.  He had to tell the class some of the highlights of a book they read.  From what I understand the teacher prompted him to answer some question about the book they read and he had to use a poster as his guide.  Reading continues to be a challenge as he mixes up some words and usually does not want to do that part of his homework.  The teacher also sent home a really cute CD with all the songs they use in class (days of the week, labeling with the alphabet and so on) to demonstrate just how much he has memorized.

I’ll be the first to admit that all that he has done has exceeded my expectations.  I thought when we met last April to prepare his goals for kindergarten that we had set a realistic standard for him and that he would be challenged.  I look at his paperwork and am delighted to say he is doing all we thought he might do and more!  He’s blowing the standard out of the water and I’m so proud of him… It is a testament to all the work he puts in and how well his teacher is guiding the class. 

As a side note, he now tells me “one secoooond” when I ask him to give me the iPad or my phone (he plays angry birds on my phone now too).  He also uses “whatever” in response to us and although many parents might be bothered we think it’s great as it illustrates just what many other kids his age are telling their parents…

Tuesday, September 20, 2011

Wit and Wisdom compilation


Today, September 20, 2011, Wit and Wisdom from the Parents of Special Needs Kids is being released.  This book is a compilation of stories written by parents that are dedicated to making a difference, and I am one of the authors featured in the publication.  As many of you know, my older son Diego was diagnosed with autism in 2008 and I am committed to sharing our story to bring about change.  By that I mean a shift in how we both perceive and act towards people that posses a different way of thinking.  The other contributors to this anthology are special needs parents just like me, relating their experiences of life with their exceptional children.  The book is available for purchase at Amazon.com, and I invite you to come discover the world of special needs parents and support our cause by purchasing a copy.  Click here or on the link provided on the right side of this page and you will be directed to the page at Amazon.

When I was originally invited to participate in this project, there were a few ideas I was kicking around, trying to decide which particular topic I wanted to discuss.  A few weeks later, the decision was made for me.  We had just attended a meeting to discuss Diego’s placement for kindergarten for the upcoming school year.  During our meeting, the education official (who was actually a school psychologist) made some very negative comments, leaving me to wonder how someone working in that capacity could know so little about autism.  I left that meeting saddened by the way he spoke about Diego’s future but determined not to dwell on the negativity.  Later that same day I decided that my entry in the book would be about our encounter that morning.  That story and everything else I write is intended to foster hope for the future by slowly chipping away at what seems to be a mountain of ignorance that exists in regard to intellectual disabilities and autism in particular.

Tuesday, January 25, 2011

Focusing on our son's health

Today I am a guest blogger over at "I'm Just That Way and That's Just Me", a wonderful blog edited by another special needs parent, Dani G.  She is the mother of a sweet little girl who, like my son, has autism...

Even though I will remember 2010 for progress that Diego has made, I will also remember some scary moments, hospital visits and ear infections.  In order to move forward and focus on helping him, I wanted to take the time to reflect on some of the concerns and tough moments of this past year.  We know 2011 will be bigger and better! Please click here to read my post...