Showing posts with label autism. Show all posts
Showing posts with label autism. Show all posts

Saturday, August 9, 2014

N.W. Arkansas Angel Pageant

God Made Everyone Special!


2:18 a.m.
  I simply can not sleep.  Today I will be taking my 'special needs children' to their very first pageant.  They will not be performing a talent, nor speech.  They will simply be showing up.  They will get their names called, walk up on stage...and a cue card will be read with my thoughts as to what is special about them.  All children are special.  They all have different hurdles then others - and so do their parents.  A certain person close to me was appalled when informed that I was taking them.  This individual was afraid that everyone will know about 'their conditions', and 'they will get labeled in our new town' among some more harsh words.  I'm second guessing a lot rite now, including taking them...

8:20 p.m.  
  Guess What!?!  News flash - It is okay to be different!  I can't even sum up the words for how glad I am for not backing out of this program.  The boys have been floating on air since we got home.  My eyes sting from crying tears of joy for hours.  
  My youngest was stimming from the time we arrived at the pageant.  He was covering his ears asking me to ask for the low playing music to be shut off (he can make all the noise he wants, but heaven forbid someone else make it!)... and there was a lot of separating of the boys and positive/negative reinforcements...but no one gave us nasty glares!  The other families, staff, and volunteers showed us so much love, kindness and affection.  We're not used to that in public.   Everyone made my boys feel like they are special.  A genuine, engaging.  This exercise wasn't just good for them and had them glowing and feeling accepted...but it has helped me as their mother and 'a certain close person' to look for programs in our new state to connect with other Autism Spectrum families.  We've all had a change of hearts!  Even the church that hosted the event, has an outreach ministry for special needs.  I would have never knew that if I allowed for us to stay in our comfort zone - aka hiding place home.  

While waiting...we took some photos -
The boys & table display
  Then from the very beginning, Vaughn made me cry.  As soon as we were on our way back to our seats from the stage where I explained the process several times of what to expect - Vaughn says, "Mom, you should be the one going up on stage to get a sash and crown for taking care of us."  WATERWORKS!  And once I started crying, it was so hard to hold them back the rest of the time.

Me and the boys cheesing =)

In prayer of Thanksgiving for all of the Angels
On the stage:
Vaughn behind the stage waiting for his name to be announced

Vaughn listening to his for the first time what mom wrote that makes him special <3 
escorted by BHS Quarterback Mr. Kasey Ford!

The Lovely Ladies waiting to sash/crown the Special Angels

Vaughn getting his sash by Miss Hanna

Vaughn waiting to be dismissed


Kingston started crying (he thought when he was announced as 'The Family Tinker' and everyone started laughing, that they were laughing at him...I had to explain the misunderstanding for about an hour afterwards...

Kingston getting his sash


Quick recover while inspecting his trophy with escort Mr. Kasey Ford (BHS Quarterback)

Malachi has REALLY come out of his shell in the past year.  This boy was BEAMING on (and off) the stage!  

Behind the stage :}
Miss Lakes of the Northwest ~ Hannah Gibson with Vaughn & Kingston

Miss Lakes of the Northwest ~ Hannah Gibson w/Malachi

Malachi and Miss Rodeo of the Ozarks 2014 Tori Miller - please visit her BLOG HERE

Malachi and Miss Emily Edwards that did the Crowning :)

Malachi was in his glory talking about Batman with the photographer =)

The Coffman Trio getting ready for a brother picture together

3rd Annual NWA Angels 2014

  Each family is different.  I urge you not to hide behind the labels like our family has come to do over the years.  The boys always knew they were different.  Not only did they get to feel special about being different, as an adult - I got to rejoice today with them for the first time.  I had a spiritual celebration that my kids (grocery list of diagnosis included) are who they are.  Each unique in their own way.  They do have strengths.  They are Mr. NWA Angels & my gifts from God.

James 1:17  Every good gift and every perfect gift is from above, coming down from the Father of lights with whom there is no variation or shadow due to change.

Thank you to Daphne England for starting this organization and your team of angels.  From the bottom of our hearts.
Email: NWArkangels@yahoo.com
Their Facebook Page
Please consider being a Sponsor or making a donation by clicking FUND SITE 

Quoted from their home page:

About

This is NOT your typical pageant, this pageant is for anyone with special needs. Anyone newborn-105, with a special need, is welcome to participate. We want this to be an exciting and super fun experience for these kids.
General Information
Our pageant system believes that EVERY child is a gift from God, regardless of their abilities. We love them and praise God for their life and spirit.

These pageants are not about ability. This is simply a chance for us to come together and celebrate these children's sweet spirits. There is no one winner, all of the contestants are winners! All will receive a crown, t-shirt, sash, and a goodie bag.

We welcome any special needs child that would like to participate, no matter which state you reside in.








Monday, July 28, 2014

Weighted Neck Wrap

  Most people think it's odd to see a child walk around with a 'neck wrap' in a grocery store, or out and about.  Especially when they ask your child, "What's that?" and he replies with, "My Melson!".   

Look at his smile!  Thank you Nana! 
  My son Vaughn was initially diagnosed with PDD-NOS (Pervasive Displacement Disorder - Not Otherwise Specified), and noncompliance, as well as what seemed like a grocery list of other axis diagnosis.  Later, that changed to Autism and Mild Mental Retardation.  HE is our little warrior.  We still work on his 'coping skills' when he's angry, but he's come a loooooong way.
   He wasn't given a diagnose till he was four 4 years old.  From the time he was 11 months old, he repeatedly banged his head on any hard surfaces till he had goose eggs, and built up scar tissue on his forehead, but never would cry.  I knew there was something wrong, but it took 4 years of telling his pediatrician that Vaughn was still non-verbal, refused to go to anyone but me, and refused to be near other kids.  When he was near other kids he would bite them till they moved away.  Two separate daycare facilities were telling me he needed to be tested and get help otherwise we would have to find a new center for him.  After the 2nd daycare, I asked them to put it in writing to take to his doctor.  It was a long four years before I got services started for him.  As a parent, you truly are you're child's only advocate.  It is so important to not give up when reaching road blocks.

  While my husband and I were learning about all the different faces of Autism, and specifically - how to help our son with with his needs, we found that pressure therapy worked best for him.  Every night he wrapped himself like a tight burrito with his blanket to sleep.  All the signs were there - but until I dove into researching I didn't know about Autism or what signs to look for.  

  Then one day, a beautiful angel {a.k.a. my mother-in-law} made him a gift when he was 9.  I wanted to buy him a weighted lap pad, vest, or blanket...but couldn't afford one as pricey as they are.  So she made him his own version.

  She told me about how much fun she had balancing the fabric while sewing a lavender/rice mix into each pocket.  I sure wish I could have gotten a picture of that!  Apparently it can get a little messy.  She also made the rice neck wrap 2 sleeves to slip it into like a pillow case.  He has Charlie Brown below, {he loves Charlie!} and the other is a tie-dye designed one.  It works great popping in the microwave for warming up, or leaving in the freezer for cooling/cleaning time.

  Our little sensory craver's face lit up when she gave it too him!  He was glowing with happiness!  He declared he was naming it Melson, and so he did.  Vaughn still gets infuriated if his little brother takes/hides his Melson.  I began to worry it may be a new forming bad habit, but so far he hasn't given anything else a human name.  It was also the first time ever that he named ANYTHING.  Not to mention an inanimate object!!!  For almost the past 2 years, he's toted 'Melson' around his neck almost all day and sleeps with him at night.  The weight from Melson truly helps sooth him.  We learned to never take a road trip (meaning more than 5 minutes) without bringing Melson along.    

  So, we deal with the curious stares, answer the same questions, and go with the flow with a smile on our faces.  If Melson {a weighted neck wrap} helps our son with self soothing so WE ALL can have a better day, I really don't care what other people think of it and so grateful to have this as part of our 'sensory tool box'.   
    
Close up of the pocket stitching.
Full length of 'Melson' 29.5" L x 8" W
Vaughn took 'Melson' with him to get his tonsils removed

  I hope this information can help someone else with sensory seekers!  Do you have any recommendations for other weighted or pressure devices that you don't need to refinance your home to buy?  If so, please share or leave a link below, Thanks!!