Sunday, April 29, 2012

Join Team "Nathan's Voice" In Promoting #Autism Awareness, Understanding and Acceptance In Our Communities and Online


     This coming Saturday, May 5, 2012 is the third Annual Piece Walk organized by AutismOklahoma.org and our Family and Friends Autism Team "Nathan's Voice" will be walking in support of everyone affected by autism. The Piece Walk and 5K is the largest single autism event in the state of Oklahoma. Attended by an average of 5,000 people every May, the annual Piece Walk and 5K generates monies back into the community in the form of grants or special projects and also provides operating funds for AutismOklahoma.org. Our Family and Friends Autism Team "Nathan's Voice" is very excited to be a part of such an AWESOME opportunity to "pay it forward" in the autism community!!  
     Nathan, our almost nine year old son was diagnosed with Autism four years ago. Please consider supporting our Family and Friends Autism Team"Nathan's Voice" by either walking with us this coming Saturday, May 5, 2012 and/or making a donation towards the 2012 Autism Oklahoma Piece Walk, through our team's participation. You are welcome to follow our autism team on twitter @NathansVoice for updates on the upcoming walk.

Saturday, April 28, 2012

The Life Story of Nathan's Voice



     I have been blessed with one beautiful daughter, three handsome sons, a energetic grandson and a precious granddaughter. My husband and I have been together for almost thirteen years and getting ready to celebrate eleven years of marriage. We dated for almost a year and a half before getting married. This is mostly due to the previous relationships that each of us had experienced. If I was going to commit to a relationship, it was important that this person accept my daughter, my son and I as a package deal. I quickly realized that this wonderful man was put in my life for a reason. My daughter and son were afraid that my new husband would try to replace their father, instead he offered them additional support and treated them like they were his children.  

     Vincent was born a little over ten years ago. When I returned to work after having him, we thought that we had found a good home day care. I dropped him off one morning on my way to work and there was a child with green snot caked on his nose standing just inside the playroom. The woman whom I trusted to care for my infant promised that he was just waiting for his parents to come pick him back up. I made the mistake in believing her because the next morning I was taking my son to the hospital because he was running a fever and was having difficulty breathing. My infant son was only two and a half months old and he was being given breathing treatments every four hours. He had been exposed to an upper respiratory infection by one of the children at the home day care. When my husband and I were able to take him home, we decided that I should become a stay at home mom, or most times referred to as SAHM.

     It was almost six years later, we found out that Vincent has had only one kidney since birth. This means that skateboards, trampolinesfootball, joining the military like his older brother, race car driving and motorcycle racing are things that our son should not dream of. My sister, who is a RN and works in dialysis, has already explained to him that if his one kidney is damaged, he would have to do dialysis for the rest of his life. Even if he doesn't fully understand the consequences, we did. 

     Just four months later, our youngest son, Nathan, was diagnosed with Asperger's Syndrome, one of the Autism Spectrum Disorders (ASD). I was sitting in the office of the Special Education Department at our local School Board. Nathan was playing with toys behind me, oblivious to what was happening around him. The school psychologist had just brought Nathan back into the room where I was while he was being evaluated. She sat down across the table from me and said "Your child has Autism". I felt like I had been knocked off my feet! The recent development was not exactly what we imagined for either of our sons but, our family believes in Philippians 4:13 where it says that "I can do all things through Christ which strengthens me". God has always taken care of us, even though we may not agree with His designs. 

     During the next few months, I spent a lot of time searching for answers on the internet. I became more familiar with my son's diagnosis and more comfortable with being his voice to the outside world. In the course of my search, I found that there was a Autism Speaks walk that was scheduled to happen in our area. I immediately registered and started our Family and Friends Team "Nathan's Voice" making myself the Team Captain. The four of us walked in support of Nathan the first year. Several of our family and church members joined us over the next three (3) years. That type of support was important to us as a family. 

     Nathan was going to start kindergarten in about five months and I started working with him on communication and interaction with others. This was critical because he had difficulty doing anything that was not of interest to him. If it didn't intrigue him and hold his focus, it wasn't worth his time. This is where the red CVS pharmacy savings card became more than a discount card. He was so taken with it that he kept snatching it from my purse. No matter how much effort I put into hiding it, he always found it! So his Kindergarten teacher and I came up with rules for Nathan to be able to have access to the ever so popular red savings card. When Nathan got to class each morning, he would hand it to his teacher for the day. If Nathan listened to his teacher, followed her directions and made good behavior choices then the red card would stay in one of her pockets indicating he would get it back at the end of the day. But, if Nathan didn't respond appropriately when he was asked to make the right decision, his beloved red savings card was moved to another pocket. This meant that it would stay at school, in his teacher's possession, until the next day when he would start with a clean slate. That only happened a few times. It upset him so much that I asked the store for another one and let him "visit" it for thirty minutes after we talked about why he couldn't keep it. This was a major adaptation in Nathan learning positive behavior.

     When Nathan started first grade, it was quite a transition because kindergarten had only been half a day. I spent most days volunteering at his elementary school, unless I was assisting in his classroom. With his teacher's permission, I read to his class once a week and brought a small reward for listening to the story. I went on class field trips, helped with class parties and made myself available for anytime Nathan's teacher needed my assistance with Nathan. I started noticing that I spent more time at school than I did at home but, it was worth it in the big picture scheme of things.

     By the time that Nathan had started second grade, I thought that I would be able to juggle a part time job as a substitute teacher and still help at the school when needed. I couldn't have been more wrong...it complicated things for everyone, especially Nathan! Even though I had made sure to tell Nathan's elementary school that I was available as a substitute teacher, the only jobs that I was receiving were from the middle school in the special education department. The problem was that their classes started and ended almost an hour later than the elementary where my boys attended. My dear husband was willing to help pick them up in the afternoon, at first. After a while, he complained that he wasn't able to finish what he needed to do before he had to drop everything to come get the boys. I knew that I needed to do a better job of managing my family to get things back on track.

     Nathan had begun to have problems in school and it was probably due to my not being as available as I needed to be during the day. His second grade teacher, who seemed so understanding at the beginning of the year, had evidently been optimistic when it came to working with Nathan. She was becoming irritated with everything that he did and it was affecting him to the point that he didn't want to go to school. I tried talking to her about what I could do to help her, Nathan and the rest of the class while we figured out how to get the situation resolved. His teacher kept telling me she had it under control but, all I saw was her taking out her frustrations on Nathan by taking his recess away when something didn't go as she had planned. There weren't any positive reinforcements being used in her classroom and it seemed as if she had given up on him. I was fortunate that his special education teacher and case manager had asked me to cover a month of her classes while she was on maternity leave. This was my foot in the door at the elementary school to show the other teachers that I was available to handle their classes, when and if they needed me to.

     Nathan made it through the rest of the school year with a few minor incidents. His class was having P.E. outside on day and when the teacher blew her whistle for the students to line up but, he decided that he wasn't quite ready to stop playing. He ignored her, which was wrong but, how she and her assistant reacted made the situation worse. Nathan was in "play mode" and when the P.E. teachers approached him, thinking that they wanted to play "tag", he ran away from them! This made them mad and he was suspended for one day as a result of the situation they created. I explained to them that his disorder made him process everything different than what another child would. If that type of situation presented itself in the future, to stand completely still while using a stern voice asking him to line up. This would prevent the possibility of Nathan misunderstanding what they are trying to communicate to him. Nothing like that has ever happened again.

     Over the summer break, I began to get frustrated over how the school year had gone and how misunderstood my child was. I didn't know what I wanted to do. I was on twitter and someone asked why I wasn't blogging about our experiences. It started me thinking that this might be the way to document Nathan's diagnosis and progress for him to look back on as he got older. I would be able to keep friends and family up to date on what was going on with Nathan, Vincent, Paul, Candace, my husband and I in the form of a blog. If what I shared helped other families, then that would be a bonus!

     Since I started my blog, Nathan's Voice, I have met so many wonderful parents with children on the autism spectrum. I am happy that I made the decision to start blogging when I did. It has been quite therapeutic, helped me record Nathan's progress, keep track of everything that we have been through, what worked in helping Nathan and what aggravated him! The little blog that I started almost a year ago now offers a variety of resources besides the details of our own experiences with Nathan's autism spectrum disorder. We welcome anyone that wants to check out our autism blog!

Wednesday, April 25, 2012

Nathan's Glow in the Dark Dinosaur

     On Monday, Nathan and other students from his elementary school were rewarded with a field trip to the Sam Noble Oklahoma Museum of Natural History in Norman, OK. Nathan and the other students had met the Accelerated Reader (AR) Goal and earned a partial day away from the school, the chance to tour a great museum, enjoy a picnic lunch and play at a park! Don't forget about getting a round trip ride on the legendary yellow school bus that all of the kids enjoy. I was able to be a part of the excitement by accompanying Nathan, leading him and three other great students plus take some pictures of the outing. This picture below has Nathan's older brother already asking us to take the whole family! And he wants to be able to get something cool like the glow in the dark dinosaur like his brother, Nathan!!


     It has been four years since Nathan was diagnosed with Asperger's Syndrome, one of the Autism Spectrum Disorders. This field trip wouldn't have been a success for Nathan if he had not received special education services through his school for the last four years. He used to not be able to go out in public without hitting himself and screaming at the top of his lungs. Now, Nathan can go anywhere, walk around like any other child and talk to most anyone without them knowing that he has Autism. We are so proud of what Nathan has been able to accomplish which is why I want to draw your attention to this important petition that I recently signed. The proposed changes to the DSM-V stand to rob autistic children of the therapies and services that they already receive. Please read, sign and share to advocate!


"Petition against changes to Autism Spectrum Diagnostic Criteria"
This petition is against the proposed changes to the DSM-V, which would eliminate high functioning ASD patients (PDD-NOS, Aspberger's and Childhood Disintegrative Disorder) from the Autism Spectrum. More than 3/4 of high-functioning autistics would no longer be considered autistic, placing their access to social and school services in jeopardy. Changing the name of their diagnosis from ASD to another name does not make them any less autistic. Basic formative differences exist in all autistic children's brains - including enlarged white matter growth in the first year of life leading to a large cranial size in infancy; reduced brain stem size and function, and confused neural connections, which lead to sensory and social difficulties. These formative differences exist in patients with PDD-NOS and Aspberger's as well. Changing a name will merely shift the tide, rather than stopping the epidemic, and it shifts focus from the real problem - and that is the root cause of autism, which must be addressed.





UNTIL SUCH TIME AS CAUSALITY AND DIAGNOSTICS CAN BE MORE PRECISE, WE 
THE SIGNEES ASK YOU TO HOLD OFF ON MAKING CHANGES TO THE DSM-V. WHEN DIAGNOSTICS ARE MORE PRECISE, AND YOU CAN DEFINITIVELY DIAGNOSE AUTISM
AND RELATED DISORDERS, WE ASK FOR A GRACE PERIOD ON GOVERNMENT PROGRAMS AND INSURANCE POLICY OF NO LESS THAN 5 YEARS THAT WOULD 
ALLOW ASD PATIENTS TO CONTINUE GETTING THE THERAPIES THAT THEY NEED.


I really think this is an important cause, and I'd like to encourage you to add your signature, too. It's free and takes just a few seconds of your time. Please sign the petition below and be sure to share with everyone you know! 

Saturday, April 21, 2012

How Would You Grade Me on the "30 Days of #Autism" Challenge?!?

     I have not been able to write every single day like I would have liked to and I am not trying to make excuses. We all have to re-prioritize from time to time. I just wish that I could have had a perfect posting for the "30 Days of #Autism" Challenge! So, I would appreciate it you would leave me a comment on how you would "grade" me for the "30 Days of #Autism" Challenge. Thank you for your input. It will give me an idea what I need to work on while raising Autism Awareness, Understanding and Acceptance.

     I want to take another opportunity to share with you the names of the blogs, that I know of, who are participating in the "30 Days of #Autism" Challenge.

  • 30 Days of Autism | Leah Kelley
  • 7 Yuckmouths and Autism
  • Aspergers Rules
  • C Gregory Run
  • Caden's Tale
  • Just Bring the Chocolate
  • Kat's Cafe
  • Life is a Puzzle
  • Lost and Tired
  • Making Time for Mom
  • Special Happens
  • Stuart Duncan's
  • Stuck on Shelby


  • Here is an updated list of participants in:
       

    Wednesday, April 18, 2012

    Could My Grandson Have #Autism?

         My daughter has her own children, now. I keep having to remind myself that I am a "Nana" to a very energetic two and a half year old grandson and a beautiful two month old granddaughter. My daughter and her brother that is off in Army Basic Training have grown up but, my new husband and I still have our two sons living at home, an almost nine year old and a ten year old. Our almost nine year old son, Nathan, was diagnosed with autism just a little more than four years ago. The following is a message that I received from my daughter after reading my most recent guest article Autism "How To" Guide For Parents on Our Mom Spot:

    Mom, 
    Your article has opened my eyes to what I have been missing. I'm definitely going to take Devon in for an evaluation. Almost everything you mentioned in this article points to him. I love that you are such a supporting and caring person, and I am glad to be in your life, and have you in mine. Would you accompany me to his doctors to help me know what to do? 
    Love, Candace



    OMGoodness! In the past few months, she has expressed her concerns with his garbled speech but, this caught me off guard. She said that he gets frustrated while trying to communicate with her, sometimes even grabbing her face with a hand on each side to look at her square in the eye. Because my grandson is under three years of age, he would qualify to be evaluated under the Early Intervention Program . My daughter is going to let me know when they are able to schedule an appointment for us to take him in for an evaluation. 
         My grandson's father has voiced his disbelief in his son needing any kind of educational assistance, leaving my precious daughter with little to no emotional support while she works at getting her son the help he needs. I pray that he will eventually be able to accept that his son will benefit from being evaluated now versus later. It may turn out that he might only need speech therapy. We will just have to wait to find out.  

    Tuesday, April 17, 2012

    Join Us For An #AutismAwareness Twitter Party!

    YOU Are Invited
    to a


    Tomorrow Night!
    Wednesday April 18, 2012
    8-9pm EST
    at

    Co-sponsored by

    Please share this information with EVERYONE you know in the Autism Community!

    Psst! I forgot to mention that there are PRIZES!!

    To get more details and to RSVP for 
    the #AutismAwareness Twitter Party
    click HERE!

    Monday, April 16, 2012

    Hanging Out With Friends Over At "Lost and Tired"


         I was invited by my friend, Rob Gorski, over at Lost and Tired to share the story behind "Nathan's Voice" in support of April being Autism Awareness Month. I had to put my thinking cap on to get the basic story down for everyone but, it was something that I was thrilled to do. I hope you enjoy my guest article "The Life Story Of Nathan's Voice" and that you take the time to browse the site of Lost and Tired. Please consider following them on twitter @Lost_and_Tired and be sure to check out Lost and Tired's Community Autism Support

                                                                                                           Lorrie


    *Interested in reading guest blog posts by "Lost and Tired" featured on Nathan's Voice?
     These are the posts we have been privileged to have Rob share with us!