Wednesday, October 26, 2011

Jars by Lisa

I started on a whim a few years ago by making holiday decorations for my own personal use. Til one year my DH suggested I try to sell them, I went from making them for me, to selling to friends & family. It was good for extra cash around the holidays but, being the stay at home mom that I am, in the failing economy, I decided I either needed to go bigger with my jars or find work outside of the home.

I was still really slow getting started but got a big push when we found out this year we were losing our home. I jumped on Facebook and wrestled with a name and Jars By Lisa was created. The last few years was devoted to just making jars for the big holidays, Halloween, Christmas, Valentines day. But then it dawned on me that I could be making Autism awareness jars! I searched high and low for puzzle piece themed stickers or paper punches, anything that I could find and put on a jar to create the look. But my searches always came up with nothing, I ventured into Michael's Arts n Crafts it was always my muse, I could walk into that store and get lost in all the things I wanted to do or make. But even Michael's had nothing for me, it was hard realizing yet again I live in a world where Autism isn't on the forefront of everyone's mind. It got me a little dejected, but after speaking to one of the employees I had a new plan. Why not use real puzzles?!! My pack rat mind had a box at home filled with loose pieces from my own kids puzzles, I also then turned to my friends and fellow Autism moms from a group I'm in, to donate their old puzzles to me.

I love making my jars, I love knowing that they will be in someone's home for years to come. Being able to create something from nothing has become a passion!
~ Lisa

     If you are interested in placing an order for the upcoming holiday, please click Jars by Lisa for more information! Thank YOU for your support...we look forward to hearing from you and helping you with
your purchase from Jars by Lisa!!

*Pssst! Don't forget to check out our NEW Giveaway!
One lucky person will WIN two (2) Jars by Lisa...be sure
 to tell your friends about this spectacular giveaway!! 

Friday, October 21, 2011

Bringing Awareness, Understanding and Acceptance Into Your Child's School

     No matter what learning disability a child may have, a parent's main concern is for their child to be accepted by their peers. Our eight year old son, Nathan, has Asperger's Syndrome, a high-functioning form of autism. Academically, he is where he should be but, it is the challenge of adapting socially that Nathan struggles with daily. He encounters a child every once in a while that has learned to "push his buttons". No matter how much Nathan tries to block out the actions of the other child and things that are said towards him, he eventually loses control of the small world around him.
     This is why I became more involved in our elementary school after Nathan made it through half day kindergarten. His kindergarten teacher had willingly accompanied his Intervention Team Specialist and myself to a three part training in behavior of autism during that year. If it hadn't been for those two wonderful women, I wouldn't have been able to attend due to the requirement of having two educators as part of the team with a parent. It gave me unbelievable encouragement to know that my son had such understanding teachers guiding him at school. We collaborated daily on his behavior, his strengths and weaknesses in order to help him cope with his surroundings.
     During Nathan's kindergarten year the students were joined by their fourth grade Reading Buddies during a certain time each week. Out of appreciation for these understanding students that were reading with my son, I offered to read to their class once a week. I explained to their teacher about a book I had found written from the perspective of a twelve year old girl whose eight year old brother had autism. I was so ecstatic when he agreed to let me read about a disorder none of his students had probably even heard about! I knew it would help them understand him a little better and would hopefully instill awareness and tolerance for them to draw from as they met with him each week. The fourth grade class seemed to get a kick out of it when I would either accidentally, or purposely, use Nathan's name instead of the character, David, when reading the story to them. The book was written on a fourth grade level so there were very few words or phrases I had to change while reading it aloud to them. I really looked forward to reading to them each week because I have always wanted to write childrens' books myself.
     When Nathan started first grade, Nathan's kindergarten teacher had already spoken to his new teacher about the progress he had made the previous year and what we were still working with him on. She was very open to the idea of me coming into class once a week to read to Nathan's classmates. Even though I had to substitute more appropriate words in some places when I read aloud to the first graders, I was more comfortable reading to them than the older students. Every once in a while, I purposely used Nathan's name instead of David's to see if they were still listening. To reward Nathan's classmates for letting me come read to them, I brought them a small snack towards the end of my reading time. I went on field trips, helped with class parties and continued to make myself available to Nathan's teacher whenever Nathan was up against a challenge in his daily routine. The rest of the year I became a parent that most of the student's recognized as "Nathan's Mom" when they saw me in the halls, sometimes in my work uniform.
     Before, Nathan started second grade I had decided that I would become a substitute teacher for our public school system and I could choose to work mostly at our elementary school. Nathan did so much better when he knew I was around the school, or could "pop in" at any given time. I took a few assignments at the middle school, just around the corner, hoping that the elementary school would have something for me in the near future. After the elementary teachers had a chance to get to know me better, many of them were stopping me in the halls, or calling me, to ask me if I was able to substitute for them. Both of my boys but, especially Nathan seemed more secure, or at ease, when I was on the elementary school campus during the day. Unfortunately, I wasn't always able to wait for a substitute assignment at the elementary school. Nathan struggled through the rest of the school year but, I decided that certain things would need to change in order for Nathan to concentrate on his education. He shouldn't have to worry about being bullied, because he's different.
     The last day of school, the students are recognized at a school assembly for excelling in reading, their academic achievements and attendance. Before the assembly, the State PTA President joined our school Principal in a special PTA school meeting to promote the importance parents of getting involved in their child's school. I hadn't been feeling well and, after dropping the boys off at school, I had only stayed to see each of my boys recognized in their separate assemblies. Afterwards, I just wanted to go home, make myself a cup of tea, take my medicine and sleep until I had to pick up the boys from their last day of school. I really wanted to get more involved in the elementary school but, I decided that I would sign up when the new school year started in the fall. The school Principal had spotted me and was determined to make a change of her own by nominating me as the new PTA Treasurer for our elementary school. Before I knew what had happened, I had been elected as part of a new PTA counsel for the next two years! I stood before a crowded room of parents, grandparents and teachers wearing sweatpants, a hoodie over my t-shirt, no make up and my hair pulled up into a ponytail. I spoke briefly to them in how I looked forward to working with the parents, teachers and most importantly, the students during the next school year. I have learned that God works in mysterious ways and to not question but, to be open to changes. Besides, this could be an opportunity to bring autism awareness, understanding and acceptance to our elementary school making it possible for children like Nathan to co-exist without being bullied.
     We have been very impressed with Nathan's third grade teacher and how she has been working with him. She and his reading teacher have been communicating with his Intervention Team Specialist to provide Nathan with the best possible education and daily routine. I have read to his class three times after giving them a chance to ask me questions about autism and how it affects Nathan. It has given me what some might call "the once in a lifetime" chance to help my son's classmates understand and accept other students for who they are. I had noticed in Nathan's first grade class, once his classmates understand more about him, and how each of them was special in their own way, the students were more supportive and protective of him at school. That's what I want for Nathan and every student that gets to know him...to be understood, have awareness of each other and be accepted regardless of how different they might seem from anyone else. I look forward to every chance I have to read, help or do anything with the students at our elementary school. And I make sure the students know that I am not perfect and can make mistakes but, my goal is to learn something new, use my manners and help others when I can. It is important for students to understand they are individually special and can make a positive impact in each others lives.
     For anyone that might be interested, the title of the book I have been referring to is Rules by Cynthia Lord. It can be found in almost any public school library. Or you can buy a copy for yourself at a local bookstore or online.

Lorrie

Tuesday, October 4, 2011

Nathan's Voice & little o' Me Are Being Featured In a Guest Blog on Our Mom Spot!

I can't tell you how excited I am to be featured on Our Parenting Spot as a Guest Blogger! I wasn't quite sure about venturing outside my "comfort zone" especially since I just started blogging recently. Which made me consider the reason that I started blogging in the first place...to raise awareness!! I am sharing "Bringing Awareness, Understanding and Acceptance Into Your Child's School" as my Guest Blog post because it tells what I have been doing to help my eight year old son's classmates accept him, his disorder and other children with disabilities. I encourage YOU to check Our Parenting Spot out!

Saturday, October 1, 2011

Beans, Exercise, and Thinking Aspergers

     I would like to introduce our next Featured Guest Blogger, Lisa Gallegos of Seven Yuckmouths and Autism, in an effort to raise autism awareness and continue to provide a variety of information for our readers! I hope you will enjoy the post and check out her blog, as well as the rest of mine!!
                                                                                           Lorrie

I can't yet put into words how honestly messed up things have been lately. My ability to maintain control is the only thing that hasn't set me off the deep end yet. But I have been able to see the good in the storm, don't ask me how I do it but I do. Part of it has to do with the fact that their are eight other people in this house who count on me to drag my happy self out of bed everyday and keep moving regardless of how I feel so I do. So on to other things for now.

Beans

Racer is obsessed with fruit, its the one thing I can get him to eat any time any day. But beans (seeds) stand in our way. Thanks to a well meaning comment from my 7yr old he thinks if you eat the seeds from any fruit it will start growing inside of you. But because of how Racer thinks not only can he not eat beans but no one else can either....I mean God forbid that one of us grows into a apple! So that leads me to today when Racer and the daddy partake in a afternoon snack of apples. Now Racer will carefully eat the whole top of the apple without the "wet" part touching his fingers, he will eat it down to the core and never expose the beans. The daddy on the other hand must not have heard the "beans story" and ate his apple into the core. Now its not like during this whole time Racer isn't warning him insisting he not eat the beans....with my 7yr old shouting from the bedroom about turning into a apple tree, and me trying to hush everyone. It was like a shouting match for WWE I swear, lol and people outside must think we are insane. Anyways what did the daddy do?!! He ate the freaking beans! After Racer warned him not to over and over again, not sure if at this point in Racers mind he's in high alert to see if daddy turns into a tree so we'll see.

Exercise

So the hubs has been all about getting back into shape....good for him right? He goes walking everyday and then comes home and does jumping jacks and push ups. I'm really proud of him because we are not a great will power kind of family. I'd much rather be doing anything but working out lol. The funny part about this is that the girls...CareBear and PigPen have been doing jumping jacks and push ups with him. lol mostly just bouncing and some jumping and then late clapping but its cute and funny as "h-e-double hockey sticks". The push ups on the other hand are a weird form of PigPen with her butt in the air and putting her face close to the floor and CareBear sitting and kissing the floor. lol I want in on CareBears exercise plans seems easy enough right? But great for the hubs to be working out!! *high fives and slaps on the rear!*

Thinking Aspergers

Now I've fought with my paranoia for long enough, sat thinking about how others would perceive me if I even suggested that I thought for a second that PigPen might have Aspergers. But the more I look at it and watch it the more it looks just like it. For the longest time I thought maybe she was just copying Racer or attention seeking but its so much more than that. So we are going to try and get her tested, but going on my gut on this on this one its Aspergers.

- Racers Mommy
Friday, May 13, 2011

Saturday, September 17, 2011

Why Autism Awareness is broken

After reading this post on "Autism Today" by Lost and Tired, I felt obligated to share this with my readers. I am certainly guilty of "sugar-coating" how things were with Nathan before and around the time he was diagnosed and that really doesn't help anyone understand what us parents go through!

                                                                                           Lorrie


Problem’s with Autism Awareness


I have been wanting to write this for a while but honestly it seemed to exhausting to do. This has been eating away at me and I need to just get this off my chest and move on. I’m not sure how this will turn out but I want to make a few things very clear as to avoid any misinterpretation. Everyone’s problems are relative and I get that.

I am by NO MEANS trying to belittle anyones personal experience with Autism and its impact in their lives. Now with that said, there are some things I need to say.

Autism and my family

I’m the father of 3 Autistic boys. My boys are each in different places on the spectrum (ranging from low functioning to high functioning) so I have very unique experience and perspective that most don’t have.


Gavin and Elliott are our Aspergers kids. Gavin is “functioning” but not “high functioning”. He also has a host of other mental health issues, most notably schizoeffective disorder. Elliott is our middle child and is “very high functioning”. Most people unfamiliar with what Aspergers actually is, would not know that Elliott has any problems but he does. His issues mostly revolve around anxiety. Gavin will most likely never be able to function independently without supervision. Elliott should be quiet successful in life, as he is more enhanced by Autism then hampered.

Emmett is our youngest and he is Autistic. He is “low functioning” and significantly developmentally delayed. He is pre-verbal meaning he does have a few words but little to no language skills. He was believed to be non-verbal but has picked up a few words so pre-verbal is more accurate. He is violent and aggressive but sweet and beautiful. Emmett is EASILY the MOST DIFFICULT challenge I have ever faced….

My wife and I have been walking this journey for 10 years together so far. I have become an expert (as much as possible) on my children’s disorders….and yes they are disorders. So I do have some knowledge and experience in this area.

Autism Awareness in it’s current form


There has been a lot of debate over whether or not Autism Awareness is effective. I would argue that currently it’s not effective but not for the reasons people think. Many people will say that society just doesn’t care. While that may be PARTIALLY true I don’t think that’s the problem.. There is a fracture within the Autism community itself.

We have parent’s with Aspergers kids (like myself) saying things like “Autism does not define my child”. Then we have parents of much lower functioning kids (again like myself) that don’t say much at all because we are just to exhausted, beaten down and demoralized.

Now, I’m going to say this knowing full well how it’s going to sound but I think it NEEDS to be discussed.
Raising a child with Aspergers (again which I’m personally doing) while not without it’s challenges, it’s even remotely similar to raising a truly non/pre-verbal Autistic child. You have to understand that there is a huge difference.

Again, I can say this as I am personally doing both. I have NO experience in raising a truly non-verbal Autistic child and I can’t even imagine how difficult that is.

This is the problem in my opinion. All we really ever hear are the “fluff” pieces about Aspergers from parents and large organizations. Honestly, they aren’t wrong because many of these kids will grow up to be successful or at least independent and God bless them for that. However, the problem is these examples become the public image for Autism and these parents its voice. It just doesn’t portray Autism in an accurate light and it sends the a less then accurate message.

Truly low functioning Autistic kids and their parents don’t share the same positive experiences or hope for the future. From personal experience I can tell you how demoralizing it is for me to hear people say things like “Autism doesn’t define who my child is” or something similar. The truth is, that maybe for them it doesn’t but walk a mile in my shoes (or anyone else who’s dealing with low functioning Autism) and you’ll likely walk away singing a different tune.

I mean no disrespect by this at all. I just see things from both sides. For my part, I assumed that the experience I gained raising Gavin and Elliott would prepare me for Emmett but I couldn’t have been more wrong… I could not believe how infinitely more difficult it was with Emmett and that’s after 9 years of raising Gavin, who breaks the mold in just about all areas. Honestly, it’s a night and day difference.

How can we expect Autism Awareness?


How can we as members of the Autism community ever expect the world to understand when we can’t even be on the same page ourselves. We preach to the world that every Autistic child is different and that’s very true. However, these words become empty if we fail to apply them within our own Autism community. As parents we make the mistake of generalizing things much the same way our kids do.

We generalize our experience with Autism and its impact on the family and transpose that across the board. In other words, we assume that other peoples experience mirrors that of our own. That’s a very dangerous and damaging assumption……. If we are making that mistake how can we expect the rest of the world to be any different?

The follow up to Why Autism Awareness is broken can be found here: How we can fix Autism Awareness


- Lost and Tired

Thursday, September 15, 2011

What is Autism?

I have asked our Featured Guest Blogger, Rob Gorski of Lost and Tired @Lost_and_Tired, for permission to post this article because the Oklahoma Walk Now For Autism Speaks in my area is on Saturday, September 17, 2011 @ the East Wharf of Lake Hefner in Oklahoma City. The following post has been taken in whole, as it has been posted on his blog.

                                                                                            Lorrie                                                                                                                          
                                                                                          
What is Autism?

This is directly from Autism Speaks (The original link can be found here)



What is Autism?

Autism is a general term used to describe a group of complex developmental brain disorders known as Pervasive Developmental Disorders (PDD). The other pervasive developmental disorders are PDD-NOS (Pervasive Developmental Disorder – Not Otherwise Specified), Asperger’s Syndrome, Rett Syndrome and Childhood Disintegrative Disorder. Many parents and professionals refer to this group as Autism Spectrum Disorders.

How common is Autism?

Today, it is estimated that one in every 110 children is diagnosed with autism, making it more common than childhood cancer, juvenile diabetes and pediatric AIDS combined. An estimated 1.5 million individuals in the U.S. and tens of millions worldwide are affected by autism. Government statistics suggest the prevalence rate of autism is increasing 10-17 percent annually. There is not established explanation for this increase, although improved diagnosis and environmental influences are two reasons often considered. Studies suggest boys are more likely than girls to develop autism and receive the diagnosis three to four times more frequently. Current estimates are that in the United States alone, one out of 70 boys is diagnosed with autism.

What causes Autism?

The simple answer is we don’t know. The vast majority of cases of autism are idiopathic, which means the cause is unknown.

The more complex answer is that just as there are different levels of severity and combinations of symptoms in autism, there are probably multiple causes. The best scientific evidence available to us today points toward a potential for various combinations of factors causing autism – multiple genetic components that may cause autism on their own or possibly when combined with exposure to as yet undetermined environmental factors. Timing of exposure during the child’s development (before, during or after birth) may also play a role in the development or final presentation of the disorder.

A small number of cases can be linked to genetic disorders such as Fragile X, Tuberous Sclerosis, and Angelman’s Syndrome, as well as exposure to environmental agents such as infectious ones (maternal rubella or cytomegalovirus) or chemical ones (thalidomide or valproate) during pregnancy.

There is a growing interest among researchers about the role of the functions and regulation of the immune system in autism – both within the body and the brain. Piecemeal evidence over the past 30 years suggests that autism may involve inflammation in the central nervous system. There is also emerging evidence from animal studies that illustrates how the immune system can influence behaviors related to autism. Autism Speaks is working to extend awareness and investigation of potential immunological issues to researchers outside the field of autism as well as those within the autism research community.

While the definitive cause (or causes) of autism is not yet clear, it is clear that it is not caused by bad parenting. Dr. Leo Kanner, the psychiatrist who first described autism as a unique condition in 1943, believed that it was caused by cold, unloving mothers. Bruno Bettelheim, a renowned professor of child development perpetuated this misinterpretation of autism. Their promotion of the idea that unloving mothers caused their children’s autism created a generation of parents who carried the tremendous burden of guilt for their children’s disability.

In the 1960s and 70s, Dr. Bernard Rimland, the father of a son with autism, who later founded the Autism Society of America and the Autism Research Institute, helped the medical community understand that autism is not caused by cold parents but rather is a biological disorder.

posted by Lost and Tired

Friday, September 2, 2011

My Broken Heart

I have the distinct honor of introducing our 1st Guest Blogger, Rob Gorski of Lost and Tired, in an effort to raise autism awareness and, of course, give everyone something else to read besides what I write! The following is taken in full context, as not to leave anything out.
                                                                                                      
                                                                                            Lorrie
                                                                                            Nathan's Voice

To my readers:
The story in the below post happened to me on February 22, 2011. This event has forever changed my life. Please help me share it. This is why we desperately need Autism Awareness. Thank you for reading and helping me share my story…
-LT


It’s been a few days since I have spoken with all of you. Something happened to me a few days ago that I have been struggling to deal with it. I hope you all truly hear what I’m about to share with you. I want everyone to read this and know what happened. Not because of what I did but because of what I learned… Please share this story and help spread awareness.

A few days ago I went to Giant Eagle to pick up some groceries. We had a winter storm on the way and I needed to pick up a few things in case we got snowed in again. I pulled into the parking lot and found a spot right in front of the entrance. My back is out again so I can’t walk very far. As I was pulling into the spot I had to wait for some people to move out the way. They were just standing in the parking spot. Their car was in the next spot over but they just stood there and shot me a few dirty looks, like “who was I to expect them to move”. I just waited, it wasn’t a big deal. I wasn’t even upset. They eventually started to get into their car and moved out of the way so I could pull in.

The snow had already started to fall and we were getting about 1″ per hour. I sat there a second collecting what I needed to take into the store. I just happened to look over at the people that were still getting into their car and I saw a large black man standing there. I didn’t see where he came from but in one minute he wasn’t there and the next minute he was. Then I realized what he was doing. He was wiping the snow and ice off their windshield with his bare hands. The woman looked at him, like, “how dare you touch my car”.

She was clearly disgusted just breathing the same air. Instead of asking him to stop or giving him a few dollars she tried to run him down. She gunned the car forward so fast that her friend who was trying to get into the back seat had the back passenger door slammed on him and he was left standing in the snow. The man who had been trying to clean the windshield was knocked back. This woman just kept shouting things to the man with the bare hands.


Hands_by_rE_Fuuused

I was in shock. I had never seen anything like that before and I never want to again. A few seconds later the man gets up and walks over to me and knocks on my window. I hadn’t even begun to process what I had just seen. Now he was coming over to me and I had no idea what I was going to say. Shamefully, I was thinking “please not now, I just want to get what I need and get home”. Where I live it’s not uncommon for people to approach you for money. So I knew what was probably about to happen. I took a deep breath and started to open the door. The bare handed man opened it the rest of the way, being careful not to hit the car next to me.

The bare handed man was under dressed for the weather and obviously cold. He asked me for change. I gave him everything I had, $2.37. He started talking to me but couldn’t look me in the eye. As he was telling me how cold and hungry he was, I watched as he was unable to control his hands. It was like he was playing an invisible piano. He had a very hard time talking to me and I could see he was much more uncomfortable then I was. He clearly had boundary issues but I never felt threatened in any way. He kept staring off and would occasionally look in my direction but never at me and I never saw his eyes. He stood about 1 or 2 feet in front of me and asked me to drive him to a shelter because it’s “warm there and they have food”. He informed me that he was “homeless and very hungry”. He then told me that he “was not lying to me”. He said “if I lie to you then you might not help me”. He asked me to buy him some food and gloves. I thought about what to say. I knew he would have hard time understanding. I don’t have any money. My family is struggling to survive each day. I would literally be taking away from what little my family has and I just couldn’t. I was trying to figure out how to explain to him that I couldn’t help him. I was lost for words.

Then something happened that shook me to the core and completely broke my heart. As I was trying to form the words I needed to tell him “no”, he looked me in the eyes. All of the sudden I was looking at Gavin. Gavin is the oldest of our three special needs boys (all Autistic). Gavin is 11 years old and is also diagnosed with schizoaffective disorder as well. Looking at the bare handed man was looking through some special window at my son Gavin, 20 or 30 years from now. It was a kick in gut. I was overcome with emotion. It was like I was run over by a freight train. I can’t put words together to really describe what that moment was like.

He again asked me to buy him food because he was hungry and gloves because his hands were cold. Something about him was so familiar and yet I’d never met him before. I looked at him and told him I would buy him some food. He smiled in my direction and took my hand (without looking at me) and led me into the store. He didn’t fit in with the rest of the people in there. His clothes were old, beat up and didn’t smell very good. He had clearly been through a great deal in his life and it showed in his face. I noticed the looks people gave me as I walked with the bare handed man into the grocery store. He asked me to buy him a gift card so he could buy food later on when he is hungry again. So we walked over to the rack and he picked out a Giant Eagle gift card. He asked for other ones but I just couldn’t. We went to the register to ring it up and I explained how to use it. I put $25 on the gift card and the cashier asked if I wanted any cash back. I had them give me $25 cash back. I gave it to the bare handed man and asked him to please buy himself some gloves and a bus ride to the shelter. The last thing he asked was to have the receipt so “when the police stop me, I can prove I didn’t steal this”.

He told me again that he wasn’t lying. I told him I knew he wasn’t. He turned to walk away and he stopped and looked in my direction as to say “Thank You” but didn’t. What he did said more than a simple thank you. He showed me his eyes again for a brief moment before he turned around and left. I stood there completely heartbroken as I watched my son Gavin walking away into the cold. I was beside myself with grief. How could someone I didn’t know have such a profound effect on me?

I just couldn’t shake just how much the bare handed man reminded me of Gavin. I tried to finish the shopping I had to do but I couldn’t remember anything I was supposed to get. I walked up and down the aisles on “autopilot” doing everything I could not to burst into tears. I got to the end of the store and realized I still had an empty cart. All I could think was “how does that happen”. I was smacked in the face with reality. Someday I won’t be here to take care of my kids. What if this happens to them? What if they are the ones wiping off a windshield with their bare hands and almost getting run over by someone who clearly doesn’t care.

I screwed up grocery shopping. I just couldn’t focus on anything. I got what I could remember with what little I had left and drove home. I was completely lost at that point. I just couldn’t process what had just happened. All I could think about was not allowing this to happen to my kids in the future. The horrifying truth is that someday I won’t be here for my kids and I pray they are never in that same situation. I truly hope that if they are, someone will show them kindness and compassion. These are my babies and I get sick to my stomach thinking about what their future holds.

I got home and unloaded the groceries and was in the kitchen with Lizze. I wasn’t going to say anything to her about it but I had to because we already were struggling and now things were going to be even tighter and she deserved to know why. I looked her in the eyes and told her what had happened. I just sobbed and sobbed on the floor in my kitchen. I couldn’t control myself or keep my emotions in check. That has only ever happened to me when I watched Lizze give birth to our kids. The past few days have been rough because I just can’t seem to get past this. All I can think about is my kids and their future. My heart has been broken and I live with the reality that this could be one or more of my kids in the future.

This has been very difficult for me to write. I’m still very emotional. Most parents will never know this fear but I do. Parents of special needs kids live with this indescribable fear each and every day. I wanted to share this story because we CANNOT allow this to happen to our kids. Please help me spread Autism Awareness. I don’t care what it takes but the world needs to be better. These people NEED compassion and understanding. My kids need your compassion and understanding… Please give them that much, I beg you….




- Lost and Tired
February 24, 2011