Temple Grandin cautions not to give up on autistic kids according to our friends at The Autism News!!

Temple Grandin cautions not to give up on autistic kids according to our friends at The Autism News!!

CHICO — When a young child is diagnosed as autistic, parents must move into high gear, Temple Grandin said in Chico Wednesday.

“The worst thing you can do is nothing,” she said.

Grandin, who is autistic herself, is famous as an animal-behavior expert and as an advocate for people with autism.

An author and professor of animal science at Colorado State University, Grandin spoke twice, to large audiences, in Chico State University’s Bell Memorial Union Auditorium Wednesday morning. She also was to be the keynote speaker at the Butte County Farm Bureau’s annual banquet Wednesday evening.

In her talk on autism, Grandin said young autistic children who are non-verbal should have a teacher working with them intensely from an early age.

They need “at least 20 hours weekly of one-to-one teaching,” she said. “Get them engaged. Build on their strengths.”

Autism is “a range of complex neurodevelopment disorders, characterized by social impairments, communication difficulties, and restricted, repetitive and stereotyped patterns of behavior,” according to the National Institute of Neurological Disorders and Stroke.

Grandin said autistic people have major abnormalities “in the circuits that connect different parts of the brain.”

She talked about some of the ways autistic people experience the world differently from how most people do.

In part, autism is “a sensory processing disorder,” she said. “Kids block their ears because certain sounds hurt.”

For more information and autism related news go to–> link

Temple Grandin will be in Las Vegas on the 9th of March for a speaking event sponsored by Future Horizons Publishing.

I wish Temple would help our autistic run autism tech blog and nonprofit get exposure to help us make a change for people with autism!!

Ipad 3 Secrets revealed? Maybe

Ipad 3 Secrets revealed? Maybe

I have been a Apple products user since the Apple 2’s that I used in high
school. Our nonprofit’s intent if we ever get funded is to help autism via Technology, Music and the arts. We will donate tablets to schools. Due to this we are always intrigued by the latest technology.

New Ipad 3?
Will there be a new Ipad 3 soon?

According to Techradar

The Apple iPad 2 has been out for almost a year now, so it’s nearly time to say hello to iPad 3.

The web is teeming with rumours about the new iPad 3 processor, cameras and display, so we’ve gathered together as many details as we can on its possible specifications.

Of course, some of these can be taken with a pinch of salt, but there’s definite patterns occuring and we’d say the final iPad 3 release won’t be that far removed from many of these rumours

So what’s the word on the street about the next iPad?

Apple iPad 3 release date
The iPad 3 release date looks set for March or April 2012, with an iPad 3 announcement in March to coincide with the release of iOS 5.1.

Website YourDailyMac has unearthed iOS 5.1 carrier profiles which carry the possible iPad 3 release date of 9 March 2012 in their names.

However, we’d expect the iPad 3 announcement to be in February, with the iPad 3 US release date in early March and the iPad 3 UK release date in late March.

Apple news site iMore says the announcement will be 7 March, citing sources “which have proved reliable in the past” have confirmed the date ahead of any official announcement from Cupertino.

Digitimes reported in late November 2011 that panel makers had already started shipping panels for the new iPad 3 – a million in October and two million in November.

Foxconn, Apple’s major manufacturing partner, is said to have started production of the iPad 3 in January. 2012. A source at one of Apple’s partners also told Bloomberg also stated that the company began production of the iPad 3 in January, with a view to reaching full volumes in February.

Digitimes says the new model is expected to meet the heady heights of 9.5 to 9.8 million units over the course of Q1 2012.

The Apple iPad 3 will have a quad-core processor
It’s probable that the iPad 3 will have a brand spanking new processor, Apple’s A6 – which will surely be a quad-core ARM-based processor. Quad-core designs are coming from various ARM partners and the Tegra 3 has already been launched by Nvidia, as well as the Snapdragon S4 from Qualcomm.

According to the Korea Times in November 2011, the A6 processors are to be manufactured by Samsung, despite the companies’ ongoing patent battles.

Apple iPad 3 display
A retina display was widely predicted for the iPad 2, but of course the current iPad doesn’t have a double-resolution display: for now, that’s something you’ll only get in the iPhone 4 and iPhone 4S. Could an iPad 3 Retina Display be on the way? It’s the very first thing on our iPad 3 wish list.

The exciting news is that it looks as though it is happening, with Apple reportedly testing suppliers’ current shipments of 2048 x 1536 resolution 9.7-inch displays. Now that iBooks 2 has been launched (as of 19 January 2012), we’ve also seen further references to 2x iPad screen images – these will, most likely, be for iPad 3.

However, it’s not always been plain sailing for the display – rumours continued over the summer and autumn of 2011 that the retina display in the iPad 3 was continuing to be a challenge.

Back in May 2011, we reported that the iPad 3 could launch with a Samsung-made AMOLED screen, following rumours that Apple was in talks on the matter with Samsung execs. There have also been more LG and Samsung rumours, too.

However, according to the Wall Street Journal in late November 2011, Sharp will manufacture panels for the device. Apparently Apple is investing in infrastructure at Sharp’s LCD plant. Further rumours said that Apple is looking to implement some nifty dual LED lightbar technology into the iPad 3, apparently in a bid to counter-balance the brightness issue that the Apple tablet may have, due to its super-high pixel density.

A part leak in early December again pointed to a Sharp-manufactured 2048×1536 retina display and dual lightbar.

Another source of ipad rumors is Link

The amazing folks at the Boy Genius Report also have information as well–>http://www.uswitch.com/mobiles/news/2012/02/ipad_3_to_feature_quad_core_processor_leaked_snaps_reveal/

An awesome article on autism awareness by Liz Becker on The Autism Support Network!!

An awesome article on autism awareness by Liz Becker on The Autism Support Network!!
Liz Becker, amazing article autism awareness!!
Liz Becker, amazing article autism awareness!!

I recently read this incredible and though provoking article on The Autism Support Network. Being on the autism spectrum and having 3 kids as well on the spectrum I can totally relate in many respects.

Here is a link to the original article–>link

Autism awareness is everything. The difference between being unaware and awareness can be illustrated in looking at my son’s high school experiences and the journey he took toward social interaction. In reflecting on these emotionally charged years I realized something else…. there is enormous harm inherent in a school system that does not provide autism awareness to its general student population.
I taught at the high school level years ago, during the same time that my son Matt was a student in a different high school. I would bring Matt to some of my school events and this simple act of inclusion paid off in his ability to interact socially with his peers. We attended events at his school also – but with quite a different outcome.
One of the events was an academic competition between area schools. I was one of the science judges. Matt would sit in the audience with me until the science portion was announced, at which time I would take my place at the judges table leaving Matt to stay in his seat and watch, listen, and draw. Matt always brought pencil and paper – it was one of those behaviors that calmed him – sort of like Linus and his blanket (Charlie Brown’s best friend). For the first few competitions he would draw until the match began, at which time he would then sit up straight and listen to each question and answer. After a few competitions I noticed just how much knowledge this child kept under wraps. Sometimes his answers were wrong, but most times he was right. He answered each question in a whisper as he competed by himself. Matt’s forte was (and still is) History and Geography. During these questions I would be sitting with him and he would quietly answer each question as if it each were common knowledge. He would give a long slow sigh if the students got it wrong, as if he just couldn’t fathom anyone not knowing such simple historical events or locations.
Realizing he could be an asset to his school’s academic team we had Matt join – only to be left out of the group practices. They would never allow him to compete having already decided that Matt couldn’t do it. His autism affects his speech, which is hesitant. Under stress it is even more so, and he will struggle to initiate that very first word. Once he gets the first word out the rest is not a problem. Practice was everything. By assuming he couldn’t do it they guaranteed he couldn’t do it. Matt’s stress was too much. He wasn’t fitting in and he knew it. We decided he should just drop out.
Sitting in the audience with me, and with no pressure to respond, Matt easily answered most of the questions at every match, year after year. His school missed out on a very knowledgeable competitor – Matt missed out on social interaction with a team of his peers. Each time his school was up against my school Matt rooted for mine – not his. Do you blame him? At the matches for my school Matt was in seventh heaven. You see, many of my students were competitors and they knew about Matt. I had told them about autism, what it means, what behaviors are evident and who Matt really was and they eagerly asked questions and sought information. Matt’s introduction to real peer social interaction actually was initiated by my students at the academic competitions. I had explained to my students during class that the first introduction would seem a bit strange as Matt would look downward and most likely not speak to them, but if they came over again he would actually greet them by name and look right at them. Several of the students tried it out – stopping by for the introduction before the competition and returning after the competition to say good-bye. They were amazed at the difference between the two meetings. Matt would smile and looking right at them, wave and say good-bye as if they were long-time friends.
Matt got to know my students after weeks of academic competition, so it came as no surprise that whenever I had another school event to go to (plays, sports, and dances), Matt was eager to come along. He was approached at football games, baseball games, and plays by my students every single year and that made a world of difference. He felt as if he belonged there and it made him feel good about himself.
He went out for sports at his school only to be left sitting on the bench, never once given the chance to prove himself to be just another kid. At my school, the wrestling coach wanted him to be their official videographer. At his school he was never accepted. At my school they loved him. The secretaries hung his drawings on their walls, the students asked him to come to their plays and when they saw him out in public places always stopped to chat. Student often asked to see the latest in his art portfolio which he carried with him everywhere. The differences between the students and adults at his school and those from my school were blatantly obvious. During school hours he had a wonderful paraprofessional and he loved his school, but it was at mine that he felt free to be who he was.
The most memorable event came in Matt’s senior year – his prom. He couldn’t have done that type of social event if it had not been for the autism awareness at my school. At my high school, prom was a really big deal, with decoration of the gym consuming the entire spring semester. Prom was always elaborately creative with several departments lending their expertise; art, drafting, building trades, home economics, and even P.E. (for the labor). The gym would be transformed over a period of months into magical gardens with waterfalls (real water!), sculpture lined pathways, and cozy dining areas with drink fountains and fancy appetizers. As one of the senior sponsors I was a chaperone – and I brought Matt.
The first time I took him with me to prom Matt was only 12 years old. He looked around, took pictures, ate some cookies and drank some punch. He was introduced to new people and watched the students dance, but he stayed on the sidelines and walked the perimeter. The next year he got more into it and even danced with the young daughter of one of my teacher-friends. The year after that he even danced with a few of my students. The young ladies would come over and engage him in a short conversation and then ask him to dance. Shy at first, they would gently take his hand and walk him to the dance floor. They understood what autism meant and what Matt had to deal with in regards to sensory stimulation and troubles with speech. They were gentle and soft-spoken. It didn’t take long for Matt to feel comfortable in such a large gathering of people his own age. They were friendly … and they were safe.
The years went by until finally the time arrived for Matt to attend his own Senior Prom. When asked if he wanted to go he declined at first, but when he learned his two friends were going – and they wanted Matt to be there – he soon changed his mind. Getting him fitted for a tux, buying flowers and choosing a place to eat were all minor decisions. The major decision was getting a date. Matt doesn’t date. The social mingling of a boy-friend and girl friend couple are beyond his comfort zone.
My husband and I talked it over and decided if Matt were to have any fun at his prom he would have to go with someone he knew well, someone he could have a great time with, someone he could be himself with, someone who knew him . . . like his step-sister, Sarah. We called Sarah, who was at college, and asked if she would be interested in taking Matt to prom. The request was met with a resounding “Yes!” She would come home from college on that weekend and escort Matt to his Senior Prom!
The big day arrived. Matt got dressed in his tux and at first pulled at the collar and complained about the tie, but after hearing all the great compliments on his attire, decided it wasn’t so bad. He knew he needed to wear the tux – he had seen the young men at my school each year all dressed in one. Sarah dressed in a pale lavender gown with her hair French-braided – she looked beautiful! Matt gave Sarah her wrist corsage. Sarah gave Matt his boutonniere. We took pictures of the smiling faces of a very handsome pair.
They went to dinner with Matt’s friends and sat with them at the prom. There was laughing, conversation, and dancing. For days afterward people asked me, “Who was the beautiful young lady that went with Matt to Prom?” Part of me wanted it to remain a mystery, but I was too proud to keep it a secret.
Going to Prom was a milestone. I never would have guessed that Matt would’ve been willing to subject himself to the noise and the lights. He was comfortable in that large group because he had practiced going to similar events for years. He truly enjoyed his prom because he knew how to go to prom. Matt was a senior and going to prom solidified his feelings of pride. He realized he had achieved what each of his siblings had achieved – and he was going to graduate! The weeks after prom flew by and Matt stayed on cloud-9 the entire time.
Would Matt have gone to prom if I hadn’t subjected him to all my high school events? I don’t think so. Matt found acceptance at my school that he didn’t have at his own. Classroom acceptance is limited as the other students knew he was autistic and that he was “special-ed.” They didn’t realize he was a young adolescent just like them with feelings and intelligence. After school programs are ways for students to interact socially, but he couldn’t do that at his own school. The students there were unaware and that alone can lead to bullying or misconceptions about ability. The two friends Matt had were children he had grown up with – their mothers and I are friends. Matt’s friends were aware.
I honestly feel that had he not had the many practice sessions at my school with my autism-aware students he would not have been comfortable enough to attend his own prom. Events at his own school were too stressful for him. Coaches considered him a liability. Other student’s tried to make fun of him. It was different at my school. My students learned about autism and learned about the ways in which to interact with my son. They were eager to meet him and enjoyed bringing him into their fold. Their openness to learn, to interact and to genuinely discover who Matt really was made all the difference.
The difference on how autism was viewed was determined by the degree of autism awareness students at each school had. What is needed in every school is an autism awareness program that reaches across the curriculum so that students can have the opportunity to learn and understand.
Understanding autism – isn’t that really the main obstacle parents and their children face? It’s time to bring autism awareness into the schools.

Read more: http://www.autismsupportnetwork.com/news/autism-awareness-teaches-more-just-facts-3839292#ixzz1mHBwMzO1

A nice article from Autism Support Network–>Autism & living on purpose by Lena Rivkin

A nice article from Autism Support Network–>Autism & living on purpose by Lena Rivkin

A link from Autism Support Network and the original article–>http://www.autismsupportnetwork.com/news/autism-living-purpose-3789343

I never know when to stop saying Happy New Year. I strive to hold onto the feeling of renewal, hope and fresh starts that the New Year provides. But holidays quickly recede into the rear view mirror, since the business of living demands our full and present attention, until the next round of designated pre-programmed holiday landmarks sneak up on us. Of course we all endeavor to
live as if every day were a holiday or the first day of the rest of our lives, but that eventually becomes exhausting- usually around mid-January.
However, for those of us with special needs children or siblings, we consistently struggle with how to make the every day more meaningful and resonant for them. My brother, Phillip, is a severely autistic adult and lives in a group home administered by New Horizons. I feel a certain amount of self-imposed pressure to make each visit with my brother intently unique: for his wellbeing, his development, to bring some joy into his quiet little world.
This year I’m resolving to invent cost effective yet special monthly ‘holidays’ for Phillip. And I believe this is an idea we can all build upon and re-invent with our particular families in mind. Each family has a favorite activity- whether our monthly ‘holiday’ is organized around a favorite sport or place to go, making food, music or art together; it is within all of us to find creative ways to make family time together vivid, fun and commemorative.
In my brother’s home we celebrate everyone’s birthday, even if it’s staff or a family member. This creates a loving and fun-filled family-style environment where any seemingly ordinary day is special to someone and worthy of attention. And exposing our special needs family member to variety, to change and the world outside them is as important for them as it is for us. New Horizons places a special emphasis on frequent group outings, which many of the clients anticipate with glee.
As a child I would veer from being overly protective of my brother to being embarrassed by him. Once, when our parents took us to a restaurant Phillip casually helped himself to another diner’s french fries while we were walking to our table. He was ten and figured that since he loved french fries he was welcome to them, no matter whom they belonged to. Our parents had a great sense of humor about Phillip, but I was seven and wanted to crawl under the table. We both have grown up in our own ways- I’m no longer concerned about what the world thinks of my brother and he no longer helps himself to other people’s meals!
I know it’s crucial to take Phillip out into the community. Society needs to be exposed to every kind of person. We all need to swim together among our differences and commonalities. Hopefully bringing Phillip and his friends from New Horizons out shopping will promote education and understanding as to how other families cope with life’s challenges. Our special needs siblings and children have guided us to open our hearts to people with disabilities- and out in the world, Phillip sweetly wins the hearts and minds of people who once eyed him with apprehension.
One of the myths of individuals with special needs is that there is a lack of emotional sensitivity and limited interest in the outside world as compared to higher functioning people. When someone does not communicate verbally or with socially acceptable body language, it is easy to dismiss this person as being unworthy of our attention. Besides, we are all deeply consumed with making our lives tick like Swiss clocks; it’s increasingly difficult to make time we just don’t have for those of us with complicated needs.
A thoughtful and insightful friend recently asked if I shared information about my life with Phillip. I was stunned to consider the notion of my brother wanting to know about my life. I’ve usually been so consumed with caring for him, that the one person who has known me longer than anyone living- has a severely limited knowledge of me … because it never occurred to me that the details of my life would matter to him.
On my next visit I was taking Phillip to get his haircut. Phillip truly loves going anywhere but he especially loves getting his haircut because Catalina, his stylist, dotes on him and has one of his needlepoints framed on the wall of her Dominican Salon. It’s very moving to see people take time for Phillip and for them to create meaningful moments for him. Catalina is one of these people.
In the car ride over I knew Phillip was excited because he was humming. I decided to talk to him the way I would talk to a friend. I casually chatted to Phillip about my latest art project. As I was talking, my brother stopped humming, looked me straight in the eye and held my gaze. I could tell he was paying attention to me. This was a deeply teachable moment… for me. Believing that my life is as important to my brother as his life is to me is one of the light bulb moments that make regular, ordinary days anything but.
The bar has been raised. Here’s to a new year of discovering what tiny gestures can contribute meaning and love to our deeply special families. Having a monthly celebratory goal can keep the feeling of a new year with new hopes alive longer than the resolutions that dissolve somewhere around January 15th.
Lena Rivkin, M.F.A., is an artist and graphologist living in Los Angeles.

I was really impressed by the article, my 3 kids are on the spectrum as am I. One of my son’s is similar it seems to Phillip in many respects, he is 15 almost 16 but I unlikely to live on his own, we do not know for sure but it seems likely that he will not be able to handle himself.

Read more: http://www.autismsupportnetwork.com/news/autism-living-purpose-3789343#ixzz1mH7nICtl

Read our articles on tech and autism as well–>link

We are seeking donors, and sponsors to help us to help people with autism and their quality of life.

Just a little heart attack, A video from the American Heart Association and Go Red for Women-worth watching!!!

I recently saw this nice video on Youtube in regards to heart attacks that is really informative.

We all have to be careful and aware.

Please share it with the people you know and love.

Here is a link to their site—>link

Super Bowl Sunday 2012, and an article from Autisable

Super Bowl Sunday 2012, and an article from Autisable

Though I would have liked a west coast team like the 49’ers to be in the game, in the end it is what it is. I am rooting for the underdog, can relate being a person on the autism spectrum. Go Giants. My kids and I will eat snacks and watch the game. My more autistic son will probably watch a few minutes, get bored and play video games.

Here is a nice article that I found on the amazing autisable.com site–>

http://www.autisable.com/758836588/superbowl-sunday-poems-dsm-5-and-autism-speaks/

Time for one of my favorite days of the year…Superbowl Sunday! Obviously I am rooting for the Giants! On Friday I went to the Autism Speaks Awards Reception in Princeton, it was such a fun night! They honored the top teams, individual fundraisers and shared some new studies with us. I am honored and thrilled to be the 2012 Publicity Chair for Autism Speaks (Central NJ) and hope this year’s walk is the biggest yet! I will be blogging a lot about Autism Speaks, since I have been volunteering with them for a few years now, and I think they are wonderful. I wanted to talk about a few things that some of you have asked me to blog about! Feel free to send me ideas

more–>

An interesting article from Autisable–>What does the future hold for my autistic child?

An interesting article from Autisable–>What does the future hold for my autistic child?

When you mention that your child has Aspergers Syndrome, most that have some understanding of the syndrome, just think the characteristics are a lacking in social interaction skills, literal understanding, or an intense special interest. There is so much more to Aspergers then this! One of the main difficulties for Little man is learning independence skills, the most basic everyday things that a “typical” child masters in the early years of life, such as tying their own shoe laces, Little man is only just beginning to do at the age of 11 years.

The article comes from http://aboywithaspergers.autisable.com
For the rest of the story click here–>link

Do you reside somewhere on the autism spectrum? In the near future, you may not.(Theautismnewswire) and The New York Times

Do you reside somewhere on the autism spectrum? In the near future, you may not.(Theautismnewswire) and The New York Times

http://www.theautismnewswire.com/NewsITems.aspx?newsID=954

Benedict Cary Autism Article NY Times
Mary Meyer, right, of Ramsey, N.J., said that a diagnosis of Asperger syndrome was crucial for her daughter, Susan, 37.

I found this interesting and troubling article recently from Theautismnewswire–>

One of the mental conditions facing major emendations in its D.S.M. definition is autism. If the changes go through, a recent analysis suggests that the rate of official diagnosis for autism, and related disorders like Asperger syndrome, could plummet. And that, some people worry, could be bad news for those marginalized by the new diagnostic criteria.

The revision of the D.S.M. puts the APA in the unenviable position of having to draw what the New York Times calls “the line between unusual and abnormal” in relation to mental disorders; in the case of autism, the fact that symptoms are widely believed to manifest themselves along a “spectrum” of class and severity makes the situation even more difficult to navigate. According to the Times:

At least a million children and adults have a diagnosis of autism or a related disorder, like Asperger syndrome or “pervasive developmental disorder, not otherwise specified,” also known as P.D.D.-N.O.S. People with Asperger’s or P.D.D.-N.O.S. endure some of the same social struggles as those with autism but do not meet the definition for the full-blown version. The proposed change would consolidate all three diagnoses under one category, autism spectrum disorder, eliminating Asperger syndrome and P.D.D.-N.O.S. from the manual. Under the current criteria, a person can qualify for the diagnosis by exhibiting 6 or more of 12 behaviors; under the proposed definition, the person would have to exhibit 3 deficits in social interaction and communication and at least 2 repetitive behaviors, a much narrower menu.

If the proposed changes come into effect, an analysis conducted by Yale researchers Fred Volkmar, Brian Reichow and James McPartland indicates they could have a dramatic impact on everything from diagnosis rates (some estimates indicate that autism diagnoses have mushroomed to one child in 100 in recent years), to the ability for many people — people who presently reside somewhere on the autism spectrum of disorders — to access health, educational and social services.

“Our fear is that we are going to take a big step backward,” said Lori Shery, president of the Asperger Syndrome Education Network. “If clinicians say, ‘These kids don’t fit the criteria for an autism spectrum diagnosis,’ they are not going to get the supports and services they need, and they’re going to experience failure.”

For more information on this article click here for the original story from The New York Times By BENEDICT CAREY
Published: January 19, 2012
–>
http://www.nytimes.com/2012/01/20/health/research/new-autism-definition-would-exclude-many-study-suggests.html?_r=3&src=tp

Our week long review of Lethal Audio’s High Performance Earsubs with Microphone

Our week long review of Lethal Audio’s  High Performance Earsubs with Microphone

While I was at CES 2012, I was given a set of Lethal Audio’s “High Performance Earsubs with Microphone.” They are edgy, interestingly designed, sort of appealing to the young rocker crowd. To put it mildy I am very impressed by them.

I have used them to watch Netflix videos, listen to music, and do conference calls for my full time job with Pitney Bowes.

The sound quality is very good, they are lounder than other head sets with microphone that I have used, and the microphone works well.

I like that the cords that go to the earphones are wrapped in a nice solid covering. The covering also helps to stop them from tangling as well.

I like their fit and finish, as well as the cool little bag that they come with to store them in your pocket with.

If you are looking for nice quality ear buds with a microphone for music, conference calls or gaming these are an excellent choice.

They have nice sound, great bass response, and a nice design and image.

Here is a link to their site as well–>http://lethalaudioheadphones.com/earsubs/5554/5554.htmls

A thanks to http://www.theautismnewswire.com/ for an article on us!!

A thanks to http://www.theautismnewswire.com/ for an article on us!!

http://www.theautismnewswire.com/NewsITems.aspx?newsID=944&utm_source=Autism&utm_campaign=5000e5c66b-20120121&utm_medium=email

I appreciate that The Autism News Wire did a recent article on us.

We are trying to make a difference for autism and can not do it alone.

Please check them out, their nice content.

Here is a summary:–>

I dream of establishing a national organization like the American Heart Association or American Cancer Society to make living on the spectrum better for those with autism related disorders. Utilizing my knowledge and passion for technology with my personal experience and interest in autism, I launched https://technewszone.com, on January 11, 2011 .

We are a tech-focused state nonprofit. As we get funded we intend to help those on the autism spectrum by using technology-tablets and related computer technology plus the gift of music and the arts, to make the lives of people with autism better, and to support their families and the educational facilities that serve them.

We have a unique approach, view point and ideas.

Our Plan:

Our intent is to give the gift of technology through donated tablets and along with proper training to children and young adults with autism, their families, and the educational programs and schools that could make use of them. We also plan to fund applications to use with the technology.

Tablets are a very kinesthetic device which seems to make learning easier for many people with autism. Tablets like Apple iPads aid in education and improve the level of involvement in many aspects of their lives. However, a decent tablet runs $400-$800 which is very expensive for most families of people with autism.

Our second intent is to give the gift of music and the arts. Schools are very short on funding especially for the arts and music. Most parents of kids with autism cannot afford instruments, band trips, choir events and other arts materials. We want to help.

We will donate musical instruments to people with autism and education to improve quality of life. In addition, we will give the resources to provide help to theatre programs in both private and in public schools, as well as other arts that accept people with autism in their programs. We strive to promote inclusion and acceptance.

In order to further the quality of life for people with autism we want to expose them to cultural events. We will donate tickets, to musical events, theater, and other arts to enrich their lives.

I feel that many people with autism are talented in the arts and music. Even if not talented in the arts, I feel they can definitely benefit from the exposure to arts, music and technology.

A version of this article was originally published on The Autism Spot, an excellent resource for autism related topics.

http://www.autismspot.com/blog/Guest-Piece-%E2%80%93-Autism-Advocacy-and-Technology-News-Zone

It is in our genes, Autism..
It is in our genes, Autism..