GIVING AUTISM A VOICE: Funding should be geared more for quality of life-Pahrump Valley times

GIVING AUTISM A VOICE: Funding should be geared more for quality of life-Pahrump Valley times
GIVING AUTISM A VOICE: Funding should be geared more for quality of life
GIVING AUTISM A VOICE: Funding should be geared more for quality of life

http://pvtimes.com/community/giving-autism-a-voice-funding-should-be-geared-more-for-quality-of-life/

We were in the Pahrumnp Valley Times news paper today, A mention on the front page as well as on the front of the community section as well.

Here is a copy of the article–>

By Kelsey Givens
One in every 88.
That’s the alarming rate in which children in the United States today are being diagnosed with autism, according to the National Autism Association.
People in every state, city and community are seeing the effects of this developmental disability.
Not everyone touched by it, however, has the financial ability to go out and purchase items to better the lives of individuals living with it.
Knowing the affects of the condition first-hand, one man is trying, with the help of investors, to get his nonprofit up and running in order to actively place technology and the arts in the hands of disadvantaged families with autistic children and young adults.
David Berkowitz, a Las Vegas native, has Asperger’s Syndrome, a high-functioning form of autism, and three children who have also been diagnosed with some degree of autism as well.
A retired veteran currently working in sales, he started his foundation, Autism Advocacy and Technology News Zone, last year with the hope of raising money to buy and donate technology, music and the arts to families and schools working to educate and better the lives of people with autism.
“As an individual with high-functioning Asperger syndrome and the father of three kids who are also on the spectrum for this disorder, I have always felt a need to make a difference for people with autism,” Berkowitz said in a statement.
“As we get funded we intend to help those on the autism spectrum by giving the gift of the arts and technology to make the lives of people with autism better, and to support their families and the educational facilities that serve them. We are determined to make a difference in the lives of people with autism and their families,” he said.
According to the National Autism Association, autism is a “bio-neurological developmental disability.”
Generally appearing before the age of 3, this condition generally affects the development of areas in the brain which control social interactions, communication and cognitive development.
The NAA states autism is four times as likely to affect males as females, and 40 percent of children diagnosed with the disability typically don’t speak.
Sadly, the association also reports that while autism has become one of the fastest growing developmental disorders in the nation, it is also one of the most severely underfunded.
While some organizations exist to raise funds for the study of how autism affects people, Berkowitz said he wants to focus more on helping enrich these individuals’ lives.
“Were trying to help create an autism foundation for quality of life and education because no one is really doing it,” he said.
Berkowitz explained items like iPads, other electronic tablets and musical instruments are very kinesthetic devices, which make learning much easier for those on the autism spectrum.
He hopes by being able to provide these types of learning tools to families and schools, he can help enrich the lives of those with autism, while also giving them another way to communicate and interact with the people and world around them.
“A lot of families with autistic kids aren’t rich, they can’t afford to just go out and buy these things,” Berkowitz said.
And by introducing more music and the arts to people with autism, Berkowitz said he believes it may be possible for these kids to find an easier way of expressing themselves or finding a talent they would have never known they had.
“Half the time you don’t even know if they could succeed in these areas and don’t have the money to even give them the chance,” he said.
By gaining funding through partnerships and donations, Berkowitz wants to not only purchase the tools but possibly sponsor activities such as artist meet and greets, free concert tickets or special events to help raise awareness for autism.
Lack of money is keeping the dream from becoming reality.
“The first help we need is funding for the 501(c)(3), as well as a lawyer or CPA to do the paperwork properly. We also need exposure such as TV, in the newspaper, magazines and web-based as well. We can not do it alone and need support to make a real difference,” Berkowitz writes on his website.
“What we really need is for some other organization or company to partner with us so we can get the accreditation. There’s not much we can do until we can get that and it’s expensive.”
Berkowitz said it can cost thousands to become an accredited organization.
“I’m not rich, I can’t just go out and pay for this myself,” he said. “We have to start somewhere, and maybe by reaching out to the community someone will be willing to help us.”
While the organization seems to be hitting a wall in the way of funding, it isn’t for lack of trying.
Berkowitz has gone on several news shows, Internet radio shows and use of social media in an attempt to get the word out about what he is trying to do.
“There are a lot of people spreading the word about us on Twitter, and we’ve been featured on SpecialNeeds.com,” he said.
While the name of the organization is continuously put out there, “it has been a struggle to reach people able to help,” Berkowitz said.
Currently Autism Advocacy and Technology News Zone have a board of only two people; Berkowitz and his wife Michele. But Berkowitz said he knows several people that have said they would join once the group is accredited.
The group is based out of Las Vegas, where Berkowitz lives, but he said he doesn’t want to be limited to helping only those in the city. He wants to reach out to all surrounding area families as well, areas like Pahrump, to be able to help families dealing with autism.
“Autism affects you socially, and my family understands that, we’re living those lives ourselves,” Berkowitz said.
“I am smart, different and am going about it on my own; I need support so that I can help other people with autism,” he said.
The foundation currently had its own website technewszone.com.
Anyone interested in donating to the organization or trying to help them reach their goal of becoming a certified 501(c)(3) can go there for more information.
Berkowitz can also be reached by email for more information on how you can help at [email protected].

I appreciate it a great deal!!!

Aspergers Syndrome The Hidden Disorder by Mari Nosal

Aspergers Syndrome The Hidden Disorder by Mari Nosal
autism nosal pict
autism nosal pict

This article is very valid. I am asperger’s, have always been a brainiac so was considered a bit different but normal. In 43 years, I have had few friends. I am married but other than my wife, I have had no real friends in decades. I want friends,but people do not get me. I reach out to people and ask them to help my non-profit but it is a struggle.

I hear from people all the time, that I need to work on this or that socially, or to slow down, or simplify. It really annoys me at time, why should I have to change who I am for them, why can’t they expand their level of understanding. I am told your eye contact is bad,it has hurt me many times over the years in job interviews because I talk fast, and have poor eye contact. As LMFAO says sort of, I am autistic and I know it..

I really like Mari’s article and can relate in many regards.

Lately, I haven been observing comments regarding what Aspergers is, how it effects the lives and family of individuals living with this syndrome , their family, and individuals whom they have daily interaction with. My experiences and opinions conveyed in this article are not internet and research related. They are resultant from bringing up a son who lives with Aspergers daily.

Aspergers is not outgrown, nor curable. Individuals with Aspergers merely learn compensatory strategies as they grow and silently struggle daily with their difficulty communicating, working with, and living with the neurotypical population. Aspergerers is a neurological disorder which effects many aspects of their daily lives. Because they tend to have normal to above normal I.Q.s, society perceives them as merely quirky loners.

The old phrase, “One cannot tell a book by it”s cover” is an appropriate analogy here. Ican equate their issues with a cast. When one sees an individual with a cast, they know that individual has a broken bone. In regards TO Aspergers, these individuals look like functioning neurotypicals on the exterior. I will now explain that is not the case.

Aspergians have issues impairments with communication, appropriate behavior, and socialization, or assimilation in the neurotypical society if you will. Children with Asperger’s have excellent and advanced expressive language skills. (speaking to people) Aspergians have large vocabularies and are excellent at conveying data, information, what happened on a T.V. show, etc. i.e. factual information. They often have difficulty in reciprocal conversations.

Their difficulty conversing in social situations goes beyond a lack of interest. On the contraire, they silently wish that they could socialize better. I recall my son calling from college. He attempted to join groups because he wanted to fit in with other students. He attempted to join the Frisbee club, but impaired motor skills hampered that effort. He attempted to join in at parties but difficulties with reciprocal conversation squelched that effort.

My son called me at home making me aware of his efforts to fit in, have a girlfriend and more. He informed me of his efforts to make friends and socialize. My heart broke silently when he said, “Mom I try and try to fit in but it is not working, can you teach me?” I suggested he join the computer club and he responded by saying, I only like computers because I have nothing else. My computer is my only entertainment.

Aspergers creates havoc in terms of the individual’s ability to process information, strategize, and receive information. Hence, their difficulty with receptive language. (Processing and absorbing information) Reading body language and knowing how to respond when someone is sad, despondent, or distressed is difficult for Aspergians. I recall a gentleman telling me that he wished he new what to say or do when his wife was upset.

The man told me that it hurt him greatly because he wanted to say and do the right thing in such situations but did not know how.

Individuals with Aspergers are prone to sensory overload when presented with loud noises, strong odors, office environments where several conversations are going on simultaneously, and parties where background music is playing while people attempt to converse with them. It is not uncommon for Aspergians to have tertiary anxiety disorder which rear their ugly face in situations mentioned in the latter paragraph. Aspergers is a neurological condition.

On the surface they tend to be academic prodigiesin certain areas of academia. Hence their nickname as children of the little professor. In reference to language skills, many aspergians speak in a concrete format and upon further review in a reciprocal conversation their sentences may be out of context. Due to receptive processing language deficits, many individuals have difficulty with being given more than several steps through the auditory modality at one time.

It is a misnomer that Aspergians do not warrant speech therapy. On the contrary, speech therapy can assist children in honing expressive language skills i.e. using descriptors, expressing emotions verbally, describing an experience like a trip to the zoo in more than rote terminology. Speech therapy can also assist children with deficits in sequencing. An example of sequencing would be verbally summarizing a story in sequential order.

Aspergians tend to struggle with fine and gross motor skill impairment as well due to neurological impairment. Pincer grip issues can cause issues with difficulty in cutting with scissors, tying shoes, and other fine motor skill tasks. Tasks such as bowling with one hand, midline issues, riding a bike, and climbing trees can prove difficult as well. Hand grip is generally weak and hampers ability in hanging on to jungle gym rungs, etc. Hence they tend to be ostracized by their peers not only for their social deficits, but lack of athletic prowess as well. Thus, they may benefit from physical therapy.

Aspergians may commonly present with A.D.H.D., Non Verbal processing disorder, and other maladies. They may not appear to stim. Upon further observation however on will notice that many aspergians run their hands up and down a drinking cup, have feet or legs that are in constant motion, stretch arms bent at elbows while turning wrists, tap tables and feet, and whistle, to name a few. These may be used forms of mild stimming to release anxiety.

Aspergians tend to prefer simple foods void of mixed flavors when young. This is due to sensory overload from heightened taste buds. Simplified, a spaghetti sauce can put their taste buds into sensory overload. It is extremely common for Aspergians to have tactile sensitivities. As children, a scratchy tag or rough texture shirt can drive them to the point of sensory overload, which is resultant in an emotional meltdown. A rough shirt may feel like someone is scratching their back with fingernails.

Due to mind blindness and neurological delays in development that normally place them approximately four years behind their peers, children with Aspergers are prone to being bullied. Cognitive behavior therapy may be productive in assisting children with developing emotional skills.

Please attempt to understand these children. Do not minimize nor assume that they go on to lead independent fulfilling lives. Many of these children grow up to be underemployed due to inept social skills. A college degree does not guarantee a decent due to neurologically based social, and processing difficulties. Due to popular belief not every aspergian becomes an engineer or scientist. They are as diverse as you and I. In my sons case, he is advanced in English but struggles with math and he is an Aspergian.

The divorce rate is extremely high for Aspergians in relation to neurotypical couples. Some go through life having no romantic relationship or friends due to struggling with navigating the social maze. Without society’s assistance and a nationwide education program these children will not hone their wonderful talents.

Society owes these children AND adults a fighting chance. They cannot always control their behavior and depend on us (society) to equip them with the skills, guidance, and positive support network that they need to thrive as adults. Believe in children and they will believe in themselves.

In closing, I leave you with this food for thought. Not all disabilities are as apparent as a blind individual with a cane, an individual in a wheel chair, etc. Please attempt to look below the surface and understand. Thanks and stay well.

Mari Nosal M.Ed., CECE

Help for an Arts Foundation for Autism as seen on www.specialneeds.com

Help for an Arts Foundation for Autism as seen on www.specialneeds.com

We were recently written about on specialneeds.com–>http://www.specialneeds.com/products-and-services/autism/help-arts-foundation-autism Please check them out, they are a simply great website with tons of special needs resources and articles.

Help for an Arts Foundation for Autism
Help for an Arts Foundation for Autism

This guest piece is written by a man passionate about his vision. David Berkowitz lives in Las Vegas, is an honorably discharged veteran and spent the last 20 years in sales and marketing. David lives with Asperger Syndrome and is raising three kids also on the spectrum. Looking to improve the lives of individuals with autism through technology and the arts, David wants to share a bit about his vision with our readers. He is trying to make a difference for autism, please help him in his efforts.

AUTISM ADVOCACY AND TECHNOLOGY NEWS ZONE
By David Joseph Berkowitz

As an individual with high functioning Asperger syndrome, a kind of autism, and the father of three kids who are also on the spectrum for this disorder, I have always felt a need to make a difference for the people with autism. 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 state nonprofit seeking our 501c3. Our intent is to become a national Arts and Technology Foundation within the autism community.

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

We are determined to make a difference in the lives of people with autism and their families.

Our Plan:

Our intent is to give the gift of the arts and technology through donated musical instruments, arts supplies, and 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. We plan to help the arts in schools as well as promote inclusion of people on the spectrum.

Tablets and musical instruments are a very kinesthetic devices and they 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. In addition, musical instruments, the arts such as dance classes are very costly to the individual.

We also give the gift of music and the arts, and to save the music especially for people with autism and special needs. 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.

The first help we need is funding for our 501c3, as well as a lawyer or cpa to do the paperwork properly. We also need exposure such as on TV, in the newspaper, magazines, and web based as well. We can not do it alone and need support to make a real difference.

Please help us help others for the next school year.

We need your help to donate of tech, music and the arts for the school year starting in September. We want to give tablets to people with autism, as well as gift cards and tickets to concerts to make their holidays happier. Please go to our website now and make a donation today to help us make a difference for people with autism and their families. Even a $ 5.00 gift card or a donation on our website will make a huge difference in the quality of life for people on the autism spectrum.

We are also seeking corporate sponsors who can help us in the future as well.

In addition we need media exposure so please put a link to this article on your website as well.

Our tech and autism blog is https://technewszone.com, and we will soon have our autism nonprofit site up as well at http://www.autismhelpusa.com as well soon.

To make a donation–> https://technewszone.com/tech-news-zone-and-paying-it-forward-for-autism-zone/donate-today-autism-technology-music-arts/

I am smart, different, and am going about it on my own; I am not rich and need support so that I can help other people with autism. If you are interested in helping our organization, Autism Advocacy and Technology News Zone, Please do not hesitate to contact me.

About the Author:
Autism Advocacy andTechnology News Zone, Inc. A Nevada Nonprofit Corporation

www.technewszone.com
Twitter: itechnewszone

Facebook: http://www.facebook.com/pages/Autism-Advocacy-and-Technology-News-Zone-Inc

Email: [email protected]

Tips to Encourage Development of Social Skills of Children on the Autism Spectrum in the Classroom by Mari Nosal.

Tips to Encourage Development of Social Skills of Children on the Autism Spectrum in the Classroom by Mari Nosal.
Mari Nosal
Mari Nosal

http://marimouth.wordpress.com/2012/05/29/tips-to-encourage-development-of-social-skillsof-children-on-the-autism-spectrum-used-in-my-classroom/

This is an interesting article with regards to social skills for children on the autism spectrum recently published by Mari Nosal. I wish that there were more program for autism when I was growing up, the problem is that if you do very well academically the system ignored difficulties with athletics and social skills to a large degree when I was in School in the 1980’s.

Here is the fine article–>

1) Set aside a table in the corner of the room. Make sure ample space is provided in proximity to other activities. In doing so, the child on the autism spectrum will not feel crowded or feel as though their personal space is being intruded upon.This should be left out as a long-term project and can be used to encourage non threatening solitary play during times when the child is anxious and needs space. It can also be used to gradually encourage participation in a group project, even if the child is parallel playing.Place a puzzle, snap together model, or construction project on the table. Children on the spectrum are often attracted to items like these. They are great as they can be done in groups or as a solitary activity.Children on the Spectrum will generally allow a trusted adult to assist with the project. On the first day allow the child to work on the task alone and get comfortable with surroundings. On the second day ask if you can participate in the project.Other children will inevitably wander over out of curiosity and ask to join in. When the child is engrossed in the project let him/her know that you need to step away for a moment. Make your absence short, no more than a couple of minutes. Each day lengthen the time that you step back from the group by a couple of minutes.This can be successfully orchestrated in a one on one card game as well. Play cards one on one with the child. As other children become curious and ask to join the game hand your cards to one child and step aside for a few minutes using procedures already mentioned.If this is done slowly over a week or so you should be able to start coaching versus being involved in what will have become a group project at this point. Intervening will be done at this point only during the presence of behaviors or peer difficulties.

Tabletop long-term projects can also be used to redirect a child to a solitary activity when the signs of over-stimulation appear.

2) When it is group cleanup time in the classroom, children on the spectrum can get anxious, and overstimulated if too many children are in close proximity to them. Using an example of putting wooden blocks away, discreetly place some blocks a few feet away from the other children who are cleaning up. Again, this will assist the autistic child in feeling non – threatened.Ask the child to please put the blocks away in the bin. He/she will generally comply dropping the blocks in the bin quickly and walking away. As time goes on move the blacks slightly closer to the other children during clean up time. As the child is introduced to this concept slowly and over a period of time they will generally feel comfortable after a week or two.These ideas can be adapted to group play at home as well. Invite a maximum of two or three children over as more will overwhelm a child with social, emotional, and sensory issues. Initially, sit with the children and encourage group play with a play dough kit, race track, etc. slowly excuse yourself from the activity for several minutes. Gradually extend your time without intervening in group play. Your goal will be to become a coach observing from afar, only intervening when difficulties regarding the social situation arise. This is an extremely slow process the can literally take a month or more to accomplish.

These socialization tips can be quite successful, but the child must not be pushed before they are ready. The ingredients to success are a safe non threatening environment, patience, and praise.

Mari Nosal, M.Ed., CECE

I was on Special Needs Talk Radio, Autism As They Grow with Bobbi Sheahan!!

I was on Special Needs Talk Radio, Autism  As They Grow with Bobbi Sheahan!!
Autism Help USA/Technewszone
Autism Help USA/Technewszone

I had the opportunity to speak on Bobbi Sheahan and Amalia Starr’s Special Needs Talk Radio, Autism As They Grow’s Second to last show. I really appreciate it.

We are trying to make a difference for people with autism for quality of life, education, vocation and to help them find enjoyment in their lives, and promote inclusion as possible in schools. We are trying to do this by giving the gift of music, the arts and technology and by partnering with tech like Android, Blackberry and Apple Ipad Tablets to schools and individuals, music, and arts related organizations and people to help us get funding and reach people.

We would love to be on more shows, to gain support and make a difference.

Here is a link to the show–>http://www.blogtalkradio.com/specialneedstalkradio/2012/05/24/autism-as-they-grow-1

http://www.blogtalkradio.com/specialneedstalkradio/2012/05/24/autism-as-they-grow-1

A bio on Bobbi Sheahan–>

Catch my new show, Autism As They Grow, on Special Needs Talk Radio, Wednesdays at 9:30 p.m. EST!

Do people suggest that your child is different – really different? Are you wondering how to make sense of your child’s behavior (or your spouse’s – or your own)? Don’t despair; help is on the way! Bobbi Sheahan and psychologist Kathy DeOrnellas, Ph.D., offer themselves as your scouts in the field. They have valuable information to share – from the moment you realize your kid is different (“My, what a quiet baby I have!”), to the self-righteous moms on the playground, to holding your marriage together in the realm of routines, they candidly tackle autism spectrum issues such as picky eating, bedtime battles, potty training, speech delays, discipline, early intervention, sibling rivalry, and much more!

Bobbi Sheahan is the mother of four children; Grace, her second-born, has been diagnosed with autism. Her new book, What I Wish I’d Known About Raising a Child With Autism: A Mom and a Psychologist Offer Heartfelt Guidance for the First Five Years, has been published by Future Horizons, the world’s largest and most authoritative autism publisher. Bobbi says, “Dr. Kathy DeOrnellas, my co-author, knows more about autism than anyone you will ever meet. Since I can’t bring you to her office – and I would if I could – this book is my way of bringing her to you.” In Chapter 2 (entitled Autism 101), Dr. DeOrnellas brings you more than 20 years of experience, teaching, and research in the field of autism in a readable, conversational manner.

Autism is not only a challenge to a family’s emotions; it can also be a financial drain. Bobbi says, “With families routinely spending thousands of dollars out of pocket each year, we are here to help to point families in the direction of meaningful, affordable help.”

For her part, Bobbi pulls no punches in telling the story of her family’s road to discovering Grace’s autism. “The entire family comes along on this journey, believe me,” she says. “There is a reason that my favorite chapter heading is: Fun and Folly With Self-Diagnosis: Is Asperger’s German for Engineer?”

The book is also enriched by quotes from more than two dozen families who have been breathtakingly honest about everything, from speech delays to potty training, from doing battle with professionals who are supposed to be on your family’s side; this book is an indispensable resource for families. From reading lists to guidance about building a personal and professional support system, the authors offer a crash course to families who don’t have time to waste. The wit and humor with which the information is conveyed is a much-needed breath of fresh air for families who desperately need a break – and a friend.

Available now at Future Horizons, Amazon, Barnes & Noble, Borders, and wherever books are sold!

Please listen to the show, I am on at the halfway point. Please share with people in the media.

Please help us to help others, we can not do it alone!!!

How to reach us:

Http://technewszone.com

Or FACEBOOK–>http://www.facebook.com/technewszone

or YOUTUBE–>Http://www.youtube.com/technewszone

Or Itechnewszone on Twitter!!

Thank you I appreciate it.

American Idol 2012 Who is going to win, Jessica or Phillip Phillips?

American Idol 2012 Who is going to win, Jessica or Phillip Phillips?

I really like music and American Idol. This year the talent was better than in previous years. The final 2 are both really excellent. I am leaning towards Jessica, but Phillip is great as well. I was surprised that Joshua was not in the top 2.
I wish them good luck.

The final 2 American Idol 2012
The final 2 American Idol 2012

Please help us to help autism, we are a music, the arts and tech focused autism nonprofit trying to help people with their quality of life, education and vocations.

Here are their most recent videos–>

The amazing Jessica–>

Phillip–>

May 22, 2012–> Historic Commercial Space Mission Heads off to the International Space Station

May 22, 2012–> Historic Commercial Space Mission Heads off to the International Space Station
gr-nasa-falcon-624
gr-nasa-falcon-624

http://www.msnbc.msn.com/id/47514404/ns/technology_and_science-space/#.T7whp9z3qf4

We live in exciting times, not as high tech as would have thought in high school in the 1980’s but still very interesting.

Here is a story from MSNBC with regards to the new DragonX Falcoln 9 to launch into space from NASA.

CAPE CANAVERAL, Fla. — A private space capsule called Dragon soared into the predawn sky Tuesday, riding a pillar of flame like its beastly namesake on a history-making trip to the International Space Station.
The unmanned capsule, built by billionaire entrepreneur Elon Musk’s SpaceX venture, is the first non-governmental spacecraft to launch to the space station, ushering in a new era of partnership between the public and private spaceflight programs.
“I think this is an example of American entrepreneurship at its best,” Alan Lindenmoyer, manager of NASA’s commercial crew and cargo program, said in a briefing before the launch. About 100 VIP guests were on hand to witness liftoff, NASA officials said.
Related: Private rocket launch vindicates commercial spaceflight model
Hawthorne, Calif.-based SpaceX, known more formally as Space Exploration Technologies Corp., launched its Dragon capsule at 3:44 a.m. ET Tuesday from a pad here at the Cape Canaveral Air Force Station. It blasted off atop SpaceX’s Falcon 9 rocket, a 157-foot (48-meter) booster powered by nine Merlin rocket engines. The space station was flying 249 miles above the North Atlantic Ocean as the rocket lifted off, NASA officials said. [Launch Photos: SpaceX’s Dragon Blasts Off for Space Station]
The Falcon 9 rocket’s second stage is also reportedly carrying ashes from 308 people, including actor James Doohan, who played Scotty on the 1960s television series “Star Trek,” and Mercury astronaut Gordon Cooper. The ashes were flown under a deal with the memorial spaceflight company Celestis.

Reuters
SpaceX Dragon spacecraft
The SpaceX launch vehicle is named after the Millennium Falcon of “Star Wars,” while the capsule got its moniker from the Peter, Paul and Mary song, “Puff, the Magic Dragon.”
Advertise | AdChoices

Tuesday marked only the second-ever launch of a Dragon capsule, and the third flight for the Falcon 9 rocket. It was the second attempt to launch the space station-bound test flight, after a launch try on Saturday was thwarted by a faulty rocket engine valve. Repairs were made over the weekend, and the SpaceX team counted down smoothly to Tuesday’s liftoff.
“One thing that they are very good at is being able to work through launch abort and treat those problems and be prepared to go again in a very short time,” Mike Horkachuck, NASA project executive for SpaceX, said Monday.
How the test flight will unfold
Tuesday’s launch could be the last test flight for SpaceX under NASA’s Commercial Orbital Transportation Services program, which is supporting the development of private-sector replacements for the cargo-delivery services of the retired space shuttles. SpaceX has a $1.6 billion contract to fly at least 12 unmanned missions to the space station through 2015.
More space news from msnbc.com

Alan Boyle / msnbc.com
The queen of SETI retires from research
Science editor Alan Boyle’s blog: The real-life astronomer who inspired the alien-hunting character in “Contact” is retiring from her research post — but she isn’t giving up on the SETI quest.
Your favorite views of the solar eclipse
Milestone mission to space station lifts off
Space realities keep pace with science fiction
Musk founded SpaceX in 2002 with the goal of boosting commercial access to space and aiming for deep-space exploration, including missions to Mars. Success was never certain or assured, Musk had repeatedly said.
After Tuesday’s launch, Musk said the mission’s uncertainty has eased up.
“Falcon flew perfectly!!” Musk wrote in a Twitter post from Falcon 9’s mission control room in Hawthorne. “Dragon in orbit, comm locked and solar arrays active!! Feels like a giant weight just came off my back.”
The spacecraft is due to spend its first day on orbit catching up with the 240-mile-high (390-kilometer-high) space station, where it will rendezvous Thursday and perform a flyby to within 1.5 miles (2.5 kilometers) to check its navigation systems. [Quiz: How Well Do You Know SpaceX’s Dragon?]
On Friday, the capsule is slated to perform a series of maneuvers to approach the station, with crew members onboard the outpost issuing commands to Dragon. If the spacecraft passes a set of “go/no-go” checks at Mission Control in Houston, NASA will give the go-ahead for the vehicle to approach the space station. From inside, astronauts Don Pettit and Andre Kuipers will use the lab’s robotic arm to grab Dragon and berth it to the station’s Harmony node.
The hatches between the two spacecraft would be opened early Saturday, so the crew can enter Dragon and unpack its deliveries.
Dragon is due to spend about a week and a half attached to the outpost. On May 31, the capsule will be packed with completed science experiments and other equipment, unberthed, and sent back toward Earth. The vehicle is equipped with a heat shield to withstand the fires of re-entry, and is due to splash down and be recovered by ship in the Pacific Ocean.
If this test flight is not completely successful, another demonstration mission would be scheduled later this year.
Giant leap for private spaceflight
Dragon is an unmanned version of a capsule ultimately intended to carry people as well.
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Another company, Orbital Sciences Corp. of Dulles, Va., also has a NASA contract to deliver cargo to the space station, and plans to launch its first test flight later this year.
The program is part of a larger effort by NASA to outsource low-Earth orbit transportation to the private sector, allowing the space agency to focus on a new spacecraft and heavy-lift rocket to visit asteroids, the moon and Mars.

Robert Pearlman / collectSPACE.com
SpaceX’s first space station-bound Dragon spacecraft, flying atop a Falcon 9 rocket, launches behind a high fidelity mockup of the space shuttle, NASA’s previous means of delivering cargo to International Space Station. Liftoff occurred on May 22 from Cape Canaveral Air Force Station.
The plan has been criticized by some lawmakers and members of the public, who worry that commercial vehicles aren’t as safe or reliable as NASA’s in-house spacecraft.
“It’s really easy to criticize, and it’s very difficult to solve a problem and actually do something,” said SpaceX President Gwynne Shotwell. “So I tend to focus on the business and getting our jobs done and not focus on those that want to criticize.”
NASA officials and leaders of the commercial space sector say the time is right for space to transition from an exclusively government regime to an arena open to private companies.
“I kind of see that transition as being inevitable,” said Phil McAlister, NASA’s director of commercial spaceflight development. “I believe it is going to happen at some point. If it’s not today and this mission falls short of expectations, it is going to happen eventually.”
You can follow Space.com assistant managing editor Clara Moskowitz on Twitter @ClaraMoskowitz.Follow Space.com for the latest in space science and exploration news on Twitter @Spacedotcom and on Facebook.

Here is an exciting video that they allow people to share as well of the launch–>

Visit msnbc.com for breaking news, world news, and news about the economy

A video on bullying from the Huffingpost, can relate was picked on as well, even as an adult!!!

A video on bullying from the Huffingpost, can relate was picked on as well, even as an adult!!!
bullying
bullying

http://www.huffingtonpost.com/2012/05/18/lynda-frederick_n_1527764.html


Having been picked on, excluded socially, made fun of, treated differently all of my life, I totally get the fact that Bullyinn needs to be eradicated from our society, we need to teach acceptance, of all people we are all the same, one race, Human. It should not matter what someones race, color, sexual preference, clothing, hair cut or anything else whatsoever.

A poem that speaks to it as well from The Huffington Post–>

ESCONDIDO, Calif. — A woman’s poem about being bullied in a California school 25 years ago has brought her former classmates to tears. Now, they’ve created a scholarship fund in her name and raised $800 to fly her back to California for a class reunion.

Former classmates say they were reduced to tears after reading Lynda Frederick’s poem, which she posted on the Orange Glen High School class of 1987’s 25th reunion Facebook page.

“This poem touched me so bad I could not sleep…I cried,” Frederick’s classmate, Lisa Wallace, told NBC News.

In the poem, Frederick, now a mother of three who lives in Seneca Falls, N.Y., described how the bullying she endured as a teenager “shattered her childhood.”

that little girl who came to school with the clothes she wore the day before
instead of asking why.. you picked on her

the little girl who had to walk to school while others rode the bus

instead of asking why.. you picked on her

the little girl who had bruises and was dirty

instead of asking why.. you picked on her

the little girl who was always crying

instead of asking why.. you picked on her

Classmate Kristi Malone told NBC News that she remembers how cruel the other kids were to Frederick.

“Looking at her being bullied horribly and thinking…I feel so bad for her,” said Malone. “But never thinking in my head that I could stand up for her, and not once did anyone back her up.”

Frederick’s poem has been a wake up call for many of her classmates, Malone said.

“Just people in tears, like ‘how could we have done this to her,'” she said. “[They] were just crying, saying ‘Why did I do that?'”

Many of Frederick’s classmates have since contacted her and apologized.

They have also raised money to fly her to Escondido, Calif., for the July class reunion and have set up a scholarship fund in her name.

“We are making a statement for all that bully anyone, it is not right and it feels bad on both ends,” wrote Wendy Bergin Gotte on the high school reunion’s Facebook page. “It just goes down the line and hurts everyone along the way.”

Frederick said she forgives her old classmates and has accepted the invitation to return for the reunion.

“I said, Christ forgave me..and I forgive you,” she said.

A Very Special Mothers Day To Special Needs Moms by Mari Nosal

A Very Special Mothers Day To Special Needs Moms by Mari Nosal
Aspergers
Aspergers

I really like this article by Mari Nosal. I meant to publish it but it slipped my mind. It is quite wonderful. It takes strength to be a parent of special needs kids. For some of us it is a struggle.

http://marimouth.wordpress.com/2012/05/11/a-very-special-mothers-day-to-special-needs-moms/

I was perusing the numerous racks of mother’s day cards recently. As is characteristic of me, my experience jettisoned into a silent analytical observation. I made mental notes pertaining to the responsibility afforded to a mother. It is a 24-7 job. Mothers must be on call to jump to attention for a whimpering baby with a wet diaper or hunger pangs. Mothers must be on constant alert for toddlers unrolling a roll of toilet paper that he is busily spreading from room to room with the roll unraveling behind him as he gleefully runs.

We are a tough breed who gets attacked with a projectile shot of vomit that lands on our bodies with the force of a speeding bullet. We wipe runny noses with an almost unlimited amount of tissue that seems to be pulled from thin air. We spend years of sleep deprivation from waking at all hours of the night to nurse sick children back to health. We spend the better part of our child’s teen years pacing the floor when our new drivers are past curfew , conjuring all the terrible things that might have happened to them within the confines of our mind.

Through challenges, trials, tribulations, childhood illness, mothers shrug it off and unquestionably support their children day after day. We never notice the first year of life when you smell like spit up, or that poopy diaper that leaked on your lap. If the child is out of baby food etc. we have all made a trip to the store smelling like the latter because our worries about looking presentable are blinded by the needs of our child.

There you have it. All mothers are special, but special needs moms are different. They are humbled, challenged, tough, protective, and cheerleaders for their children beyond the call of duty. They deal with doctors, teachers, therapists, and more who tell them their child will never meet a certain milestone. Milestones that traditional parents take for granted.

A word of caution, never say your child won’t, can’t, never will, or any other phrase which reeks of pessimistic projections for their child. Like a cat, special needs mothers have hidden claws behind their fingernails that will protrude when they are in attack mode resultant from any threat, or negativity aimed towards their child or the child’s mom.

Special needs parents will expect nothing but the best of care for their children. They are not afraid to vocalize and take action until their child gets just that. While other parents seek out babysitters for a weekly date night, many special needs parents silently stay home to care for their child’s demanding needs. It is much more difficult to get sitters for special needs children, and medical, and therapy issues can leave parents financially strapped. While other parents complain that their child did not make captain of the soccer team, these parents merely want their child to make the team and socialize with peers.

While parents worry about their child being popular, special needs parents worry about their child having friends at all. We shuffle our children to numerous therapy appointments, social groups, pediatricians, tutors, and specialists, while managing jobs, homes, and the stares from people in public.

Through it all we realize that we can climb mountains, make it to the summit and down again as we develop determination and strength to fight for our young like nothing else.

Now, back to my story about visiting the card shop. None of those cards appeared to be directed at special needs parents so I am providing my version that I would design for all of you out there.

I agree, never give up, keep trying, you never know what you can achieve if you really try.
==> A Mari Nosal Hallmark Card for Special Needs Mothers on Mother Day, simply brilliant.

To A Special Needs Mom (A Hallmark moment)

Mommies, you always look beyond my disability and see my talents

To you I am a diamond in the rough black on the exterior but shiny underneath

As my daily cheerleader you slowly buff me off to reach the shiny diamond that I am inside

Without you in my corner I would never have made it as far as I have

We have proved doctors and therapists prognosis wrong repeatedly

With you in my corner we will keep proving them wrong

Thanks for believing in me and helping me when others give up

Thanks for showing your love for me every day

Most of all, thanks for being my mommy

Happy Mothers Day Mommy from your special needs child to my very SPECIAL mommy

And from me – I wish all fellow Moms a happy Mothers Day

Mari Nosal, M.Ed., CECE