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Shoplifting…made me smile today

0 Comments | This entry was posted on May 17 2012
 

A good friend of mine writes about her daughter who has autism
“Priceless literalism from Lea in Sainsburys – Grabbed a box of coco pops of a shelf and announced full voice ‘I’m shop lifting’ – After a brief discussion she agreed that maybe that was not an entirely accurate description.”
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Mother cannot cope

0 Comments | This entry was posted on Jan 21 2011

** Disabled girl's mother attacks PM ** A mother who says she may put her disabled child into care criticises Prime Minister David Cameron on respite care provision. 

http://www.bbc.co.uk/go/em/fr/-/news/uk-england-bristol-12237100 >

Gold.

0 Comments | This entry was posted on Jan 18 2011

“A gold Blue Peter badge, the highest award you can ever get said his little sister and brother today very gravely as they watched Blue Peter .  “You only get a gold one for saving someone’s life.”

You both should get one then i  thought,  you saved my life.

Watching the telly…

0 Comments | This entry was posted on Jan 04 2011

The boy has developed a new behaviour,  for the moment,  until another one arrives.  He seems to be just sitting on the sofa and  staring into the distance for a few minutes a day  When asked  what are you doing he says.  “Watching the telly”  Yes, that’s true I think…even though the telly is off.  He is quite literally watching the telly.

Autistic Child writes to Family and Friends

0 Comments | This entry was posted on Dec 24 2010

Dear Family and Friends-

           I understand that we will be visiting each other for some get-togethers this year.  Sometimes these visits can be very hard for me, but here is some information that might help our visit to be more successful.  As you probably know, I am challenged by a hidden disability called Autism, or what some people refer to as Pervasive Developmental Disorder (PDD).  Autism/PDD is a neurodevelopmental disorder which makes it hard for me to understand the environment around me.  I have barriers in my brain that you can’t see, but which make it difficult for me to adapt to my surroundings.

            Sometimes I may seem rude and abrupt or silly and out of control, but it is only because I have to try so hard to understand people and at the same time, make myself understood.  People with autism have different abilities.  Some may not speak, some will write beautiful poetry.  Others are whizzes in math (Albert Einstein was thought to be autistic), or may have difficulty making friends.  We are ALL different and need various degrees of support.

            Sometimes when I am touched unexpectedly, it might feel painful and make me want to run away.  I get easily frustrated, too.  Being with lots of other people is like standing next to a moving freight train and trying to decide how and when to jump aboard.  I feel frightened and confused a lot of the time.  This is why I need to have things the same as much as possible.  Once I learn how things happen, I can get by OK.  But if something, anything, changes then I have to relearn the situation all over again!  It is very hard.

            When you try to talk to me, I often can’t understand what you say because there is a lot of distraction around.  I have to concentrate very hard to hear and understand one thing at a time.  You might think I am ignoring you – I am not.  Rather, I am hearing everything and not knowing what is most important to respond to.

            Get-togethers are exceptionally hard because there are so many different people, places and things going on that are out of my ordinary realm.  This may be fun and adventurous for most people, but for me, it’s very hard work and can be extremely stressful.  I often have to get away from all the commotion to calm down.  It would be great if I had a private place set up to where I could retreat every time I go to get-togethers.

            If I cannot sit at the meal table, do not think I am misbehaved or my parents have no control over me.  Sitting in one place for even five minutes is often impossible for me.  I feel so antsy and overwhelmed by all the smells, sounds, and people – I just have to get up and move about.  Please don’t hold up your meal for me – go on without me, and my parents will handle the situation the best way they know how.

            Eating in general is hard for me.  If you understand that autism is a sensory processing disorder, it’s no wonder eating is a problem! Think of all the senses involved with eating.  Sight, smell, taste, touch AND all the complicated mechanics that are involved.  Chewing and swallowing is something that a lot of people with autism have trouble with.  I am not picky – I literally cannot eat certain foods as my sensory system and/or oral motor coordination are impaired.

             Don’t be disappointed if Mom hasn’t dressed me in the best clothes there are.  It’s because she knows how much stiff and frilly clothes drive me buggy!  I have to feel comfortable in my clothes or I will just be miserable.  When I go to someone else’s house, I may appear crabby.  Things have to be done in ways I am familiar with or else I might get confused and frustrated.  It doesn’t mean you have to change the way you are doing things – just please be patient with me, and understanding of how I have to cope.  Mom and Dad have no control over how my autism makes me feel inside.  People with autism often have little things that they do to help themselves feel more comfortable.  The grown-ups call it “self-regulation” or “stimming.” I might rock, hum, flick my fingers, tap a string, or any number of different things.  I am not trying to be disruptive or weird.  Again, I am doing what I have to do for my brain to adapt to your world.  Sometimes I cannot stop myself from talking, singing, laughing, or doing an activity I enjoy.  The grown-ups call this “perseverating” which is kinda like self-regulation or stimming.  I do this only because I have found something to occupy myself that makes me feel comfortable.  Perseverating behaviors are good to a certain degree because they help me calm down.

            Please be respectful to my Mom and Dad if they let me “stim” for a while as they know me best and what helps to calm me.  Remember that my Mom and Dad have to watch me much more closely than the average child.  This is for my own safety, and preservation of your possessions.  It hurts my parents’ feelings to be criticized for being over-protective, or condemned for not watching me close enough.  They are human and have been given an assignment intended for saints.  My parents are good people and need your support and not rude remarks.

            Gatherings are filled with sights, sounds, and smells.  The average household is turned into a busy, frantic, festive place.  Remember that this may be fun for you, but it’s very hard work for me to conform.  If I fall apart or act out in a way that you consider socially inappropriate, please remember that I don’t possess the neurological system that is required to follow some social rules.  I am a unique person – an interesting person.  I will find my place at these celebrations that is comfortable for us all, as long as you’ll try to view the world through my eyes!

 

            -Author Unknown

 

 I do not know who wrote this, I do feel it can help so many. Bless the child  whose caregiver wrote this letter.

 

 

 

    Riding!

    0 Comments | This entry was posted on Dec 14 2010

    It was so nice to receive a photo of him on his pony at Riding for the Disabled.  He is so happy when on horseback and is progressing very well indeed they say.  It was also nice to hear that apparently he is loved by everyone who works at our local branch.   At the beginning of the session, once they have mounted,  all the riders are asked to say “Walk on” to their ponies.

    He always says “Walk on please”

    www.dailymail.co.uk/…/How-mothers-cope-autistic-sons-grow-sexually-aware.html

    0 Comments | This entry was posted on Dec 11 2010

    Warm feet for Fred

    0 Comments | This entry was posted on Dec 07 2010

    The year before last Fred’s Mum was aware that he wasn’t sleeping well and seemed to be in pain. Watching him carefully she could see it was something to do with his feet. A visit to the shoe shop confirmed that his shoes were the right size. What was the problem?  Unable to guess what it was she took him to the doctor. He said that poor Fred had the worst case of chilblains he had ever seen – almost frostbite. Every Time his feet warmed up he was in agony. He had not been able to tell his Mum that he was cold in his wellies when he was outside, despite warm socks and clothes.

    That year The Celtic Sheepskin company came to Fred’s rescue and sent him a free pair of cosy sheepskin waterproof boots. Well Fred is a growing like every other little boy and has finally outgrown the boots. His mother was dreading this very cold weather was going to give him chilblains again, but The Celtic Sheepskin company have again come to the rescue and sent Fred another pair of cosy boots.

    The Celtic Sheepskin company is a British firm based in Cornwall. Please take every opportunity to tell everyone you know about how kind they have been, and buy your boots from them!

    www.celtic-sheepskin.co.uk

    Felicity

    Free donation for Fred

    0 Comments | This entry was posted on Nov 29 2010

    Don’t forget when you are doing your online Christmas shopping, to enter the easyfundraising site first. The Fred Foundation will get a donation without it costing you a penny!
    Forgotten how to go about it?

    Go onto www.easyfundraising.org.uk.
    If it is your first time – register and choose ‘The Fred Foundation’ as your charity. ( Very fast to do)
    Start shopping! All the major on line retailers are on the site, including M+S, John Lewis, Boden and Amazon. For every pound you spend they give us a donation. Very simple, but it just requires you to remember to go through the site to reach your retailer.
    Thanks in advance.

    thefredfoundation@googlemail.com

    Stan the Man

    0 Comments | This entry was posted on Nov 18 2010

     he is the most

    beautiful

    man in the

    world.

     

    when he laughs

    i am happy

    for him

    when he sleeps

    i am happy

    for him

    when he hugs

    his mum and dad

    i am happy

    for them.

     

    a stranger

    may not see that

    he is the most

    beautiful

    man in the

    world.

     

    to us

    the world is

    confusing

    but to him

    it is like

    clouds

    on a clear day

    or blue sky

    when it should be

    grey.

     

    his mum sits

    on the sofa

    crying

    she is tired

    because her son is

    alone

    not from lack of

    love

    but because his

    burden

    is to be

    alone.

     

    to be the most

    beautiful

    man in the

    world

    you must be

    alone.

     

     his brother Victor

    loves him

    his brother cares

    for him

    when he cries

    Victor says

    mum

    dad

    Stanley is

    crying

    he cares for his

    brother

    he loves him

    dearly.

     

    to suffer this

    a punishment

    the rewards must be

    great

    a reward

    unseen.

     

    the boy

    on his dads back

    is the most

    beautiful

    boy in the

    world.

     

    sometimes you feel

    that you want

    to get

    hold of him

    to squeeze him

    to squeeze him

    so tight

    that you might

    squeeze out

    of him his

    condition

     

    but this may also

    squeeze out his

    beauty

     

    for he is the most

    beautiful

    man in the

    world.

     

       Daniel Cockrill

    Inspirational people on the Autistic Spectrum

    0 Comments | This entry was posted on Nov 18 2010

    http://www.stephenwiltshire.co.uk/download_video.aspx?Id=2527

    http://www.metacafe.com/w/cb-oDmsSeoKxe4tbVpYX0ZDnrgR0jprDvxG/