Tag Archives: sensory sensitivities

The Do’s And Don’ts When Parenting A Child With Aspergers Syndrome

15 May

Its not easy being a parent to a child on the autism spectrum! Actually… It isn’t that easy being a parent full stop!

Below are some dos and don’t, all based around the stuff I’ve learnt while parenting my little man. Remember, I’m just another parent like you! No, I’m not doctor or child psychologist and what works for us may totally not work for you. But why not have a read anyway… If anything you won’t feel do alone. Please, feel free to add anything within the comments sections:)

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So… Here it goes…

Don’t feel guilty if you failed to spot the signs at an early age.

Do remember that this is common for children diagnosed with Asperger’s syndrome with many of them not gaining an actual official diagnosis, till their teenage years.

Don’t be to proud to ask for help!

Do fight for it, if those who are meant to provide it, withhold it!

Don’t force your child to be someone they are not!

Do show them you are proud of them for being the person they are.

Don’t assume its easy!

Do remember that parenting any child can at times be challenging.

Don’t feel you have to explain your child’s behaviour, every single time they do something that makes others stop and stare.

But do educate those who are willing to listen! The important issue here is, not to get stressed when out and about. this only makes things more difficult for both yourself and your child. Remember its ignorance and sadly many are guilty of displaying it!

Don’t restrict the activities you do as a family.

Do prepare your child for such occasions with the help of visual resources and schedules to avoid unwanted challenges on the day.

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Don’t forget you have a life too.

Do take time out for you, whenever the opportunity arises.

Don’t assume that any two children diagnosed with Aspergers will experience the exact same traits.

But do make yourself aware of such traits, preparing yourself for what may lay ahead.

Don’t assume a diagnosis is your child’s ticket to the support and services they may need.

Do be prepared to battle for them, services! Yes, you’ll be expected to provide evidence showing why it is the help is needed.

Don’t just expect others to instantly understand your child’s diagnosis

Do be prepared for ignorance & denial. Sadly many find that its friends & family who display the worst reactions to the news of a child’s diagnosis. As for strangers…. I not don’t even notice the states as my son displays a screaming match at the local train station. Ok its never easy, but you adjust and get used to it.

Don’t freak out if your child develops an interest in something considered to be strange or unusual.

Do embrace and encourage all that your child loves regardless of its wackiness.

Don’t assume your child will have learning difficulties.

Do celebrate the subjects they excel in, and offer help and support to improve in those they are not.

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Don’t base decisions on what you want for your child!

Do base decisions on what is best for them.

Don’t beat yourself up if you lose it! Meltdowns that go on for hours are likely to make you crumble.

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Do remember that your human and your child still loves you ( regardless of what they may say).

Don’t be surprised if your child announces to the lady sat on the bus, that she’s old, wrinkled and looks close to death.

Do play games and work on activities designed to help your child avoid social mishaps like that of the above.

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Don’t waste money buying your child the top branded toys, especially if they have failed to express any interest.

Do make them happy on Christmas morning if padlocks, staples and rulers were on their Christmas list.

Don’t be too disheartened if your child shows no interest in making friends.

Do have hope that one day that will change!

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Don’t force your child to play with other children…

… But do teach them the social skills required to do so! Most children on the autism spectrum will eventually show a desire to interact and play with others.

Don’t waste your time looking for cures

But do look into therapies that have been designed to help your child better develop the skills required to succeed in both child and adulthood.

Don’t assume that just because your child doesn’t display certain traits during childhood they won’t during adulthood.

But Do remember maybes are not certainties.

Don’t try to make your child fit into society!

But do mould them as you would any child so society fits with them.

Don’t use complex language (metaphors and sarcasm) when talking with your child

But do try and teach them that others will to avoid miscommunications.

Don’t force your child to wear certain clothing, eat certain foods or attend certain activities.

Do be sure to research sensory processing disorders as their refusal to do any of the above could be and likely is related.

Don’t assume that your child with Aspergers will have the abilities to cope in a mainstream school (not all can)!

Do make sure you are open minded… Sometimes special schools are all your child needs to succeed within education.

Don’t use your child’s diagnosis as an excuse for unwanted behaviour.

Do remember that all children can be challenging and all are not autistic… You will learn the difference, I have!

Don’t forget to be mum to everyone

Do remember that siblings of children with Asperger’s syndrome may display unwanted behaviour or mimic their siblings traits as a way to gain the attention they crave.

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Don’t assume your child will be bullied.

But do look out for the signs as statistics have shown that it is children like yours and mine who become targets.

Don’t force your child to believe in the mystical world of make believe.

Do remember that many child with Asperger’s syndrome like things based upon facts, the type backed up by evidence. If you can’t prove how santa gets round the world in one single night then chances are he will never believe. Just make sure he doesn’t share his findings with his siblings… Like little man has tried.

Don’t ask your child if you look good in a new dress unless you want blatant sharp honesty…

Do be prepared to be shown your love handles and chubby knees if you do.

Don’t believe everything the books tell you.

Do remember that every child has the capability to at least try and lie… Well, at least the desire to try and do so, is usually there! Its just that children with Aspergers are not all that hot at it! Little man usually cracks within minutes.

Don’t be so serious…

Do crack a smile, your child with Aspergers is more than capable of making you proud… Mine does.

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Don’t just assume your child will tell you if something is wrong! Aspergers is a communication disorder after all!

Do be ready to put on your investigation cap, as you try to discover just what has upset your child… Remember they will expect you to just know.

Don’t feel that everything has to become a mission in life because of your child’s condition.

Do be prepared to be pleasantly surprised when your child shows you that something you thought would be impossible for them… is actually totally possibly.

Don’t waste time asking yourself “What If?”

Do remember that we have one life, Our own unique and special story. All children deserve to be brought up happy with stacks of love and great memories to support it. Our children will eventually grow up and fly the nest… Yes even those with Aspergers Syndrome! My point? Just enjoy your kids, never taking a single day for granted… Even those not so good ones!

A Sweet Smelling Home

25 Aug

When being contacted by the guys at Zoflora I wasn’t at all surprised by their findings

Freshly cut grass’ and ‘flowers’ are the most loved smells by us Brits.

Brits spend £7.7 billion each year maintaining the outside space around their homes.

Ensuring our home smells fresh and clean is also a top priority for us Brits according to a survey commissioned by Zoflora. Half of all Brit’s agree that smell is the first thing they notice when they walk into someone’s home.

More than three quarters of us admit that they would judge someone with a bad smell in their home or look at them in a negative light.

The smell of garden flowers are known to be the source of many pleasant recollections and the way that your home smells is just as important.

I’m already a big fan of Zoflora. Their range of concentrated antibacterial disinfectants are small but mighty when it comes to killing gems. The small bottle surprisingly goes much further than one would expect. The formula can be diluted 1 part Zoflora to 40 parts water to make full strength disinfectant for large areas, such as floors and bathrooms, making them hygienically clean and welcoming

With a child in the house who experiences numerous sensory sensitivities the smell of disinfectant can be one that is quite over powering. For this reason I will always try to use it while his at school but with such long holidays that luxury is taken away.

This is why I choose to use Zoflora! It floral fragrance amongst others is one that doesn’t upset Little man in the same way as other disinfectants. Bouquet, is a rich scent of warm wood and musk notes creating a heady seductive fragrance. We were sent a bottle to try and we found that it gave our home a really present scent.

I want my children to be able to get involved in chores, its a really important life lesson and for this reason I want the products we use to be pleasantly fragranced and safe for the children to use.

Zoflora’s has two new fragrances I can’t wait to try and these have been formulated inline with the above findings.

The two new scents will recreate the smells of British Country Gardens and Summer Bouquets. So, we can experiences some of our favourite smells all year round regardless of the weather.

Zoflora’s two new scents are that of Country Garden and Summer Bouquet.

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The new fragrances are now available as 56ml concentrated antibacterial disinfectants at Wilkinsons, independent local stores and pharmacy visit www.zoflora.co.uk or www.facebook.com/LoveZoflora

Our very own “school” trip

5 Nov

So this week myself and little man had our very own school trip.
Ever since all this horrible business of little man missing out on school trips started his confidence has been at an all time low.

“Ok it may not be a “real” school trip but it’s our school trip” and I had to do something to help repair his dramatically disappearing confidence, to make him feel better about himself & more confident in who he is! I’m not saying little man isn’t sometimes a bit of a handful when out & about, his no “angel” but then again what ten-year old boy is? He does have difficult times & always will when his out on school/family outings but a great deal of his difficulties are caused by anxiety, over excitement and more recently… Pure apprehension of what’s a head. It’s like he won’t allow himself to look forward to anything as his learnt how quick it can be taken away. On a recent trip to swimming (sadly only his second time attending since the new school year) he suggested we didn’t walk with the class as a way to avoid something going wrong resulting in him missing out! How crazy is that? Sadly things didn’t go well at swimming but that’s another post for another day,and one that’s to long and upsetting to report on just now.
So the point I’m trying to make is… All the above is directly connected with his Aspergers and let’s face it he was born that way he didn’t ask to have the condition so therefore he shouldn’t be treated as if he has himself to blamed every time something goes wrong. If little man is just being a ten-year old boy then I will be the first to put my hand up in agreement and have done when needed.

Well, to be honest I was quite excited about taking little man on a trip! it was only possible due to the fact his currently on half day schooling. So as this was the perfect opportunity we went for it.

So… wondering where it was we went? “No…. for once it wasn’t buses riding on the 450!” though that’s not far off! We actually visited London’s Covent Garden where you can find the all exciting Transport Museum. Not only was this ideal given that it was full to the rim with little mans interest, *buses* followed by tubes, trams & trains, but it was also very educational. The Museum does have learning facilities within the building and after a little conversation with a helpful member of staff on the Ins & outs of little mans situation he was shown into the learning lounge where he could use the IT software or read one of the many transport reference books. What made it even more great was the fact he did these things a long side children on a more “formal” school trip. He didn’t try to interact with these children but he didn’t abuse any off them either. I was grateful to that member of staff, he didn’t judge him and regardless of my shared information on the good and the sometimes challenging behaviour associated with his condition, he responded by stating “Everyone deserves a chance, and just because his not responded well before, who’s to say he won’t this time?” I stood thinking “Wow, people like you are like gold dust”

Well, Lucky for me my friend had come along on our “school trip” I was in need of some adult non bus based conversation and while little man did his stuff on the PC me and my friend grabbed a ten minute break (that turned out to be our only break of the day) Still I’m not complaining we did have a fantastic day, especially little man and that’s what we were there for, to give him something to enjoy! Of course there were times when little man was a little over excited, hyper or even frustrated (mainly because he wanted to be on the next item of transport before he had even left the one he was currently sat on) but through a collection of strategies we were able to successfully keep him on the right track. We did encounter a small episode towards the end off the day when leaving the Museum at closing time (yes we were there that long) but it could have been a whole lot worse. It was essential to spot any potential triggers and remove them or him before they had any undesirable effects. undoubtedly there is no need to explain why this is to any parent(s) of children on the spectrum, because they are likely to be the ones that “really” get it! But for those who don’t or just think they do….. Let’s just say.. if I hadn’t approached issues in this way the outcome would have been explosive!!!


I’m so…. pleased with the way our creation of a school trip planed out. After some essential planing that took place in the weeks leading up to the trip, these included little mans ideas and views on all aspects of the trip, a social story, countdown tick chat (visual aids), and journey planing (Little mans job, of course!) things went remarkable well.

And the fun didn’t end there! After the Transport Museum we went for dinner, followed by a short walk around the city, a fun-filled visit to Trocadero where we experienced the realisation of the 4D simulator and drove the bump a cars till I felt sick, finally hitting Starbucks for an espresso followed by a large skinny latte with cinnamon sprinkled on the froth  yummy.

After waving my friend off at Charing Cross station. Myself and the little dude boarded our train. We found a spot that just had the two seats (little man hates having to sit with all these “strange commuters” his words not mind!) and as I suddenly realised I was beat and was potentially asleep I felt his arms interlock around me, very tightly. Then came the kiss that he gentle placed on my forehead. “Thanks mum, I love you” came a voice… Wow getting kisses is like getting a night on the town (rare) “I Love you”, well they normally pop along when his done something wrong or wants something. This wasn’t the case today! And it felt so great that it wasn’t. Me and my little man were happy… really…really happy, and that my friends is priceless!

 

 

 

APRIL IS AUTISM MADNESS

8 Apr

So Autism Awareness month is here. April is said to be the month to best get heard when reaching out to society when trying to raise awareness for Autism. I consider every month to be awareness month! I blog, talk, share, link, tweet and more It seems to happen naturally now and it just comes easy to me. I am proud to say im passionate about autism. I love autism solely because its part of my son.  Aspergers don’t make little man! Little man makes Aspergers. So for this reason I’m going to blog like mad this April! I’m looking to do at least one interview this April. I really enjoyed them last year and I’m considering bringing back the feature permanently. Guest post will also feature on the blog this April and throughout the rest of the year. The first Guest post is in relation to my day in Court on the 30th March 2010. A friend who attended Court with me has written an interesting  post. She makes fantastic points and has strong opinions it’s in my view a wonderful read.

Over these past few months I have discovered some great links and excellently good blogs that I’m keen to share with readers. Some have been added to the links already.  Pass through regularly?  Then maybe you noticed and gave them a preview. You will also see that a few more blog buttons have been added to the sidebar. If  displayed then in my opinion they are worth a look. With it being April I will be highlighting some fantastic campaigns and non-profit charity’s So if you’re looking for an Autism  charity to fundraise for this April then please I urge you to check these out. The last few months it’s been nothing but doom and gloom within these blog walls. That’s not what I want the blog to be focussed on. I don’t want new visitors, parents of  a newly diagnosed child to look and feel that life is set to be a never-ending challenge. I wont lie when I say with every closing door another seems to open and behind it is a new battle. It seems to be that way  for me right now! But ASD or not! We will always as parents try to gain the best in everything we aim for when it’s for our children. No day is the same! As is no child on the spectrum.  We need less negativity and more positive Input. As little man don’t return to school in till 21st April that gives me plenty of time to spread a little sunshine over the blog.  And lets hope that some day soon school will bring more positive days for little man clearly resulting in a few more uplifting post.

Well in my quest to create a totally  jam-packed Awareness month and not being able to take on the challenge single-handed, I’m gonna need readers help. This is what I’m looking for.

  • A Father of a child on the autism spectrum. I want to hear from the dads who would be interested in sharing their story in an interview with me. Covering diagnosis its impact and what everyday life is like. Check out some of the interviews from 2009. John Kirton from the documentary Autism x6 on Discovery Health was interviewed on the blog last April. Did it raise awareness? Hell yes and it still continues too giving that it’s still one of our most popular post on this blog to date. John a father to not one but six children all placed along the spectrum of autism made for a truly inspirational interview. I’m not requesting you need six children in order to participate in an interview I’m just requesting you’re a father to a child on the Autism spectrum. Email me or comment if interested.
  • Mums tell it how it is. This was a feature due to start last month. However this never happened with the craziness of whats been my life lately. So any spectrum mums who wish to voice important opinions or advise other parents and caregivers on ASD related issues then let me know. I am hoping that the lovely Rachel author of the blog Strange and beautiful would still be happy to share her insights in a talk relating to Sensory sensitivities 🙂
  • Kids art to be put up on the Autism and Art page. Please refer to the page for details.
  • help in our ever-growing Autism Love list. All it takes is for you to visit the page and state your reason for loving Autism. After all it’s within somebody we love. For this reason I say we embrace it. Thank you for the recent comments on the page. If you were one of them commentors then I’m pleased to inform you that your comments have been transformed into something beautiful and are now ready to view as part of the Autism Love List.
  • Now for my big ask!  Are there any autism professionals willing to be interviewed? By professionals I mean specialist teachers, Dr, Educational psychologist, speech and language therapist, behavioural therapist, child psychologist, mental health practitioner or other. There would be no payment for the interview. It would be done by yourself solely for the purpose of helping raise awareness for autism. And for that I would be truly greatful.

Anybody who participates on any part of this blog are very welcome to have a link back to their blog or website.

Autor Clairelouise82 parkinson.claire@yahoo.com

The Big Interview with Cale Irwin

27 Feb

At last it’s here! The Big Interview.

This month I’m speaking to Cale Irwin a 20 year old with the condition Aspergers. Not only did i enjoy this interview but i learnt a great deal from it’ so thank you Cale.

Hi cale. so you have Aspergers? Is that correct? How old were you when you discovered you had Aspergers? And how old are you know?

I have Asperger’s Syndrome, diagnosed by a psychiatrist in 1997, when i was 8. I was informed about the diagnosis when i started asking about it when I was 17. Since my brother has classic Kanner’s, and autism is genetic, and I know my social skills were awful, it seemed Asperger’s was a possibility. So that’s when i found out about it directly from my parents. im almost 20 now.

Did you ever see yourself as different when growing up? Do you remember what age you were at the time these fellings came about?

I felt different from my peers from the moment I started meeting my peers; the age difference between us was the first factor. Because I was fully conversational at around 14 months, Iwas involved in programs for late toddlers before i’d even learned to walk. By kindergardenthe differences between myself and my peers began to lead to bullying which continued on into my late teens.  However, it was not until 14 that I began to understand just how different I was from my peers. I always knew I was smarter ( not in a cocky way, but in a testable IQ way ), and less socially competent. But  it wasn’t until then that I realized I perceived the world differently then they did. It was then that i become aware of how they perceived me, as an other, and one who had always been an other and simply hadn’t realized it. I would compare it to when the ugly duckling looked up for the first time and realized he wasn’t with his family, but rather with individuals who bore some similarities but also major differences from himself.

Cale what was school life like for a child with Asperger’s?

I obviously can’t speak for all individuals with AS, but for me, all elementary classes besides my gifted-LD class were hell! I was physically assaulted daily from K-4th, and verbally abused from 3rd on. I knew the material before we learned it in class, but teachers became angry when i sat and read rather then paying attention to their lessons. My gifted-LDclass which was all individuals who would later be diagnosed with Asperger’s or PDD-NOS was the major highlight . I was surrounded with kids who were like me. Offered material that challenged me intellectually, and in a classroom built for kids with sensory sensitivities.

Could you tell me is it true that all children with Aspergers develop special interest?

I think most do! Though i know i didn’t develop my special interest ( which happens to be ASDs ) until I was 15 or so. Before that I sort of bounced around, reading a bit of everything, but never finding anything that stuck. Now I eat, sleep and breathe books on autism, and no one can make me shut up about it.

Do you have any sensory sensitivities or problems with moter tics?

I have both! I can’t be suddenly touched or be around loud noise ( classifying loud as at or above normal television volume ). I can’t filter out background noise so i need conversations to be in a quiet environments. I have proprioceptive difficulties, so I stim almost constantly to gain information about the location of my body in space. I also have prosopagnosia ( face -blindness ), but I’m not sure whether that’s classifiable as a sensory issue in the same way.

Recently I have developed a slew of moter tics, and very recently some vocal ones, which would warrant a TS diagnosis in any country but the US (as DSM says 18 or under onset, but ICD-10 says 21 and under). It would be difficult to say whether the TS is more bothersome because of the activities it prevents me from doing ( I’ve had to change my focus in neuroscience as i can no longer operate needles/scalpels ), or because of the unkind and judgemental remarks i get from others.

So Cale, What’s life like for you now, how are you spending your time, are you happy with where your life is heading?

Life for me know is better then it has ever been . I’ve gained a position in the college which allows me to utilize my devotion to and fascination with autism ( my professors were quite excited to find an Aspie with a special interest in ASDs. Now i can do all their grunt work for them, because it’s far more fascinating to me then to them. ; ) I spend about a quarter of my working hours in class and doing hw, a quarter reading informative materials for fun, a quarter reading informative materials for research purposes, and as of late a quarter with autistic children, one of whom I’m setting up an ABA program for. I tend to get the majority of my social interaction with peers during meals or in the half-hour before sleep, but i do try and schedule a few hours each weekend to associate with friends.

I’mvery happy with where life is heading at this point. Academia was made for Aspies and i’ve certainly found my place within it. I have found a job goal to aim for ( BCBA) which I know will be immensely personally satisfying. And adopting children is certainly in my future, either with or without a partner.

Wow they are some pretty amazing goals! I wish you every luck in succeeding  with them. It’s been fantastic speaking with you Cale. Your a person with a strong sense of where his meant to be in life. Your story is one of a young man that never gave up on what he wanted no matter what was but in his path Maybe the years of bullying have made you the strong man you are today. I hope so!

Please come back again some time in the feature with an update on your journey through life, But before you leave would you be so kind to finish by giving us a cool  Aspie fact! one you would like to express to the world?

I can’t think of a cool fact off hand ( other then the speculation that both Steve jobs and Bill Gates are Aspies ), but i will offer my favorite Aspie quote: “For success in science and art, a dash of autism is essential.” – Hans Asperger.

I could not agree more:)

Want to read more on what Cale has been up to? Visit http://frogger11758.wordpress.com or follow frogger11758 on twitter .

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