Tag Archives: Neurodevelopmental

7×7 My Favourite blog post’s

25 Feb

I was recently tagged by the lovely Jennifer, an awesome talented blogger, who blogs over at Jbmumofone to give you my 7×7 low down.

First I must share the seven top blog posts, I’ve read over the last week (please bear in mind this has sat unpublished a good week, due to careers brain)!

Next, I’m to share 7 things about me that you don’t know already (if that’s actually possible)!

Lastly, I’m to share the meme love and tag another blogger, who hopefully isn’t already tagged (if I’m lucky)!

Ok… here it goes… the seven blog post I’ve enjoyed this week!

1) Kate Vyktorian wrote about her amazing experience as an attendee at the Elle Style Awards 2012, over on her blog Snugglebubbly. Yes, this jammy blogger bagged herself a ticket to this celeb fest as a result of her recreation of a red carpet look, with the use of items from the Next directory… Lucky girl!

2) Lexy from Mammywoo in her emotional, yet inspiring post, ‘Forgiveness with extra cheese

3) Angela, a talented new mummy blogger wrote a beautiful post of love, dedicated to her 9-year-old son, in the post, ‘A letter to my loved one’s – Part one

4) Autism Mums & Dads is a brand new blog displaying some talented, inspiring words. I read the post, “Everything but the kitchen sink” and had to share!

5) From Fun to Mum, the funniest post I’ve read all yet, let alone week. If you haven’t read, “The Day That Shit Happened” I’d run off and read it now!

6) Bluecrisps, a fellow parent to a child with autism wrote the post, “Does this buggy cause offence” when speaking how our societies ignorance get going when she takes here daughter out and about in her special needs buggy. It’s a strong message from an empowering parent of a child with a hidden disability.

and finally…

7) “Missing my Grandad” a beautiful post written by “a mummy too” as her weekly gallery post. Filled with emotion and love, it’s a really lovely piece.

Next: Seven things you may not already know about me!

  1. I hate eggs, any type but the chocolate type
  2. As well as my love for writing, I spend time drawing and painting too.
  3. I own so many shoes, that they need their own wardrobe
  4. I did plastering and brick-laying at college and passed my first and only exams on the two subjects (no bloke tells me it’s a man’s job)!
  5. I laugh when Nervous
  6. I’m rubbish at icing fairy cakes
  7. I’ve been in a relationship for 15 years and I’m only 29 years old… Goodness me!
  8. Lastly, I tag

The lovely Kylie Hodges over at “Not even a bag of sugar” to list her 7×7

Questioning your coping mechanisms

3 Jan
One of Those Days

Image by rosefirerising via Flickr

Some days are great and others… not so great… yesterday was one of the latter!

Unfortunately a family row commenced at home yesterday (something I wont go into on the blog) however I do believe that as a result of this, a series of high-profile challenging behaviour was demonstrated by my little man. In all honesty, the behaviour was off the scale and I really did struggle to maintain sanity!

I do understand that arguments should not break out in front of children, especially those on the autism spectrum, already easily tipped into an overly anxious state of being, but I’m human and there are times certain situations commence, especially when you find half the arguments are caused by something or another your child on the spectrum may have done or said, worse the person who is arguing with you just can’t leave it a lone, refusing to stop!

I thought it would properly be a good idea to take the children to my mothers, we could see my mum and chill for a bit! Little man could spend some time playing the PS3 with my sister’s boyfriend and all should convert to something far merrier! My plan was going ever so well, though as the evening approached, little man began getting worse and worse… before I knew it, he was throwing a load of nasty swear words at me, why proceeding to kick, punch and lastly spit at me.

God I felt like running away and staying away! When your child has a tendency to throw a load of offensive nasties in your face, you tend to get used to it (in a wrong kind of way) though sometimes such obscenities hurt a thousand times more than any violence… and this time his awful name calling was becoming much to hard to bare. Little man finished his almighty meltdown with a hard punch in my arm and a thump in his sisters back, all while his little brother of two sat screaming! It was at this moment I actually thought… Maybe it would be better if his not here any more, maybe he should live some place else!

I felt such a mix of overbearing emotions as I tortured myself over the thought that had entered my head! I felt assumed and heartbroken how I could even think such a thing! Yet.. at that time as he stood showing no remorse for his actions and I watched how he continued to lash out at his sister, I know I couldn’t help it, I just couldn’t! Every time I stood trying so hard to reason with him, he’ll just laugh and swear! I seriously felt complete despair, lost on where we go from here! I just felt like going to bed forever!

Day’s like this, I wonder what happened to my Little red-haired boy? Though he was always noticeably different, he would sit watching his favourite Thomas video or sit happily playing (even if it was mainly alone… he seemed happy, that’s what counted)! Not anymore! I just see an angry child, who gets anxious, depressed, violent, and often acts in quite an evil and scary manner!

As my Little man grows into someone who actually doesn’t resemble that of a little man at all, I fear for him, I fear for us as a family! At 11 he is reaching the stages of puberty and with it I notice so much more anger, the ability to care less about the people who get hurt in the cross fire. I therefore question my ability to control such behaviour, longing for an answer! As the little man grows bigger, stronger and sadly more violent, I worry he will hurt himself, me or his siblings! Though there is one thing that I fear that little bit more…. Asking for help!

Guest post and Competition: A safe day out for a child with Aspergers

28 Nov

Days out with your children don’t have to be stressful and a safe day out for a child with Asperger’s doesn’t have to be stressful either.

A close relative of mine has four children. He has two girls and two boys. All of the kids are happy, loving and lots of fun. Both girls go to mainstream schools. They have no difficulties whatsoever, but they certainly understand that everybody is different and that we all have our own challenges in life. One of his sons is autistic and the other has Asperger’s syndrome. Tom who is autistic needs to be monitored pretty much most of the time and to look at him you know that he is autistic and the majority of people do make allowances for that. Steve on the other hand, is the older of the brothers, he has Asperser’s syndrome. To look at him you would not know he has it.

When the family go out for the day, all of them take turns to mind Tom as he does wonder off and no matter how many times that they tell him he still does it. Steve does not normally wonder off but becomes extremely engrossed in something and does not realise that everyone else has moved on. There have been numerous occasions that my cousin or his wife and even I have gone racing back to the last place we were only to see Steve looking very bewildered. Because of his condition he will not ask anyone for help as he finds interaction difficult. So he is for want of a better phrase ‘left stranded’.

To overcome this and to be able to have a safe day out for a child with Asperger’s my cousin now uses a child locator with Steve. The child locator is made up of two pieces. One for Steve and one for my cousin or his wife, if they move off without Steve there is a chirping sound and they realise that Steve is not moving on with them. All of the children carry a personal alarm for kids anyway so the child locator was not something that was a big deal for Steve.

One of the other things that can sometimes a bit of a challenge for my cousins’ family when they have a day out is that both boys tire quicker than the girls and they tire at different rates themselves. To minimise the impact this can have on the day out my cousin plans the day ahead of time. He schedules meal and break times. This gives the boys some R and R time and means the boys have enough energy to keep up with the girls.

A safe day out for a child with Asperger’s is as simple as a day out with any other child.

Post written by Andrea mother and owner of Safe girl http://www.safe-girl.co.uk

The teddy bear child locator is on sale reduced from £29.99 to just £19.99 till Christmas

WIN A CHILD TEDDY BEAR LOCATOR

The lovely Andrea is offering you all the chance to win one of this fantastic safety child locators.

If entering please leave a contact email or tweeter idea so I can contact you in the event you win.

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All I’m asking you to do is visit Safe-Girl website and tell me what Alarm or Locator you like best

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DISCLAIMER: This competition will close on the 15th December at midnight and will be drawn at random! Once notified the winner has 48hrs to email (email in the sidebar) there postal address. Prize will be sent direct from Safe girl. Competition is open world wide. 

The power of positivity

25 Oct

 A pretty exciting thing happened to me yesterday. I was contacted by a reporter for the “Weekly News” which is part of the D C  Thomson  &  Co (a Glasgow Newspaper and media group)

 lovely guy interviewed me over the phone and had a particular interest in my attitude to Little man’s diagnosis of Aspergers Syndrome.  

 It was my positive outlook that got him, he was interested to hear all about how I know embrace my sons condition instead of fighting it! 

 Now, what took me by surprise, was his interest in this side of things. You see, since I first started the I’ve had a number of journalist from the media contact me wanting a story on our most difficult & trying times. Now don’t get me wrong, I’m happy to discuss this, after all it gives those who are currently experiencing them same difficulties, the feeling that they are not alone, and yes they can come out the other side! But to have someone contact me with an interest I’m my positive approach to Aspergers was somewhat refreshing. 

 You see, if this same reporter had read my blog this time a year ago, he wouldn’t have come anywhere near me for a positive story (well, I wouldn’t have that’s for sure)! Ok, I’ve long had the attitude that I will never change little man, but during them long hard days of dealing with a school that didn’t give a donkeys rear end, or while fighting the never ending battling to obtain a statement, positive I was not! 

 I’m proud to say that I’ve come a long way since pre-diagnosis and the day of diagnosis itself.

When I look on my dressing table and see that glass award with the words “Mads Most Inspiring” I can’t help but break out in a smile, and here’s why! 

 My son’s difficulties were the reason I started using a computer, my god back then a snail could type faster than me and yes, I know a snail has no fingers, so what does that say about me ah? Now I’m so fast at typing I could do it with my eyes shut. Back then I was looking for answers and support, why? Because their was nowhere else to find them! That was in 2008 and that’s when I one day found myself blogging… Blogging, the girl who said she would never write through choice, My goodness, I actually love it now! My point being is it was the online community that provided me support and taught me one of the most important lesson of my life to date, one I will always hope to teach another… 

“My child may have Asperger’s but his still the same child, he is no different! The label will not change this” 

 From that moment on I looked at things differently! Once I got that diagnosis, the one I knew he would get (let’s not forget it was two year prior to his formal diagnosis that the child psychologist first told me he was 99% certain my child had Aspergers) I didn’t see it as something we needed to fight through, I was already past the stage of asking myself, “Why my child” or “Was it something I did?” I leant quickly that their would be a lot of battles I would need to fight as a result of the diagnosis. I learnt not to take it personally, it was all about money when obtaining the right support, not the fact nobody believed me, like I first thought. The system didn’t wish to believe any of us for the same reason! The cost to them to give our children that little bit extra support each one desperately required!

 Yes, I wouldn’t change my child, he is who he is and taking his AS away would change so much about him. However of course there are certain things I’d wish away in a second, things that would make his life a little easier, who wouldn’t? I’m his mother after all!

 I don’t blame the parent of the non verbal child or the child who has great developmental delays, when they state they would want to cure autism if they could! How could I, my child can speak and is that bit more high functioning! However I would state that just because he can speak or has the ability to do Math, doesn’t mean his difficulties are not always as trying. So… yes, I’d take away his anxiety, I love him to sleep better, but I wouldn’t take his brilliant mind, his interests and his inquisitiveness as these are parts of his wonderfully personality. 

 It was a really nice interview and I put down the phone feeling positive and positivity is the way forward when your child has a diagnosis of Asperger’s Syndrome.

 If anything, it’s the only way forward!

Feeling a tad proud

28 Aug

Wow, can you believe it? I managed to get my article, “Big issues for Little Man” published in SEN magazine!

Back in late May I sent some press releases to the Media relating to the Mad Blog Awards. I was overjoyed when, ‘Peter’ the editor for ‘SEN magazine’ emailed me stating he really liked the blog, “Especially that of my latest article” (remember this was late May). Peter then went on to ask me  if  I would be interested in writing an article for the magazine based on my experiences parenting a child on the autism spectrum. 

Umm, Yes Please! 

SEN Magazine is a great resource for parents and professionals alike. It contains all the latest information on Special educational needs, as-well as host of other areas.

SEN contains resources and articles relating to a number of different conditions and disabilities. It provides contact details and links, pointing you in the right direction of all them need to know organisations! SEN, shares all the latest events and exhibitions and even has an online resource that shares extracts from the mag as-well as breaking news in the world of special education. 

The magazine is delivered via a subscription but is given as a free resource to all Special school. There is a free trail taking place at the moment, meaning you can have a copy of SEN delivered free of charge (try before you buy). I recommend this magazine to anyone with a child with special educational needs, (and no, it has nothing to do with my contribution what so ever) it’s just an awesome resource throughout!

I really didn’t think I would be able to upload a pdf file of my article on a,’wordpress.com’ blog (I have only been blogging here for like three years :))! 

Well, to my surprise and utter delight it turns out that I can! This means that I am able to now share my article with all my lovely online friends and anyone else for that matter! 

So, before you click the link and see the article I’m so very proud off, let me thank all my wonderful readers, new and old. Yes, its every single one of you guys that has helped me through the many battles I’ve faced as a parent to a boy with Aspergers.

 Could I see myself writing an article about the subject a year ago? No way! Life was far to messy to even contemplate such a thing! (Having your article published in a magazine, somehow feels a tad scarier then on the web!)

Writing this article actually shows just how far we’ve come as a family!

 The link will open a pdf file (Note: please feel free to download if you wish)! It would also be great if you could help me spread the news by sharing the link to my article online.

Thanks and enjoy

Claire-Louise 

SEN54 autism

Do your homework!

20 Aug

As a parent I’ve read many articles floating about the net, all written with the aim of assisting parents who have children returning to school this September. I find that many do not offer any information to assist those parents of the “non typical” children, the child with autism or aspergers.

 In some respects I kind of think, “Well, why would they” but when I  think about the high numbers of children being diagnosed as being on the autism spectrum, I ask myself, “Well, why the hell haven’t they!” I’m no expert, “Far from it” but as a parent of an almost 11 year old  boy with a diagnosis of Aspergers syndrome who has been through both mainstream and special school (where he thankfully now resides) a child who was an active school refuser, who had been excluded more times than I care to remember, I have needed to tried one or two techniques aimed to ease the whole returning to school situation! It’s these few little techniques that I am willing to share with you here today! Sadly there are no quick fixes, believe me I know!

  I Hate this uniform

 Uniform, a total nightmare for the child with autism, especially the one who is tactile defensive! We all like to buy new school uniforms at the beginning of  the new school year (we often don’t have a choice what with the rate they grow)! However, if that uniform still fits, don’t change it! Of course there are those times it unavoidable, change of school, the start of secondary school is one great example that a new uniform will need to be brought! When little man was at his mainstream school, they suddenly introduced a new school uniform policy. Uniform posed a massive problem for little man causing all sorts of issues (even exclusion). He went from no uniform to full uniform, a huge change for any child! So, Here’s some tips on ways to make wearing uniform that little bit easier for your child on the autism spectrum!

 Get it washed

That’s right, wash new uniform in your usual detergent, not once but a good few times prior to your child returning to school. Use a fabric softener and if possible dry in the tumble-dryer as opposed to the washing-line, where clothing tends to become stiff. The tumble-drying of uniform will help to create maximum softness of garments.

 Test run

Get your child wearing the uniform for a few minutes each day increasing the time as you go. This enables your child time to get used to uniform rather then expecting them to wear it for the first time when returning to school. Think of it as wearing in a new pair of  shoes to ensure they don’t hurt your feet when you wear them on your big night out for the first time.

Let’s not go Shopping

 Most children with autism hate the prospect of shopping, even those that enjoy it fail to cope with it well. If you are lucky enough to be in the position of leaving your child with a loved one when doing your, “back to school shop” then do so. If something don’t fit you can always return it! Shopping online is another good idea. Try to buy from those you have brought from before. This way you will have an idea of the ranges they stock and the service you will receive (fast delivery, good  returns policy , etc.) Your child will also be familiar with the texture, material of the clothing, important for those who are sensitive to certain tactile input. If you do find you have to take your child shopping then go at a quieter time/day. Have the aim of buying everything in the one shop (if  possible). You can also check stock before hand if stock is in! Some stores will be helpful enough to check and then hold the items back (especially if  you explain your situation) This means you can pretty much do an in & out job which could save your child from experiencing a sensory related meltdown!

 Advanced preparation

 Most schools will introduce all children to a new teacher or learning environment (classroom) before the last day of term. This is fine for the typical child but those on the spectrum may require that bit extra!  If your child is in a special school then it’s my guess lots will be done to prepare your child for even the smallest transition.  Mainstream schools also have a duty to make reasonable adjustments for the child on the autism spectrum and this would be considered one of  those adjustments! Speak to your child’s teacher or school senco to see if the child  could maybe spend extra time with the new teacher in the run up to the end of term (school year). Maybe arrangements can be made for your child to spend a  few hours per week in the new classroom starting a few months before hand ( though there are times that schools will not be aware of the child’s new learning arrangements till the last few weeks of term, nonetheless, careful preparations need to be made). All the above and more should be done for a child making the transition from pre-school to reception and those off to secondary , etc.

 Social stories

 A great idea would be to create a social story for your child. This could be done with the help of your child’s teaching team. A picture of the new classroom  in-which your child will learn and even a photo of the new teacher could  prove a massive help. You can spend time going through your child’s social story with your child during the school holidays. If this is something you haven’t done already, don’t panic! You can create a social story with the focus of change and returning to school with cut-outs from magazines, newspapers or from visuals downloaded from the net, it’s never to late!

 Visual aids

It’s important to use visual timetables at home if used in school, this helps to create some level of consistency. Many children require images & picture symbols where others do just fine with words. Visual timetables can be expensive but you can get creative and make your own (maybe I will show you how in a post one day). Be sure to highlight during the holidays how many days are let till the return to school (Children on the spectrum like to know what’s coming next). We had this highlighted at the side of  little mans home made magnetic timetable. We just used the symbol for school with the correct number next to it as to indicate how many days remained till he returns to school. This is also a great way to avoid school refusal.

Consistency 

Another good thing to do is remain consistent throughout the school holidays. I mean keeping the bedtime routine the same. Sadly little man has trouble maintaining bedtime routines at the best of times which  technically puts me in no position to advise on the matter! Still, the concept is a good one, which is basically to keep things the same! Who knows it could work for you.

 Well, that’s it, I have an arm arch from the typing, so I’m done! I hope my little tips assist you in some way, even if it just makes one thing less trying that’s got to be something?

 Little man has just two and a bit weeks left. Here’s hoping we have a  good return to school.

Are you really brave enough to put the word Aspergers down on your job application?

9 Jul

The power of the internet is truly amazing, for me it’s brought information, peace, opportunities, comfort, experiences, support, education, understanding and friends. (Those and so many more!) 

 Yesterday, I got to meet one those friends in the flesh, over a fabulously delicious skinny latte, with lashings of cinnamon generously sprinkled over a layer of froth. (No, that wasn’t a snip-it from the Marks & Sparks commercial, but me really appreciating a good mug of coffee!) Thanks Neil 🙂

 Star bucks was the ideal setting to chat to a new friend, one I had been wanting to meet for sometime but life being life just made it an impossible task… Well till now! 

 I suppose to classify Neil as a “New friend” isn’t quite right! You see, I’ve known Neil for sometime now, though conversations are only ever exchanged in the land of cyber-space. Neil, an adult on the autism spectrum who was given a late diagnosis of Aspergers syndrome, is a regular contributor in discussions and a massive supporter of the support page, ‘A boy with Asperger’s’ the Facebook page in which I created some few years back as an added addition to this very blog (hence the name of course). His opinions are always given in a frank and honest manner, his certainly given some great advice to many of our members, including that of myself. To be honest Neil has provided me with a sort of insight, highlighting how things could possibly be for my own child in adult life (an important issue to which I will elaborate on soon enough)! 

 Here I was, finally about to meet Neil who yes as mentioned has Aspergers. Just, after 1.30 lunch time I arrived to found Neil awaiting my arrival at the entrance. I knew it was Neil and his profile pic on Facebook had sod all to do with it! So… What gave him away? Only the fact he checked out my footwear as I entered through the door ensuring I had no sandals upon my feet (Yes, Neil hates sandals) There was no awkwardness having only previously met in cyberspace, well… this was the case for me and Neil seemed just fine too! Having got passed the shock that was caused by the similarities of my common London girl accent to that of someone you would likely find staring in the soap ‘Eastenders’ We chatted about life in general. Honestly, Neil is a genuine guy who is extremely interesting and speaks from his heart. He says exactly how it is (Which is an aspie trait you cannot fail to appreciate). 

 Everything Neil said was of interest, I found it a privilege to have him tell me about his life on the spectrum. He put the myths to bed and although I myself  always knew it possible, it was just so good to hear that the best part of his life has been a great success! How else can you describe a good education, (through it wasn’t always easy) a happy marriage and a beautiful son. However, there was something that had never been quite right! At no fault of his own Neil has never been able to hold down a job! Why because society wont allow him that right, the basic human right to make an honest living, to be the loving husband and father who provides and I should add ‘Wants’ to provide for his family… WHY? Its simple! Neil is not seen as a) a “Team-Player, b)  a big communicator  and c) one of them (you know part of the click) Yes, that’s right, those that will a least give him a chance assume his some kind of character from the film ‘Rain man’ sitting him in the corner alone, far away from his colleagues, drawing the conclusion that it’s for the best as this is what those with aspergers want and need to be social isolated from the ‘world… Well, isn’t It! 

This alone screams out loud how little those in the work place, especially that of senior staff really know about AS!

 Neil isn’t under-qualified in-fact he proves that yes, people with AS have great minds and given they put everything into it just as one would who isn’t on the spectrum, they can go on to obtain good qualifications, even having excelled in many areas of  their learning. Is it right that many people on the autism specturm or those with learning disabilities, mental health problems, especially those who’s condition is characterised but that of a difficulty with social communication, are taught by society at large that it is at there utter best interest to go to collage and then university, for god knows how many years, to obtain a degree only to face to total disappointment on the discovery that they are completely unemployable? Even when they do get their foot in the door ready for the challenge of the world of work, a large number of employees with a disability are treated just like my friend Neil (Though you haven’t yet heard the half of it)! Note: I’m not stating those with autism or any other form of disability shouldn’t go to university, obtain a degree! Maybe one day that of my own son will, through that’s his choice and his alone! Nor am I stating that all employers treat employees who have autism/aspergers or other, in this same manner… That would mean I was writing this in a discriminating way! I acknowledge that there are many that do not discriminate and actually do take the time to get autism aware and inflict that awareness on all of its employers! But sadly the number that do not are still far to high, just ask Neil or better still,  just go back a few months when MP Philip Davis outrageously called for all disabled to work for less then the minimum wage… Something he must have unquestionably considered fair in his discriminating little brain! 

 Neil’s last job ( in IT) saw him and around approximately fifteen other employees, employed on a fixed term contract! Neil once again was sat in a corner, left to his own devices. Where was the structure? Of course there wasn’t any. As a woman who isn’t on the spectrum, though I often like to be left to my own devices, I like to know exactly what it is I’m supposed to be doing, how, when and how long for in order for me to do it and do it well, who don’t? For someone like Neil this is imperative! This didn’t happen, like many people with a social communication difficulty he didn’t feel to ask, he didn’t want to, this wasn’t the comfortable thing to do. Failing to see that In-fact Neil was human and would kind of appreciate come social interaction… No one took notice! The results… Neil’s work wasn’t at its finest (but still good I must add). 

 The very end result…

You guessed it, (If, u didn’t after such a long rant then you’re clearly not following.)  Neil’s contract came to an end as planned and just as it did for those fifteen others! Well, fair game then, a contract ending is just that, a contract ending! Where is the problem? Here’s the problem… The other fifteen, all except Neil that is, found themselves happily celebrating the fact they immediately had their contracts renewed for a much longer period of time by their once more praising boss. What a sack of crap!!! Seriously can you imagine how that must have felt? Maybe It felt something like how my own son felt when he was taught in isolation, away from others, left to his own devices, maybe it kinda resembled that same feeling like when my son was told he wouldn’t be allowed to attend educational trips or participate in activities alongside that of his peers! My point… From class room, to office, child to adult discrimination due to others inability to except the person you are, that of disability discriminate still delivers that same devastating blow! Was it Ok, after all the contract had come to a timely end? Crap! This was wrong and Neil for one knows it. Lets not forget its not his first job and likely wont be that of his last! He was told, Sorry you are not much of a team player and yes your work wasn’t always up to scratch. The fact is, having they had made the work place that bit more accessible, made adaptions allowing for his Aspergers from the word go, with the added courtesy of  some instructions, which would have been much appreciated, Neil would have produced the work expected and would likely have been a great deal happier in his working environment!

 My very last point… Promise!

 Not only did I learn from Neil that my son could possible get married, have children, ride a motorbike and hate sandals as much as him! I also learnt he could possible found himself unemployable and yet again the target of discrimination. Yes, my child may have got in to our desired school but like Neil showed me… To get into his desired job is something his yet to face! 

 Neil is looking to make a stand! His words to me, “I want to change things so children like your son don’t have to grow up and be treated in the same way!” My opinion… That was spoken with passion! Please help. I don’t often plea for your help (Ok, Ok excluding that of the Mad blog awards) but this is so very important and its life changing for him and so many others. Neil is searching for other adults both young and old who have autism or other related conditions to get in touch. He wants to collect your stories and get them heard… I guarantee that this will be a campaign he will fight to the bitter end but to do it alone just makes it harder! Neil is looking for people who feel they were discriminated against at work due to their disability, who wants change and wants it with a passion. 

Contact me here by leaving a comment here on the blog

To visit Neil’s Blog: Click HERE

Contact me on twitter: @Clairelouise82

 

revolutionary device designed to keep children from wandering could benefit families of children with autism

4 Jul

Scrolling through my twitter timeline I came across a link that lead me to a site called, ‘Safe Girl Security’ who were promoting a really great product. To my delight some few weeks later I was approached and asked to review that same product, to share my views with my readers, to which I was happy to oblige!

Why?

Because I could see a great idea that could benefit families of young children especially those with autism

The Mommy I’m here teddy bear child locator is designed to give parents like me a little extra piece of mind!

 The locator is designed in a fun teddy bear design making it more appealing to a toddler or small child!  The locator is offered in a choice of two colours, pink or brown

 This locator is designed to send a signal from a hand held transmitter to a receiver that will give off a high pitch chirping sound allowing a parent to successfully locate a wandering child.

Given you notice that your child isn’t where they are meant to be in a reasonably good time after they have wandered off the locators chirps are loud enough to lead you to your child avoiding a potential accident or even fatality.

 When I first read about the Mommy I’m here locators my first thought was for parents with children on the autism spectrum and those with other special needs. I have sadly read one to many stories in the news and social networking sites that highlight a missing child with autism or sadly one that has had a terrible accident after becoming lost. This locator itself can of course be used for an older child however the product does seem to be aimed more at mothers with younger children. Nevertheless it’s my view that it all comes down to safety and the locator can do what it does for a younger child just as well for the older one.

 Putting it to the test

 I received the ‘Mommy I’m here’ child locator and was pretty keen to give it a go right away. However this wasn’t possible and it was a few days till I got the privilege of putting it to the test. Although my little man who has Aspergers syndrome has done a bit of wandering in the past his learnt as his grown to stick to the no wandering rule. He can be very rule bound and now tends to seek permission before going anywhere

So, the obvious choice for me was my 19 month old toddling terror Harley. Yes, he is at that wandering age and don’t I just know it!

 There was however one little issue! The teddy bear locator we received was pink and little man being so rigid in his thinking laughed continuously for some hours branding his little brother a little sister! Not like this mattered in anyway whatsoever to Harley… After all who says boys can’t do pink?


 I thought Harley would happily participate in my little test but he seemed to be in one of his little moods. I put the teddy receiver on to his shoe but he just wanted it off in-order to discover and play with it… Trust Harley!

Plan B was to attach the teddy receiver to the belt loop in Harley’s jeans. My trick… To do this before actually putting them on him! I made sure the teddy receiver was  switched on by switching it on at the back and checking that its tummy was displaying the bright red light. With this I opened my street door and waved him off (Seriously guys I’m joking!)

 I did in-fact open the back door allowing Harley a little explore time in the garden

 I went back inside and stood at the kitchen window watching Harley trying to pull the washing of the line (not impressed) I then took the transmitter out of my pocket (that comes on a key chain and has a little extending arial) and pressed the button.

 Well, it worked and pretty well too!

 Tip! let the little one get used to the noise or at least make them aware that they are wearing it. What started of as a good idea actually back fired on me when Harley almost jumped out of his skin. What’s great is you control the receiver, once you have your child in sight you can quickly stop the chirping at the touch of a button. The noise was extremely high pitched and I guessed it could be heard from a distance (every dog on the street barked that’s for sure)! I later tried it out again at the park! Daddy took Harley and walked ahead, after five minutes once out of sight I hit the button and tracked them down like a mother in the special forces. It was fabulous, one mother even asked where I got it from to which I happily told her.

  It’s worth noting that the noise produced by the locator may upset a child with auditory sensitivity but for me the safety aspect would far outweigh this.

I would suggest that you try to get your child as familiar with the sound as possible in order to avoid any distress. This is worth any time and effort.

 Although we mothers hate to think about the possible risk involved with children we need too in order to keep them safe! The world today doesn’t only offer our growing children a host of adventures but a host of dangers too. Like it or not there are some very unpleasant people in the world and this alarm could help keep your child that bit safer. If somebody attempted to snatch your child the noise is so high pitched and loud that this would possibly startle an abductor.

The thick Velcro strap is designed to keep the locator in a secure position throughout your child’s wear. I found the strap allowed you to secure the receiver in such away that someone attempting to remove it quickly would have to do some fumbling around to achieve this. The fact that it can be discretely hidden under any layers of clothing made this even better.

 This is a great product that I would highly recommend for toddlers, young children and those with special needs and autism. Just imagine having your child wear this when shopping in a busy supermarket, at the park or when visiting the beach.

The locator would also be great to use when your child is on a school trip or when out and about with a group of children, when its much easier for a child’s wandering to go unseen.

 You really can’t put a price on your child’s safety. Yet living in the real world I’m fully aware that piece of mind often equals a huge price tag! Not all parents including myself are in a position to part with a load of cash, especially when you’re a stay at home mum or dad or a  carer for a child with a disability.

That’s why I recommend the, ‘Mommy I’m here child locator‘ that  little bit more! At £29.99 I think it’s a great price that is very affordable allowing all parents regardless of their income the ability to keep their child safe from possible harm.

 Recommended: Check out the mommy I’m here child locator with new alert feature. This means the locator will send an alert to the key chain transmitter when the child wanders out of  range .

Visit the safe girl security website or call 0844 579 1129 where you can find a number of other fantastic products for all ages. Panic alarms, blinkies and child locators are just a few.

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