This Is My Child - the new MNHQ campaign. Everyone come look please!(305 Posts)
MNHQ have commented on this thread.
As lots of you will already know, we've spent the last few months working on a new campaign called 'This Is My Child' - and it's launching on Monday. (We're letting you know about it now because there's a rather nice piece about in in the Guardian this weekend.)
You can read about the background to the campaign here, but in essence it's about myth-busting and awareness-raising - so we'd really love you all to share it as widely as possible. We've consulted with Mumsnetters and the material is supported by input from some of the leading charities in the field: Mencap, Contact A Family and Every Disabled Child Matters.
Over the years on Mumsnet, parents of children with SN have described how their lives are made more difficult by the occasional (or not-so-occasional) judginess of members of the public. They've described how this can contribute to their isolation, placing limits on their social opportunities because they can't face the stress and disapproval that comes with public interactions.
That's why we came up with This Is My Child. Its aim is to support parents of children with additional needs, inform everyone else, and open up a conversation about how we can all act together to make day-to-day life a bit easier for these families.
The input of parents caring for children with special needs has always provided a fascinating perspective for other MNers, encouraging empathy and giving real insight into what life can be like. We're hoping that our myth-busters, tips for non-experts and strategies for parents and carers, along with our background facts and figures, will help to bring the wisdom and perspective of Mumsnet SN posters to a wider audience.
So if you like what you read and think someone you know would find it interesting or useful, please share it as widely as you can (you'll find our impressively large sharing buttons on each page ).
And for the Tweeps among you, we'll be holding a Twitter party on the #ThisIsMyChild hashtag on Tuesday between 1pm and 2pm; please join in if you can.
As ever, we'd love to know your thoughts and hear your feedback, so please use this thread to post up anything that occurs to you.
My daughter has adhd,odd, dysgraphia, hypermobility and other learning difficulties. She stuggles in school and melts down when home or out and about and we get the funny looks and the comments; such as control your child or a good smack would sort that out. But its not that easy especially when they get frustrated to the point where they cant actually communicate and its so hard as you just need to let them calm down so they can tell you
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good..it was eventually deleted..but other similar ones, were not.
To answer "yes out of consideration to people that want to see the film that they paid for without those distractions!" to the question "should people with disablities causing them to make noise stay away from the cinema" is not deleted in the interests of "not stifling debate".
I thought MNHQ had moved on from the old days and took a harsher line on disablism now but clearly I was wrong, sadly.
"this is my child"..but people can talk disparagingly about her noises being annoying in cinema and even say she cannot go..because we wouldn't want to stifle debate.
Shocked to the core by recent responses from MNHQ when had been impressed with campaign and recent support for posters affected by disability.
Thankyou thankyou thankyou!!!! I've just stumbled across this campaign after reading an article in the guardian.
I have a severely disabled 15 year old boy and you have basically wrapped up all my thoughts and feelings into this campaign!! Someone is finally listening and doing something!!! This is kinda an epiphany for me to come across like minded people and genuinely know what it is like to experience what me and my family do on a dally basis!
I've had someone tell me I should have let him die after a traumatic birth and weeks in intensive care and I had no right to bring him into society and burden taxpayers with our problems. (It was hospital errors that caused his disabilities)
That's the most hurtful thing that's ever been said to me but there is a long long list of other people's negative and damn right rude remarks. I've had people walk in lamp posts for staring so much (we got the last laugh there, my son foubd that very funny!) and a woman with young children have a physical fight with me as his wheelchair was protruding from a till and she couldn't get her buggy! Pathetic!
Thanks once again!!!
I made it quite clear that it was unacceptable to put a child in detention in that situation. What makes me quite and is that there are obviously other children being treated this way at that school. Thankfully, DS1 is at a lovely school, but not all children are that lucky.
Triggles, that really makes me that you were treated like that.
When we went looking at our local junior school, in the process of deciding whether or not DS1 could cope, the SENCO there told us that they were very inclusive - then proceeded to point out the separate lunch room, the separate classroom if needed, kept hearing the word "separate".. And she capped it off by showing me the DENTENTION room, saying "if he is having difficulty coping, he can sit in here for awhile." The detention room?!?! So basically, he'll think he's being punished for struggling to cope? No thanks.
He is now in a lovely specialised school that is brilliant for him.
Vivi - my ds is walking across a log tightrope at Heligan. Did you spot his insulin pump?!
I would definitely recommend that anyone who has concerns obtains both their child's school and LA records - it's absolutely shocking some of the things you can uncover. Most people (apart from those on those on the SN board) would be totally horrified by the things I've uncovered.
I am waiting for the SS knock at the door as that seems to be the usual tactic to try to silence 'troublemakers'.
I agree. It is impossible to prove that this kind of thing is happening because you might be able to say 'SENCO whinged about how much he would cost the school if we placed him there and told us that his 1:1 support wouldn't be used exclusively for him as there are children much more
deserving disruptive', which is all they would have to say to out a parent off.
But that is hardly a media story. And when the LA were questioned they'd just say 'well the school got an outstanding rating and the SENCO has a good reputation and wouldn't have said that'.
sunny it's a nice idea about publicising this sort of practice in the media and it would be nice if some big names with legal clout could protect those that want to speak out. The problem is that you still have the LA to contend with if you dare to criticise a school that has a reputation for being very inclusive. They will back their schools all the way and, as I've found, even cover up for them. Complaints go nowhere - I've even been threatened with legal action if I dare to speak out about certain things. I've uncovered various illegal practices but it's all been denied.They think that no-one will actually believe you if you tell anyone as 'where's the proof?'. Usually it's their word against yours and as they are 'professionals' society prefers to believe them than the parent of a disabled child. I happen to have however a huge amount of written evidence about what happened to my ds and how appallingly he was treated - they're not as clever as they think they are. I'm just waiting for the right moment to publicise it.
Jake - I know what you mean about secondary schools. When I went to talk to a Senco she totally blanked my ds. She looked and said 'is that him over there? I heard that he might be coming here'. She then wittered on about various 'woo' strategies that she used to help her 'special children'. She said that she had a child similar to ds but he had always managed very well there. When I asked what strategies were used for managing meltdowns or angry outbursts she said ' we don't have those in school - I call the parents to collect the child so there's no disruption'.
Needless to say the school is thrilled to have recently received an 'outstanding' Ofsted rating.
The thing is that my DS has to go SOMEWHERE, he is deemed too able for the special schools and having visited them I agree as socially he is very able....of a bit odd.
It is very dispiriting to think that I have to send him to me of these schools which really don't want him.
On a positive note one of the schools I visited has a very good name for supporting children with SEN. Again the SENCO is of the "he is going to struggle all the way through" variety but I know enough of the experience of other parents to know the school does a good job.
I have reported my post to MNHQ and asked if there is anything they think they could do to highlight the plight of families where dc with SEN are forced out of school.
Hmmm....pondering on visiting all the local MS secondary schools with a question sheet and a tape recorder.
My experience seems to be all too common then sadly. What makes me crossed is that the SENCAN seemed utterly horrified by what I have experienced.....and seemed to indicate it was out of the usual order f things but it isn't from what I can glean from other parents.
I CAN understand why they do it but.....
Is yours the owl child, Tidy? I've become somewhat enchanted by him.....
Thank you MNHQ for including a picture of my ds in the gallery. It makes me very proud.
No incentive should be needed for any school or teacher other than the desire to do the best for every child.
If, as it seeks is the case, we have created a system where that incentive is in competition with others, we need to do something about it.
I think it is also easy for a potential school to see the availability of 'elsewhere' or not beyond their concern as they have quite enough to do with the children that are IN their school, with the hoops they are required to jump through and the ever-increasing demands and lists of criticisms.
I honestly can't see what a child with SEN, can bring to a school except extra work, extra hassle and a cost. In some ways I think it is less problematic for schools admitting children without a statement because their legal entitlement to support isn't a statutory responsibility of the LA to be delivered by a school.
Those without statements can be admitted and then 'managed' rather than 'educated', through the school system for as cheaply as possible, so not having a statement can make it easier to get place. If you so much as hint that you have expectations for your child at the show-around you'll be sent packing.
Interestingly, having a statement means you can chose your school. But who in their right mind would send their children to a school that made it clear from the outset that they would in the best case, tolerate your child, but in the worst refuse to deliver on their statutory duty and fulfil the provision in the statement?
The statement is the child's protection of their provision, in law. But those of us on the SN boards have story after story of schools having no regard for what is written in the statement, with the key to enabling schools to do this the closed doors to parents, and the inability of their children to communicate what goes on.
Sadly Starlight, I think what many in the general public still think is that all children with any degree of SEN should be educated in Special Schools. They do not realise the places don't exist.
I have to add though that many SENCOS and teachers have very little training in either SEN or the law, and what they do have rarely comes from unbiased or independent sources.
Often they can truly believe that a child would be better placed elsewhere. Unfortunately they don't understand that 'elsewhere' just doesn't exist.
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