Of course she might not describe herself as a disabled person... but I caught a glimpse of a very animated new CBeebies presenter today and all of a sudden noticed she was an arm amputee. Of course Ben, my 2 year old didn't notice, although interestingly he did remember her name when he saw her again later in the day.
When I googled to find out more about her it was interesting. Some posts were from parents not knowing how to answer their offsprings questions eg how does she cut up her food, get dressed, what happened to her etc.
Others were from people saying how great it was just to have a disabled person presenting, getting youngsters used to the idea of disability in a very casual way.
The rest were from people saying how attractive they found her because she was an amputee... devotees. See previous post.
Disabled presenters are not new to BBC Children's TV - Ade Adepitan being the best known example but they are rare/non existant for no valid reason on adult programmes. The big question is when are we going to see equivalent presenters on adult programmes because it's actually adults that are more prejudiced and ignorant about disability, children just accept it.
Contact details
As well as being a freelance writer I am also a qualified counsellor and I work for a low cost counselling service in Exeter and for the NHS Gender Clinic also in Exeter.
Simultaneously, I work as a Disability Member of the First Tier Tribunal, Social Entitlement Chamber sitting on disability benefit tribunals on an ad hoc basis.
My articles have been published in the Guardian, Times, OUCH! [BBC disability website], Disability Now, Broadcast, Lifestyle [Motability magazine], The Practising Midwife, 'Junior, Pregnancy & Baby', Writers' News, Able, Getting There [Transport for London magazine], Junior, Community Care, DPPi [Disability, Pregnancy & Parenthood International]. I have also had articles commissioned by Daily Mail.
For more information about me and for examples of my writing please see below.
If you would like me to write an article for your publication, about any aspect of disability, please do get in touch:
emma@emmabowler.co.uk
Simultaneously, I work as a Disability Member of the First Tier Tribunal, Social Entitlement Chamber sitting on disability benefit tribunals on an ad hoc basis.
As a writer I specialise in writing about disability and health.
My articles have been published in the Guardian, Times, OUCH! [BBC disability website], Disability Now, Broadcast, Lifestyle [Motability magazine], The Practising Midwife, 'Junior, Pregnancy & Baby', Writers' News, Able, Getting There [Transport for London magazine], Junior, Community Care, DPPi [Disability, Pregnancy & Parenthood International]. I have also had articles commissioned by Daily Mail.
For more information about me and for examples of my writing please see below.
If you would like me to write an article for your publication, about any aspect of disability, please do get in touch:
emma@emmabowler.co.uk
Monday, February 16, 2009
Monday, February 9, 2009
The perils of being disabled on Facebook
Like many others I eventually succumbed to the lure of Facebook and have steadily built up my list of friends - some are great friends of old, others I have met more recently, mainly through work.
The danger I've found of being open about your disability on facebook is that you can attract 'devotees'.
For those of you not in the know 'devotees' are apparently aroused by disabled people not because of their vivacious personalities, sharp wit, intelligence or flirtatious nature, but purely because of their disability.
Perhaps devotees think they are doing us a favour because they think no one else will go for us. My personal experience is that there are plenty of very 'normal' people who do want to go out with disabled people because of their positive qualities, rather than just because they have a disability.
There's far more to me than my disability so when a 'devotee' picks me out and asks me to be their friend it is really not flattering in the slightest. Ironically in my younger, less experienced and at times more deparate days I might have been flattered.
Nowadays it just seems perversed that someone should pick me out when they don't even know me and for some reason has the audacity to think I might be so desparate as to sign up to be their friend. Who's the saddo, not me.
The danger I've found of being open about your disability on facebook is that you can attract 'devotees'.
For those of you not in the know 'devotees' are apparently aroused by disabled people not because of their vivacious personalities, sharp wit, intelligence or flirtatious nature, but purely because of their disability.
Perhaps devotees think they are doing us a favour because they think no one else will go for us. My personal experience is that there are plenty of very 'normal' people who do want to go out with disabled people because of their positive qualities, rather than just because they have a disability.
There's far more to me than my disability so when a 'devotee' picks me out and asks me to be their friend it is really not flattering in the slightest. Ironically in my younger, less experienced and at times more deparate days I might have been flattered.
Nowadays it just seems perversed that someone should pick me out when they don't even know me and for some reason has the audacity to think I might be so desparate as to sign up to be their friend. Who's the saddo, not me.
Thursday, January 29, 2009
Finding an accessible home - what a nightmare!
We're currently lucky enough to be living in a very modern, spacious, single storey home, in fact it was built on Grand Designs so you can imagine what it is like - think lots of glass! Unfortunately it has also recently been sold so we have to move.
This is actually the first time in my 38 years that I've lived in a house without stairs, I'm not sure why it's taken so long for me to realise that it is a good idea. At least in our house in London we did fit some stairlifts, just as well as there were 4 flights of stairs...
Having to rush to find an accessible home is not a situation I would recommend. We've had to stretch our search to two counties to increase the likelihood of finding somewhere.
The problem is that single storey homes are near next to impossible to find. When I say single storey I'm thinking of the more modern concept of single floor living, more 'Grand Design-esque' than bungalow...
Bungalows you see seem to be a very different beast to what might be described in estate agent speak as a 'single storey home'. I've only seen one property described as bungalow that was spacious, modern, inviting and that was a new build. Most seem to be stuck in some bygone age, multicoloured carpets, borders halfway up the wallpaper, pink bathroom suites... arggghhhh.
Anyway better get back to house hunting...
This is actually the first time in my 38 years that I've lived in a house without stairs, I'm not sure why it's taken so long for me to realise that it is a good idea. At least in our house in London we did fit some stairlifts, just as well as there were 4 flights of stairs...
Having to rush to find an accessible home is not a situation I would recommend. We've had to stretch our search to two counties to increase the likelihood of finding somewhere.
The problem is that single storey homes are near next to impossible to find. When I say single storey I'm thinking of the more modern concept of single floor living, more 'Grand Design-esque' than bungalow...
Bungalows you see seem to be a very different beast to what might be described in estate agent speak as a 'single storey home'. I've only seen one property described as bungalow that was spacious, modern, inviting and that was a new build. Most seem to be stuck in some bygone age, multicoloured carpets, borders halfway up the wallpaper, pink bathroom suites... arggghhhh.
Anyway better get back to house hunting...
Thursday, January 8, 2009
Am I bigger yet?
Archie is now 4. I've told him he is a little bit bigger now he is 4 but I get the impression he had expected to shoot up on his birthday. Indeed on the day he asked "can you see me growing bigger"...
He is now increasingly aware that although he might be older than some other children, including his younger [but not little] brother, he isn't bigger than they are.
I find it's a balancing act - not wanting to make him have a hang up about his height whilst at the same time not wanting to pretend that he will end up as big as everyone else when he won't be.
The bottom line is that he could do just fine in life if it wasn't for the prejudice that exist in others....
He is now increasingly aware that although he might be older than some other children, including his younger [but not little] brother, he isn't bigger than they are.
I find it's a balancing act - not wanting to make him have a hang up about his height whilst at the same time not wanting to pretend that he will end up as big as everyone else when he won't be.
The bottom line is that he could do just fine in life if it wasn't for the prejudice that exist in others....
Wednesday, December 10, 2008
The Power of the Internet
When you have a rare condition [and/or a child with a rare condition] the internet is such a powerful tool for finding others with the same condition. That can then be an amazing source of information, support and comfort because having a rare condition can be quite an isolating experience.
As Archie's broken a few bones recently I e mailed an e mailing list for people with Kniest/SEDc and asked if this was a common occurance, seems like it is. Although I'd rather he didn't break bones, knowing that it is 'normal' for some Kniest children [wasn't a regular occurance for me I have to say] was reassuring.
I've also come to realise through belonging to that group how lucky we have been with Archie in terms of him being able to walk, as there are other children with Kniest who can't walk or who use wheelchairs. I'm not sure how much that has to do with the fact that we never contemplated the idea that Archie wouldn't walk, because I can walk. And I wonder how much can your expectations of a child's development can influence their final ability?
As Archie's broken a few bones recently I e mailed an e mailing list for people with Kniest/SEDc and asked if this was a common occurance, seems like it is. Although I'd rather he didn't break bones, knowing that it is 'normal' for some Kniest children [wasn't a regular occurance for me I have to say] was reassuring.
I've also come to realise through belonging to that group how lucky we have been with Archie in terms of him being able to walk, as there are other children with Kniest who can't walk or who use wheelchairs. I'm not sure how much that has to do with the fact that we never contemplated the idea that Archie wouldn't walk, because I can walk. And I wonder how much can your expectations of a child's development can influence their final ability?
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