Showing posts with label International Day of People with Disability. Show all posts
Showing posts with label International Day of People with Disability. Show all posts

03 December 2013

Disability has meant finding my tribe.

 

While disability comes in different forms, I have found there's a collective sense of empathy in the disability community. Putting my condition in a box - ticking that box 'yes I have a disability' - has been more empowering than I imagined it could be.

I never identified with any words to describe my appearance when I was younger. The nicknames I was called hurt, and I wasn't disabled enough to go to a special school so I never had an affinity with the word disability. In the era and town I grew up, the definition of disability was either so severe you went to a special school, or you weren't disabled at all. I too had limited perceptions of disability.

When I first started mentoring young people with chronic illnesses, I was only a year older than the oldest members of the program. They talked about their experiences of having a chronic illness - things like constant hospital stays and appointments, time off school and a lack of understanding from their peers. I realised that these were my experiences too. We were different, we didn't have to talk about our conditions, but we just understood each other. It didn't matter that our conditions varied, we could learn from and support each others experiences. It was then, in 2008 I realised that I have a chronic illness. I always knew I did, but that was the first time I felt like I belonged in a group.

And then, when I was on No Limits, I'd listen to the stories from people with all types of disabilities. I'd nod and laugh, and sometimes tear up, because I just knew. I don't know what it's like to be in a wheelchair, but I do know what it's like to be asked intrusive questions.

Every time I mentored, or spoke on that TV panel, I had an epiphany and felt the greatest sense of empathy ever.

I'd found my tribe.

I went to Quippings on Saturday - it's a disability performance night. The theme was 'Piss On Pity'. I read out my piece on normal. Lots of people came up to me to tell me they enjoyed and/or identified with my words. The audience featured various disabilities and expressions of sexuality - everyone raging against the normal stereotype. It was brilliant. Kate Hood spoke of the patronising conversations she has with people who pry into why she's in a wheelchair. She mentioned how someone chased her down the street to give her a piece of paper featuring the number of a faith healer in Indonesia on it. It's happened to me too. Another performer, 'And Deathray', who has a variety of invisible disabilities, ranted that its so hard when she just doesn't fit neatly inside the box of disability. She's more than a wheelchair accessible sign. Why is she so sore today when she looked well yesterday. Again, I haven't experienced Fibromyalgia, but I've experienced the reactions she's received - the assumptions, advice and especially the sheer lack of understanding.

A person with Ichthyosis asked why I Identify with having a disability. She seemed surprised - she told me she doesn't believe she has a disability. Maybe she was surprised at me because of the negative connotations that the word disability has, or the assumption that disability is a limitation on mobility only? I told her that while I can do so many things, the disability surrounding my condition is external to me. It's the curiosity, attitudes, reservation and hesitation towards my skin, and occasional harassment - all from other people. These experiences are what my friends with disabilities face too. We are all different but so much of us is the same through our collective empathy.

Disability is a little bit about what I can't do, a little about the discrimination and attitudes I face and yet so much about what I can do. I don't want to diminish the harsh and often sad reality of disability. But I - and so many of my friends with disabilities - see the word and the condition in a positive light.

Since I've identified with having a chronic illness and a disability, my life has become enriched. I've met great people and done so many things that I may have missed out on if I'd dwelled on the negative connotations and assumptions around disability.

For me, disability is pride. it's individualism and not giving a fuck about non conformity. Disability is showing them - the underestimators. It's a sense of community. It's friendship and a strong sense of empathy with a big dose of laughing at the ignorance of others' reactions. Disability is a place to belong. It's finding my tribe.

Today is International Day of People with Disability. I've done a couple of interviews - one for 3CR radio and another for ABC Online. You can see what events are happening near you on the IDPwD website.

 

06 December 2011

Noteworthy

There are a few things I want to share with you this week. Maybe I'll start doing a regular 'noteworthy' post of the things that have made me smile. Blogging is all about sharing, right? What do you think?

Ivy's wish
First and foremost is a blog entry by Tiffany Treganza at Three Ring Circus that is possibly the most beautiful thing I have ever seen. Her little girl Ivy has a rare and severe chronic illness that affects her immune system. Ivy was recently granted her wish from Starlight to dance on stage with the Australian Ballet at the Opera House. In her blog entry, Tiff writes about the joy brought to Ivy and the rest of her family.

Ivy's smile is so cute, and seeing her dance and in awe is heart melting. I have read the entry three times now, and cried just as much each time. Amazing. Please, please read this post and be reminded at the joy in the world.

Please also consider donating to Starlight, to grant other sick children their wishes. I donate and am so glad to see my money bringing smiles to those who need them.


Tiff has given me permission to share some of the gorgeous pictures with you on my blog.

 Ivy and her twin brother Noah.
 
 Ivy received some signed ballet shoes.
 
 She danced on stage.
 
 And more dancing and spinning. Just gorgeous.

28 November 2011

Woman of the Week on The Hoopla

I am Woman of the Week on Wendy Harmer's website The Hoopla!! It coincides with International Day of People with Disability.

It is a great honour to be up there with Tracey Spicer, Gorgi Coghlan and Rebecca Gilling. So awesome! I am very proud of this one :)

Thanks for having me Wendy and Team Hoopla!

You can read my whole interview here.

21 November 2011

International Day of People with Disability - blog carnival

International Day of People with Disability is on 3 December. I am participating in the Pin Post and Pose initiative. I hope you can get involved. (See below for further details.)


International Day of People with Disability (IDPwD) is a United Nations sanctioned day that aims to promote an understanding of people with disability and encourage support for their dignity, rights and well-being. The day also seeks to increase awareness of the benefits of the integration of people with disability in every aspect of political, social, economic and cultural life.


IDPwD brings together individuals, businesses, community organisations, and governments from every corner of the world to celebrate and acknowledge the contributions, skills and achievements of people with disability.


In 1992, at the conclusion of the United Nations Decade of Disabled Persons (1983-1992), the General Assembly proclaimed 3 December as the International Day of Disabled Persons. (From the IDPwD website)
The ribbon I am wearing signals my support for International Day of People with Disability.

While we have come a long way in the developed world with disability policy and support, so much more can be done. Increases to funding, improvements to accessibility and changing of attitudes are continuously needed.

I have not identified with having a disability (or chronic illness as I view it) until recent times. The social and medical challenges I've faced with ichthyosis are the same sorts of barriers as my friends with much different disabilities face. I guess my ichthyosis has always been a part of my routine, but I didn't define it until recently. I realised that it can be a barrier to some aspects of life, and also a competitive advantage. Without it, I may not be able to do all the exciting things I've been doing - writing, TV presenting, getting noticed at concerts...
And I'm so glad to be involved in the disability community. I've made some great friends.

For me, International Day of People with Disability is not so much about making people with disabilities aware of the day, but educating and including the people without disabilities.

For three years, I've been coordinating International Day of People with Disability events at work. I have given several speeches, and invited members of the disability community (young people from the ChIPS program) to speak about their experiences. This event is the one I love to run the most. I love giving our guest speakers the chance to tell their stories - for too often, people with disabilities don't get the chance to be heard. And I also love the way the audience - my colleagues, most of which don't have a disability - engage with our guest speakers. The talk in the office after the event is about how the guest speakers inspired them - changed their perceptions and taught them about different ways of living and positive outlooks, despite their challenges.

And I think this is one of the most important issues around disability - challenging the way people without a disability think about disability.

Aside from holding an event at work, I'll be celebrating International Day of People with Disability by attending an official State Government event in the day and at night, celebrating my 30th birthday with family and friends. The doctors didn't think I would survive much past birth, and look where I am now. That's a pretty cool way to spend International Day of People with Disability!

If you want to get involved in a small blog carnival I'm running, write a blog post about what International Day of People with Disability means for you, and post your link below.

  Facebook event here.


Pin, Pose, Post & Ribbons 


You can also take part in a community effort to show support for this years IDPwD.

As part of celebrations for 2011 a colourful ribbon pack has been developed by Nican in partnership with the Australian Government. We hope this ribbon will develop as a recognised way for people across the country to signal their support for the day.

People across Australia can signal their support for International Day of People with Disability by wearing a ribbon in the lead-up to 3 December or on the Day. 

You can also take part in a community awareness effort in the lead up to IDPwD called Pin, Pose, Post for IDPwD. This will involve a range of Australians, including Disability Community Leaders and prominent people from all walks of life, donning a ribbon in advance of the Day, capturing an image and providing a single sentence beginning with “I support IDPwD because”. This might indicate why you support IDPwD and its message of breaking down the barriers as well as supporting access and inclusion. 

If you choose this option, your Pin, Pose, Post for IDPwD will be shared on a Gallery of Supporters via the IDPwD website and Social Media to represent a wave of enthusiasm leading up to the Day across Australia. 

To take part please email idpwd@nican.com.au


07 December 2010

My radio interview where I talked about sex and dating

I did a radio interview on 3CR community radio where I talked about sex and dating. The interview was a part of 3CR's feature on International Day of People with Disability. The other women who did interviews were so moving.

I was a bit worried about my responses - I was quite nervous, but I am happy how it turned out!

You can hear it here:

http://podcast.3cr.org.au/audio/3CRCast-2010-12-03-10502.mp3

Thanks for producing, Clare Burns!

03 December 2010

ABC online's Ramp Up launch + International Day of People with Disability

It is quite fitting on this International Day of People with Disability that my own chronic illness has somewhat disabled me. I am writing this from under the covers (even if you imagine really hard, it's not a sexy situation I am in). I am sore, finding it hard and very painful to walk, a little bit miserable, and unable to go to work. The chemist gave me a doctor's certificate, and suggested home-based treatments. I am now on a second dose of antibiotics and nauseating pain killers. If I am not better by Sunday I will take myself to the emergency ward for a consult with the dermatologist, to receive IV antibiotics rather than a hospital stay. And I'm concerned that I'll be too unwell to go to my own birthday party tomorrow night. It sucks.

I had a shower at my friend's house this morning. As I mentioned, I never look my best first thing in the morning, so to have kisses blown to me and smiles from her beautiful one year old daughter made me feel good about myself. There's nothing like the unconditional love from a baby to cheer you up when you're feeling your worst.

Something else that's put a smile on my face today, and made me very proud is the launch of the ABC's disability portal, Ramp Up.

Ramp Up is a website dedicated to news, opinion, broadcasts and discussion about disability.
My introductory article has been published.

You can read it here.

My online friend Todd has also written an article which I recommend reading. And check out my real-life friend Pauline's article too.

I've not had a lot to do with International Day of People with Disability until very recently. I never thought it applied to me. But it does, and even if I didn't have a chronic illness, it should apply to me. This day is very important to raise awareness about disabilities and chronic illnesses, and to celebrate ability.

For the past three years I've had greater involvement in International Day of People with Disability. I coordinate events for it in my workplace. I've spoken at some of these events in 2008 and 2009. This week I have coordinated and assisted with two events at work - giving the opportunity to young staff and friends to share their stories about their disabilities. Hearing their stories - some struggles but mostly triumphs - moves me to tears.

In her editorial welcome on Ramp Up, Stella Young writes 'In a lot of ways, International Day still doesn't mean a great deal to me. It's just a day. I'm proud of who I am every day, and I know dozens of other disabled people who feel exactly the same way.'

I feel a bit the same. But this year International Day of People with Disability feels more special for me because I am now a contributor to Ramp Up, in the company of many other talented writers.

I am going to rest up now, under the covers. Read the newspaper and sleep. And hope that my infection heals soon.

29 October 2010

Feature on the International Day of People with Disability website

This just in!

I have been featured on the International Day of People with Disability website.




So many exciting things have happened this week! More news to come soon.
International Day of People with Disability (IDPwD) is a United Nations sanctioned day that aims to promote an understanding of people with disability and encourage support for their dignity, rights and well-being. The day also seeks to increase awareness of the benefits of the integration of people with disability in every aspect of political, social, economic and cultural life.
IDPwD brings together individuals, businesses, community organisations, and governments from every corner of the world to celebrate and acknowledge the contributions, skills and achievements of people with disability.
In 1992, at the conclusion of the United Nations Decade of Disabled Persons (1983-1992), the General Assembly proclaimed 3 December as the International Day of Disabled Persons.
Since 1996, the Australian Government has provided funds to promote and raise awareness of IDPwD around Australia, through the Department of Families, Housing, Community Services and Indigenous Affairs (FaHCSIA).

More information on the Australian Government's support for people with disability can be found on the FaHCSIA website and the Department of Education, Employment and Workplace Relations' website.
(Source)

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