Showing posts with label curlypops. Show all posts
Showing posts with label curlypops. Show all posts

16 September 2013

Walking Alongside Someone With A Visible Difference

It seems the more people I meet, and the more friends I make, the more I am reminded that people do treat me both normally and differently. Almost all of the new people who come into my life comment on how much they notice the staring. I never realised staring is that prominent until people remind me.

Tash, a friend I met through blogging, once said to me that she often forgets why people stare at us when we go out together. I am so used to being stared at and commented on that I forget what it must be like for my friends. Of course, I don't feel like my appearance is a burden on them, but I imagine the stares we receive must be just as tiring for them as it is for me. Camille has said that since her lung transplant (which means she no longer carries an oxygen tank with her), she's noticed a lot more stares when we go out together, because she no longer gets stared at alone.

James Partridge, CEO of and author of Changing Faces (the charity and book of the same name), wrote about how when people with visible differences are in the company of people with 'normal' looking faces, it can put strangers at ease during first time encounters - it shows that we are accepted by society. Partridge also wrote "being in a crowd with normal faced friends will almost certainly protect you from abuse and assure your integrity; the very fact of being with a normal-looking person will give you credibility." Furthermore, Partridge writes about implied slurs - people worrying their status of attractiveness could slip by you being in their presence. Partridge uses the example "You aren't pretty enough to be seen among us"; and adds "Nothing may be said, but the looks tell it all." Lifelong experience of having a visible difference has taught me how to read looks and hesitant behaviour from strangers (and sometimes people I know). I am not being paranoid, or thinking the worst of people - I just know these looks. There have been occasions where people have hinted they don't want me in their photo. And I'm certain that a reason for relationships not getting off the ground is that some boys have been embarrassed to be seen with me and not sure how to handle strangers' reactions.

My friends can also see reasons for me to be frustrated with ignorance, hurtful comments and discrimination, and how sometimes I can't keep on being polite. Recently I had dinner and a long, long chat with Kath, a friend who is missing part of two diagonal limbs. She is incredibly smart and funny, and very comfortable and confident about her disability. We were chatting about disability, and how it is just so tiring explaining and defending the way we look, and how we prefer to educate people on our own terms. She said that she is happy to stand in front of a lecture hall or write an article, but she doesnt want to educate people in her every day life just walking down to the shops. Which is the way I feel. I believe it's ok to only want to educate people on our own terms. When the taxi driver thing blew up in July, the things that annoyed me the most were that people expected me to educate everyone I meet - that I should be ok with answering every question that comes my way because I experience this all the time; and that I should also be polite in all my encounters. And for those who know me, and experience what I do by being a friend, can see that sometimes that's just not possible.

Tash has written her perspective of having a friend with a visible difference - it's one of the nicest things anyone has written for and about me.

"Carly and I have been good friends for over a year now, sharing laughs, going to new and different restaurants around Melbourne, attending movies and talks, and even travelling to Canberra together for the Human Brochure weekend. We have bonded over blogging, social media, and disability and other social justice issues we are both passionate about.

When the spotlight hit Carly amid the treatment she coped from a taxi driver a couple of months ago, and the positive and negative responses she got from highlighting this treatment, I was reminded how people see her and treat her differently. Because I often forget – she’s Carly to me! A vibrant, fun and funny friend, who is interested in many of the things I am.

I forget when we walk down a street together, or walk into a crowded restaurant, and people stare. Blatantly! I never remember why….I’m always so self conscious when it happens - “do I have my skirt tucked into my undies?” or “Do I have bird poo in my hair that I didn’t notice??” Oh no, I forgot, my friend is red and shiny….

This realisation, which also occurs at times when I read comments and tweets directed at her from the broader community, reminds me about how tiring it must be for her to be nice and pleasant in the face of such stares, comments and treatment by strangers, and how amazing it is that she does not react as most people would automatically react in such a situation. Given the volume of comments, intrusions and stares, she seems super human to me to withstand the Chinese water torture that is the constant drip drip drip of abuse and horrendously thoughtless comments. How lucky so many people think they are, to be in a position to judge someone else, because of their appearance.

I have also had a couple of different friends of mine talk to me about Carly and her story, and ask after her as you might after someone you know is in the hospital or someone going through some horrible time. It stops me in my thoughts, and makes me wonder if she may have been in an accident I didn’t know about, and thus the voice of concern. But then I always just mention that Carly is just living her life, just like everyone else – maybe I am too flippant, but I don’t see her as any different, in all seriousness! She’s working, socialising, chipping away at goals and dreams, writing, raising awareness for the things important to her, and things that matter and that should matter to all of us.

I have been told that because of my working history in disability and mental health, and my varied roles as a Social Worker, that my views are different to most people. That the average person doesn’t have the experience with people with disabilities that I do, and so it’s an unusual perspective. But I disagree.

You don’t need experience with difference to treat people as you would want to be treated. With dignity and respect. You don’t need a degree in disability to have empathy. You don’t need to work in the industry to have gained a glimpse into the experience, and recognise that people are people, regardless of each person’s range of abilities and challenges.

Am I wrong?

I wonder about people who are rude or horrible to Carly. Do they really not know anyone with a physical or intellectual or mental health difference? Really? The stats about our population would suggest otherwise. And so then I am even more baffled by people’s treatment of others.

I am endlessly in awe of Carly’s patience and resilience in standing up for herself, and other people with a visible difference. But she is still Carly to me! I will always take the piss out of her for her different music tastes and her complete ignorance about sports, just as I would anyone else. I will challenge her on things I don’t agree with, just as I would with any other friend. And I will banter and laugh along with her at the range of things we come across every day. Because surely we are all the same, in the end."

You can read Tash's blog, and follow her on Twitter and Facebook.

 

 

25 February 2013

Donate Life. The most loving thing you can do for a stranger



It's Donate Life Week from 24 February - 3 March, and I urge you to consider registering to be an organ or tissue donor, as well has having the conversation about your wishes with your family.

The Donate Life website states:

"In 2012, 354 organ donors gave 1,052 Australians a new chance in life. The number of organ donors and transplant recipients in 2012 was the highest since national records began.

and

The majority of Australians are generally willing to become organ (80%) and tissue (78%) donors. Only around 1% of people actually die in hospital in the specific circumstances where organ donation is possible. The circumstances in which you can become a tissue donor are less limited. In Australia the family will always be asked to confirm the donation wishes of the deceased before donation can proceed. In Australia less than 60% of families give consent for organ and tissue donation to proceed. The most important thing that helps a family's decision is their knowing the wishes of their loved one."

As at 31 December 2012, just over 1 Million Australians had registered their decision to become an organ donor. You can view the registration statistics on the Medicare website.

Around 1600 people are on Australian organ transplant waiting lists.

 

Until recently, my beautiful friend Camille was on that transplant waiting list, desperate for new lungs. She is in her 30s, so very talented, and lived life to the fullest that she could, with chronic lung disease and being restricted by the waiting list. She was given the gift of life from an incredibly generous donor, with their family's permission.

She writes about her gift of life over here

I can't imagine what Cam went through while waiting for her new lungs. She is the bravest, least complaining person I know. I saw her frustration at times, and wished that she'd get the call soon.

After she got the call from the donor coordinator, she texted me in the middle of the night, to tell me she was on her way to hospital. "Fingers crossed, I love you" I wrote back. The day was long - I checked in with her sister for news every few hours. Her own wait must have been tumultuous.

Her recovery will be long, but my gosh I've seen progress. I went to visit her two weekends ago. She was in high spirits, talking a mile a minute. I am so happy she's here.We took some photos of ourselves together - the first we have taken in our three year friendship. Because we are too busy taking pictures of food.
I gave her some presents- a toy cat and some art supplies and nail polish, because now she can paint her nails! Look at the colour in her cheeks! Isn't she beautiful!

She's made considerable progress since my first vist. She's now able to breathe without the assistance of oxygen.

I said to Camille, I met her because of her old lungs. She and I both write for the disability website Divine. I tracked her down on Facebook after I read her article about being a blogger. And we became friends. The first time I met her in person she was in hospital too. I also said to her that her new lungs will enable us to share laughs and cake for years to come.

Cam has a pinboard next to her bed in the hospital ward. It's filled with pictures from her nephews, cards and pretty coloured paper. There's also a list of things she will do now she's got new lungs. Ride a bike. Walk. Go on a holiday. Shoot hoops. The things that most people take for granted. I added to that list. See bands with Carly.

And we will. I can't wait.

Camille is a huge INXS fan and I can't help think how apt the line "we all have wings, but some of us don't know why" is to her situation. I am so grateful to her donor and their family.



Please consider registering your decision to become an organ or tissue donor. Those on the waiting list need the gift of life. They're someone's daughter, someone's sister, someone's friend. My friend. It's the most loving thing you can do for a stranger.

Visit www.donatelife.gov.au for more information.



FilmLife.

There's a little competition for Donate Life Week called FilmLife. Now Camille is recovering from her transplant, I've been appointed a judge of the competion. You may want to enter, or know someone who is eligible to enter. 

FilmLIfe project is using creativity to spark vital conversations about organ and tissue donation in young people. Using filmmaking and blogging to create awareness provides a fresh approach to this life saving social issue. 
 
We are inviting young filmmakers aged 16-28 to submit a film using the theme of DonateLife Week 2013: Make your wish count. Discover, decide and discuss organ and tissue donation”.

The deadline for all film submissions is midnight on 25 March. Winners will be announced at the FilmLife Festival official screening on 13 April.

Awards will be given for the Best Film, Best Interpretation of the Theme and the People’s Choice award. Filmmakers get national exposure for their work through the DonateLife network and be in the running for great prizes including the Canon 5D and over $2500 in prizes. This we will also have a prize for the best blog in our Blogging challenge.

For more details and information about FilmLife workshops, blogging comp and film festival please go to www.filmlife.com.au, join in the conversation on Facebook and Twitter.

19 September 2012

When Kirk Pengilly from INXS called his biggest fan, CurlyPops, on my phone.

One of the big highlights of my Layne Beachley Aim for the Stars experience was being able to make one of my best friends' dreams come true.

You may be aware that Camille from CurlyPops blog is a big INXS fan. You may also be aware she needs some new lungs. Sadly she isn't able to get to an INXS concert due to her illness, but she has not stopped loving the band.

Camille and I have become great friends after meeting through blogging, and we have bonded over cake and pretty clothes and accessories and more dessert. She made my Western Suburbs bag that I took overseas and also my gorgeous capelet for the Aim for the Stars ball.

You may also be aware that Layne Beachley is married to Kirk Pengilly from INXS. And he was at the ball. I mentioned Camille to Layne the previous night, and she told me he would be there.

After a couple of drinks I went up to Kirk (he was the man that the young ones couldn't quite recognise!) and introduced myself. I told him about Camille and asked him if he could call her. "Make sure you introduce yourself as she doesn't answer the home phone" I told him.

"Hello, can I speak to Camille please? Is Camille there?" She said she realised it wasn't a telemarketer and picked up the phone.

And oh gosh! Camille was beside herself!!!



They chatted for a few minutes. He asked her if she was ok and if she was watching the Manly Sea Eagles play (Yes and No). She told him she has all of their albums. I was crying with excitement! And when I got up on stage to make my speech, I told Layne.

Here are some selfies right after the call.

A little while later I told Kirk that Camille was beyond excited! He was so pleased to have made her day :)

Thanks Kirk for making this incredible woman so very happy!

"Too often we underestimate the power of a touch, a smile, a kind word, a listening ear, an honest compliment, or the smallest act of caring, all of which have the potential to turn a life around.”

Read about Camille's excitement here. As a huge fan of Darren Hayes, I completely understand and love the excitement she felt :)!

18 January 2012

FilmLife Project Blogger Challenge for organ donation

This post is part of the FilmLife Blogger Challenge


 (Picture by CurlyPops)

The FilmLife Project was created to create awareness and conversations about organ donation through short film.

 From the FilmLife Project website:
"FilmLife Project is a collaborative project in conjunction with Donate Life Week 2012 (19-26 February), that aims to inspire and encourage young people to have conversations that ask and find out their loved ones wishes around organ and tissue donation.
FilmLife exists to capture the stories of organ donation and transplantation through the eyes of young filmmakers.
We believe that more people need to be asking and knowing their loved one’s wishes, and we’re inviting passionate people to spark these conversations by creating films about organ and tissue donation."
My wonderful friend Camille asked me to take part in the FilmLife blogger challenge. 

I think it is so important to give your organs and tissue to those that need them after you die. I also think it's important to donate your organs and tissue to research to help others. Your organs and tissue could save the lives of up to 10 people, and improve the lives of many more. (Donate Life states "in 2010, 309 organ donors gave 931 Australians a new chance in life".)

Camille needs a new set of lungs and I want to raise awareness about organ donation so that she gets a new set of lungs. She's on the transplant list, so I hope she receives new lungs soon. Camille's life would be made so much easier with a new set of lungs - spending time with her has certainly opened my eyes to how much we take our breathing for granted. I'd love for her to get a new lease of life, and for her not to wait too long.
One of my friends' brothers passed away a few years ago - it was so very tragic as he was so young and it was very unexpected, but he believed in organ donation and spoke to his family about his wishes when he got his drivers licence. Through the donation of his organs, the lives of seven other people were saved. You can read his story here. 
I think knowing people who have been impacted by organ donation makes the decision to donate easier. You can see the importance of donating life to someone who needs a chance. 

While it isn't strictly organ donation, I have donated my time and body to research - when I go to the hospital, I see many doctors in training, and them examining my body and me talking about my condition helps them learn about ichthyosis (from physical, emotional and humourous aspects too) and treat future patients. So if you have the time, say yes to talking to student doctors - it helps them, and it helps others.

If I were given the opportunity to donate my organs, firstly, I hope my lungs can go to Camille. The hospital can take the lot - my eyes, heart, teeth - whatever's useful and needed. I am obviously going to donate my skin to research. People are quite envious of my breasts, so perhaps if anyone's in the mood for an implant, they can have those too! ;)

I have spoken to my parents about my wishes for my organs and tissue. I am registered on the Australian Organ Donor Register via Medicare. If you have registered, or are considering, make sure you speak to your family too.
Camille has a blog link up happening here. You can join the blogger challenge too. 

More information:

19 June 2011

The Hottie Challenge (or the creative exercise I wish I could enter a written or cooked product)


I love to create. In my head. In reality my crafts turn out nothing like I envisaged. When I craft on my own I can't wait for the session to be over. I am impatient, and coupled with a (still) sore thumb, my creations look very pre-school artist. I wish I could write or cook my way out of crafting. Having said that, crafting as a group is so much fun and I really want to do it!

I was crafting as a part of the Hottie Challenge run by Open Drawer. It's a challenge to create hot water bottle covers to raise money for the The Margaret Pratt Foundation. Camille from CurlyPops is coordinating a blogger Hottie Challenge.

From their website:

The Margaret Pratt Foundation Heart Lung Transplant Trust is a registered charity whose aim is to encourage, develop and maintain Australia’s world class expertise in the field of organ transplantation by supporting research that addresses the problems faced by children and adults after heart and lung transplant. 

The aim of the research must be to improve the outcomes for heart and lung transplant recipients.  

The Margaret Pratt Foundation has donated $700,000 to date in 2011 to promote research into the causes and prevention of chronic lung rejection.
Read more about the Hottie Challenge at CurlyPops' blog.

Of course I wanted to take part, in order to support Cam and others needing heart and lung transplants.

I wanted to make a panda hottie. I imagined it'd be grand. Cute and panda looking. 

Like this.

But it turned out like this.

My friend M sewed the main part. I sewed the draw string bit. So proud given I am not a sewer, and my thumb was aching.
I used a hand puppet template for the panda's features. I glued them on.
It's not a functional hot water bottle cover, but it doesn't have to be. I wish I was a better, more patient, and more skilled crafter. Post thesis resolution!

What should I call him?
Check out the other Hottie Challenge creations - they are AMAZING!

In corporate terms, I discovered three learning gaps doing the Hottie Challenge. I need lessons in craft, patience and hot glue gunning.


23 May 2011

Perceptions of disability

I read an article about the perceptions of disability by Cam from CurlyPops last week. The article is about how we can forget we have a disability because we get so used to living with it and it's when we encounter curious people that we remember there's something 'wrong' with us. She pondered how people perceive her.

While I am used to the chronic illness component of my disability, and only notice half the stares and comments, it is often my friends who notice it more than me. And I guess it's then I am reminded I am so visibly different. When my friend and I went to Jebediah she asked me in a serious tone "when we are out tonight do you mind if I just let loose and give someone a serve?". I was puzzled at this, thinking she had a behavioural problem I was not aware of. I asked what she meant. She said she'd heard some guys making comments about me in the restaurant. I had not noticed. The night didn't ensue a chance for her to give anyone a serve. Maybe next time!

Since doing work in the disability community, I do notice the way people stare at my friends. Actually, before that, I was fiercely protective of a colleague I am close to at work - a number of people were asking me about her illness. I realised that this is probably what people who know me may experience. I mentioned this to my colleague, and she said that so many people ask her about me too! We had a laugh. I digress. When I am with my friends with disabilities, I notice the stares, the parting of the crowds, the condescending ways in which others speak to us, the pity faces, the low expectations of us, and the assumptions made.

I wonder whether people warn others about their friends with disabilities - to quell their surprise and to mitigate questions. Perhaps.

I went out with a friend recently - she used a wheelchair. We met one of my friends out, one she had not met before. When my friend in a wheelchair left, my other friend said to me "so, is she always like that?", making a hand gesture. "Like what?" I asked. "In a wheelchair", he said. I was a bit surprised he felt the need to ask. There was no malice in his question, just curiosity. "No", I replied, and left it at that. I wondered why he needed to know, why was it important? And why did he ask about her wheelchair when he's never been concerned about my appearance (to my face).

Cam made a great point in her article. She saw someone else with a similar disability to hers, and wrote "Then I had my most ridiculous thought. I was sad that someone so young had to live like that." While I haven't thought this about people with disabilities, I once said to my Dad that I thought it was sad that Muslim women in Australia felt the need to wear hijabs or niqabs. He told me that they are so lucky they live in a country that allows them the freedom to dress how they want.

This wisdom has stuck with me and I think it can be applied to people with disabilities too. We're in a society where disability isn't something to be ashamed of, or to take pity on. When I meet someone tells me it's a shame I look the way I do, I tell them that I am not dying from my illness, I am living with it the best way I can.

30 March 2011

Giveaway - Able and Game, Curly Pops and more!

I picked up a few goodies at Finders Keepers to give away on the blog :)

Able and Game cards. I love these cheeky Melbourne designed cards. Lots of funny illustrations and puns. I have a pack of three to give away.
And this cute purse. I don't know who it is by. But I love it, and have one of my own. I have one to give away.
And the lovely Camille from Curly Pops, who I saw at Finders Keepers, has given me a handmade iPod holder. Isn't she talented?!

To enter, please become a subscriber to my blog via Google friend connect or my Facebook page or Twitter, and leave me a comment, with your preference of prize, and your email address.

Entries close 6.00 pm AET, Wednesday13 April 2011.

Good luck!

26 February 2011

A few kind words

Hello! You may have noticed my new blog header. Isn't it awesome?!

It was made by the lovely creative Camille from CurlyPops. Thanks Cam, I love it!

And this morning I woke up to read some kind words about my own blog. I took part in a blog carnival on the Chronic Babes website. I submitted possibly the most personal blog entry I've written. And Jenni, host of the carnival wrote this about my blog:
Carly Findlay at Tune Into Radio Carly writes about Sex. And WOW, am I impressed. I kind of want to be her new best friend. It's about time someone in her position (see? I made a sex joke!) wrote a frank article about sex, disclosure, and the particulars of her life. LOVE. THIS. POST.
Wow! Thanks Jenni :)

You can check out the blog carnival here. There are some great blogs to be read :)

PS: don't forget, you can interact with me on my Facebook page.

23 February 2011

Donate Life Week

I am an organ donor. Are you?

I can't donate blood while I'm alive, but I want to make sure I give life to others by hopefully donating my organs, and give hope to people with ichthyosis by donating my skin to medical research when I pass away.

My friend Camille posted a very moving blog entry which I want to share with you here.

"I'm a couple of days late, but this week is Donate Life Week in Australia.

It's the perfect time to not only join the official Organ Donor register, but to sit down and have a discussion with your family to ensure that they are aware of your wishes.

Just in case you don't know my story, there's a very good reason that I'm so passionate about this issue..... so here's the very short version:

I'm 36 years old and I've had a chronic lung disease since the age of 15. I was then diagnosed with panhypogammablobulinemia about 11 years ago which just added further complications.

At the age of 28, I was told that I would need a lung transplant at some time in the future. That was a huge bombshell and the first time that I really took the time to think about my future (or lack thereof). Well that was eight years ago now, and I've managed to keep plodding on with my own very dodgy barely working lungs, connected to a never-ending supply of oxygen.

I often think about what it would be like to be able to breathe again - to ride a bike, to go for a run, to walk up a hill, to go shopping, to pick up my nephews, even to mop my floors! All those normal things that I can't do.

At this stage, I need to keep my own dodgy lungs for as long as I possibly can. But, I'm hoping that when the time arrives that I can't go on any longer, I'll receive the ultimate gift.


There are over 1700 Australians waiting for an organ transplant at any time, and the wait can be anywhere between 6 months and 4 years.

The Donate Life website is a wonderful resource full of information, including the family discussion page.

Please spare some time this week and have that conversation...."
(From Curlypops' blog, 21 February 2011)

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