1000 Voices Speak For Compassion, Bucket List, Guest Blogs and Featured Spotlights, IN THE NEWS AND ON MY MIND, Kerry's Causes, Memoir and Reflections, Piece of Cake, Spotlight Saturday, The Insightful Wanderer, Travel

International Day For Persons with Disabilities 2016, #IDPD2016

Helen Keller…Stevie Wonder…Ray Charles…Rick Hansen…Stephen Hawking…

The Rick Hansen Foundation

There are so many more of us out here, only looking to have rich, full lives like anyone else, but what often stops us is not only society’s barriers, but our own.

***

Since 1992, the United Nations International Day of Persons with Disabilities (IDPD) has been celebrated annually on 3 December around the world. The theme for this year’s International Day is “Achieving 17 Goals for the Future We Want” . This theme notes the recent adoption of the 17 Sustainable Development Goals (SDGs) and the role of these goals in building a more inclusive and equitable world for persons with disabilities.

***

One note on the society part – some of you may not want to think a lot about it, if you don’t have to, because then it becomes clear that the possibility for anyone to become disabled is indeed a possibility for anyone..

I am a Canadian woman, living with a disability. I didn’t acquire my disability through an accident later in life. I did not develop it overtime, but from birth and still, who knows which direction my remaining vision might take.

On the day before the
United Nation’s International Day For PErsons with Disabilities
I felt a tired feeling that I sometimes get. I panic and assume my sight is worsening, but I am not sure, if that makes any real sense. I close my eyes and decide I will try to get back in to see my retinal specialist soon.

I don’t know what, if anything, he will be able to tell me, offer me as hope that I won’t be completely blind one day. He will probably see no changes or signs of the mysterious eye disease that took my left eye twenty years ago. He will speak to me of gene therapies in various stages of development, but I don’t know what hope lies in that for me. Maybe it will be my future. Maybe not. I’ve learned not to bank on anything.

That’s a part of my DNA, just like the genetic eye disease. I am conditioned to either think the worst or simply not want to hope for the things I may really really want, always fearing that the disappointment from possibly not getting them will break me. It hasn’t broken me yet, which does give me reason to be optimistic though.

I wanted to be able to see the truly unique show violinist Lindsey Stirling put on recently. Instead, I listened to all I could and relied on my helpful sister to fill in the blanks. I wanted to throw my white cane away and yelled my displeasure, and through the wish, but instead I sat and listened even harder.

I want to draw like I used to when I saw colours and when everything in my world was more clearly and brightly defined. I can’t. I want to scream in frustration but I’m resigned instead.

I want to take up the latest craze of adult colouring books, but I don’t.

Of course, nothing is really stopping me. I may not, as an adult, see the lines I may have hardly seen as a child, which are now nearly invisible to me. I could still get myself a Harry Potter or any number of other themed colouring books with a theme which fits my interest, and be damned if I miss colouring in the lines by a mile.

But I don’t. I don’t scream or rail at the world in an uproar. I find other ways to spend my time.

I want to travel and to go through life with an independent spirit and loads of self confidence, but I don’t. I try and I work at it, but I’m scared.

I find a travel series, a BBC documentary, available to me on Netflix. It’s Stephen Fry, whom I love, and he is doing a road trip across the United States in his British cab. I know him from his narration of the Harry Potter books and for his intelligent and witty character. After watching him visit all 50 states I now know he hates being on a horse, dancing, and skiing. He loves science and culture and literature.

Stephen Fry In America

I watch him on his trip and I long to go on one of my own, but I fear getting lost in the big, expansive world and I worry that my white cane will attract only pity. I want to grip it with extra determination and go anyway. It’s all in my attitude, right?

I can’t drive a cab across the country. I want to believe I will see more of the world anyway, even without definition of sight.

I don’t try to revisit childhood experiences of mine by colouring. Instead, I watch a travel show which I’ve heard of but only now decided to give a chance.

HELLO GOODBYE, #HelloGoodbye

The host speaks to one woman in her sixties, widowed after her late husband’s long battle with illness, but who has now found new love with a man from England. Her happiness is infectious. Her newly found love walks down the ramp in the arrivals terminal at Toronto Pearson International Airport and gets down on one knee. Love is lost and can be found again.

I feel warm just by watching and listening to her story.

The host also speaks to a young man and his parents. The son is on his way to participate in Rio, at the Paralympics. He was paralyzed from a diving accident and now plays wheelchair rugby.

And then there was the grandmother, daughter, and grandson saying their goodbyes. The young guy and his mother are heading back to Britain after a visit with Grandma. The mother has RP (Retinitis Pigmentosa). She carries a cane, but the son speaks of wanting his mother to have companionship with a guide dog, as he will soon be going out on his own and doesn’t want her to be alone. He has worried about her safety all his life. She admits to being unsure about going for a guide dog once they get back home, but her son’s words cause her to rethink things.

She grips her white cane. I grip mine. She has been losing sight for years. I’ve been blind since birth and losing since. Am I any further along in accepting my circumstances and my white cane than she is?

People ask me all the time if I am ever going to get another guide dog. I don’t quite know what to say. Yes, they may provide the necessary confidence boost for many. I consider it.

I don’t think any dog will ever compare to my Croche, But is that all it is?

I can’t put another animal through what I put Croche through. She was so well trained and so fittingly suited in temperament. She was given to me and I was trusted with her. A lot went into all that. We were a team, but I failed her.

My ever growing illnesses caused me to sleep and her to dutifully stay by my side, but she was prevented from shining. She was my pal, but I don’t take the responsibility of a working dog lightly. I don’t know what my future will bring and I can’t bring myself to bringing another animal into that.

I want to curse what stops me, but what often stops me is me. And so I would just end up cursing myself, again and again.

Or, I could take hold of my white cane and use it for betterment, for working for some of my dreams, and for hardening my resolve and building my often feeble confidence.

My feelings of shame when I walk with my cane are hard to describe and hard to fight off. I will never be happy if I don’t try. Fear and disappointment stop me from even trying. What a waste that would be.

Standard
Guest Blogs and Featured Spotlights, Memoir Monday

Dating in the Dark

All joking aside:

Blind Bonus.

There are some questions I’ll probably never totally come to a decision on.

***

Q: In what other ways are your interpersonal relationships affected by disabilities?

Examples might be that it’s harder to form or maintain relationships or that people treat you differently once they realize you have a disability.

A: Yes. Yes. Yes.

🙂

One way this is the case is in dating, but today I will speak specifically about online dating.

I could write a whole book on this subject, with the experience I have had with it over the last five years, but up until now I have resisted writing anything to do with this fast-growing method of finding love.

I have resisted, not sure why that is.

Dating is one interpersonal relationship issue I have yet to write extensively on.

It is, indeed, harder to form this kind of relationship when you can’t locate a stranger, out of a crowd, with whom you might have an interest in. It can narrow down the places where meeting someone is possible. All of this, and yet I was determined and I have had some success.

The question here is one I struggle with every time I begin speaking with a new guy online.

Of course, in person it is obvious, often glaringly so. I like to think I can fit in, in public, and not stand out as the blind girl. This isn’t always very realistic for me to think.

Online, I have never been able to decide when and how to bring it up.

Do you, perchance, know the answer to this?

🙂

Do I mention it first thing in my online dating profile? Do I casually attempt to sneak it in the middle somewhere? Or leave it until the last few lines?

Am I looking like I mean to hide the fact, if I don’t come right out and say it? Do I ruin things before even getting started, scaring someone off, if I make it the first thing they read?

I don’t want my blindness to be all I am; it’s not.

I want to be able to show that I am a well-rounded person, with many interests and passions. My blindness is a factor, for sure, but it can’t be how I define myself overall or that is how others will start defining me too.

Yes, people do treat me differently when I do reveal this one detail in particular. This, I understand. I can empathize.

Whether I reveal it in my first message, during a subsequent phone call, or when they show up to meet me face-to-face.

I have experienced different amounts of shock and surprise. I have heard it all, from the pause of several seconds, to the stuttering response, to the normal array of curiosity and its companioning questions.

Like anything else, it isn’t a good idea to leave it out and just show up for coffee, cane in hand. This, like being less than honest about current weight or age, it can result in a bad rapport from the start. I know not to pull this on anyone. It really is not fair and it leaves me awkward and fumbling too.

I like to know, somewhat, what I am getting and I want the other person to have the same courtesy from me.

At the moment I am watching a tribute special for Stevie Wonder.

Of course, it is no secret that Stevie is blind. He doesn’t seem to have had any trouble meeting partners in his own life. I doubt this “wonder” has never had to utilize online dating to find women.

then again, who knows.

At one point, host LL Cool J asks everyone to take a moment and close their eyes, even going as far to darken the screen, while the song Stevie wrote for his baby daughter years ago is being performed by a few fans and fellow performers.

http://entertainthis.usatoday.com/2015/02/16/stevie-wonder-tribute-beyonce-john-legend-lady-gaga/

This is certainly an interesting part of this special. I was wondering when they were going to address his blindness. I figured they would.

Now I am no Stevie Wonder.

🙂

I haven’t had his talent or fame to help me meet people.

Stevie Wonder has been the main spokesperson for the blind community, world-wide. When most people think of blindness, they think of him. He has been extremely successful in his life, blindness notwithstanding, but dating, love, and children are experienced differently when unable to see the faces of loved ones.

I know it is a touchy subject sometimes. I wish there was a one-hundred percent agreed upon answer to my main question of this post.

I know online dating works. If I keep my eyes open, pardon the pun, I can and have found those who are willing to be flexible and give dating a blind woman a shot.

I have never been accused of trying to hide my blindness when commencing conversations with anyone online. I’ve found the right time to slip in my blindness in there. It works and I am always navigating the turns and the bumps of dating online.

I guess some questions will never have definitive answers to them. This, I greatly dislike. I like to know which way to go when I am struggling with a question and when no answer presents itself to me, I rail at the uncertainty.

I don’t want to be treated different, but unfortunately this is unavoidable in most instances.

Someone who has never before spoken to a blind person will not usually know, right off the cuff, how to handle themselves.

I try to make them feel at ease, by simply speaking of your normal, run-of-the-mill things that anyone who’s just getting to know another person might discuss.

This is often all it takes to keep things moving forward. And forward is the only way any hoped-for relationship will have a chance.

Sure, some may halt any further conversation, but there’s always more out there. Sometimes, the shock of it is just too much for a person to handle. That is their prerogative.

I could always start a new series on this blog, online dating adventure series, but i think I’ll continue to resist this impulse.

🙂

You never know. Maybe this week’s question will have started something, but then again I am not sure people want to hear about such things on a regular basis.

I wonder if there’s a site out there, devoted only to online dating stories, good or bad.

Well, while I’m off to investigate that further, please offer your thoughts and/or opinions on my question and I will leave you with my favourite of Stevie’s lesser well-known hits.

Stevie Wonder – PArt Time Lover – YouTube

***

Have you ever tried online dating?

Did you ever find out something about someone you were talking with that surprised you? When is it important, do you think, to provide certain details?

How have others reacted when you’ve offered up something you’ve been nervous to mention?

On next week’s Memoir Monday post, for the

Redefining Disability Awareness Challenge,

is a question that is at the heart of this whole thing.

Do you have preferred language when it comes to disability?

Standard