Blogging, Fiction Friday, Guest Blogs and Featured Spotlights, IN THE NEWS AND ON MY MIND, Interviews, Kerry's Causes, Memoir Monday, SoCS, The Redefining Disability Awareness Challenge, Throw-back Thursday, Travel Tuesday, TToT

2015 October Platform Challenge: Day Nine, #platchal

I missed a few days there, or a little more than that, as I already have both a Facebook page and Twitter, but I’m back for more of a refresher.

Create An Editorial Calendar

I outline what I want for my blog, in my very first post,

Bucket List,

but I had no clue how it would really be to have a blog, day in and day out. I couldn’t have known then.

I do like to keep a rough schedule, more in my head, but the categories I select before each post help me keep things straight.

I stayed up, into the night, before I actually launched this blog, coming up to my thirtieth birthday in 2014 and mapped out which days I wanted to post.

I would let alliteration lead me.

Memoir Monday: My Fear of Going Blind

Fiction Friday: An Old Woman’s Regret

Spotlight On Saltz

From there, as the months of blogging went on, more weekday categories were added.

Touching Landscapes: Feel the Vibrations

This was my regular post, my growing favourite, Travel Tuesday as I called it. This was how I eventually decided to branch out further, creating

The Insightful Wanderer

and my blogging schedule continuing to change.

Slowly, my favourite weekly posts have become

In The News and On My Mind: #1000Speak Edition

because these allow me to focus in on what may be going on, in the moment.

It is a difficult question, how often to post on a blog. I don’t like to box myself in by telling myself I have to post, but I understand consistency and regularity.

I have not run out of things to say, like I’d feared in the beginning, and only really the opposite is true.

Every day is too much, but I hate to go more than a few days and not publishing something.

My Mondays have become a series on disability, for which I have a vested interest.

When It Rains It Pours – The Redefining Disability Awareness Challenge

I do the well known TBT thing.

Throwback Thursday: World Kidney Day

My weekends were where I featured interviews. I wanted to give the spotlight to other people who write, blog, and make a difference in some way.

She’s the Bomb

Eventually, my weekends would evolve into what they currently consist of: Stream of Consciousness Saturday and 10 Things of Thankful on Sunday.

SoCS: Engraved

and

TToT: Extra Thankful For These Last Eighteen Years

So this is just a selection of my posts, an example of the kind of blogging schedule I keep to. This won’t be the way others can or choose to do it. I don’t know. Is this too much? I know it’s enough and I am happy because my blog, its content, style, and all other elements, including number of weekly posts is me…just me.

When an idea hits me I make a note of it, trying to decide when and if it might fit. I plan things, sometimes weeks or even months ahead of where I am. It works for me. Writing is a lot of hard work, more than people realize, but the weekly practice is the best thing for me. I like to have a plan wherever possible, but yet I also like to go with the flow and let things happen naturally.

A blogging calendar, like a yearly one, has certain markers of importance and note. What might take place in between is anyone’s guess.

I am enjoying this challenge for the month of October. It has given me more to think about. It is now a part of my month.

Follow the guy who runs the challenge.

@RobertLeeBrewer

Dates to make note of, things to come on my blog, of course always subject to change:

**More posts for Redefining Disability, including my thoughts on a woman who made the news for making herself go blind.

**An “In The News and On My Mind” post about voting. Will I or won’t I?

**A post about love (tentatively titled Somebody That I Used to Know), a list of songs to help with heartbreak and how to get past lost love.

**Halloween themed posts about spiders, werewolves, and ghosts.

**My story about a giant book fair, by the lake, in Toronto.

That should get us through October anyway.

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Blogging, Guest Blogs and Featured Spotlights, Kerry's Causes, Memoir and Reflections, Special Occasions, Writing

One Year and Counting: Kind and Generous

Happy Birthday to me and here I am – I made it one year as a blogger.

I didn’t give up, I didn’t give in, and I did not burn out or run out of things to write about. It felt somewhat like a floodgate that was opened, spilling out all the things I’ve ever wanted to write about but didn’t for so long.

I liked the idea of pairing my actual birthday and what would become my blogging anniversary and that is just what I’ve done.

I never could have imagined, when I wrote my

very first post – Bucket List,

that I would have come so much farther than I dared believe I could and that I would have so much to show for it.

I thought a lot about how I wanted to mark this occasion and I decided to take this opportunity to thank all those who have made this, creatively, one of the best years of my life.

🙂

***

CANDACE JOHNSON

One of my biggest supporters, almost from the very beginning, has been Candace at:

Change It Up Editing and Writing Services

She gets the first spot in my list of thank you mentions – well deserved. The tagline from her website reads: “I love words. Especially yours.” This clearly shows her dedication to helping others.

When I was only debating and throwing around the idea of starting a blog in the first place I discovered her

Facebook page.

You can tell, or I soon learned how to, when someone genuinely wants to help you and to give you a moment of their time. I recognized, right away, that she was and is someone who is happy to help whenever, wherever, and however she possibly can.

Not everyone is willing to listen and do what they can, but when I reached out to Candace because I was, with my iPhone and its VoiceOver, unable to click on her Facebook links, she made a point of listening to what my issue was and doing what she could for me.

Ever since then, she has repeatedly put an extra copy of each link in the comments, where my VoiceOver recognizes it and allows me to read all the interesting articles and blog posts she shares on writing and editing.

I have learned so much from her. She granted me an interview, my first on Her Headache, and generously gave me the exposure, allowing me to write a guest post to explain to her readers some of the particular issues with technology that I face.

Since then she has continued to read and share my blog posts whenever she can. I will never forget her kindness and her support, the belief she has shown in my writing ever since.

I guess you could say that the bloggers and writers I have discovered and who have come to mean something to me, showing me kindness and assistance along the way, fall into a handful of different categories.

MAXWELL IVEY JR.

There’s the first blind seller of carnival rides I’ve ever met, who started a website to help advertise his business:

The Midway Marketplace

He is the friendliest person I have ever come across and he has done so much to show me how to open up, online and off.

He has introduced me to places for my blog and my writing to fit in, all while introducing me to other bloggers and writers, always there to answer any blogging or social media questions I might have.

Since I’ve begun talking with him he has started a second site (The Blind Blogger) and published his first ebook (Leading You Out of the Darkness Into the Light), which can be found here:

http://theblindblogger.net/ebooks/leading-you-out-of-the-darkness-into-the-light

STEPHANAE MCCOY

Then there’s the lady who has lost a lot of sight later in life, but who has not let that stop her. Instead, she has come out with this incredible resource for all women who are visually impaired and blind, but who still wish to be fashionable and stylish:

Bold Blind Beauty

Stephanae has again been someone willing to offer me support and an exchange of interviews. She has a site where she discusses things like makeup, shoes, and other accessories all girls like to indulge in from time to time. She includes not only photographs of these items, but the descriptions necessary for all women, even those who can not see, to be able to enjoy the things she recommends.

Sure, I may not wear makeup, but I still love to visit her website and especially I love to read about the interesting women she highlights on her Fierce Friday posts.

😉

She draws me in with the alliteration her blog name possesses.

🙂

I have met some wonderful authors and writers along the way too:

Alana Saltz,

Jordan Rosenfeld,

and writer, activist, and feminist:

Julie Zeilinger, from The FBomb.

The blogosphere is an amazing place; however, I sometimes feel like I stand out or I don’t quite fit into any particular niche. I guess this isn’t the worst thing in the world because I enjoy a number of areas of the blogging world and its many varied subjects.

I am in my early thirties, for those unfamiliar with me and my blog, but I am not a mother.

Parenting blogs are one of the most commonly found on the internet.

I have grown quite comfortable sandwiched between two groups in the blogging universe, all of which I do read for the array of different perspectives offered.

The second group are those twenty-something writers and bloggers, writing about the decade of exploration and self-discovery that the twenties has become. I guess I continue to return to blogs like these because, in some ways, I feel I am living some part of my twenties over again in my thirties, learning and growing and still so easily able to relate to the struggles these ladies are experiencing.

These bloggers include brilliant and insightful young women such as:

Young and Twenty,

Scarlet Wonderland,

Flowers and Wanderlust,

and

Single Strides.

Other blogs I love to follow include a Canadian writer and mother, a French blogger now living in the US, an Australian visually impaired travel blogger, a wizard with words, and a guy who lives with his illness and disability as best he can and who is a tireless activist for others with rare and debilitating conditions:

Carrie the Obscure CanLit Mama,

French writer and life coach Sylviane Nuccio,

Maribel of Touching Landscapes,

Lorraine of Wording Well,

and

Michael at Migraine Discussions.

What have I learned from one year of blogging and what advice would I give to those just starting out, who are where I was one year ago at this time? Hmmm.

I think this post from Scarlet Wonderland says it better than I ever could:

Advice For New Bloggers,

The best and only thing I have learned, think I knew all along, and would advise would be to remain authentic. I only know how to be me and that is all. If I ever did have those moments of watching what another blogger was doing, and the thought to emulate them crossed my mind, I soon realized that I have to stick on my own path and do things my own way.

Thank you to every one of my loyal family who read this blog and any friends and family, those who I know are reading, even if I sometimes don’t realize it.

Also, I want to take this time to thank everyone else. If I forgot you, I apologize. Just know I am grateful for your collective presence here and for each and every time you return to read one of my posts.

Whether it’s 100 or 1000 followers – I’m lucky to have you reading this. I appreciate every comment made, good or bad, because they’ve all taught me some powerful lessons, being able to hear other’s thoughts on what I write helps me to grow my voice.

This blog has sustained me through the hard times of the past year, gotten me through multiple rejections in love and in writing, and captured some new experiences and some lasting memories.

Half-way through this past year I got the crazy notion of starting a second one.

What was I thinking, right?

🙂

Kidding. I may have come a long way since I published my first post here, but I still have a long ways to go when it comes to the blogging side of things.

Now it’s each year of this blog that marks my life, more than New Year’s Eve does for most people.

I have goals I’d like to have reached this time next year.

I have a stubborn streak with the publications I was turned down from this past year. Maybe those serve to make me work even harder or, perhaps they are meant to be lessons, serving to teach me that not everything is meant to be.

I have a few exciting things in the works at this very moment. I hesitate to say anymore than that.

I know, I know – don’t you hate when people do that?

🙂

I will say as much as I believe I can, without jinxing myself completely. Yes, it’s happened before.

I hope to continue to write about new, different, and interesting subjects here and share even more fascinating people with you through the interviews I love so much to do.

Currently, what I can say is that I am in the midst of participating in two things, specifically:

The Redefining Disability Awareness Challenge

and

1000 Voices Speak For Compassion

Both are causes I believe deeply in.

Finally, I couldn’t end this post without thanking the one who first got this blog up and running for me and who encouraged me, helping me get passed the tricky and the technical.

Thanks BSK.

***

Now then…

*Clears throat*
Now that I’ve come full circle.

Love and life are scary sometimes. I am scared a lot of the time frankly, but this blog is one of the greatest rewards for all that fear.

Jennifer from Young and Twenty sums up fear best in this way:

The Power of Being Scared

**I truly believe that where I am right now, at this moment in time, is where I was always supposed to be.**

This line from my very first post (February, 2014) was true then and, hey – it’s just as true today.

What do you know?

🙂

Through all the hard times and the struggles – I still believe it and I can’t tell you how comforting that thought is.

An so – one year and counting and here’s to many more.

Natalie Merchant, Kind and Generous, on YouTube

I want to dedicate this anniversary post and this song to you all.

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Blogging, Book Reviews

Blind Bonus

Discrimination is not uncommon with disabilities. I try not to focus on it, but it can happen.

I wrote about my handful of experiences with this in last week’s Memoir Monday post:

Discrimination Happens.

This week’s post, I hope, will be a lot more fun and lighthearted.

And now – the story of a little something my family and I have coined “The Blind Bonus”.

***

Q: Have you experienced preferential treatment because of disabilities?

A: This will be a lighthearted post, as I say, although, for me, the line between having a sense of humour about these things and feeling sensitive is tricky for me.

In my family, with my brother and I both being blind, we have our inside jokes. He is much more easy-going than I am when it comes to it all. I want to be normal, just like everyone else, but I work and hope for equality, which all takes time.

This can be a tricky balance to achieve.

Until then I can say sometimes I grow tired of looking at my life and striving to fit in as an ongoing battle and I let down my guard and look for the humour.

Preferential treatment, as is worded in the above question, is an interesting way of putting it. I suppose, at times, you could say that I have received things others did not, from people I know and from strangers alike.

This brings to the forefront the notion of pity. If someone pities me, even with the best of intentions, it’s because they feel badly for “the poor little blind girl”.

I used to think this in my head. My grandparents were good examples of this.

They knew me and loved me, but they did feel bad that I got such a lousy lot in life, to be born blind. Because of these feelings, because they loved me, I sometimes received material things or special treatment.

This is how it goes for a lot of things in life. Life is not fair and we’ve all experienced that firsthand, at one time or another.

My oma may have cut me some slack in ways she did not others. She could be critical at times, as she got older especially, but I was always her precious little granddaughter. She rarely, if ever, criticized me like she did others.

My grandmother was the nicest woman you could ever find, but pity is one way of looking at the preferential treatment she sometimes showed toward me.

My grandparents had twenty-one grandchildren and they loved us all equally, but they did feel like we had it harder and wanted to do what they could to make our lives just a little bit easier and happier.

For example, they took us all on a night away to Niagara Falls, spread out in groups of three or four kids at a time over the years. All the others only got to go once, but they took my brother and I twice.

They used to bring a little keychain or other small souvenir for each of us with every vacation they took, but as the years went by and more and more grandchildren came along they didn’t keep that up.

Understandable, right? Who could blame them. After all, even the smallest of souvenirs can take up practically an entire suitcase when bringing back twenty-one of something.

However, I have several dolphin and whale sculptures that they brought back for me from the last few tropical locales they traveled to. They did not do this for everyone else.

My mother once confronted hers about this, saying they really did not need to bring me anything. My grandmother’s response had something to do with how she knew they didn’t, but she really just wanted to bring me something anyway.

I don’t say this here to tattle on my beloved grandparents, who are both gone now, or my evil mother for spoiling any chances I had of receiving anymore special presents.

🙂

I say it just because I know, again that life isn’t fair, and so did they.

My mother wanted to prevent any possible jealousy between me and any other siblings or cousins, if they were to find out and because she knew I didn’t need those things when none of the other kids got them.

Also, my mother has always done her best to treat my brother and I the same as her other two children and she worked hard to teach us that we were really no different. This is the best gift anyone could have ever given me.

As for my grandparents – I always knew they loved me, in all the ways they felt it or showed it, and I know how hard it was for them to see me dealing with some of the extra things that I did, fair or not.

Then there were the “blind bonuses” my brother and I received, say, during our trip to Cuba.

We went for a week, with parents and two grandparents.

By the end of the week I’d received a doll from a Cuban woman and a rose made out of a napkin, from a Cuban man as we sat listening to live music near the resort.

Of course it’s hard to know their true motivation, due to the language barrier, but these are only a few examples of what I’m talking about.

In this case, the term preferential treatment, to me it means someone feeling badly for me being blind and either offering me something or giving me something they wouldn’t normally give.

It’s difficult sometimes. On the one hand I strive to show the world around me that I can do most anything else anyone can do and that I want to be treated the same.

On the other, I occasionally need things to be modified so that I can keep up.

In school I would get extra time to do tests and assignments, because sometimes I required specialized equipment or technology. These things often took longer. My teachers, for the most part, understood this and did their best to accommodate.

Then, how did I ever expect to convince the world that I can fit in and contribute?

I’ve never wanted to be treated differently, good or bad. However, at certain moments I resign myself to the unfairness of life. It’s at times like these that I tell myself I miss out on so much and struggle enough that if I sometimes get breaks others do not: so what?

A “blind bonus” is alliteration at its best and I love me some good alliteration.

🙂

Sometimes I probably think I am getting this when I am not (all in my head) and other times it is blatantly obvious to anyone.

***

Next week’s question:

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

Note: I have been blogging for exactly one year and I am thrilled to be doing just that, involved in such projects as the

Redefining Disability Awareness Challenge

and I still have many more questions to go on it.

I am honoured to be able to use a vehicle like blogging to speak on the issues raised in this extensive set of questions that Rose has put together.

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