Thursday, 29 December 2016

RIP George Michael

This is my favourite George Michael song. "Faith" brings back fond memories of my teen years.

Thursday, 1 December 2016

Kelly MacDonald’s New Radio Show Makes For Great Company (Enables Me story)

http://enables.me/kelly-macdonalds-new-radio-show-makes-great-company/

Kelly & Company
Kelly MacDonald (right) with co-host Sharon Caddy

There is a new radio show that might sound like a typical daytime talk show, but at the same time is unlike any other right now.

Kelly and Company, on AMI-audio, is the first-afternoon talk show to be hosted by a member of the blind community. Kelly MacDonald, a veteran radio and TV broadcaster, has been a part of the Accessible Media Incorporated family for the past 15 years.

“The show came to be on the heels of our morning show, Live From Studio 5, and the need for people who want more than just a reading service,” he says. “They want information more spontaneously.”

Unlike the morning show, Kelly and Company is a lifestyle centered show. MacDonald hosts the program with veteran broadcaster Sharon Caddy (formerly of CTV News Toronto and CTS). They are joined by a weekly group of panelists and correspondents, focusing on topics such as employment, nutrition, sexuality, personal finance audiobooks and sports.

“The Company part of our show is really our way of asking people to give us ideas, subjects and ask questions, and give their own opinions. We don’t come across as experts, but as contributors lending experiences and to combine information with entertainment.”

For Kelly MacDonald, you could say that he has now come full circle in his career as a reporter and broadcaster. A graduate of Fanshawe College in London, Ont., MacDonald started out in radio which he says is his first love. He later moved into television including a show he created and hosted for AMI TV called Blind Sighted before returning to radio for Kelly and Company.

I asked him what the secret is behind his success in a field where people with disabilities aren’t always heard or appreciated.

“I try (to be both serious and funny) because it’s too depressing to be only one way," he replies. "It has been an interesting  15 years for me to do production work, be a volunteer coordinator, do TV work, and now forging on to do what I actually set out to do when I went to college to do radio.”

Kelly and Company debuted on October 31. It airs live weekday afternoons from 3-5 pm ET on AMI-audio.

You can listen to the show live online at http://www.ami.ca/listenlive. AMI-audio can also be heard on digital TV at Bell Fibe 49 and Rogers 196.

Tuesday, 1 November 2016

RIP Dave Broadfoot

I met him once when he performed with the Air Farce crew. May he continue making people laugh in the life to come.

Tuesday, 25 October 2016

RIP Bobby Vee

My mom used to have some of his music back in the '60s. He had a good voice and sound. Rest in peace, Mr. Vee.

Tuesday, 16 August 2016

Tuesday, 21 June 2016

There is more to Maayan Ziv than AccessNow (Enables Me story)

http://enables.me/maayan-ziv-accessnow/


People who have learned about Maayan Ziv through her recent TV appearances or through her online app AccessNow know she dreams of a world without physical barriers. But there is so much more to her than that.

Born with muscular dystrophy, Ziv grew up in Richmond Hill, Ontario. She credits her years spent at the prestigious Waldorf School for nurturing her creativity. During this period, she got into acting and even writing short plays. Ziv applied to Ryerson University’s Theatre Arts program, despite the fact that its building was inaccessible.
In 2013, she accepted the opportunity to act and collaborate on a production with Toronto’sSoulpepper Theatre, called Borne. “It was a good experience, and even though I’m not acting in anything right now, it’s still a part of who I am,” she says.
“Photography is my first love,” she says. According to one of her blog entries, her love of photography was established in 2006 while in New York City. Her wheelchair got damaged on the flight to New York. “I wasn’t able to make it to all the places I had planned but instead found myself spending the rest of my trip observing people, taking in the streets of New York… and taking pictures.”
She taught herself photography at age 16. Her portfolio includes everyday people, fashion models, and even celebrities (e.g. Edward Norton, Keri Russel and David Onley, former Lieutenant Governor of Ontario).

Beginning of AccessNow

In 2014, Ziv was accepted into Ryerson’s new Digital Media program. It was during her year as a student that she came up with the idea of AccessNow, an app highlighting barrier-free places. I told her about other apps focusing on accessibility similar to her AccessNow. (I sent her my story on the Wheelmapapp prior to the interview.)
“(Creating AccessNow) wasn’t scary for me,” Ziv says, adding that it didn’t discourage her from wanting to make her own app. “There are many different apps now. When I started there were three or four prominent ones, and within a year of AccessNow’s existence, they’ve been popping up everywhere.”
AccessNow was launched in August 2015. Ziv says a mobile version of the AccessNow app is in the works. “People have been asking for it since day one! It will be launching this summer. I’m super-excited about that because it will allow people to pin and share experiences or review a place from wherever you are at any time.”
Prior to taking Digital Media, she completed a Radio and Television Arts degree at Ryerson. She has presently struck up a relationship with CBC. She hosted and produced a radio special for them (Shifting Space), and occasionally writes for their website. “I’m interested in telling stories about access, and bringing forth the perspectives of people with disabilities in the mainstream,” she says.

So what enables Maayan Ziv?

“What enables me are levels of understanding, where people understand that everything is possible. I’ve believed that, and having a community of people who believe that enables me to go out and do whatever I want.”
A week after I interviewed her, she was honoured with David Onley’s Youth Leadership Award for Accessibility, at a ceremony held at Queen’s Park. She was also honoured with the UJA (United Jewish Association) Federation’s Inclusion Award of Excellence.
Maayan Ziv and her portfolio can be found online at www.maayanziv.com. AccessNow’s website is accessnow.me.

Friday, 3 June 2016

Farewell, Canada AM

Canada AM was my favourite morning show on TV. It was also Canada's longest-running morning show, airing from Sept. 1972 to June 2016. My earliest memory of watching it was somewhere between 1979-80. The show was abruptly cancelled by CTV this week after a 43-season run. Another morning show is scheduled to debut on CTV soon, but weekday mornings won't ever be the same!

Saturday, 7 May 2016

A Mother’s Day Testimonial from a Mom

Recently I invited my mom to contribute to a blog series on Mother’s Day. My mom and I are close, yet I wanted to have more information on what her experience on being a mother has been like. I am her only child. Here, in her own words, is the testimony by my mom, Sherry Barrie.
Sherry Barrie and the young Donald Barrie
I have always wanted to be a mother. As a young girl and teenager, I was the one who always wanted to take care of other people’s babies and toddlers. So, I was very happy and excited to learn that I was pregnant in the fall of 1972!
After initially having “false labour,” then the ‘real thing’, Donald was born on June 23, 1973, a breech birth. The doctor immediately knew that something was very wrong and Donald was quickly transferred to the Hospital for Sick Children. Later in the day I was informed that he had a rare condition, (that I had never heard of) called osteogenesis imperfecta (OI). Commonly called ‘brittle bone disease,’ the bones do not develop properly and are weak and brittle and fracture easily.
Donald was born with broken arms and legs and skull fractures, some suffered in utero and the others during delivery. During his lifetime, he has sustained many fractures and had several surgeries. There is no cure for this condition but today there are more treatments and medications available than there were 40 years ago.
I was shocked and devastated when the doctor told me that Donald would not survive. Wrong again. Although I had met a few families raising children with disabilities, I was not involved in their lives and was too young to appreciate what they must have been going through. To me, motherhood means that there is someone I have to watch out for and put before myself and worry about 24/7!
This will be my 42nd Mother’s Day. I usually am treated to a meal out, a gift and usually a funny card! I enjoy being pampered! I believe my first Mother’s Day has to be my favourite.
I have no regrets about being a mother, despite the many challenges. Some things I would change, if I could, but I cannot.
What gives me the most joy and satisfaction about being a mother? I love to hear Donald laugh! He has a great sense of humour!
I am very proud of Donald and all his accomplishments and love him dearly, although he sometimes drives me crazy, and vice-versa, I’m sure!
Sherry and Donald Barrie today!
Donald and his mom says, “CHEERS” to mothers everywhere!

Tuesday, 3 May 2016

Top 10 Myths About Osteogenesis Imperfecta


Top 10 Myths About OI - 2016 (taken from an OI parent)
10) They don't have blue sclerae so it's not OI. (White, gray, gray-blue, or blue)
9) Kids with OI will "grow out of it". (Genetics)
8) OI is contagious. (Genetics, not infectious)
7) You think you can control a child's innate/biological instinct to move, crawl, stand, climb, explore. (You can't. Safe environment)
6) Every person with OI is affected the same way and presents the same way clinically, so should be treated the same way (spectrum condition, unique genetic information for each individual, individualized context based clinical care plans)
5) Toddlers are too young to have rodding surgeries (Fassier-Duval Rods - pulling to stand, weight bearing child)
4) Infants are too young to be started on medical therapies like IV Pamidronate. (Montreal Shriners - Glorieux, Plotkin, Rauch studies of late 90s/early 2000s)
3) The increased ambulation, activity levels, reduced pain levels, improved quality of life in children over the last 20 years are due to "nutrition". (See 4 & 5)
2) Infants, toddlers, children, adolescents, adults do not feel pain with fractures the older they get and more they have them. (Pain is real and affects recovery and long term outcomes)
1) Drinking more milk will cure OI. (Really?!)

Tuesday, 19 April 2016

Enables Me Live! – Donald Barrie – What I Learned Through Enables Me

http://enables.me/enables-live-donald-barrie-learned-enables/



Enables Me Live! – Donald Barrie – What I Learned Through Enables Me







Donald Barrie is a published writer, blogger and editor, web designer, Diamond Jubilee Medalist and aspiring podcaster/voiceover guy. His personal interests include faith, movies, music, reading, writing, chocolate, a good laugh and socializing.
Enjoy the moment, well that’s self explanatory, enjoy the present time you’re in
Donald has spent the past two years with Enables Me and has had the opportunity to interview amazing people from para-athletes at the 2015 Toronto Parapan Am Games, such as Priscilla Gagne, Canadian musicians, such as Justin Hines, and advocates such asTim Rose and picked up a variety of life lessons from them.
The definition of the word the enable, is by being a part of Enables Me, I learned a new definition healthier more positive definition
He takes great pride on the research that’s required in preparation for the interview and development of the story.
In this Enables Me Live! talk, Donald shares his experience as a reporter for Enables Me and what he has learned from the interviews he’s conducted.

Tuesday, 22 March 2016

RIP Rob Ford

Today I remember former Toronto mayor Rob Ford. He served as mayor from 2010 to 2014. Earlier this morning he lost his battle with cancer. I met him once back in 2013, and he was friendly to me. No bad stories here. His long season of suffering has ended. He made a difference in my city, and he will be missed.




Tuesday, 9 February 2016

Tim Rose has a rosy outlook on love and life

Tim Rose
For Tim Rose, everything’s coming up roses as another Valentine’s Day approaches. What makes Tim Rose most happy, aside from being a successful entrepreneur, is that he is a person with a disability who is happily married.
Rose, a 29-year-old entrepreneur born with cerebral palsy spastic quadriplegia, met his wife, Natalie, through a mutual friend during the summer of 2010. Prior to meeting Natalie, he had attempted to have relationships with other women, but most of them weren’t interested because of the fact that he has a disability.
Natalie, like the previous women he approached, does not have a disability. Their relationship was confirmed one night when Tim and Natalie attended a party hosted by his brother. “She wanted to go with me, and we realized that we really liked each other.” After leaving the party, Natalie returned the feelings Tim had for her when she told him she had a crush on him.
“We hung out together a couple of times before I moved to England to attend university,” he says.  With the exception of a three-week period, most of their communication during their first year together was done across the miles.
“It was tough at times, but it made our relationship stronger,” he says.  When Tim returned to Toronto from the University of Nottingham in August 2011, he and Natalie dated for five months before proposing to her in 2012.
“I knew by the second date that she was the one,” Tim says. “I organized a scavenger hunt the night that I proposed to her. I think she knew I was going to propose but wasn’t sure how or when” he says. When he presented her with the ring at the end of the scavenger hunt, she said yes immediately.
I asked Tim what they like to do on Valentine’s Day since this interview was conducted in the days leading up to February 14. “We’re not huge Valentine’s Day people, but we always find time to do something together, either on Valentine’s Day or around that day. We may go out for dinner, play board games or do something not too extravagant.”
Tim says that since he and Natalie have become busy with their respective careers, it isn’t always possible to plan a date. Tim, however, stresses that they set aside a date night as often as they can, schedules permitting.
“We always want to maintain communication in our marriage,” he says. “We’re always talking and saying, ‘I love you’ to each other. We try not to hide too much from each other. We always find couple time during the day because it’s so important.”
While he is aware of the struggles people with disabilities experience in finding love, Tim has this advice. “A disability, while it can present challenges to dating other people, there’s also a lot of good things it can bring to a relationship.” He also adds that “once you find that one person, you find the advantages that having a disability can bring to a relationship. It makes you a better person, and more desirable in general.”
To learn more about Tim Rose and his consulting business, you can visit http://www.disabilitypositive.com/.
Tim Rose with his wife Natalie, and their dog Rush.
Tim Rose with his wife Natalie, and their dog Rush.