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September, 2010Archive for

The iPad as an Affordable Communicator: Initial Review

Monday, September 13th, 2010

By Glenda Watson Hyatt

The Apple Store in Chicago

While in Chicago, I made a short trek to the Apple Store. My mission was to try out an iPad to see if I could reliably use the touch screen with my shaky athetoid cerebral palsy. The reason for wanting an iPad is to use it as a communication device while I’m out and about.

I spent an hour playing with the thing, not quite sure what I was doing. Although I did manage to get a tweet out with minimal typos:

A twitter update reading: Trying an ipad NOW. Test 123. Man, My arm hurts now.need more practice!

Once I had had enough playing, I attracted the attention of the young Apple employee Courtney and indicated that I was ready to buy one. She said they were sold out. My heart sank. Then she found one in the back room, and when an employee looked surprised, she said that one was special. (I sensed a shipment had just arrived, but had yet to be inventoried.)

Continue reading The iPad as an Affordable Communicator: Initial Review

Confessions of a “control freak” – my life as a mom of children with special needs

Friday, September 10th, 2010

text on wall that reads: fear
As the mom of 2 children, one with autism, both with type 1 diabetes, I have had my fair share of challenges to face over the years.   One of the biggest issues that I struggle with is that of control, or at least the illusion of control.

This control freak pathology is a common one among parents of children with special needs.   We have been faced with a lot of things in our lives that we didn’t have a say in or control over, so we throw ourselves head on into trying to control every other thing in our lives.   No one could possibly care about our child as much as we do, so how can they be trusted to do the critical work of caring for, teaching, treating our vulnerable children?

Trying to control everything, however well-intentioned our efforts might be, is an exhausting and isolating effort.  The reality is that it’s not so much about control as it is about FEAR.  Fear about who will care for our children when we are gone, fear that the systems and professionals involved in that care will not be available or properly prepared, fear that something else, something even worse than what we’ve already faced, might happen at some unknown, unanticipated time in the future.

For me, the thing that best tempers my control/fear issues is reaching out and asking for help and sharing my fears with other parents, friends and family. Even in the act of asking for help I have to overcome a bit of fear, the fear that I am NOT the supermom that people expect and that I really can’t do it all. Overcoming that particular fear and letting go of a little control has made a huge difference in my life.

Go ahead. Give it a try. We can help each other.

Wheeling in Rome: Are You Serious?

Tuesday, September 7th, 2010

Food in RomeIf you’re not really one for challenging environments, taking on Rome in a wheelchair is not something I’d advise. Of all the cities undertaken on my Wheely Big OE, Rome was by far the trickiest. And, crucially, one of the most expensive. And it’s not like I can say I hadn’t been forewarned! Plenty has been written about Rome’s unsuitability for wheelchair users, especially those in power chairs. Unperturbed, we decided to go anyway.

I cannot stress this enough: when travelling to Rome in a wheelchair, planning is essential. In order to take the Leonardo Express from Rome’s Fiumicino Airport to the main station, Termini, you have to email the Sala Blu team at trenitalia.it in order for them to arrange the requisite lift service at Termini. Unless you’re comfortable being hauled down steps, don’t forget to do this! Also, don’t expect a readily-available wheelchair-accessible taxi service! We had a few muckups with our flights, and after ringing what seemed like every taxi company in Rome, we ended up spending 140euro (which is around $280NZD) on a taxi to the airport. Absolutely criminal.

Continue reading Wheeling in Rome: Are You Serious?

Part II: Assistive Technology and Accessibility Research in the Developing World

Thursday, September 2nd, 2010

Establishing AT research in the developing world is not going to be trivial, especially given the overall lack of existing scientific research capacity. Building this capacity must be based on a significant long-term investment and a commitment from the state and higher educational institutions to reward research both academically and commercially.

AT and Accessibility represent a massive breadth of work – building expertise in speech synthesizers for new languages requires a very different skill-set from building automated wheelchairs of currency readers. The most successful AT research centers have typically had connections with university, and thereby tapped into faculty with a range of interests. These have also bridged the connection between academia and industry, but from a funding perspective have almost always been kickstarted by the state. State commitments of inclusion to their vision-impaired populations cannot be realized without an investment in building an indigenous and inclusive research culture.

In an ideal case scenario, this would mean building a scenario where people can think of research as a career – from graduate studies onward either towards academic careers or industrial research positions. Given that the larger goals of building scientific research can be anything between very challenging to completely infeasible for a number of smaller countries, for the purposes of AT research there are three short-term possibilities.

Continue reading Part II: Assistive Technology and Accessibility Research in the Developing World