Last week, on March 29, I was a keynote speaker at the Monash Human Library which was held in the Peninsular campus. This was conducted to an audience of about 100 OTs – both students and professionals. My keynote speech explored the individualistic pursuits of Friedreich’s Ataxia which can be summarised as follows: Continue reading “Monash Human Library and New Book”
I want to discuss a disorder that afflicts me. Friedreich’s Ataxia (FA) will eventually leave the person afflicted with severe socioeconomic and medical restrictions. And because of this many people with FA are constantly subjected to stereotypes, as losers. We are unfairly harassed, and our abnormal features and functions as a result of the disability doesn’t make our life any easier. Believe me. My experience is that many people – it doesn’t matter what walk of life – believe they know best for an FA suffered and will then apply the stereotype to tell them what they can and can’t do.
Does this sound fair to you? Continue reading “Furthering Mutual Respect: Some Thoughts on Giving Sexuality its Due and Friedreich’s Ataxia”
My ongoing request is a complaint, like the persistent complaining of a broken record. It is simply pointing out the fact I have no cognitive impairments, just purely Friedreich’s Ataxia.
Mutual obligation was a political buzz-word during Prime Minister Howard’s leadership from 1996-2007. Let me be frank, when we are talking about mutual obligation, the political definition of the term describes it as such: ‘Mutual Obligation is based on a concept that welfare assistance provided, should involve some return responsibilities for the recipient’. Continue reading “Another Hurdle I Must Get Over”
This was sent to me by a friend.