Says Ross: “It’s not purely about disability because I don’t like being put in that box. Recent articles, for example, have included a look at trolls online and covered Ross’ lockdown diaries. I think people enjoy the honesty and the comedy of it.”Ĭrucially, his wheelchair is incidental, not central, to the content. I am a bit of a cheeky chappie, so I say anything and everything on there. “It grew and grew and it is now a real passion of mine. “It started as a hobby, just a way of documenting my life as a young man with a disability that I could look back on in years to come,” he says. The blog, which covers lifestyle topics and reviews events and products, was even nominated for a National Diversity Award last year. “When you think that something like 22% of the population has some form of disability, you have to question how that counts as representation”Ī Life on Wheels started out as Ross’ hobby back in 2017 and has been growing steadily ever since. “The next generation need a better level of representation so they know they know they can achieve what they want to achieve,” said Ross. Just because we have to do things a little different, it doesn’t mean that we can’t succeed. There are people in the world who look a little different or who have mobility issues, but we are just the same as everyone else. “We need to learn to break down those barriers. It matters, he tells pharmaphorum, as it creates role models and lets young people know that their disability does not define them. “When you think that something like 22% of the population has some form of disability, you have to question how that counts as representation.” “There are some positive disabled characters, but nine times out of ten their sole purpose in the programme is based around their disability,” says Ross, who was diagnosed with spinal muscular atrophy (SMA) Type 2 when he was a toddler. They tend to be portrayed as struggling with their disability, rather than dealing with all the same highs and lows of life as everyone else. On our screens, for example, people with disabilities are often one-dimensional, he says. But disability is one thing that always seems to get left behind.” “On TV and in the media now, you are starting to see all sorts of people: people of different shapes and sizes, different races, different sexual orientations. He says: “While we still have such a long way to go, I think things have improved over the last few years. None of this makes sense.From #MeToo to Black Lives Matter, as a society we have been discussing the relationship between representation and equality more than ever over the last few years.īut while progress is being made in so many areas, people with disabilities are still struggling to find a voice above the accepted narrative, says Ross Lannon, the 27-year-old blogger and multi-media content creator behind A Life on Wheels. Yes something about this whole story does. I can smell a rat, and it is the two legged variet. I just watched today an hour long documentary by L. I can smell the same two legged rat also, have don. Especially with this year being election y.īe strong let them know you will no longer fight f. I would also like to know of alternative sources.Ĥ:12 PM: Guatemala suspends flights of Salvadoran. Thanks to both Bb9 and Jan for this memory. Russ, you do not understand the situation. Yes you must stop consuming their media and paying. I never knew of this invasion! Thank you very much. I have a new comments system so your com. That's very much! I hope you are still viewing the. ![]() Translation: Europe is going to be the place where Whites can go to live!Ĭountries By European or White Percentage 2030 □Ĭountries By European or White Percentage 2010Įuropa gaan die plek vir Witmense wees om te gaan bly. ![]() ![]() Interestingly in Afrikaans, Europe is called Europa. Then Europa will still be more than 80% White. Translation: This is not unfamiliar: USA’s Whites will be a minority by 2040. Dis nie vreemd nie: VSA gaan minderheid Wittes h teen 2040.
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