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by Katelyn Leader
Join Day Undefined for a webinar with the National Ataxia Foundation on everyday products that might make daily life more accessible. This hour-lon...
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by Liam Dougherty
Navigating today’s society means needing easy access to money. But having a disability that affects my fine motor skills means money is inherently ...
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by Keri Hanson
One thing I swear by is the use of a Lazy Susan. No, this doesn’t mean grabbing your snoozy sister Susan and asking for help! They are versatile tu...
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by Jake Tompkins
As I lost my long term personal care assistant (PCA), I was approved for an accessible apartment I had been on the waiting list for for the better ...
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by Keri Hanson
I could name quite a few things that have made my life as a wheelchair user easier. I could also name quite a few things in life that greatly inhi...
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by Liam Dougherty
Water is easy to spill, can be difficult to imbibe, but must be drank oh so frequently. It is plain to see how it could be a pressurized topic in ...
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by Liam Dougherty
As someone with progressive ataxia, I have lived through different levels of access. What worked for me in high school doesn't work for me as an ad...
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by Liam Dougherty
Urination shapes my life more than most parts of my disability--it impacts what I do, where I go and what I put into my body. Peeing is a very high...
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by Katelyn Leader
My family loves their condiments. Fries without ketchup? Forget it. Hamburgers or hotdogs without ketchup, mustard, or sauerkraut (depending on who...
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by Liam Dougherty
I gave myself second and third degree burns on five percent of my body the last time I tried to make hot coffee in a french press. I don’t want to ...
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by Katelyn Leader
I love head scratches. I was the kid who used to beg any aunt or uncle or babysitter or parent for a head scratch. And so did my siblings. In fact,...
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