Disabled DS Members - what's your disability?
[Deleted User]
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Reading the "what medication are you on and why?" thread has made me curious as to how many disabled DS members there are, and what disabilities we all have.
I am paraplegic. A lot of people seem to presume this mean I only can't use my legs, or that I'm paralyzed from the waist down. Some paraplegics ARE paralyzed from the waist down, but I'm not one of them. I can't move or feel anything from the chest down.
My hands and arms are fine though.
As a youngish (early 30s) active fulltime wheelchair user, I get a LOT of stares. I can fully understand people want to know what's wrong with me. Heck, even I look at other people using wheelchairs. But, I don't like blatant staring. That's just rude!
So yeah, that's me. How about you?
I am paraplegic. A lot of people seem to presume this mean I only can't use my legs, or that I'm paralyzed from the waist down. Some paraplegics ARE paralyzed from the waist down, but I'm not one of them. I can't move or feel anything from the chest down.
My hands and arms are fine though.
As a youngish (early 30s) active fulltime wheelchair user, I get a LOT of stares. I can fully understand people want to know what's wrong with me. Heck, even I look at other people using wheelchairs. But, I don't like blatant staring. That's just rude!
So yeah, that's me. How about you?
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how has it impacted on your life? did you get help when at school?
I thought it was Top Trumps!!
How do we determine the winner?
Enough questions for a dull day on DS i think
I certainly wouldn't have noticed any discernable difference if I wasn't diagnosed that's for sure. Before I knew abouyt my conditoon, I could have lived quite happily considering Dyspraxia is considered an invisible disability. I was diagnosed not long before I did my GCSE's.
Now that I know I can see what my problems are and were. I learned a lot more about how I was as a child and the problems I had. I used to get all sorts of childhood treatment through occupation therapists and up to my GCSE's I was on a Statement of Educational Needs.
My parents were told that because of my problems I would never cope with mainstream education. However through hard work over the years i've always overcome the odds, even through the hardest times. Now, i'm in my Final Year at University.
I feel my Dyspraxia every day... inside my brain messing me up, but I don't let it win and I only do things I know I'm capable of.
thanks for answering
i do wonder sometimes how much have a diagnosed 'thing' actually helps some individuals, i don't believe it does help in some cases, particularly if it's a mild case of it
I doubt it could do much harm. If can give a person a sense of ease knowing that they now have a label for what's wrong with them and it can give you the help and support that you need.
true, sometimes the labels can be unhelpful tho'
The Symptoms I get are
Balance problems & never being able to walk in a straight line
Headaches & pressure pain behind the eyes
Dizziness
Blackouts
Constant tingling (pins n needles sensation) in the body
Sleep Apnea & other sleep issues.
Loss of feeling down 1 side of the body
There are 2 ways of getting Chiari, 1st is that you are born with it & secondly is via head trauma like a car accident. I was born with it but the majority of my symptoms started in my early 20's.
There are sufferers who have different symptoms & some sufferers have died from the condition as their brain suddenly collapses .
There is no daily treatment for the condition & there is no cure. There is only risky brain surgery which I have had done with no success.
The symptoms are a bit similar to Fibromyalgia or part Chronic Fatigue, I'm not actually sure what's going on.
sounds like you have 2 separate things going on there
Also my speech is slower but everyone understands what I say.
Other than that, i'm as 'healthy as a horse' as the saying goes lol
:D:D