(Dsylexai*)
It’s another May post – because now University has finished my life has no meaning anymore – and, sticking to the lovely votes bloggers gave me, this will both a personal blog and one containing my utter contempt for all those around me (as if this is a new concept within my blog). So today my DSA delivery is finally arriving, the DSA is the Disabled Student Allowance and depending on the level of mental or physical disability you have will decide whether you qualify for DSA equipment (which is just free equipment suited to your disabilities). I have mild Dyslexia, or at least that is where I fall into when I do psychological tests, where as my brain scan says that I have minor brain damage of the limbic system… which really isn’t as bad as it sounds, it just mean that my hippocampus and hypothalamus don’t spark up when they should be. I had a lot of ear infections as a child, which caused the damage, but because of the generally open format of what Dyslexia is I fall into the bracket, in the same sense that most people could fall into the Autistic spectrum if tested. I’m not too keen on being classed as Dyslexia, simply because the majority of people have no idea what Dyslexia is – and I swear to cow if another person asks me “oh yeah, Dyslexia, so does that mean you can’t spell and count?” I will kill you with a pencil – and I’m also tired of hearing people diagnosing themselves with Dyslexia because they have poor mathematical skills or grammar, sometimes you’re just plain stupid so don’t go clinging to disabilities. But anyway, despite the fact that I do doubt how useful these things will be for my studies, you know being that it is now a month after finishing University, the DSA wanted me to have these things to counter any impairments so during the end of the first year I took the assessments and sent my results off, two years later they finally contacted me with approval, so during the start of third year I finished the applications and now at the end of my Degree (TODAY!) I will actually be getting the fabled equipment.
Or at least that is what I have been told, I cant help but question it after not only waiting two years to finally get to this point, but also after suffering through three years of Edge Hills and Student Finances “Oh, you wanted us to actually do something… Yeah, no that isn’t going to happen” approach. I’ve been told it will be delivered at 12, so I should get it around 5pm. Edge Hill you once again have made me the most suspicious when giving me free things, not many Universities go the extra mile of getting you used to the real world by taking £9,000 of your money and then laughing at you, as they walk away with it. But to give me equipment for my Degree, after I’ve already finished the three years really adds new levels to the mismanagement found in Edge Hill.
Oh another note, I have RSI (Repetitive Strain Injury) in my wrist from whisking cake batter, and it hurts like a bitch, I decided that learning how to knit, and therefore knitting wrist cuffs would be the best idea to cope with this… It wasn’t, if anything it has most definitely aggravated it further. I may have myself tested for mental retardation, it would be worth it to see what free shit they give me then… Three years after I needed them.
After Thought:
The legendary DSA equipment has actually arrived, and even an hour earlier then scheduled, I therefore take back all my bitter comments... not the ones aimed at Edge Hill, just the ones aimed at Wyvern Business Systems. So I now have a PC, printer and scanner and a shiny Livescribe (for those wondering: http://www.livescribe.com/uk/smartpen/echo/) but now I really don't have anything to do on any of the equipment, I could have used it to do my essays, that would have been really useful, but instead I'm left editing a blog post.
Despite the delay on my own equipment, I do think it is worth getting yourself assessed if you feel you may have any form of disability, few people know the extent to which the SpLD team can help and what things you may be 'entitled' to because of your impairment. You'll have to go through a psychological assessment to gauge where you fall in the disabilities brackets, mine cost something under £100 and after this it should take around ten days until you get the results back and then it will be decided whether your disability requires any specialist equipment or personal assistance throughout your studies. After the psychological assessment you will also take a needs assessment test with your supplier to find out what equipment is out there and whether you would ever find it useful, I was given a PC (but you can choose yourself whether you would prefer instead to have a laptop) and Inspiration (http://www.inspiration.com/) and Claro Software (http://www.clarosoftware.com/index.php). Originally the DSA had intended to rent all the equipment to me, or I could pay £108 pounds and instead buy all the equipment - and as they have planned to rent it from the 24th of May to the 16th of July it was by far the best option for myself to pay for the equipment outright - all in all you will end up spending a maximum of £200 on a lot of equipment suited to what you need the most, so it's worth the cost of the assessments.
I think when it comes to any disability it really is best to get yourself tested, I was always aware I had an impairment, but it was only through taking the test that I realized to what extent it had gone. For example: I have what a lot of people with Dyslexia and Dyspraxia have, a visual impairment that makes any colours on paper or screen produce a glare that makes it difficult to look at, but I wasn't aware that if I was to attempt to read black or white lettering's on a red piece of paper the glare would swallow up the writing and as far as I would know I would be looking at a plain piece of red paper. When it comes to disabilities I've noticed people tend to reject any form of diagnosis because they don't want to be labelled, and in fairness even I don't like telling people that I am (because suddenly people assume they know more about Dyslexia then you do, and actually try to tell me my own symptoms), but without testing you'll never fully understand the symptoms you have - which means you can never actively counter the limitations you may have.
So in short:
Things that will make me feed you your own tongue;
"Oh yeah, I have Dyslexia too"
"Oh, ok. What where you diagnosed with?"
"... Well, I haven't actually been tested but I always misspell words so I obviously have it"
"Oh yeah, Dyslexia - so can you not do mathematical equations?"
"Mine is more colour and memory based"
"Oh. But isn't Dyslexia just about spelling and counting? Are you sure you have Dyslexia... maybe you have a visual impairment"
Things you should be doing;
If you think you have a disability, go get yourself tested - instead of just putting a label on any limitation you feel you have to make yourself feel better.
Never assume knowledge on disabilities because you have heard it mentioned once, in the same way you wouldn't say this -
"Oh, you have cancer. So sorry to hear that, have you started chemo yet?"
"No, that's just one of my options but for now I'm hoping that my medicine can help hold it off whilst I wait for my surgery to remove the tumor"
"Oh... are you sure you have cancer then, because I'm pretty sure you go into chemo once you're diagnosed with cancer"
- give others the same courtesy.