Okay, this one has been coming for a while because subtly discriminative job adverts are an issue of mine and sometimes less subtly.
Because finding a job with a disability is hard enough and in the UK the Equality Act 2010 is meant to prevent disability discrimination in the workplace – from the application stage.
I’m not going to get into a debate about whether it does this well enough or not but I am going to discuss some of the parts of job adverts I’ve seen that are somewhat discriminatory.
We are looking for a high energy individual – My condition causes fatigue but it doesn’t mean I can’t do the job well.
Must be able to drive – If the job doesn’t require significant travel and is in a place accessible by public transport why do I need to be able to drive? There are many reasons why someone with a disability wouldn’t be able drive and this exempts you from the job even if driving isn’t necessary to perform the job well.
Must be able to lift X amount – If it’s an office role requiring mainly desk based work it would usually be a reasonable adjustment to delegate the lifting part of the role to another member of the team
Must be physically fit – unless it’s a role that actually requires this I think this one is self-explanatory
Good health record
Physically and mentally healthy
Flexible – flexible in what sense? How flexible? This may also be discriminatory to women who often have more childcare needs than men. Yes we may be flexible but only within certain parameters.
We need to work with employers to ensure these phrases don’t crop up in job advertisements, recruiters and disabled candidates are aware of the range of adjustments that may be considered reasonable and that recruiter are open to recruiting disabled candidates and understand that we can be valuable members of the workforce.
I hope that when the next generation start applying for jobs they won’t face these barriers.
This week I went out in my manual wheelchair for the first time half being pushed because I live on streets with uneven pavements (which I’ve learn’t as long as the pavements straight but not if there are any bends!) and I still can’t get myself up a drop curb. I thought I’d write about some of the things I’ve learnt from the experience.
My arms are stronger than I thought they were. I knew my arms had better function than my legs. I trust them more and can feel them properly. But I genuinely thought I’d only manage self propelling 5 feet on a v flat easy surface before they just gave up.
Why can’t all pavements be level?
People were a lot nicer than I expected. I didn’t encounter any Karen’s on this trip.
Can people please put signs for COVID entry and exit sides at a wheelchair users eyeline before they have to choose a side of ribbon to go on.
Can we have counters at banks at a height that is more accessible?
Sometimes people do expect you to try and weave around them which is interesting as a new wheelchair user on a busy high-street. Was definitely scared I may run someone over at these points.
I didn’t feel like I was about to pass out or collapse as much, I could feel my legs and was much less grumpy and more chatty (so clearly it’s doing it’s job or atleast half the job)
The skin on my hands, my wrists and my shoulders surprisingly survived but there were deffo a couple of finger dislocations!
I somehow ended up with a bruise on the inside of my upper arm? (EDS skin)
I’ve come a long way in accepting myself since that time last year I had to be wheeled around A&E in a chair.
The advice a can give so far. The practicalities of navigating pavement in a manual wheelchair are a lot harder than you think and you have to go a lot slower than you think or even want to if the ground uneven (Maybe not for the seasoned manual wheelchair user). If you think you need to use a wheelchair you probably do need to and don’t let anyone tell you otherwise.
I made the decision the other day to get a wheelchair. It’s a decision I really should have made years ago but I was too scared and I could walk okay when I needed to…. so it was fine right? I mean not really but it’s hard to come to the realisation that you need a aid that many people see is only for people who are paralysed or otherwise literally cannot walk when you can. Adrenaline will keep you on your feet it just really hurts, the pressure in your head gets exponentially worse and it cases payback which limits your ability to do other things. It’s also hard to justify needing a wheelchair when you can climb. I don’t know why because climbing and walking are two completely different types of movement and your able to sit on the mats and rest inbetween.
It’s scary anticipating neighbours simultaneously seeing you walk to the car to go to your nans or the climbing wall or wherever else one goes in the car, but go out in the chair to go to town or the doctors or wherever once I have built up the ability to self propel I may go on my own.
There’s definitely a lot of people my parents included who don’t understand how chronic illnesses fluctuate. If I pace myself okay I can function and with my ME feel okay. Not healthy person okay but ME/CFS okay. Like the day I’m writing this. There’s some inner energy but the symptoms are still there. With my EDS yes my joints would be better if I could get myself more conditioned by climbing more but even then some days they are worse than others. Some days I can’t go into the freezer without partially dislocating a shoulder, others I can.
There’s also a lot of people who think people in wheelchairs somehow also have an intellectual disability – like we can’t speak for themselves.
And the awful “wheelchair bound” no for me it would be some freedom outside of the house with less payback and I know others feel that way.
It’s difficult navigating spaces that aren’t really made for us but it’s better than being stuck in the house.
And that. That would be amazing!
Does anyone else use a wheelchair for certain outings? What ableism have you faced?
So I thought this would be a fun lil project to work on, working my way through various TV shows/episodes and reviewing them on the disability representation in the show. To start, The Story of Tracy Beaker because it was a childhood favourite and I’ve really enjoyed rewatching it! I also now want to read Jaqueline Wilsons newer Tracy Beaker books even though I’m 22 and currently am struggling to find time to read but that’s beside the point. The two characters I want to focus on for this are Layla and Millie.
Layla has Cerebral Palsy and a big positive is that she is played by an actress with this condition. Disabled actors playing disabled characters is rare in TV and film so I definitely appreciate this! Other pros are:
She has a great personality and is a solid character whom viewers can easily become endeared with for reasons other than her disability
We get to see the reality of missing out on things when your disabled or have a chronic illness in the episode where she has to miss an exciting day of school for a physio appointment that ends up getting cancelled. Layla not wanting to miss school helps debunk stigma that disabled people are just lazy or the belief that they are lucky to get to miss days of school
We see issues with accessibility and when Duke says “first one to the table” and Layla is unable to run as fast as the others.
Tracy uses her age and height as well as able body to get her wings back from Michael. Seeing Layla fit in with the other kids so well and seeing the other kids help her when she needs it but not being overly pushy or protective or pitying sends an important message that disabled children are just children and deserve to be treated with the same respect and in the same way as any other similar child, providing necessary accommodations are made.
She seems independent and intelligent for a child of her age through her lines and the fact that she does household chores like everyone else – this is very important for two reasons, one to help dispel the whole disabled people are a burden myth and secondly to show that not all disabled people are stupid.
The only con I really have is that she didn’t get fostered but that’s reality sadly. Although she’s young and cute, having a disability does make her less likely to get fostered.
Millie is non verbal until she gets fostered and then she says the best line to Elaine.
The other dumping ground kids suspect her of weird goings on and think she’s scary but eventually realise she’s a scared kid and they should be nice to her
Her friendship with Marco and her eventually getting fostered with him
Even without lines we see her personality and emotions
I wish she got more screen time
I know Elaine is a pain but I really don’t like how she pity’s and patronises Millie just because she doesn’t speak.
Overall I would give the representation of disability in The Story of Tracy Beaker an 8.5/10! Although this is only my opinion.
There will also be one coming on Tracy Beaker Returns/The dumping ground some point soon so watch this space!
If you have any TV shows and characters to recommend for this series leave it in the comments.