Don’t Ask, Don’t Assume…

The government has launched yet another useless campaign. This time they claim the aim is empowering & dispelling myths about disabled people.

In my opinion Ask Don’t Assume is a big fail. I don’t seem to be alone in that opinion. Many disabled people agree that encouraging the public at large to ask us whatever questions into pop their heads is a terrible idea. The government claim to have done extensive research. According to Minister for Disabled People, Health & Work, Tom Pursglove that ‘extensive research was with 500+ people with lived experience of disability. To be honest I’m surprised they found 500 people who thought this was a good campaign. However, with 6.3 million people currently entitled to disability benefits*, consulting 500 does not qualify as extensive.

One of the problems I encounter as a disabled/chronically ill person is maintaining boundaries. So many strangers don’t think twice of asking personal & invasive questions. Almost every time I leave the house someone will ask ‘what’s wrong with you’. In recent years Tory policies regarding disability benefits have led to more people holding hostile views. Disabled people are often viewed with suspicion, which leads to strangers demanding information from me. People who know nothing about me or my circumstances feel entitled to my private medical information just incase I am somehow ‘scrounging’ benefits. A government campaign with the tagline, Ask Don’t Assume, legitimatises this behaviour.

Further, a lot of the campaign materials include toxic positivity/inspiration porn content. I watched a video with a woman describing her disability as a strength and as something that ‘can give back’. Everyone is of course able to decide what disability means to them, but none of this resonates with me. My disabilities make my life much harder. There are lots of thing I simply can not do. Even the most mundane of daily tasks are negatively impacted by my conditions. That doesn’t feel like a strength to me. I also cannot comprehend how a disability ‘gives back’. Do my defective knees perform acts of service? Or is my daily fainting somehow contributing to a greater good? If so, I haven’t seen the evidence or benefit.

I do not believe that this narrative is advantageous to the disabled community. Our value is not tied up in how well we overcome our disabilities. Disabled & sick people require accommodations. There will always be things we cannot do without assistance or at all. Our bodies do not function like the average person. There is no amount of determination or strength that can change that. The onus should not be on us to make abled bodied people feel comfortable with that. Disabled people should not have to be grateful, inspirational or make themselves ill trying to prove their worth.

There have also been calls for our government to address their obvious failings with regards to disability rights. The Tories have spent over a decade attacking disabled people. Their continued battle to deprive people of vital benefits has done untold harm. Purposely making it incredibly difficult for those with mental illness to qualify for support is intolerable. Their persistent refusal to acknowledge UN reports on the circumstances of disabled people in the UK. Along with long-standing inequalities such as disabled people being unable to live with a partner or marry without losing disability benefits. There are many urgent issues this government could address if they truly wanted to empower disabled people. This is very poorly executed lip service.

If someone wants to share about themselves, they will do so. If a person requires your assistance, they will request it. There are very few instances in which is imperative to know the details of someone’s disability. The exceptions, health & safety in the workplace, safely accessing facilities and so on can all be handled discretely & professionally. There is never a reason to intrude on a disabled person’s privacy. This campaign does the opposite of its stated objectives. Considering it is a Conservative initiative, no one is surprised.

* UK Disability Statistics Feb 2023.

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23

Dear Son,

Today would be your 23rd birthday. I can’t imagine that I would be top of your party list. Mothers tend to cramp one’s style. Still, I think about how you would celebrate.

Would you feel too old for cake with candles? I wonder if a family dinner would be on the agenda. I picture your Gran fussing over you. Your Aunts & Uncles buying you drinks & taking the piss. I see you surrendered to your little cousin’s nonsense entreaties. It’s all perfect. Of course I know life wouldn’t always be that way, but this is what I hoped to give you.

Recently I’ve been wondering what would come next. When I kissed you goodbye, where would you be headed off to? I was self sufficient by 23. I graduated that year, I was living alone in a flat I hated & working a crappy job to get by. My mental health was a mess & adulting was a learning curve. It wasn’t all bad. I was young & answerable only to myself. I had good friends and we made the most of our youth. I partied as many nights a week as I could afford. I felt such satisfaction; paying the bills, managing a home. Living life on my terms. Always, though, you were missing.

I thought of how my life would be with you then as much as I do now. The younger years were easier to imagine. I don’t know what decisions you would have made. I’d have wanted you to go to University. I’m sure I’d be happy to still have you at home. Perhaps you’d have a partner. You could be just like me. A new graduate balancing a job & the clubs. Or maybe you’d have taken an entirely different route. I’d support anything that made you happy. I’d be proud of the man you would be becoming.

I only write today, but you’re in my thoughts every day. I’d have done whatever it took to give you everything you needed.

Love always,

Mum.

The Last Supper…

Season 2 is complete & I would like some credit for knowing that Aidan was a very bad idea from the get go.

We’ll get back to my i told you so later. Let’s kick off with the good, eh? Anthony is in love. Excellent. I’m not convinced by the whole internalised homophobia plot, but I am pleased he has a happy conclusion.

Miranda & Steve finally have the closure I was begging for. A recognition of what they shared & a promise of a friendly future. I loved Steve’s ‘I was right for a really long time’. It is lovely to see a relationship breakdown being portrayed as something other than failure. It doesn’t always last forever, but that doesn’t erase all the good that people share. Another big tick.

Che remains annoying. The tequila in Carrie’s kitchen, their insistence that those jokes were funny & to be honest their presence at the dinner wound me up. Nya’s (I had to remind myself of her name, which is not a good sign) handsome bar dude being the chef was a bit too romcom convenient. Similarly Seema’s I love you’ freak out was cliche, but I can let some things go. Carrie acquiring a kitten pleases me immensely. Bonus points for naming her Shoe. Samantha’s cameo was a let down, however at least in keeping with her character.

Which brings us back to where we started; Aidan. Now that she has sold her home & purchased a giant place he’s about to make redundant, he can bear to enter that apartment. The minute Carrie upends her entire life, he discovers that he can’t possibly take his eyes or thoughts off his kids for a second. Obviously a parent should always put their children’s needs first, but I’m not sure constant supervision is what his teen requires. It’s now that we learn that the ex wife is not a constant in the lives of the kids she flew to NYC to warn Carrie off. Aidan literally clicks his fingers & expects Carrie to freeze. There is only one possible answer to his 5yr wait proposition; FUCK OFF.

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