
Question Time
If you are not at all familiar with ABI/TBI or even disability, let me give you a very simple piece of advice. Never, ever, ever bombard someone with questions without time to answer. Actually, that’s relevant to decent human behaviour, however it’s even more important to people with an ABI or simply a disability.

Now, I’m very lucky I think and process quickly, however it’s not normal for anybody with a brain injury.
My mum has been known to ask a question when helping me move house and by the second question, I answer with a further “Yes, No, No, Yes, No” and she will ask “what are they for?” to which I inform her “Your next three questions. We laugh and all is well.

However, it’s common someone else I’m related to who doesn’t spend much time with me will throw a question at me. (Note; How I’ve kept writing this topic? Because what the hell, my family don’t read my blog anyway.) I suspect that’s common for a lot of bloggers.

Moving into an apartment has meant over the winter I will need to rely on a clothes dryer to get things dry and I don’t have one. I’ve already upgraded my washing machine to a brand-new front loader, so I use less water and it spins better. I now need a dryer which will sit directly on top.

‘Someone’ stated to me. “You probably don’t need one.” Then proceeded to attempt to convince me I could visit a laundromat and rather than wait for me to explain how that just couldn’t work, I am assaulted with reasoning and assaulted with reason’s why going to the laundromat with a pile of clothes, towels, sheets, heavy blankets (they wouldn’t go in the dryer).

Eventually, when this person paused to take a breath, I pointed out I would injure my back carrying a plastic tub of heavy damp items. In reality, I would have trouble getting it out of my apartment as the door is heavy and awkward.

I would need to put it down to dig out my swipe card to use in the lift. Again, putting down my laundry basket (these days a square plastic cube) and picking it up again. Once on the ground floor, I have to press a button to close the entrance door, then get the door open, pick up the cube and get outside.

Did I mention, I use a walking stick when out? Do I need to finish describing the ludicrous mess (is that a word) of that suggestion?

Sometimes, family will do their very best to convince you of another way so you don’t need to spend that money. They don’t need to help you do ‘that’ thing and then they don’t feel inadequate or pressed to fit you in their lives.

It’s great to be loved.

I don’t mind listening to other’s ideas but that doesn’t mean they should get pushy! It must get tiring taking in a lot of information with a brain injury…
Love, cheers, HUGS! xo
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It is the making of migraines! Cheers,H
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