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stickmancomms.bsky.social
Stickman Communications
@stickmancomms.bsky.social
Stickmen helping to build understanding and acceptance of hidden disabilities and chronic illness, in a way that empowers us. (Run by Hannah Ensor - who has #hypermobility #PoTS and probably other stuff.) +talking about personal experience of #disability
I realised I'd to need a recharge afternoon following a longer-than-usual stint in the office. I filled a laminated 'recharging ladder' in for today to help me recharge more effectively.

The 'recharging ladder' is available here: www.stickmancommunications.co.uk/product-page...
November 27, 2025 at 5:09 PM
Excellent news! We are now shipping to the USA again! - Shipping prices are slightly up as we have to pay an additional fee and there's a maximum order value of £60 due to the tariffs, but at least we can ship there again!
November 26, 2025 at 5:21 PM
One hidden challenge of #AutonomicDysfunction is heat intolerance - the body can't cope with being too warm, and it causes all sorts of symptoms (for me: brain fog, coordination loss, speech and word finding difficulties, and reduced consciousness). It often catches me by surprise in winter. -
November 25, 2025 at 5:09 PM
Oh my. Just had an excellently productive zoom call....but it was nearly two hours and I forgot to move! OW! Totally didn't notice the pain during it. I don't when I'm concentrating. Now it's done...OW! I think in the future I might keep a copy of this on my laptop or desk as a reminder!
November 24, 2025 at 5:09 PM
I really do love spending time at events with a high proportion of autistic people! I always meet a few kindred spirits there. Sunday's Bicester Autism Craft Fair was, as usual, lovely. Exhausting, but lovely. I only took a few sample cards and the status squares, and a stack of leaflets though -
November 24, 2025 at 11:14 AM
At the Bicester autism craft fair - lovely stuff as usual. I have a massively paced down stall because it’s all I can manage at the mo - alongside my sister-in-law’s fab 3D creatures. Come visit at littlebury hotel, kings end, Bicester! 11-3pm.
November 23, 2025 at 11:06 AM
It's been a busy day - happy but busy. By midday I needed to rest- once relaxed I completely flolloped, couldn't face moving. Not quite asleep, not quite awake. 2 hours later I started to emerge, and by 4pm felt SO much better. Society mistakenly makes us think stepping back is a failure, but -
November 22, 2025 at 6:21 PM
Christmas decorations are up! And the rain. All the grey winter rain. I’m so thankful for the cosiness that brightens it! - I even quite like the rain when I can watch it from warm, dry, cosiness.

Also loving being able to see it from bed and living room! #studioFlat #disability
November 22, 2025 at 8:56 AM
Pavement parking is a real issue across the UK. People don't want to block the road, and so they park on the pavement. Which makes sense - until you realise that this usually means making the path so narrow it becomes impossible for wheelchair users and pushchairs to get past!
November 20, 2025 at 6:45 PM
My PA helped me give the floor in my room a proper clean for the first time since I moved in, and sort out a few more things into proper places. A tidy/clean space really does help me, especially when my fatigue Is high. So thankful.
November 19, 2025 at 4:25 PM
Although in some ways I'm very good at self management - I find I easily forget strategies if I don't use them for a while. And if I'm really stressed. Cards like these can give a much needed - and comforting - reminder of how to help myself.
I love this particular exercise for overwhelm and pain.
November 18, 2025 at 11:22 AM
One challenge of having a disability that means you sometimes struggle to speak, is that it also means you can't tell people when you can't speak!! I find these Status Squares so helpful in allowing me to let whoever I'm interacting with know - without needing to try and talk.
#Fatigue #Autism
November 17, 2025 at 7:45 PM
Spending time with someone else who also experiences brain-fog can be quite special. There's no need to explain. A look and a nod can be all that is needed. It's can still be very inconvenient- but it's met with a shared acknowledgement that this is a limitation that is part of our lives -
November 15, 2025 at 7:30 PM
I can’t believe how mild it’s been! Went out for a wheel this afternoon, and it was beautiful.
November 15, 2025 at 5:17 PM
We have many cards relevant to autism, all of them created because autistic people asked for them - and had a say in the design. Below are a few of them. Many more can be found on our website - 'browse by condition' - 'autism' section. www.stickmancommunications.co.uk/autism
November 14, 2025 at 6:45 PM
This is such an important concept for many of us disabled people: Sometimes we can do something - and other times we can't. We aren't lying or being dramatic, we genuinely sometimes can't. And, ironically, often the reason we can't do something now is *because* we did it before. For example,
November 13, 2025 at 7:58 PM
My current top pain management tool: mini heated blanket. I can apply it to the most achy/stiff/crampy part of me without overheating all over. And I don't have to keep reheating it in the microwave. What are your current top tools for managing pain?
November 12, 2025 at 8:15 PM
knowing I'm hypermobile, and that hormones have a big effect on symptoms means I now adjust my expectations and activities around periods - and it's massively helped my fatigue management and reduced the number of injuries I get.

(image from The Pocket Book of Pacing - a practical guide to pacing -
November 11, 2025 at 5:09 PM
Drafting a blog with tips on house-moving with fatigue, and wrote "Wholeheartedly having a couple of days of cosy is a much nicer experience than spending that time doing nothing while guilt-tripping myself for not doing what I can't!"
Yep. That's how to deal with a post-overdoing hang-over
November 11, 2025 at 4:59 PM
When #BrainFog hits and no matter how hard you concentrate you can't process what is being said, it can lead to all sorts of misunderstandings - ppl thinking we're lazy/selfish/not trying etc. Being able to explain what's going on is really helpful - for both sides of the conversation!
November 10, 2025 at 5:09 PM
to get food first, or drink". But it was absolutely fabulous that each time, my friend was able to recognise my look and say something like "Ok, shall we try it this way?" - so I just had to nod - rather than trying to force me to reach a decision then verbalise it.
November 9, 2025 at 5:09 PM
like on arrival, getting food and the like. It made SO much difference to me as a powerchair user - but also as someone who get's a lot of brain fog and difficulty finding words as my fatigue increases. By the middle of the evening I was struggling to answer simple questions like "do you want -
November 9, 2025 at 5:09 PM
I had an absolutely lovely time at my church's bonfire night yesterday - I'm an autumn-outdoorsy person so the time of year when it's getting colder, and the colours are golden, and you can sit by a fire is a time I love.
This year, I asked a friend if they'd be my assistant at certain points
November 9, 2025 at 5:09 PM
One of my key self-management tools is movement while 'sitting still'. Tensing and relaxing big muscles, and wiggling my feet helps get the circulation going and reduces my #PoTS symptoms, and gentle position changing using my core muscles reduces my back pain. It's easy for people to assume -
November 8, 2025 at 2:31 PM
It's easy to think 'my fatigue is less today, so I must now do *all the things*' - when in reality it's still having a big effect on my capacity. Pottering at low-brain tasks is something that I can do very nicely at particular fatigue levels - For me -
November 7, 2025 at 5:09 PM