Margo
@mserenity.bsky.social
1.2K followers 1.1K following 4.1K posts
Disabled fibre crafter and chronic illness advocate. #WrexhamAFC
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Sadly I can't do markets because of my own disabilities, I struggle to even attend them. (The last time I tried I was uninvited because they wanted to have wax melt and scented candle sellers instead.) But if they decide to have a raffle at that I'll send them something. 🙂
Wow that is horrible. It seems like there should be rent controls on such vital community organisations. Between the rent and NI increases it's just non stop. 😢 If they're doing any raffles I can contribute some handspun wool.
This is sad to see. Services like this receive constant referrals from the local authority - they need consistent funding to survive!
Yeah, I definitely will be! And possibly head to a pub to watch the second half. 🙂
I can't help but wonder if the flu and covid wave everywhere is impacting the team too, so many of them have young kids in nursery and school. I just hope Wednesday is better, but I'll be across the Uni at the comedy festival that night (booked before matches were out).
Would be worth contacting ifollow for a refund imo. You're not getting the service paid for on these matches.

I had my ears injured by the audio problems earlier in the season so I am glad they are replacing the equipment!
It's £4.50/mo for the audio, but it's more the principle than cost. (have sky for the broadcast matches) I understand why the 3pm blackout exists, but with a team that consistently sells out and that I can't physically watch in person - it's frustrating to say the least.
I think I've read elsewhere that BBC radio Wales announces are Cardiff fans... Between the tone of their voice and the attitude, just a no for me.
All 3pm Saturday matches are blacked out here, but it's usually slightly better with Mark's audio (when it works).
Mrrr. We can't watch the match *and* don't get our comms team? I can't handle the BBC Wales commentary, it's putting me to sleep. I hope our boys put in a good performance, I'll have to keep up with the text updates. #AskWxm
Reposted by Margo
Hi, all!

A small group of people with long COVID is hosting a virtual rally on Saturday at 2:30 pm Pacific. We recognize that not everyone is able to participate in person, so we started hosting protests online in April.

You can read more here:

www.motherjones.com/politics/202...
1/9
For some disabled protestors, “Hands Off” went virtual
"We know we have to teach everyone how to include us."
www.motherjones.com
Have to sleep on old mattress in the living room until new bed is aired out enough, cat made her displeasure known by leaving me the biggest poo on the mat outside her litter box (in same room) at 4am. Not a fun way to wake up!
And with upfront payments you don't get back for the cars and adaptations! The right wing hates the scheme, but it's the only way many disabled people can access cars and it is *not* a good value for them, just essential.
Yeah, it definitely will be worth it because the current one is broken 😂 and then when tradespeople come around they confirm much wasn't installed to code. But the house price kinda reflected that, we haven't decorated yet knowing the funds had to go to other things.
Thanks :) my hairdresser does a great job with it!
This is her etsy 🙂 she runs sales occasionally too! www.etsy.com/uk/shop/soph...
www.etsy.com
Has lots of storage space underneath too! We didn't get a bed frame for it which was definitely a good idea given the fact my room is also my fibre studio space, and the bed cost enough as it was!
It's new bed day and almost match day, so wearing my cute Sophie Nina (Wrexham artist and Creu shop owner) dungarees. 🙂 Hard to believe how comfy the bed is, just have to wait for it to air out for a few days to be able to use it.
You heading to Stoke tomorrow? This is busy Friday here, can't wait for the work to finally start on our new shower. Only a couple more decisions to make!
Very well written thread about life with ME (and many of us with long covid have ME). The degrees of hot garbage comment resonates a lot, even feeling slightly less bad is a win.
Brutal truth: having a relationship with a person with ME requires a paradigm shift.

- we will not meet you halfway, bc we can’t. I give what I can, when I can, and the other party must close the gap. It’s unfair and obnoxious.

- we will often not back up our words with actions. Ex: I care
😂😂 They're a pretty big bathroom supplier but that was also my first thought!
R&F have a few fabrics but their stretch twill is so comfortable! Definitely need a second layer when it's cold but I love my trousers from them.
GP tried getting me pushed up the NHS waiting list for neurology, but without a way to get to Liverpool I'm out of luck. At least 20 weeks to go. 😢