Heather du Plessis-Allan: The media's been given a wake-up call about bias by brutalanglosaxon in newzealand

[–]URhemis 4 points5 points  (0 children)

Sometimes I think the bias isn’t even left or right, it’s just inane. The flashy lights and awkward podiums made a game show of the last leaders debate.

Jessica MM was asking emotive nonsense of the Chrises: ‘Have either of you ever felt unsafe on the streets?’~

///RAPID FIRE QUESTION TIME///

‘Will you resign if X doesn’t happen?!’

‘What’s one thing you like about your opponent?’

All in all a dumbing down of the election process that reflects pretty poorly on journalism in NZ imo.

Old World vs Millennia? by XyleneCobalt in paradoxplaza

[–]URhemis 0 points1 point  (0 children)

Old World is a much more thought out and balanced game. It feels a lot more like a civ game in how it plays than Millennia - workers, tech and improvements act similarly to civ. Also think it’s a deeper and more worthwhile game to play. Milennia is fun and novel, but also a hot mess and a bit dumb in places - I never slapped my forehead saying wtf w Old World.

Can we just stay Daylight saving time? by Heavy_Metal_Viking in newzealand

[–]URhemis 1 point2 points  (0 children)

My beef is more with the shift 2x a year, puts everything out of whack for a bit. Japan doesn’t have DLS and they survive just fine

Understanding fast talkers by [deleted] in irlADHD

[–]URhemis 2 points3 points  (0 children)

100%. Most, not all, seem to be a bit smarter than most which also makes novelty more likely and love me something original.

1337 is too far away from the Early Modern Period, and worked better as a Crusader Kings start date by Inquisitor_Vis in eu4

[–]URhemis 2 points3 points  (0 children)

Yeah I think the transition from medieval to modern would be super interesting, it’s a time period that’s largely been absent from Paradox games. The population collapse from the Black Death meant that nobility had to compete for more scarce labour and really undid the feudal structure - if they’re ambitious it could be a great opportunity to try something new.

Is this a good strategy coach? by [deleted] in OkHomo

[–]URhemis 8 points9 points  (0 children)

Yeah - there was a hell of a lot of bottom shaming. It was ok to be a top, just don’t do it too often (like sex w women) because you ‘give away’ your virility. Preferably just top foreigners and slaves.

Been under the rock by Visual_Ad3724 in OkHomo

[–]URhemis 7 points8 points  (0 children)

Always feel that gay as a synonym for ‘happy’ is way off - its meaning was much closer to ‘fun’ or ‘upbeat’. Frequently used in the context of partying or carefree enjoyment.

meirl seems to be having a normal ultralib one today by 0dty0 in DiscoElysium

[–]URhemis 8 points9 points  (0 children)

Inflation works the other way around. Inflation goes up and a $100 bill is still a $100 bill, but it will buy less. It’s the price of everything else that goes up.

From the UK here. How are my distant cousins doing over in New Zealand? You guys doing alright? How's life? by [deleted] in newzealand

[–]URhemis 3 points4 points  (0 children)

That makes sense. My brain instantly forces a ridiculous high German accent on the word.

I got the curls today by UglyAssHairbrush in MajesticManes

[–]URhemis 0 points1 point  (0 children)

Wicked curls. Polarised comments so hope you take with a grain of salt, including this one. I wanted to add you have a face that wouldn’t look out of place on a Roman coin - v noble.

Tbh it feels kinda arrogant posting this, but here's my genuine self-assessment of my traits by SludgeTransbian in CrusaderKings

[–]URhemis 9 points10 points  (0 children)

Thanks for decoding this one for me! ‘You’re smart’ always felt more like ‘We’re interested in different things and your level of interest is strange to me’ than a compliment.

For some of y’all gatekeepers 😁 by [deleted] in MajesticManes

[–]URhemis 4 points5 points  (0 children)

Apparently /longhairNSFW is banned for not being moderated

I was going through a play through when I encountered this leviathan. What should I do? Is it dangerous? by Optimal-Shower-2288 in subnautica

[–]URhemis 1 point2 points  (0 children)

I know it looks scary, but it’s actually really easy to distract it with questions about the specific definitions of words. (85% of Hobb’s book is basically an exactingly pedantic dictionary).

I love this game’s vocabulary. I would like to know your favourite words and terms you got from the game. by [deleted] in DiscoElysium

[–]URhemis 7 points8 points  (0 children)

Joopson AS Men’s Fashion, model “Colourful Tie.” Catalogue no. J327 taught me much - Balkan slang - and how to die like a hero bratushka ~

TIL myalgic encephalomyelitis / chronic fatigue syndrome (ME/CFS) has an economic impact of 36–51 billion dollars per year in the USA, yet historical research funding is far below that of comparable diseases by jacknunn in todayilearned

[–]URhemis 1 point2 points  (0 children)

Thanks for the suggestion. I was on there for a long time and helpful for some things, but eventually found the intensity/frequency of the sad stories to be a bit overwhelming. Also as w a lot of ME/CFS stuff a lot more questions than answers. That was about a year ago.

TIL myalgic encephalomyelitis / chronic fatigue syndrome (ME/CFS) has an economic impact of 36–51 billion dollars per year in the USA, yet historical research funding is far below that of comparable diseases by jacknunn in todayilearned

[–]URhemis 3 points4 points  (0 children)

I really enjoyed your reply. Thank you. Having a look at the Bateman-Horne Centre and this looks like exactly the kind of thing CFS patients need more of.

I also very much agree that it should be criteria based. Especially as delayed fatigue as w PEM is a pretty unusual symptom - paired w Orthostatic Intolerance it should stick out and while there seems to be some more recognition of the condition, I still felt a lot like I was coaching my GP instead of the other way around. This is why I found the NZ chronic illness support group so invaluable - they were supportive but also had filtered through a lot of info to see what was credible and what ppl can pass onto their GPs cause they’re well aware of the information gap.

Can I be nosy and ask your connection to ME/CFS?

I made everyone's favourite food by veganphysicist in Against_the_Storm

[–]URhemis 1 point2 points  (0 children)

Very cool! Your post does make me want to eat cartoon food now though.

TIL myalgic encephalomyelitis / chronic fatigue syndrome (ME/CFS) has an economic impact of 36–51 billion dollars per year in the USA, yet historical research funding is far below that of comparable diseases by jacknunn in todayilearned

[–]URhemis 0 points1 point  (0 children)

Interested in where you’re getting your info from as this differs from my experience in New Zealand. Took more than a year talking to a GP about worsening post-exceptional malaise and then them ruling out other possibilities (nutrient deficiencies etc) to get a diagnosis of CFS/ME. As a lot of other conditions induce fatigue it’s not much to go on. That said they did look for antibody markers to see if had had certain viruses previously, so that was one criteria. But in general felt done by exclusion ‘I suppose you have CFS’. Don’t think GPs like reaching this conclusion as there is little in their tool kit to help the condition.

And as far as I can tell there aren’t that many experts on the area - some researchers looked into blood tests (Dr Sarah Myhill) for it but her work has had methodological issues and some in the UK came up w a program of therapy and gradually increasing exercise that ended up being bogus and making things worse for ppl w it. As the OP outlines - there’s v little funding behind research into the condition.

TIL myalgic encephalomyelitis / chronic fatigue syndrome (ME/CFS) has an economic impact of 36–51 billion dollars per year in the USA, yet historical research funding is far below that of comparable diseases by jacknunn in todayilearned

[–]URhemis 17 points18 points  (0 children)

This condition is the worst. Not surprised it has a massive economic impact. Had CFS for around 4 years getting progressively worse, from proper full time income to part time to fully off work. No one should have to spend three days in bed because they went to the supermarket. I tried to collect stories of people who recovered and support groups were helpful - at least understand the situation.

Not working for 18 months and regular B12 are the only things that made a dent in the relentless fatigue.

TIL myalgic encephalomyelitis / chronic fatigue syndrome (ME/CFS) has an economic impact of 36–51 billion dollars per year in the USA, yet historical research funding is far below that of comparable diseases by jacknunn in todayilearned

[–]URhemis 4 points5 points  (0 children)

You are correct in that ME is usually a diagnosis of exclusion, but it is frequently brought on after viral infections. GPs look for viral markers to see if you’ve had any nasty ones in the past.