Please enlighten me
Tight-laced
joined 1 year ago
Plus people commuting less = less pollution and less congestion.
Good for people, good for the planet, bad for profit for some.
As the parent to a 5 year old, I feel this sooooo much.
I'm having to change my "just-a-second", as she takes it literally - a second is counted. I now say just-a-minute. Frozen got it bang on when Anna says "just give us a minute " and you can hear Olaf quietly start counting to 60.
The idea behind calling it CSAM is that "porn" has become synonymous with something desirable - foodporn, earthporn as examples.
Child porn needs to keep it's status as abhorrent, however the term is changing its nature (as language can).
This is it.
I've had an awful experience recently with an ex-friend, caught having an "affair" with his 16yr old employee. He's mid 40s. Turns out, the only illegal part is that there's pictures. He can fuck girls still at school legally, but he can't send her or request any pictures. It's insane.
Another layer is that the age of consent rises 18, but ONLY if you're in a school, healthcare, care-taking, Religion or sports club setting. According to the law, being her Boss doesn't mean he's in a Position of Trust or a Position of Authority over her. Yet, he plainly is.
Luxembourg has a gay Prime Minister. While not Head of State because Lux still has a King, he is rather up there in terms of practicality.
I'm on kbin, really hoping that the new Sync will work here. However, given the way Lemmy works, I believe that it won't really matter as its just another instance in the Federation
Google Maps is now showing me routes which will get me there in minus minutes. I'm intrigued.
Ask me a month ago and it would've been Reddit Sync.
Now - WhatsApp, kbin, YouTube
I hate to say it, but while hopeful, it's unlikely.
I've been around the CFS/ME community since my husband got it 6 years ago. There a small handful of people who have recovered, but generally they've been "misdiagnosed" with CFS and then correctly diagnosed/treated. The majority live with it for the rest of their lives. It's also why the life expectancy is only 50 - many simply cannot live with that level of pain/suffering day in, day out without any real hope of improvement/relief. Its a dreadful illness.
My husband has ME/CFS, like the Physics Girl. It's an absolutely devastating illness. He was a very active 35 when he was told there's no cure, not even a treatment, and that pain/fatigue was his life now for the rest of his days.
We've been around this long enough to see promising drug/cure/treatment/diagnostic tests come and disappear, month after month, year after year. The influx of funding/awareness linked to Long Covid is incredibly welcome, but many instances are repeats of previous ME/CFS research, so it holds up previous findings but doesnt drive anything forward. There's not been any real progress in the last 2 years, and the funding/focus is waning. I may be jaded, but hopes are low. I also sincerely hope I'm wrong.
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Thanks! Tried the Google reverse image search to no joy.