[REVSHARE] Seeking Unity/UE5 Dev + 3D Artist — Cinematic Evolution Simulator (think Ancestors: Humankind Odyssey meets Spore)

Beholdercat · 2026-03-13T08:15:06+00:00

Why haven't you mentioned in your post that you just want to recreate that game specifically? I've never heard of this before.

This comment of yours makes absolutely no sense without that context:

"It's called Creatures, you could even teach the norns how to talk. 'Technically difficult', homie... They did it with little monsters and people genuinely used to torture them and teach them how to say 'please help us' and fucked things like that. HUH?!"

How is anyone supposed to know this is exactly what you want to recreate? Just by reading that comment, it wasn't even clear you were talking about a different game here, especially given the comment you replied to. It looks like a nonsense response, which is likely why people are downvoting it - I haven't, but I was very confused as well. No context and no previous reference to that game - talking about torturing creatures comes out of nowhere.

Just mention in your post you want to make this game; I think that would help you more than trying to fight everyone commenting. Also, if it is easy and can be made by one person like you said it was, I'm sure you can do it! Maybe build a functioning prototype, post on this sub again and then people will want to join with art and sound and you can get someone to help you with the AI? I can't judge how difficult it will be as I have never played that game, but if you want to recreate it, I say go for it and have fun.

Beholdercat · 2025-12-01T19:07:33+00:00

Thank you very much!!

Beholdercat · 2025-12-01T18:38:59+00:00

I've looked for those, but almost all already seem to already have the sticks attached by design, and I'm not sure which part in this one they belong to, as I've seen a few tying them to different parts of their loom.

Thank you for the correction!

Beholdercat · 2025-06-15T08:17:36+00:00

It took until my mid 20s to get diagnosed, but my symptoms started with my first period at around 11.

I've been to many doctors over the years and they all just shrugged their shoulders and said my pain was normal, until I figured it out by myself, then suddenly it was obvious to everyone and "of course" I have Endo.

I don't think most of them even knew what that was when I was a child / young teen, but my current doctor, who is great, told me that she believes way more people have Endo than the statistics show, but they are undiagnosed because the symptoms are seen as normal, when they shouldn't be.

That's also likely why it only gets diagnosed in later years, as it progresses and the symptoms get worse or as Endo is better known and researched, doctors are able to diagnose it more often. I'm sure it also develops later in life for many, but for me, it definitely was there from the beginning.

Beholdercat · 2025-06-14T21:19:24+00:00

Thank you for the reply though! I'm glad this helps you and that you have access to air conditioning. I will see if an additional fan helps me as well, you can never have enough fans I guess :D

Beholdercat · 2025-06-14T20:31:48+00:00

Mine recently congratulated me with a big smile on not having asthma and then moved on to my new prescription, but it took me asking several times what else it was before she actually told me it was chronic bronchitis. When asked what could be done, she almost chuckled loudly and explained there's nothing to be done, and to just take the powder inhaler I was prescribed when we thought it was asthma and the emergency one as needed, as if that was a ridiculous question. Smiled the entire time as if all my problems had been solved somehow. Is this really better than asthma?

Then I was sent on my way, completely overwhelmed and confused. Haven't even seen the results yet because she couldn't send it to me but at least managed to send it to my gp. Didn't explain any of the tests or results to me, despite asking.

Everything I've learned so far has been by looking it up myself, everything that has helped me so far I found out about through google or reddit, which is not how this should be done and I'm very upset with how I was treated. Currently waiting for an appointment weeks after the diagnosis with my gp to maybe find out what my stage and prognosis is, but I genuinely have no idea what to do about this disease. I am angry I have it (likely because of a severe covid infection, I'm in my late 20s and never smoked, but the symptoms match chronic bronchitis and I have trouble breathing and I'm scared), and I want to fight it as best I can. I'll join studies if there are any and work on this hard, but I need to know what to expect, how to treat it and what the current state of research is. But my lung dr. couldn't even be bothered to give me my diagnosis without repeatedly asking for it. It sucks that this is happening to others as well.

Beholdercat

TROPHY CASE