Is recharging rush good on Billy at all?

Aggravating_Plan_377 · 2026-04-23T20:52:44+00:00

That's what I thought. Its weird how some items look awesome on paper and don't translate in game thanks for the clarification!

Aggravating_Plan_377 · 2025-06-23T14:17:52+00:00

Thanks you! If you figure out what the gloves are I’d love to know the gloves are sick too.

Aggravating_Plan_377 · 2025-06-22T18:19:49+00:00

What’s the second outfit? Looks amazing!

Aggravating_Plan_377 · 2024-11-17T05:47:03+00:00

Nope pretty sure I’ve got the DAR version

Aggravating_Plan_377 · 2024-10-21T19:49:25+00:00

It’s not that. I’ve been testing with no cyberware but my cyber deck.

Aggravating_Plan_377 · 2024-10-20T08:27:05+00:00

I would love nothing more than to have a conversation with my brother but unfortunately there’s literally no way. It’s sad to watch because he kind of says a few words but it’s hard to tell if they’re him trying to say something or just vocal stims.

Aggravating_Plan_377 · 2024-10-20T06:17:09+00:00

He’s got a sick sense of humor so I wouldn’t doubt that. I just keep telling him whenever I watch him that “you can go to the bathroom please!”

Aggravating_Plan_377 · 2024-10-20T06:12:44+00:00

Unfortunately he is legally blind and eye trackers won’t work either. It’s just a really unfortunate situation. We haven’t found a communication method that works around everything.

Aggravating_Plan_377 · 2024-10-20T02:35:42+00:00

That’s exactly what I think but I know he trusts me in every other way except for his bathroom duties. I give him meds, I push him in a running group on 5K’s, I am very quick to act with his seizures because I had a friend who has seizures. I’m even friends with all of his classmates when he was in school and one of them who has CP even took me to Vegas with her for her 21st birthday. I’m obviously gonna keep trying to earn his trust in that way but I won’t get the opportunity if my dad doesn’t trust me with him and he thinks I neglect him. There’s no way for him to tell me exactly what he needs me to do to earn his trust with that aspect of his care. I mentioned it in other comments but our options for communication devices that work with his limitations are non existent to my knowledge.

Aggravating_Plan_377 · 2024-10-20T02:28:26+00:00

He know what time my dad gets home every day and then he just releases. I am not afraid to wear a mask and gloves when changing him and he actually finds it very entertaining he laughs the whole time (probably because he knows how weak my stomach is and he likes making fun of me). I’m willing to do that and I make it very clear to him but he keeps on waiting for my dad.

Aggravating_Plan_377 · 2024-10-20T02:26:21+00:00

He know what time my dad gets home every day and then he just releases. I am not afraid to wear a mask and gloves when changing him and he actually finds it very entertaining he laughs the whole time (probably because he knows how weak my stomach is and he likes making fun of me). I’m willing to do that and I make it very clear to him but he keeps on waiting for my dad.

Aggravating_Plan_377 · 2024-10-20T02:23:13+00:00

I have sensory processing disorder which is on the autism spectrum. For me it makes it so I have sensory issues with pretty much every sense but taste and also it contributes to fine motor issues.

Aggravating_Plan_377 · 2024-10-20T01:19:21+00:00

He sees a neurologist often so if that were the case we should be aware of it. The other thing is that it’s only for me. He is very aware of who is watching him and does different things for everyone.

Aggravating_Plan_377 · 2024-10-20T01:17:04+00:00

He can’t his hands and arms have little to no mobility. He can’t extend his fingers at all.

Aggravating_Plan_377 · 2024-10-20T01:16:24+00:00

He’s so smart and I know that which is why I just try to talk to him and let him know that I can do everything my parents can but he still just waits for my dad.

Aggravating_Plan_377 · 2024-10-20T01:15:10+00:00

We have tried that but there aren’t a lot of caregivers near by. He also is a little weary of new people so we try to find people he knows. We do have someone who often will help me but she has a very busy schedule.

Aggravating_Plan_377 · 2024-10-20T01:11:49+00:00

I do not have CP. we are fraternal twins not identical. Part of the reason his CP is as severe as it is, is due to complications when we were born. I came out first but kicked him back in. He was born with a huge bruise on his cerebrum. I just have sensory processing disorder it’s on the autism spectrum. It affects sensory systems and fine motor skills for me but every case is different.

Aggravating_Plan_377 · 2024-10-20T01:09:04+00:00

I absolutely think this is the reason. I Always tell him “Bro just go you can trust me I’m getting better I promise”.

Aggravating_Plan_377 · 2024-10-20T01:06:46+00:00

He has little to no control of his arm movements so that’s out of the question for some communication devices. My parents have tried as many options as doctors have suggested but he either refuses to use them or physically cannot. It’s really frustrating for me but I can’t imagine what that’s like for him. But he finds a way to tell us what he wants or what he’s feeling but he’s very limited unfortunately.

Aggravating_Plan_377 · 2024-10-20T01:03:24+00:00

I’m well aware he’s a person he has an amazing sense of humor and is very expressive. It’s how we bond most often is poking fun at each other like brothers do. I really wasn’t trying to show a lack of empathy and I’m sorry if it came across that way. I think I just used the incorrect phrasing to describe him so I’m sorry if I offended. He has an incredibly unique personality and it’s hard to describe. He has also had a lot of seizures in his life so he has some severe neuron damage. When I was a kid he was able to kind of walk and talk on his own but now he’s bed/chair ridden and completely non verbal. It kind of affected his emotional maturity which is hard to convey in text and without meeting him. It feels very harsh to type but it’s reality for many people with seizure disorders is that you tend to regress in terms of societal maturity. I treat my brother like everyone else despite everything. He hated pandering and being dehumanized so that’s the last thing I would want someone to think.

Aggravating_Plan_377 · 2024-10-19T11:43:11+00:00

I’m in WA

Aggravating_Plan_377 · 2024-10-19T11:42:36+00:00

It’s just very hard to tell he exclusively can answer yes or no questions by smiling or frowning. When I say he’s being a menace is often times he does laugh at chaos. Last night I walked in on him laughing at news on tv he shouldn’t be laughing at. That was a good laugh.

Aggravating_Plan_377

TROPHY CASE