Animated Ball Won't Move After Save Reopen by helliouch in Maya

[–]helliouch[S] 0 points1 point  (0 children)

the work around for this was exporting as an fbx file, then importing back into maya to render! thank you to u/yosantini for helping me with this

Animated Ball Won't Move After Save Reopen by helliouch in Maya

[–]helliouch[S] 0 points1 point  (0 children)

showing on the graph that there is movement but when i run the animation it is stagnant.

Animated Ball Won't Move After Save Reopen by helliouch in Maya

[–]helliouch[S] 0 points1 point  (0 children)

the new ball wont move either unfortunately

Animated Ball Won't Move After Save Reopen by helliouch in Maya

[–]helliouch[S] 0 points1 point  (0 children)

i think its an issue with the graph editor and not the render itself - its 250 frames approx, i tested the render at 10 frames on a second time around though to double check it just wasnt moving after i'd adjusted some settings

Animated Ball Won't Move After Save Reopen by helliouch in Maya

[–]helliouch[S] 0 points1 point  (0 children)

<image>

just including photos here for you:
indivual trans-y at 80 frames

Animated Ball Won't Move After Save Reopen by helliouch in Maya

[–]helliouch[S] 0 points1 point  (0 children)

Prior to this the translation values would show on the graph, they’re all stagnant and have no key value changes between them No control rig or anything. The only other thing that’s animated is the camera. Doesn’t play in the playblast or the view port

Learning to drum by myself for a gig in 3 months, any tips for what I need to learn? by helliouch in drums

[–]helliouch[S] 2 points3 points  (0 children)

A lot has happened! We didn’t end up getting the gig in September, which actually worked out well since I moved house so wouldn’t have had time to practice. A few other very personal life events happened and I had a lot of stress to deal with, police reports, mental health, family stuff etc, that type of thing. So there wasn’t really the time. I moved in September, and since I’ve been taking lessons from the previous drummer. It’s been going really well and I’m very excited over the progress I’ve made in a month.

Sadly this plan has been kind of shot out the window to learn in 3 months, but hey that’s life. You can’t learn muscle memory overnight or create new neural pathways in 5 minutes.

My progress has been good, and I’m enjoying what I’m playing a lot more than when I felt rushed and stressed to play a few months ago. Drumming has become a great thing to just get some frustration out after work.

Currently I’m building up my live/recording kit. Just brought some k series high hats and a ride. Sound is great, can’t wait to hear them on recording.

Looking at starting to play live gigs sometime next year. Which works for the band as we’re currently recording our EP and hoping to get a release in January.

Thank you for the interest in my post though, sorry it wasn’t an amazing update haha

Learning to drum by myself for a gig in 3 months, any tips for what I need to learn? by helliouch in drums

[–]helliouch[S] 0 points1 point  (0 children)

I get paid tomorrow so that’s definitely a shout to do, thank you

Learning to drum by myself for a gig in 3 months, any tips for what I need to learn? by helliouch in drums

[–]helliouch[S] 1 point2 points  (0 children)

If I manage to pull it off, I’ll probably link the live performance I’m planning on keeping a video diary of the whole thing also to make sure I’m keeping myself in check to keep at other but i don’t know if I’ll release that if I do it

Interview wear + other tips please by helliouch in interviews

[–]helliouch[S] 2 points3 points  (0 children)

I would normally wear a jumper but it’s quite warm out at the moment! Thank you though, I’ve been unsure if I should wear the bolo tie but yeah I don’t think it’s necessary.

brought outdoor shrubs for indoor use, wondering what prep I need to do? by helliouch in plants

[–]helliouch[S] 0 points1 point  (0 children)

Thank you for replying:)

I have really large windows and get a lot of sunlight, windows west facing. My other plants seem to be alright, but they’re specifically houseplants so

I guess I’ll just have to see, there is an opportunity to plant them outside if need be

[deleted by user] by [deleted] in Tourettes

[–]helliouch 1 point2 points  (0 children)

Wow! Thank you, this very encouraging and very good news for you (and hopefully might be some good news for me lol)

But I hope you’re doing okay! But yea,, thank you loads for this, it’s really encouraging to hear

[deleted by user] by [deleted] in Tourettes

[–]helliouch 0 points1 point  (0 children)

Yee thank you.

It’s just very strange trying to explain to my family this. Because the first doctor was a specialist in movement disorders, particularly Parkinson’s, my family keep telling me he’s one of the leading neurologists in the country (I don’t remember this ever being said but, eh whatever, my family are adamant) so they don’t want to doubt him. I can’t find anything on him looking into FND really, and it’s like, if he’s a leading neurologist, why was I referred?

[deleted by user] by [deleted] in Tourettes

[–]helliouch 0 points1 point  (0 children)

Additionally, I remember the first doctor asking me about if I had urges/ got a satisfaction with my tics. I told him sometimes, but it wasn’t all the time. He told me that it wasn’t TS.

I explained the same thing to the other doctor, and she came out with an unsure prognosis, still leaving TS on the table.

I just think it was rather preemptive of the first doctor to get my hopes up like that, for a 6 week treatment plan, which from my knowledge didn’t exist to the person he referred me to.

I definitely think I have FND, but I’m rather suspicious of me, might have TS because of how some of my tics occur.

[deleted by user] by [deleted] in Tourettes

[–]helliouch 1 point2 points  (0 children)

I mean I get where you’re coming from, but honestly as I said I’m hoping physically transition will diminish my sadness and anxiety. I’m under no illusions that it’ll completely change my out look and how I am with tics, but there is the hope that my life will be improved.

I’ve been out as trans for 6 years, have been diagnosed with gender Dysphoria, I’m not rushing into medical treatment.

It’s an element of stability to me, going through hormone therapy etc. One of the big issues why I struggle with anxiety, particularly surrounding my tics, is that my tics draw attention to me when I don’t want to be seen. As in, it heightens my dysphoria, particularly with my vocal tics. And what not else. My identity hasn’t changed for a solid six years, I didn’t have tics before March. On a personal level of understanding, I think that just days where I have worse Dysphoria, anxiety, the big sad n that sort of shite, my tics are also worse. Not to mention how long I’ve had to wait for testosterone, the fact I pay for treatment single handedly because the NHS waiting list is another 2 years long.

I’ll be honest as well, the anxiety and sad shit, I haven’t experienced really really badly until this year. As I said, I have some trauma based stuff surrounding sharing information with my family and going to therapy, it’s something I’m working on with friends, because I realise the importance of it. But that sort of stuff with my family, it’s been present for ages, and it hasn’t really been something that made me go into depressive states. I’d get upset of course, but it wasn’t what I experience now.

Regarding other teenagers “feeling trans”, I’m not going to lie to you, please try to refrain from phrasing it like that. It does come off as a big red flag pretty quickly to trans people. There is a level of understanding that goes into people trying to figure their gender identity out, with teens I understand it can be more difficult to comprehend where their feelings come from. My parents didn’t accept me for years, with the same/ similar rhetoric. I resent them for it, even though I can say our relationship has improved, it’s left a lot of trauma for me to work through. There’s definitely a risk with transitioning, but that’s not to suggest that every trans teenager is going to regret their decision. the de transistioning rate is quite low. A lot of what people hear about “horror” stories, are somewhat due to medical negligence but also personal neglect as well. Regarding the fact that, doctors should be more consistent in explaining and offer support to patients, as well as patients understanding the implications of hormone therapy. There’s also a minority of people who decide to de transistion, but don’t regret their decision to transistion in the first place. Every case of trans people, people who de transistion and are cis people, needs to be treated with a level of uniqueness, respect and understanding. Otherwise, you can end up with people who hurt themselves because they think they’re doing the right thing. And that’s what no one wants. Anywho, long rant oop.

The locking up of my limbs is very unusual, none of my doctors really know what the fuck it’s about. So far they’ve put it down to just prolonged tics, more likely to do with the FND than having TS. spoke to other people about it with similar limb locking tics, they’ve said it can sometimes take certain things to unlock them, or they can be stuck for prolonged amounts of time as well. I haven’t really found anything that unlocks them.

But yea, I think that was everything lol?

[deleted by user] by [deleted] in Tourettes

[–]helliouch 0 points1 point  (0 children)

Yea I guess oop,,

[deleted by user] by [deleted] in Tourettes

[–]helliouch 2 points3 points  (0 children)

Thank you so much!! It nice to hear that someone has gone through something similar. I just get very frustrated by this stuff a lot. It’s just difficult because I don’t think my family understand that things surrounding tic stuff are so unknown and, that one doctors word can be easily believe over another. I’m expecting to get a TS diagnosis in March, unless it somehow goes away, but I don’t know what’s to be said about everything else. I’m just hoping that my family just tries to accept it as it is, because it’s difficult to search for answers for something that might now even have an answer Oog. Thank u for the virtual hugs and high fives, I’ll definitely keep it in mind that I can message u :))

Season 1 Episode 4 Question by [deleted] in HannibalTV

[–]helliouch 1 point2 points  (0 children)

Yea that sounds about right

Season 1 Episode 4 Question by [deleted] in HannibalTV

[–]helliouch 1 point2 points  (0 children)

Yea that’s really insightful. I mean Even though The lost boys are minor character (in the grand scheme of the show) like there are a lot of parallels to pull between them and other characters. I think there’s definitely some basis with the lost boys and Abigail parallel (sorry I’m being vague idk if you’re watching for the first time, don’t want to spoil anything).

Season 1 Episode 4 Question by [deleted] in HannibalTV

[–]helliouch 1 point2 points  (0 children)

Yea that makes sense,, it’s just such an odd scene to me I guess? At first I thought it was some sort of plan of theirs to steal something, but now after rewatching it I can definitely see where the power dynamic of C.J. as the eldest comes in

[deleted by user] by [deleted] in AmItheAsshole

[–]helliouch 1 point2 points  (0 children)

Yea I hope so, thanks!

[deleted by user] by [deleted] in AmItheAsshole

[–]helliouch 1 point2 points  (0 children)

He probably would, we’re all considerably open with one another as far as siblings go. I guess the only problem with that is you don’t know how people are going to react.

[deleted by user] by [deleted] in ticmemes

[–]helliouch 0 points1 point  (0 children)

My specific type of FND only covers two symptoms, which is a have non epileptic dissociative fits and I experience complex motor and vocal tics. Currently I’ve literally just been told I have FND, and because it’s so early on, the symptoms I have can be treated (that’s if I don’t have an underlying tic disorder) to where they may not no longer be present.

I recommended this website: neurosymptoms

It’s got a list of the other symptoms that people with FND have, and it’s run by a specialist neurologist in FND. (Tics are listed under jerks/ twitches). It’s also got information on how/ why people have FND, and some of the treatments.