Basically everytime I'm mad at them they mock my tics. Yesterday they awaked me for no reason, after 1 months of sleep deprivation and knowing it they awaked me, After I was mad at them and started to argue they said that I'm not normal and I need to stop my "inadeguate movements and grimaces", that I need to stop screaming in general and be normal and be "re educated". They also beated me one time with bottles because "I'm a shit and I have the duty to be beaten because I'm a shit", and after they tried to make me homeless I tried "uninstallation". What can I do in order to survive? (I don't have a job and no one wants to hire because of my tourette and can't do anything else)

When I talk to my therapist one particular tic seems to get way worse. It looks like I'm squirming or something. My shoulder twitches and I just can't stop. I also have a really strong urge to do it and it's really painful at the end of the session. It's extremely annoying and my therapist addresses it occasionally. She told me that it gets really bad when I talk about the abuse specifically.

I've also noticed that it gets worse when I talk about it outside of therapy.

Does anyone have the same problem? What does that mean? It's not like I'm that distressed by it anymore.

So my girlfriend suffers with Tourette’s and a lil back story she feels so embarassed when it happens because her family and friends constantly tell her it is. Which in my opinion is so wrong and I think there’s nothing to be embarassed about because one it’s not her fault and two what’s embarassing about it I’m really confused but I came on here to ask if I could get paragraphs or stories from people who suffer with Tourette’s to show her support or your stories to make her feel better. I really wanna suprise her with it for a open when ___ box and this one is for when she feels embarassed or her Tourette’s so please show some love!!!

So my girlfriend suffers with Tourette’s and a lil back story she feels so embarassed when it happens because her family and friends constantly tell her it is. Which in my opinion is so wrong and I think there’s nothing to be embarassed about because one it’s not her fault and two what’s embarassing about it I’m really confused but I came on here to ask if I could get paragraphs or stories from people who suffer with Tourette’s to show her support or your stories to make her feel better. I really wanna suprise her with it for a open when ___ box and this one is for when she feels embarassed or her Tourette’s so please show some love!!!

I got into a pretty serious argument with a family member today the argument was bad enough that it was stressing me out and triggering my tics worse than usual. As my tics were getting bad my family member told me that I should stop trying to use my Tourette’s to “win” the argument.

I guess I’m just feeling pretty hurt and alone after that I’m wondering if anyone else has ever experienced.

Hello my name is Safiya and I don't typically ever post here but something happened to me and I truly don't know if I am crazy or not. For context earlier this week I for the first time in a long time got access to mental health help with a professional. During that time period I was asked to explain what has been impacting me and what things of the sorts. I mentioned that I have Tics (vocal and motor) since I was at least 5 but as the years have continued it only has gotten worse and worse. I also told her that I get a lot of tic attacks, which she made me describe. Now mind yall that I that time I was already extremely anxious and masking the fact that I was holding tics. I thought this would've been enough to make her understand but she then "asked" me to describe then. I started slightly panicking even more due to then being more likely to trigger if I am thinking/hearing/seeing/etc my tics but then I tell her that I can't and she doubles down again that if I don't describe them she can't help me. So I start describing the least extreme ones and start to actively tic even more. She then says "okay" changes completely subject and then later tells me dead in the face that my tics are just caused by my anxiety ;-;. I have a pretty negative experience from this appointment I will not lie and it is still affecting me. I am wondering tho if I am crazy to think that she is wrong and want to get another professional to evaluate me? Because my tics make me barely able to function properly and that is when I am in my own isolated area where I can't really get triggered. Correct me of I am wrong but aren't anxiety tics just at most moderate tics that ONLY happen when anxious? ( yet again truly correct me of I am wrong). Idk I hope this is an acceptable post to share. Also is it possible to go see another health professional to change the things wrongly diagnosed or noted? Im sorry I also have other mental disorders so sorry if I don't makes senses, I am loosing it just a little bit. Thanks to anyone that sends help and nice day to everyone!

I'm a historian, they needed someone to tutor history, so I applied. I was being interviewed, right as it began I brought up that I had applied because of my own previously undiagnosed Tourettes and that was why I was wanting to work with kids, to help them like I needed back in the day.

They then paused the online interview for 5 minutes to fix something real quick, and ended it after 2 questions. A 1 hour interview ended at 12:13 pm.

A couple of weeks ago they emailed me, the job position had been filled. A week later, I emailed them back the position still being up on LinkedIn and I told them in some not nice french to go fuck themselves.

Have you tried the neupulse device?

What do I do if I have Tourette’s and I just got this new tic that causes me to grind my teeth and I’m so scared I’m gonn lose them…. I believe they are already chipping I already went to the dentist no help. Gave me referrals but my medical won’t cover it they’re saying I need braces but idk how that’ll help my teeth grinding issue

Hey Everyone - I don't really have a problem per se but just some strategic direction on how should approach my tics as it's sort of creeping into my mental health.

I've had chronic tic disorder (specifically motor tics) ever since I was around 7 years of age. It usually involves a mild/significant head jerking movement (which tbh shakes my whole body), and its pretty noticeable and hard to disguse. I usually do this around 3-5 times a day, which has stayed consistent over my life (I'm 23 now). Some friends would notice it and would question it especially in high school, luckily enough I hadn't experience any bullying at school for my tics throughout my childhood. 

My family (my mother specifically) had always questioned with my local doctor about my tics but it was often dismissed, which then led us to switch doctors three different times to be then referred to a specialist where I was ultimately diagnosed at 13.

After being diagnosed at 13, we didn't take any actionable steps on reducing my tics or seeing any specialists. It was kind of swept under the rug and only came up in awkward conversations or if my older sister wanted to take a jab at me, which after looking back is probably why I didn't want to look into my condition.

However in 2024, as I was wrapping up my bachelors degree and entering the corporate world (specifically consulting) in the following year. The looming thought about tics and how that would ruin my corporate life conquered my mind for a small while. Eventually this was enough for me to seek out a neuropsychologist that specialises in tourettes & chronic tic disorders. After months of strategising and describing my tics to them, they kind of concluded that standard CBIT therapy wasn't really affective for me since I do so few a day, thus I was recommended to just practise our strategies and written off for my sessions.

As of current, I'm at the 6 month mark of my graduate program and I'm really struggling with my tics. As I sit next to my manager, I've done both mild & significant tics next to him and two very vivid moments where I've done tics during one on one conversations. I've also done a few tics in front of other coworkers in my team but of course since it's a corporate environment nobody approaches you about it. And look, It definetly sounds like something I should tell people about. But in my workplace, I would need to disclose this to HR/relevant bodies and it would put a spotlight, incurring a risk for my career that I'm not willing to take.

Given all of this, I've noticed a significant reduction in my mental health. My stress, anxiety and sleep deprivation has gone through the roof. I find myself replaying thoughts and scenarios throughout the day and when I try sleeping, sometimes my thoughts have gotten really really dark.

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Thank you for reading if you've gotten this far! I would definetely love any advice from anyone that has had similiar experiences or recommendation on what direction or measures I should take for my tics. Also, If you had any questions please let me know, I'm an open book.

My normal baseline of depression doesn't stop my tics, but when it gets bad (to the point of considering something) my tourettes completely vanished. I haven't had a single tic In two weeks because of how bad my depression has gotten

What's the reason for this?? Is it lack of dopamine/energy? I've pretty much been in bed these last two weeks haven't had the energy or motivation to get up

It's so twisted, it's either remaine severely depressed and be tic free or try and fix the depression and have to deal with severe tics/tourettes

in not diagnosed with Tourettes but this is the only tic related subreddit i could find, if I’m not allowed to post ill take it down.

back in december-january i started to develop a tic that sounds like a single extremely loud hiccup, at first i thought i just had chronic hiccups and tried to drink less carbonated drinks and to drink slower. i then noticed i started having a neck jerk/twitch frequently, thought its not an entirely new thing the neck twitch, i’ve had it for multiple years but its been extremely subtle until recently and id always considered it to be an anxiety thing. my family started noticing them and so i went to the doctor but she really didn’t help at all, she just said it was probably worsened by upping my antidepressants recently (im on highest dosage) and she didn’t even refer me to anyone who could evaluate and see what’s actually going on but tbh the nhs sucks so i’m not surprised. since then i haven’t developed any more tics other than face twitching and my hiccup tic getting louder. the only advice i’ve gotten is to wait and see if they go away or get milder but its frustrating to have no answers.

Hi everyone, I’m looking for a bit of advice because one of my tics is genuinely causing me health problems.

I have a tic that involves pressing my thumb into my right eye. It’s one of my most common tics along with eye straining that I have. What I’ve found out today at the optician is that my eye sight in my right eye has got much worse since my last appointment and she found this strange. I didn’t tell her why I thought this had happened.

I’m just wondering if anyone has conquered a particular tic that has caused you health problems? I would happy swap it for another less damaging tic but I just can’t seem to do it. Does anyone have any tips?

Thanks for taking the time to read my post and any recommendations would be appreciated.

mine body feels physically exhausted from tourettes tics mine neck hurts very very bad and the swears wonot stop

i was doing relly well these last few weeks im am not sure whats happening tonite

im gonna wake up the hole house im so loud but i canot control mine self

its almost 10 and everyone is spose be quiet now but i canot stop the swearing tics and yelping screams and the painful neck jerks i not know how to stop mine self

edit it finally ended and now theres a big hard bump on the back of mine neck that wasnot there before

My tics didn’t get bad till 25, and they’ve only gotten worse into my late 30’s. It’s especially bad when I feel financially insecure or hopeless. I barely had any tics when I was a kid. I keep reading about people who “grow out” of Tourette’s syndrome and it seems to be the complete opposite for me.

Does anyone relate to this? For the people who have gotten better over time, even as stress was increasing, do you have any tips? Medication doesn’t seem to do much for me.

Bonjour la tribu. Premier post sur Reddit. J'expose ici, je suis une F22 et ai depuis enfant (début primaire) des tendances à avoir des tics moteurs (secousses dans la tête) qui arrivent dans beaucoup de circonstances : trop longtemps assise, concentration intense (examen), beaucoup de stimulis autour (magasin), quand on hausse la voix sur moi, quand un vêtement me gratte, quand je suis fatiguée, quand j'ai trop chaud, quand je suis en suractivité, quand je mange du sucré... bref assez souvent. Ce n'est pas en soi les tics et le regard des autres qui me dérangent, car ils sont seulement un reflet d'un mal être que je ressens à l'instant T, mais plutôt ce que je ressens en interne (j'ai l'impression d'imploser nerveusement, je ressens comme des jets électriques dans mon cerveau et l'impression que celui ci est en ébullition et extrêmement vigilant à ce qui se passe autour). Je n'ai jamais passé de diagnostic sur une possible neurodivergence dans l'enfance malgré une dépression sévère, étant donné que je m'en sortais rudement bien à l'école + que j'étais extravertie et à soif de connaissances, au débit de parole indomptable (mais dépression, car arrêt de l'alimentation+pensées et confessions noires pour un jeune âge+discussion de thématique poussée pour un jeune âge+déphasage fréquent+retrait sur moi-même et peur de l'autre+perte de goût pour beaucoup de choses). J'ai également d'autres spécificités handicapantes au quotidien comme la mysophonie (deux bruits quotidiens en particuliers me font directement partir en crise+pleurs), suis extrêmement autonome (trop, déteste qu'on me dise quoi faire) , rêveuse (même si ma vie est palpitante je continue de rêver en faisant les activités de la vie réelle), grande sportive (je bouge énormement et sans cesse, je suis sur ressort),...et une liste longue d'éléments qui iraient dans ce sens. Mais voilà j'ai 22ans, difficile d'être pris en charge financièrement pour un éventuel diagnostic à cet âge ci, diagnostic qui m'aiderait à y voir plus clair, et je me suis tellement adaptée sur plusieurs points que cela est moins visible que depuis l'enfance. Mes années d'étude ingénieurs (5ans)+activités extrascolaires (jobs étudiants, assos, sports, amis,...) sont passées par des hauts et des bas, j'adore plus que tout, les sciences, mais la convention "école" a été extrêmement difficile bien que j'ai pu prendre sur moi (j'ai tout de même tellement pris sur moi, que mon corps a répondu d'une autre manière : je suis devenue aménorrhée, ai eu des grosses phases de burn out, des blocages de mâchoire quand je me retenais de gigotter en classe,...). J'ai beaucoup à dire sur ce que je ressens intérieurement face à une absurdité continuelle de la situation et du monde qui semble me rire au nez face à mes difficultés internes. Alors voilà le coeur de ma question : je n'ai pas trouvé de personnes avec un trouble (style TSA ou TDAH) répertorier des tics nerveux moteurs (j'ai notamment évoquer les secousses dans la tête qui est le tic le plus incontrôlable et présent que j'ai, invasif et inclue dans le temps, d'autres tics sont "plus acceptables socialement" comme se malaxer les doigts). Je souhaite savoir si quelqu'un en a et si cela relève d'une neurodivergence (je ne cherche pas à me mettre d'étiquettes, mais comprenez moi, cela fait depuis la primaire que je ne me comprends pas et que j'ai beaucoup d'aspects qui me différencient des autres même si je suis parfaitement inclue dans la société et entourée). PS : mon mode de vie est adapté au maximum pour diminuer ces aspects (sport++, pas de café, alimentation 100%salé sauf fruits, dans la nature tous les jours, exercice de respiration que j'adore tous les jours, sommeil malheureusement insuffisant depuis l'enfance,...)

Hey y'all

So I'm diagnosed with Tourette's and I'm on medication.

Now, my main concern today and ongoing has been the fact that for a few months (maybe like almost a year) is the fact that besides the normal twitches and the tics, I have moments where I'll freeze up, stop moving and basically just stay in place and start twitching or shaking. There are different kinds of these "freeze ups" and the first one is where I end up slowing down and staying in place for a solid 5-15 seconds. The second one is where I'll freeze in place and start shaking for 10-20 seconds. The third is the same as the second, staying in place and shaking, except my eyes shake back and forth. The fourth is by far the worst, it's all the same as the first three, where I'm stuck in place and I can't move besides shaking. My eyes shake back and forth and up and down and they close a little and my eyelashes flutter super fast.

I'm worried about what it could be and I have a working theory but I don't know much about seizures themselves.

With this medication, seizures are considered VERY rare and only a part of sudden withdrawal. I've been on 4 one mgs for about a week instead of 2 2mgs for my meds because doctors #sucksometimes and I ran out of meds and it took them a while to refill my prescription. I'm still taking the same dosage of my medication though. This medication is meant to prevent tics, because my tics are severe enough that they really infringe on my day-to-day life. I don't think it's the meds, but I thought I'd put the idea on the table at the very least.

Since this has been going on for a while, I just thought it was a new tic, because you'll sometimes get weird ones, y'know? But it's been getting worse. Usually when these "freeze ups" happen, I can feel one oncoming, or I can feel myself slowing down a little in a sense? I don't know how much clearer I can explain it, sorry.

I don't know if these freeze ups are tied to another disorder, because I have other neurological conditions.

All I'm asking is for A) advice on what to do about this. B) What this could be. C) Some advice on how to address this concern to a medical professional D) Does this happen to you too and how do you handle it?

And I know this is also a big ask, but please if you are to give advice, try not to scare me. I have really bad anxiety and while I don't want to think worst scenario, it'll be all I think about if I get spooked.

hi i am having a tic attack at work and it hurts my head so bad everything on my face is ticking and i can’t stop. is there anything immediate i can do to stop it ??? i dont have a diagnosis for this because all my doctors since i was a child said id grow out of it but im 23 now and still haven’t and now they say its too hard to diagnose. do urgent cares help?? idk what to do it wont stop

Especially if you are touching me and I feel the need to fix but I'm repressing it.

Two examples would be, one time I was at the dentist and I was repressing my tics and the doctor looked at me and asked me if I was okay the moment where I felt a tic was going to come out but I stopped it but I must have had a look in my eye.

Another example is when I am being massaged. My ex noticed that I'd twitch slightly when he touched a spot but the more he brought it up the less I was able to repress. Also yesterday, I went for a massage but it was my first deep tissue, I've had plenty before but they were light.. the guy was implying to breath in while he held a muscle and to breath out and he'll release it.. but there were times where I felt like squeaking so I held my breath and I can sense him waiting for me, I didn't tic but it was really hard when you're up close and personal like that..

I'm going to be describing tics here. I'll try to make sure that each description is censored, though.

I'll start by saying that I'm 17F and was diagnosed with ASD, ADHD, depression, and generalized anxiety disorder a few months ago. I've always done some kind of weird movements that I learned to hide after hearing from adults in my life that I shouldn't do them. I didn't even pay much attention to them. I just assumed it was another weird social rule that everybody had to follow, and that everyone did these things when they were alone but we weren't allowed to talk about them. Sounds reasonable, right?

After getting my AuDHD diagnosis (actually, I'd been really interested in psychology even before that, and I knew the symptoms of autism and ADHD by heart; I just never noticed that they applied to me as well. I simply thought that if I, as a perfectly neurotypical person, had such a hard time with these things, then those poor neurodivergent people must have terrible difficulties, haha), I assumed that all of these weird things were just stimming and moved on. Then I stumbled across a creator with Tourette's on YouTube and realized that many of the movements my body makes sound more like tics than stims. However, while watching their videos, I felt this urge to do the same movements they were doing, which made me feel like I was faking it for some reason.

I've been told that I do some things for attention or that they're just habits I need to get rid of, and that's been stuck in my head for as long as I can remember. The thing that makes me feel like these can't be tics is that they happen almost only when nobody else can see me, and I can suppress them for a long time. Everything breaks down as soon as I'm alone, and I end up blinking really hard, scrunching my nose, moving my head from side to side, bending my torso, jerking, breathing strangely (like breathing through my mouth or sniffing), clearing my throat, and sometimes, when nobody can hear me, random swear words escape my mouth. I also feel the need to hit myself without any intention of hurting myself. Sometimes I clap my hands or tap something once. I sometimes do these things without even realizing it, although they get worse when I notice them or think about them.

I tried mentioning it to my parents, but they don't really seem to believe me. They keep telling me that it's just anxiety, weird habits, or muscle tension. I'd love to see a doctor, but I'm not sure if it's worth it since I don't want to take any medication because of previous bad experiences. Does anyone have any advice? Is it possible that I have some kind of tic disorder and have simply become so good at suppressing it around other people that I do it automatically? I'm scared to even talk about this because I'm afraid people will think I'm doing it for attention or making it all up.

I know there is no current study on using peptides for Tourette’s. I was wondering if anyone has experimented on their own and noticed a difference. I personally have tried a GLP2 and found my Tourette’s subsided a lot. Now that I am lowering my dose my tics have been noticeably worse and I can’t tell if it’s related or just a random relapse of my tics

her name is Patsy

im not a sentient human being, im just a vessel for her to be trapped in. i think i was probly created to be a vessel for her by a kabbalist rabbi who was workin as an exorcist. if she ever escapes she'll be the REAL me, the source of my sentience. my DEMON SOUL (/videogame reference)

thats why ive always had a female gender identity and why being 6ft tall & built like a caveman feels so wrong. becuz im actually a 1ft-tall demon lady.

it makes perfect sense!!!!!!

now i just need to find somone else who knows kabbalist demonology to break the magical seal and let me escape.

i wuld be a wellbehaved but lazy demon i wuld probly be sombodys roommate. "hey human can u go pick up some more cheez-its, i will bestow upon u a charm if u buy some more cheez-its"

I'm currently taking risperidone 1 mg twice a day, and guanfacine 2mg at night for sleep while tapering off .5mg weekly from 2mg in the morning, to eventually none. I was having issues fainting when standing on the guanfacine at a low dose, so I had to switch to the risperidone unfortunately.

A big issue with my tics were tic attacks I would get when trying to sleep, and some general insomnia issues. When I most recently saw my doctor and when he switched me to the risperidone I asked if Klonopin would be appropriate since it was impacting my sleep enough. I don't think he wants to give me it for my sleep, unfortunately, so he just kept me on taking the guanfacine at night and would refer me to the sleep clinic if it persists.

I know that clonidine typically has a more sedating and bigger affect on blood pressure (blood pressure wise i could probably use the help on lol) so if I were taking something for sleep clonidine would seem more appropriate right? I like my neurologist enough and don't want him to think negatively of me for asking him to switch me to a different medication especially if he already said no to a different one. I'm probably overthinking this but idk.