Autism, Life & Learning
So this week I am releasing three post. Yes, three. This is because I am doing something for charity so I can’t do one then but I will be doing it for a week so just in case I do can't do next weeks I have made three for everyone to read. So for this post what am I going to talk about Autism? Disability? None of that, from at least this post going live. The blog is now going to be on Google!!! Unlike Blogger this should be actually on Google. I haven’t released this on to Google until now just to make sure everything is going okay first and I have understood how to use the website. That is all for this one. There will most likely a follow up to make sure this has worked. So hopefully this should be up by the end of the month.
So if this the first one you have seen. Hello I am The Autistic Gecko. I talk about Autism and Disability. I blog about my life and how my autism changes my view on things, compared to someone who isn’t autistic. I also do some reviews on Autism related TV shows/films. As you will find out I like Pokémon and I adore Eevee and all its Eeveelutions. Thank you for reading this. If you would like to see more please click Gecko Base to see all of my posts. If you want to find more then please look at Gecko links to see the links I have provided from previous posts.
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So a couple weeks ago I was in another car accident this time the car. So the car was damaged again... this time the car got hit side on, but it was between both the cars sides so there wasn’t much damage. A few dents and a very shaken mother. I am going to say one of many times I wasn’t driving, at the moment I am not allow to drive as I have no license. I hurt my shoulder and hip, I did the maths on it and worked out if I wasn’t on my 2DS and wasn’t looking after my Eevee. It could of been slightly worse. Anyway. I have to go through the solicitors... again. I swear these people don’t understand how autism can affect people during accidents. I can record lots of information as soon as an accident happens, but before that happens I shut down or else I would have to remember every single road, signs and all the car, lorries and vans I see. To me that seems like way to much information.
So as I am typing this up, the 28th March, we have just got the car back and it has been repaired. So the car is again fixed and now all we have to do is mind every other car on the road. I think that might be easier said then done. There is other things what I don’t think people take into account when they talk about autism and road safety or road accidents. It is probably my biggest pet peeve is the signs that say “my child is autistic they may run into the road”. Lets get this cleared up we don’t run into the road. We don’t see the car or the danger whilst on the road. I have been in two car accident now and yet I haven’t ran out in the road. I am yet to see over the news that hundreds of autistic children have been run over by cars because they ran out in front of the road. I am just guessing here that those who do are on the lower end of the spectrum. Either way this doesn’t really matter because I can see two different scenarios play out. 1) The driver hits the autistic child because he didn’t see the sign saying that there maybe a child who may run out into the road. 2) The driver sees the sign for the child, as he is reading the sign, they hit the child because they weren’t paying due care and attention to the road. So either way they aren’t any good. As they won’t get seen or they cause a distraction. All this causes is a point of reference so people can bully someone. This also cement the idea that all people with autism are going to run out into roads; and this is how sterotypes are formed. Thank you for reading this. Please like, share or comment if you have enjoyed it. Please message or comment below if you want to me to talk about some thing. I am going to pre- writ some of this from now on so they may be a slight delay between comment and content. Also around May time I am going to restart all the Atypical reviews so please message if you want to review something else. Please click gecko home to see all my other post or click Gecko links to look at some the links provided. My last post of this three post mammoth is... well... its here, I have it. My Sigrid CD, my Signed copy of Sigrid’s Debut album Sucker Punch. This has made a Gecko really happy, so happy I jumped through my door and smacked it on the door frame. Don’t worry I didn’t have the CD in my hand it was put somewhere for safe keeping. At the moment I am typing this I haven’t had chance to listen to it. Although I am going to guess, it something I rarely do on here, and say that most if not all the songs on here are good and most or at least some from this album will be part of my music list for my races.
Why am I blogging about this? Well if you haven’t read a few post. I am a massive Sigrid fan. I know I mainly talk about autism, but this time I thought I would give the whole system a ‘Sucker Punch’ instead of using ‘dynamite’. I thought that I could use this to remind everyone that people with autism are still normal people that still listen to music, so please ‘Don’t kill my vibe’ and no I am not going to apologise for any of the titles that have been use for any puns mainly because I ‘don’t feel like crying’ in laughter from doing this. I am a bit of an music lover anyway but Sigrid is brilliant, I will link all the titles I have mentioned below. I am really looking forward to seeing what she does next. I would like to see her live at one point, but I know there are going to be flashing lights and I am photosensitive. So until I can find a way round it will be YouTube and going to her store to get her album. Its a bit of a 'plot twist' which still a little 'raw' for me. The next thing to do at some point is get the vinyl... and maybe anything else I could find. I mean to me she is like Eevee in Human form, so I can see me having some things. If I do it will be posted on here. I thought this would be a change of pace rather then talk on and on about autism I thought I would talk about some more of my likes and well besides Eevee, Star wars and Sigrid’s music (or just music in general) there isn’t much I have a massive passion for. This has been the end for this schedules of posts, so please; high five. Thank you for reading this. If you liked it please like, subscribe or share it. If you would like to see more please don't 'strangers' so please click Gecko Base or if you want to see my links I have provide in other post please click Gecko links. Sigrid Links: Sucker Punch (album) https://store.thisissigrid.com/*/Music/ Sucker Punch (song) https://youtu.be/1uHt2LrCSWg Dynamite https://youtu.be/hKvbaZTAQN0 Don’t Kill My Vibe https://youtu.be/xzonQoON9eo Don’t Feel Like Crying https://youtu.be/w5x93pXSmRM Strangers https://youtu.be/cIriwVhRPVA Schedules https://youtu.be/RrRDEleMo5g Raw https://youtu.be/BkpwPKZb_Zo High Five https://youtu.be/z6A2LHGx8_A Plot twist https://youtu.be/bNuCNZK-r5A Right a little catch up and then I will be on the next topic. Sorry for not posting last week I was in Milton Keynes. Right I am going to gloss over this, but I will come back to it later. Me and my mother had another car accident. I swear we are magnets to cars, again it wasn’t are fault and we are both okay. I will talk about this again later on. I started volunteering, its really good so far. I like helping people and with what I am doing I am but through little changes. I also practising how to use my senses to detect different emotions, its are but in the end I can see this being useful. Finally I have got a Pokémon game – other than Pokémon Go. I have no idea how far in I am. I am guessing halfway, but I have lots of Eevees.
I have just about a week left before I start my fundraising challenge. It is a little scary and I am a, little nervous but I am confident in my abilities to paddle the distance. The issue I face is more can I keep paddling without twitching or panicking because I have had a meltdown in the sea. Again I thought I would talk about this topic no the meltdowns; but twitching and stimming. There is lots of things I could talk about but lets focus on two things: - The harm it can cause - Also what it can look like I am only doing this again because I am cleaning this up. So my twitching includes: flapping, my fingers moving, I am waving or twisting my wrists, slapping or thumping my chest, weird facial moments and verbal outbursts. Okay so why is this so harmful? Well... with most of them I am guessing most people have figured out that hitting yourself is quite bad. In my case it is quite costly. I can often bruise or brake things like ribs, knuckles and fingers. This is why I wear gloves. To stop this, it doesn’t do much but it does stop most of the impact. Also the verbal outbursts can be dodgey, not because of what I say... most of the time... but because people have finally realise someone odd is next to them. I have seen lots of funny things because people have realised that someone odd is next to them. I have been in a shop and kept repeating ‘Pika’ and the person just carefully moved around me. I have had parents pull in their children in to them because I had an outburst and they thought I was a danger to their kids. There was an issue for that parents though; they had to ask me to move. So in their heads they had to ask the crazy person to move because you think the crazy person is a danger. In this situation I was a completely opposite to what the parents thought their face dropped. I have also ha my fair amount of abuse because of my twitching or verbal outbursts. These are part of me and people need to take people for being individual not collective group or labels you pick for people. To make the world a tiny bit better just don’t judge until you know the person. I may twitch but I want to help people. I am doing a psychology degree so I can become a psychologist to help people. If you judge you me as odd or different you forget the many people am hoping to help or will do if pass me degree. How often do you judge someone? Just count and post it below. That is it for me I know it wasn’t funny but it needs to be said... unfortunely. Please like, subscribe or comment below. If you know someone who would like this or you want to tell people please share. So... This is going to be my new home for my blog 🙃. I hope it's functional and looks at least a little colourful.
I know Sunday is meant to be the time to see a new list but alas I lost track of dates and even time at some points. Anyway I am now here your very spaced out yet odd gecko🙃. I thought I would change somethings around. So other then Autism I will be time to time talking about other topics such as mental health😱, disabitly ♿and maybe the odd bit of putting them together so you get some of this multi-faceted Gecko. So to start this new page of I thought I would tell you a story, becasue everyone likes a good story. So it started around the end 2016. I kept seeing a couple go up towards the hospital, just as I was heading to do some training. At least once a week I would see them go to the hospital. Then every so often I would see them come back from there. The first times they looked sad😔, both of them did, then around the start of 2017 I saw them come back from the hospital. I looked at them again and this time the woman I saw was crying😭, I doubt she could see through her tears and the man, he was trying to support her. So first time I got out the way and just smiled because I didn't know them or anything about them, but I felt that was the right thing to do. The man looked at me and just said thank you. That was all. To me I felt like I did something. Then I kept incountering them as I was going to the shops or coming back from training I kept doing this, and the man and sometimes the woman as well said thank you. Then I saw the man and the woman walk up to the hospital, this time it was a little different. Instead of the were sad 😔 on the way up and crying on the way back down. They were both crying 😭on the way up an holding each other like they never wanted to let go, also the woman was also pulling a suitcase. I figured she going to stay overnight. But through all of their weeping they stumbled slightly instead of smiling or just moving out of their way like I so often do. I decide to try and help, I wasn't needed but that wasn't the point I had seen these people go backward and forwards to the hospital at this point for just under six months. For that whole time I must of been one of the only 'strangers' who saw them between going to and getting back from the hospital. People forget that when we are around other people then someone can see us and it is in that moment we can make them feel found when they are lost, surrounded when they feel lonely and make they happy when they are sad. I just be autistic but through watching people I must of overheard so many convosations or seen so many glimpes into peoples lives it hard to notice some of them let alone all. Every so often I still see them, most of the time it is just the man and I still give way and they still say thank you. I remember one time it must of been when the woman was staying overnight in the hospital. The man walked into me accidently, usally I would have been a little annoyed but I would have shaken it off. Instead I didn't do that I made sure he was okay and then I carried on walking, but I still checked behid me just to make sure he was. I have an odd gift which everone belives it is through my autism where I can feel how someone is, so if anyone lies about their mood I know. I just don't know what it is. I think it is so important to see people who think that they can't be seen. It could be someone with a terminal illness who thinks that now they have been given this terrible diagnosis. It could be someone who is on the street looking for somewhere safe to go to sleep. It could be a person with mental health issues. It could be your bestest friend in the whole wide world who may have one, all or none of this issues. They may just friend a friend to speak to and to acknowledge that they have been seen by someone. Someone to them that cares. Thank you for reading this blog🙃. If you liked this please subcribe ( it works this time), share to friend or if was bad share it to people who you don't like ;) . Also if you have any any mental health issues please look at my gecko links and find Young Devon. If you live in Devon, UK and are under 19 they can diffently help. If not they definitely know where to get help. I am firstly sorry this one is late by nearly a week😶. I was waiting to talk about my experiences at the DANA Post Diagnostic course. Then I had a meltdown💫🙃. That was from the DANA Post Diagnostic course😶. Anyway, the course it self taught me not much else I didn't already know. For anyone who hasn't been to one. A post-diagnostic course is where you learn some bits about your condition, in my case autism (Asperger's), you learn about the strength you can have being autistic, learn how to control certain issues and how to fit into a neurotypical world. And we did this for 3 hours💥 and have this again next Tuesday. Well, anyone who knows my thoughts will know that I don't think we should fix it, we should be able to thrive alongside neurotypicals; all we need is a little kindness and support from people around us👪. My 'superpowers'💪 are to mimic anything I need to be to get by, alongside some others but I want to focus on this one. I know some people will say this is masking, but mine isn't I can mimic different genders and sexual orientations- that isn't part of masking neither is being able to copy peoples writing styles. This doesn't mean I don't understand why people need to fix it, in fact, I think it informs me more. It shows someone with autism can be seen as a neurotypical or as a person, rather than a problem or a condition. There was another thing that got me they kept calling it ASC (Autistic Spectrum Condition). This goes back to the cure argument so many posts ago. In short. If neurotypicals see the word condition they think it can be cured. If neurotypicals see the word disorder they don't think it can be cured but managed, although some see it as a way of avoiding autistics. The last thing to control certain issues they must be aware of our issues. That brings me on this part I was looking through Facebook and I got this ad... It's from NAS talking about autism awareness day, they are hoping to make a change by promoting autism awareness towards autistics and/or their families😂. Isn't that the part of the market that knows about autism? I mean they might promote if they like NAS. I promote autism every day I walk out my front door. I think anyone with autism does exactly the same. So a week of promoting us is silly. Then they add special prizes which means people have been bought to promote autism. That bit I see as bad, but essentially you are buying your own people to promote something they are😳. It's like Coca-Cola paying diet Coca-Cola to promote the whole Coca-cola as a business. This is from neurotypicals, so how bad is it that! They say we have small imaginations and are slightly limited. I think the business model on this definitely is😶.
Post Diagnostic Meltdown I know I said I would fill you in on my PIP form; why I am so angry and what is happening. I will that is for Sunday as I now got most things sorted out...ish🙃. Thank you for reading this🙃. Hey everyone, I know this has taken a while. I am still going through the process so I will keep updating this post as I go through it.
Before I go any further I should say the PIP stands for Personal Independence Payment. This is a benefit that helps people with any form of additional needs to be independent. And now prepare for an onslaught of stupid decisions and pointless reasoning. So, PIP has been a bit of a pain. There were some things I have spoken of; like the 30 minute ‘interview’ when it took 3 days for me to get diagnosed with autism. Also, the questions or should I say the answers to those questions are just silly. Example: how far can you walk taking into account any aids you use? A) less than 20 meters B) between 20 and 50 meters C) between 50 and 200 meters D) 200 meters or more E) it varies. So, they haven’t said where you are walking to. They haven’t given any issue of how hard walking could be. They haven’t even said where you are walking. For most people, it doesn’t matter, but for a lot of autistics where we walk is part of our environment. If it has cars, then we know it to be a hazardous or dangerous environment. If it is a lovely green field as far as the eye could see, then that is going to be different. Especially if that road is just outside your door. Let's take another ‘Do you find it difficult to mix with other people because of severe anxiety or distress?’ A) Yes B) No C) Sometimes If you read a lot of these blogs, then you will know that I can’t tell most emotions. So, when they put things like severe anxiety I get stumped. I have to be taught that it’s a negative emotion, then there is distress… ah yes, the vaguest of emotions because it varies person to person. Someone might like jumping into fires but most really wouldn’t. Most of the time I have therapy sessions they were about people. So, mixing with people do I find it hard… I’m guessing yes. For some their autism doesn’t affect them in this way it's in processing what people are saying. So, they may jump in and then go off guesswork. These questions are not made for neurodevelopmental disorders/conditions such as autism and ADHD. They don’t measure independent its more how well are things. I am quite independent; I train in the gym and on the water, I go to town, I volunteer for a few things and do my degree. On paper, I look ‘normal’. If you look closer; I train in the gym and on the water by myself, I go to town to get a specific thing and then I am straight out, I volunteer for a few things to push my boundaries and I am doing my degree because school didn’t help me because they thought I was hard to teach. So, these surface questions aren’t needed in this day and age where we can scan people to make 3D images or can video call people over a wave connected to a networking source, that’s internet video calling if you were confused. If you have to do things this way, then why not ask straight forward questions. Let's try the ones I used. how far can you walk with any aids you use near a busy road? A) less than 20 meters B) between 20 and 50 meters C) between 50 and 200 meters D) 200 meters or more E) it varies. What happens after the implied distance?................ How far can you walk with any aids you use on a public walk path away from any motorised vehicles? A) less than 20 meters B) between 20 and 50 meters C) between 50 and 200 meters D) 200 meters or more E) it varies. What happens after the implied distance?................ How hard is this? Let's try the other one next. Do you find it difficult to mix with other people? A) Yes B) No C) Sometimes If No or Sometimes, why do you find it difficult to mix with other people? ………. This way you could help the interviewer knows where to look rather than prodding in places where we don’t have any issues. Now we come to the PIP timeframe and order. You have a month to fill in a 40 page booklet filled with yes/no questions. Plus, you have to send it with evidence to back your claim. These can be medical reports, care plans and letters like assessments. These can’t be appointment letters. So, if you have a mental health issue its going to be hard to find information because not everyone is given a care plan, medical reports or assessment letters. So, it’s something to remember the whole time. If you have hearing aids you can’t use the review sheet because that isn’t proper evidence to them, but it is what you are given which your hearing aids. Also, all the evidence as to be in English, so if you read in Makaton signs you can’t use them. So there goes their care plan. When it gets to things like this, it's bad. When you have gone through the drama that is all of that then you have to wait for anywhere between 3- 8 months to get an interview date. That’s not to go to the interview that just to get a date. The date is usually a month after, so change the 3-8 months to 4-9 months to get an interview. Then they talk about what you put in your PIP form and test you from the moment they say hello. My appointment was late, not by a little bit like 1-3 minutes, by just under 10 minutes. So, I start ticking, from that ticking I bruised my intercostal muscles (the muscles around your ribs) on my left side. These muscles help you breathe and stops the bones from being broken. The person who saw me was a nurse, but most of the time it is a health assistant of some kind. These types of injury are common to me, this won’t go on their report. So, something that actually harms the person WILL NOT go on the full report. Nor will, walking into the road, meltdown related to self-harm or just meltdowns/shutdowns. All of these are what makes autism so hard to understand or to control day to day. I have the extra of issues of living in multiple realities; which I got given an odd stare because they couldn’t understand it. I know this is uncommon, but the next question really shouldn’t have been are you on any drugs? This is just stupid. I have stronger words, but this is meant to be child friendly. Also, I should stress that the interview room is usually free of any distractions, so you have two ways out to function you either talk or you shutdown and become a turtle and say nothing and either way they can say that you have shown that you are ‘well’ enough or you haven’t co-operated and won’t get anything from this. If you sign, you will need an interpreter because they will not talk to you through BSL (British Sign Language) or Makaton. I know this one from experience as one of my parents had to translate, but they decided to wait until I could talk because I went mute. If you need to lip read have someone else with you. As they will not listen or even attempt to understand you if you sign. The appeal procedure is abominable. You have to send any new evidence in via post, you can’t email or deliver by hand. It has to be through the post. The Royal mail are extremely good at not losing things. If you want to you have something like 28 days to appeal, via phone or textphone, so if you are anxious about talking to a stranger over a phone prepare to do it again. I am now going to run through what you need other than evidence for PIP. For PIP you need: to have a national insurance number, this is okay if you have one, everyone in the UK gets one but no they are on one bit of paper so if you have lost it the process is going to be even longer. It helps if you have photo ID because otherwise for the interview you need to bring 3 pieces of ID, that’s all I had as I can’t drive and you need money for a passport and that’s what my PIP was hopefully going towards. So, this seems really silly. Finally, you need to bring all of your aids if you had any. So, if they are small or can get lost easily I would say get a bag to put them all in. So overall the PIP isn’t about helping to be independent it is about helping those who fit into the label disabled. People who are autistics are still seen by this as normal and fully independent. Really!? If someone could please explain who is scared of people is being independent. Tell me how everyone but you can cross roads is independent. In my view, most autistics are independently separated just so no one can help us. There is a hidden taboo with being autistic because we look ‘normal’, but we act differently to what people think so they choose not to help in case they do something wrong. I have been taught to speak out if I think something is wrong. I am one in a few. I don’t have to, but I choose to, and I do it for people like me with Asperger’s but also non-verbal autism because I haven’t seen much for them. It seems a shame that over the nearly 70 years autism has been looked at and explored we haven’t adjusted or even seen autism as any handicap now the times are changing, and people are being more vocal the reasonable adjustments have gone out the window as people are not seeing autism as nothing more than an excuse. PIP proves this in the extreme points because through all the issues I got I scored 0. I have done it with an independent person and I got 60. So how did they miss that much!? This isn’t just happening to some, but to the majority. This is the real joke within the first pages they talk about equality and diversity, but they can’t even cater for this from the application process. Thank you for reading. I hope this has been helpful. I won't leave any link because I think if you have read this far you need a nice break. Christmas day had been an unusual day, as it is the day something goes wrong and it didn't. Everything is there pretty much on time. I had my presents🎁- which included an adorable Eevee. I gave my presents🎁 to my parents they both enjoyed them. We also were host to a guest- Which was something we don't normally do. It was nice to host for once, we rarely do it. I hope they had a good Christmas day.
For my family we celebrate Christmas from the 24th December - 31st December then celebrates New years on the 1st of January. Which is a little odd I know, but also why I haven't posted anything for that time? We aren't a religious household we go off me and my dad's Taoist ideas of; Peace, understanding of people & togetherness. They sound simple, but they can be hard to keep by, especially if it is for a week😑. We little to no arguments and understanding of everyone. For Boxing day I had to cook, luckily no one got poisoned😌. I like this part of the year because it shows how independent I can be💪. Although I usually hurt myself, it doesn't matter as I get to cook a meal for the whole family. This had been an interesting year for me. I started this blog💬, I was able to do an apprenticeship & I am halfway through my first year of university🏫. I hope next year is even better and I get to do more for promoting autism awareness. At the start of the year, I got my formal diagnosis of Asperger's Syndrome/ High Functioning Autism. I looked at lots of places to see where I could get help, without people talking down to me and will give advice if you haven't got the diagnosis on paper. Clue; there are little to none😕. The day after I posted my last blog I got a letter from the people from PIP saying they want me to come in for an assessment. This is meant to be the last step if the person doesn't say that I need some help to be completely independent all the work will have been for nothing, although I know I can appeal, but it shouldn't come to that. So I have to show how bad my tics, my scratching and my anxiety are just so people understand. This is just annoying I have to set everything off and hurt my self just so someone can see. I think the assessment is around 30 mins to 1 hour. So I have to handle a new place, a new environment, new people and I don't even know how people can handle me. I am so used to people thinking that if I tic too much that I am having a seizure of some kind. If I say something out of the blue like I'm a hamster or Pikachu. People look at me oddly and I have to show all of this because someone doesn't believe you. I have enough of this just going through town or trying to help other people. Then next year I can apply for my blue badge then I have to do that all over again. Most autistics can't lie, so without putting us through two or three layers of torture, which could be over in weeks or months. Isn't there a way of making it easier to test people without causing this much harm. There have to be people lower or higher than me who suffer from really bad self-harm, does that mean they must show all their scars or harm in front of them? In pure logical form they would, but this isn't a pure logic world.
Saying this I don't know what is causing this but, I have been phasing more and more it like things are at a certain point. It most likely just me, but I can see me worrying about this PIP test just for it not to exist or for the person to disappear. Then I would have to wait... again. I went to my lecture yesterday and I understood everything although that had to make it hard by giving me four different lecturers for three topics. It seems a little silly to me. Anyway, that's all from me. Thank you for reading this. Hopefully, I will get the Atypical season 2 stuff done but it is around the time of my PIP test so it may be a little late. If you like this please subscribe, like and share it with other people. Let's do this one out of the gate, as you are more than likely going to hear this the whole way through. I HATE SPEAKING ENGLISH! My first language was BSL, British Sign Language, so coming from a non-verbal form of communication to English is like doggy paddling to swimming the English Channel😨. BSL has very little grammar and well... English is full of it😱. You have words that are easy to say like to, but this comes at the cost of what meaning does it mean. I know that in different places of the UK have accents and with this comes lots of different words that have different or new meanings. Did you know that BSL also has accents, it's the same words just signed differently. To this makes more sense. Also I normally don’t call people by their names and almost never will whilst processing because if I had talked to 5 Alice’s and 10 Bens and processed them all the same then I would lose which Alice and Ben I talked to about what🙄, so if I call them all by different names, no I don’t mean like calling them Ali, Alice, Alison etc. I am talking about calling them cat, twizzy, deck etc. Because that is more normal. I assign names that fit them or their personality, so they can’t be confused with someone, this can mean it takes a while to not confuse the person's name with what I call them. Also let's get something else sorted, when you do an English speaking exam, remember BSL doesn’t count.😕🙃
Even if you speak BSL fluently it doesn’t work. I mean I can’t understand why. You are speaking English. Anyway, I don’t like speaking English. (As that doesn't make me sound like a 6 year old) Names is another thing I have eluded to. Names are okay but if you have a bad name you get picked on. If you have a good name no one cares. Also, people are giving their children really odd names, like peaches. In my mind, if you are called that I’m not giving a nickname I am just going to brand you like fruit. Imagine talking to a fruit bowl🍎🍌🍇🍊🍐. That would be odd. Saying that I nicknamed someone as Io, (that's capital i), and that’s a moon🌝. So... talking to a fruit bowl could get quite normal then...maybe in the future. Names I know can be anything, but there is a limit. I know I have said I hate English, but this is why I use my own form of this. I may have talked about it before. It is based on a basic form of binary, this means I process the noises through clicks and chirps (imagine R2-D2). As each word has a different sound to it. I will use this to make the words sound like they are, this also allows me to talk and communicate quicker. I usually speak English, but only when I am not on a slow day or outside the house. So languages are hard to learn, well English is. At least I know everything I now do in English is wright😉🙃. Thank you for reading this. I know I haven't done an atypical review, that is down to me doing assignment things. They will be coming don't worry. Hopefully, the next one on the list to be done, it should be making changes. Let's hope I remember. |
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September 2019
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