Interview with an Autistic Child

Interview with an Autistic Child

One of the things I find most difficult to try and explain to people, is what it is like trying to hold a conversation with my son Jack. That’s where the inspiration for, interview with an autistic child came from. Nothing I could ever write, could capture Jack’s personality and his “autism” as this has. Me talking will be in bold, and inside Jack’s answers there will be comments from me, these will appear in brackets and italic, to be easily distinguished. I apologise if it gets a bit confusing, but that is kind of the point of this hah.

I explained to Jack what we were doing, and what it was for before we stared. He was very happy to do it, indicated by the huge grin on his face. Jack loves showing off, and as with most kids these days it seems. He wants to be famous online, YouTube, TikTok etc. So jumps at any chance to be part of this blog. So let’s get on with the interview.

Interview with an autistic child
Jack training to be a ninja

What is your name?

You know.

Yeah, but what is it?

Jack. That’s a dumb question you know.

How old are you?

You know.

I know, but the people reading don’t. So you need to tell them (-pause-)how old are you?

I told you, you dummy.

No you didn’t.

What? You know, come on.

Yes, but you need to answer the question for the readers.

(At this point Jack is giving me a funny look, so I whisper to him 12 and he nods his head and we move on.)

Who do you live with?

You know, dumbass. (You might have noticed there’s a trend to Jacks answers.)

I know. But you need to answer for the people reading, remember? Because they don’t know.

Guess who’s over you’re head?

(At this point Jack has put one of his favourite teddy’s on my head, and wants me to guess which one it is. If you aren’t aware of the snuggly’s you can read about them by clicking here. A little panda has been added to the gang, so we went through this 4 times before I repeated the question.)

You know dummy. You say them I will nod.

Mummy (Jack nods), Daddy (Jack nods), Lily (Jack nods), anyone else? Biscuit. (Result! An independent answer!! Biscuit is our pet guinea pig.) And you know who else? Who? The Snuggly’s (You can never forget the Snuggly’s.)

Do you like going to school?

Yes. (That’s all Jack had to say about that.)

Do you have friends at school?

(Jack nods his head.)

What are their names?

(We have to wait for a minute, as Jack wants me to watch something that happens in PokeMon, that is on the TV.)
Jimmy, Alfie, Bonnie, Jack, Dawid, Jacob.

What are your favourite things?

(Jack points at the TV for Pokemon.) Minecraft, SCP’s don’t forget about that.

Anything else?

That’s all I can think of.

What about dogs?

Yes. (Jack nods his head and makes dog noises).

What do you want to do when you grow up?

I don’t know. I’m already a Pokemon trainer, I want to become a Pokemon master.

Thoughts on the interview

That is the interview with an autistic child brought to you by myself and Jack. Some of the key things, that I believe it shows far better than I could ever try and explain are. Just a simple question, isn’t so simple. If Jack knows you already know the answer, he just doesn’t see why he needs to tell you.

Staying focused is a difficulty, the TV was a distraction, but it would have been worse without it. The TV in the background actually helps Jack to focus. Without it, he would have been up and out of his seat within a minute.

Jack’s understanding is limited, and he needs a lot of prompting to help him give answers. He wants you to answer for him, why exactly i’m not sure. Perhaps it’s to do with anxiety. But as he proved a couple of times, he can give answers independently sometimes.

One of the big things comes in the last question, and is something I will do in more detail in a future post. Jack can’t differentiate between reality and fiction, to him Pokemon are real. He is a Pokémon trainer, and he wants to travel the world catching Pokémon.

I hope this gave a little insight into how Jack works, and also how we work with him. 7 fairly simple questions that took a lot more effort to get through than what would be perceived as “normal”. I think that sums up well, what life is like for autistic people and those that care for them. Thank you for reading.

Dad Does Autism

Family Check Up

Family Check Up

I’ve been busy with my editing the website, doing what I call “proper” blog posts about specific subjects. Plus trying to master Pinterest, so I thought it was about time I did a “family check up”. This blog started with me just talking about how we are all doing, and what we’ve been up to. I’ve learnt a lot about blogging, and writing blog posts since then.

However, I still do just want to do the posts where I’m talking about what’s been going on in our life’s. So let’s have this “family check up”.

Family check up

School

We will start with the major one. Jack is back at school full time. It feels really weird, and I don’t know if I am comfortable with it yet. He was really struggling and was desperate to go back, and we are fortunate that he goes to an autism specialist school. He is in a class of only 7 when it’s full, at the moment there are 3 of them attending. Due to this we decided to send him back, and he is much happier. It had to be full time or not at all, otherwise the confusion in routine would be too much for him.

This of course meant Lily wanted to go back to school, though not full time. At the moment she is going on just on a Monday, with the key workers group to do a outside classroom. She really enjoyed going on Monday. and was asleep by 5pm! It felt weird having a quiet house on Monday, in my head I was foo to get lots of stuff done. I ended up just enjoying the quiet time, and did nothing.

Times have been hard

It’s been a difficult few weeks, especially for Lily who is the one really struggling at the moment. We’ve got quite good at reading Jack, and knowing what’s wrong, and how to solve it. Lily is a complete mystery still, and one thing the lockdown has made really clear. Is just how much being autistic affects Lily.

There’s a lot of work coming up to get the understanding of how Lily works, so we can help her the best way we can. Natalie is back working too, so there’s going to be quite a bit of time where it’s just myself and Lily coming up. I’m hoping to be able to spend some time talking to Lily, and hopefully work put some ways to help her. Too give you an idea, whilst talking to her this week. She said things like “you know I don’t understand things” and “I sometimes wish I wasn’t hear”. Which is a frightening thing to hear from an 8 year old.

How am I doing?

Obviously I am stressing about Lily, but getting her to talk is actually a good thing. We now just need to work things out. Other than that I think I’m going a bit stir crazy, I really need to get out more. Even if it’s just for those walks I set in my July goals post, hopefully next Monday I will make more of the day without the kids.

I am pleased with how this blog is going though, which is keeping my spirits up, as well keeping me busy. Though i’m currently having trouble leaving comments on other people’s blog posts. I think Akismet has me marked down as spam, so I’ve emailed them to try and sort it out. It might seem a minor thing, but it has really stressed me out.

I think that will do for this family check up, hopefully in the next one I will be a bit more cheerful. Hope you’re are all doing well, and staying safe, take care.

Dad Does Autism

5 things you need to know about Autism

5 things you need to know about Autism

I’ve compiled a list of “5 things you need to know about autism”. The idea being to give you some idea of what autism, and being autistic means. Whilst also dispelling some myths about autism. On with the list.

An autistic child turns into an autistic adult

If you think this sounds obvious I don’t blame you, but I can’t remember the amount of times I’ve heard. Won’t they grow out of it? The answer is no you don’t grow out of it, unfortunately that’s still not fully understood by some people.

Including the it seems our government etc.. as as soon as an autistic person hits 18, they seem to go completely off the radar. Services, care and benefits are suddenly stopped, and a transfer to adult services appears to be as easy as cracking an atom. When will this change? Hopefully sooner rather than later, but I won’t be holding my breath.

Autism isn’t a learning disability

An autistic person may or may not have a learning disability (and other diagnosis) alongside autism. What autism is, is a very complicated and disputed matter. The simple version of how I try and explain it is, it is a condition that affects communication and social interaction. Is that accurate, and the best way to put it? I don’t know.

5 things you need to know about autism

Anyone can be autistic

For a long time autism was seen as a condition for white boys, one of the main reasons for this was the diagnosis procedure. It was tailored towards symptoms shown by white boys, leaving girls and people of different ethnic backgrounds completely overlooked. It’s now becoming understood that girls display symptoms differently, and progress is being made. 10 years ago our daughter probably wouldn’t have been diagnosed.

Not every autistic person is amazing at maths

More than once have I been asked, does that meat they are amazing at maths? When I’ve told people about Jack and Lily being autistic. No it doesn’t! Jack doesn’t do maths at all, and whilst maths is Lily’s favourite subject, she is still working behind her “expected level for her age” at the moment.

This applies for any other “special ability”, there are autistic people out there who have some unbelievable talents. Which should be celebrated, but I’ve also seen autistic people feeling bad about themselves for not appearing to have a special talent. That shouldn’t be the case, everyone is different and unique in their own way. Autistic or not.

You don’t need to feel sorry for parents of autistic children.

Thankfully no one has ever said, “oh I am sorry” to me, when I’ve told them my children are autistic. But it does happen a lot, as well as “awww” and the look of pity. My children aren’t ill! They find some things more difficult than others, but they are perfectly healthy.

There have been some difficult times, especially with Jack. I think they are coming with Lily, now she’s older her issues are becoming bigger. But I’m not sorry for who they are, so no one else should be.

What is autism?

They are my 5 things you need to know about autism, obviously there is a lot more to it. This I think is a good start for people who don’t know much about autism, to gain a bit of understanding.

Lastly I’d just like to mention that I’ve updated the website and integrated WordPress into the website. So I now have a nice new shiny like button at the end of posts, and a follow button to follow this blog on WordPress. Any support as always would be hugely appreciated, thanks.

Dad Does Autism

What’s it like being an autism Dad?

What’s it like being an autism Dad?

I mostly like to talk about Jack & Lily when it comes to autism, but today I’m going to talk about myself. I will be answering the question what’s it like being an autism Dad? It’s not a term I generally use for myself. Going around saying I’m an autism dad (or mum/mom) is not for me. But I wanted to open up a bit, and show you what it’s like to be a parent to two autistic children. I don’t want it to come across as having a moan about what’s difficult either. Sure I will have a look at the difficult things, but I have plenty of reason to be happy too.

Before I get started, these are my experiences with my autistic children. Every autistic person is different, the experiences we’ve had as a family wont be the same for everyone.

What’s it like being an autism dad?
photo of me worn out by the kids

Family and Sacrifices

First of all, we have been pretty lucky to have an understanding and supportive family around us. This is not always the case. I’ve heard some absolute horror stories, of people being completely abandoned by their family. Just because their child is autistic, and that doesn’t fit with how they want to be perceived.

This has not been the case for us, but there have still been challenges, and sacrifices made. We have missed lots of family outings. This is due to Jack’s anxiety, we are always invited, but whether Jack will go depends on the situation. Where is it? Who’s going? And how busy will it be? The last major one was my brothers wedding. We tried to prepare Jack for it, the day before the wedding he tried his suit on and said he was looking forward to it. Then on the day of the wedding, he just flat out refused to go.

Having to split the family

I ending up going with Lily, who gets a bit anxious in busy places, but settles if she’s with people she knows. Ideally I wanted Natalie and Jack to be there, I was disappointed they weren’t. But you can’t let these things get to you, it’s part of being an autism dad. We have to do what’s right for Jack. I rang later to see if he would come to the evening part, but he still said no.

Several birthdays and celebrations have been missed, or one of us have taken Lily. It’s nobodies fault, that’s just how it is. They’ve not all been missed, Jack has been out for family meals at restaurants etc.. Why can he do it sometimes, but not others? My best guess is it depends where his anxiety is? If he’s been having a difficult time at school etc, he will be less tolerant.

Jack & Lily
Jack & Lily our for a walk

Going out

Some families have real trouble ever doing anything, so again we don’t have it so bad. What you do need though is a thick skin, and if you’re like me and don’t have that, you need to develop it. Natalie has been around disability her whole life, so she was somewhat used to it. I wasn’t ready for it at all.

When we go out, even on Jack’s best days he will have some little moments. We will have people stare at us. It’s happened every time up until now, and it will happen every time in the future. If Jack has a full on meltdown, then we will have people gawking at us, and no doubt some will be judging.

To give you an idea of a meltdown in public. Imagine being stood outside the giraffe pen at the zoo, trying to calm down a 6ft tall 13 stone child. Who is just growling, whilst kicking, punching, head butting and scratching you. Whilst people stop to have a look, and then if Jack’s catches someone looking at him, he will go for them. So I have the added stress of stopping him hurting other people.

Learning and improving

After many years of learning we are more prepared for things like days out, which can mean preparing weeks in advance for a trip out. A spur of the moment day trip is not on the agenda. Jack needs to be prepared for it well in advance, whilst Lily tends to be okay, she too is more comfortable with this approach.

We get social stories and PECS ready so Jack is fully aware of what to expect. Then whilst we are out, we have to really watch Jack’s anxiety and sensory input. Where necessary we will apply deep pressure to keep him modulated. This might involve holding his hand, whilst we walk around and squeezing his hand repetitively. Or stopping to squeeze his arms and legs, jumping up and down together. Holding each other’s hands and pushing into each other, or waving your arms around like some sort of demented jellyfish. Sounds fun right?

Like I Said you need a thick skin, and it’s no good being shy, or worrying about what other people think. Days out are always stressful, but we do enjoy ourselves. I certainly have no intention of hiding away, especially when the kids want to go out and explore as much as they can.

Family
At a fireworks display

My own social life

Now I am going to talk about my own social life. To be honest I’ve barely had one, and that’s not completely down to the kids. I’ve had my own struggles with depression, and spent 10 years working full time. Then as soon as I’d come home Natalie would go to work, and I’d have the kids to look after. We basically had no money, so even if I felt like meeting up with friends, which wasn’t very often. I’d just wouldn’t be able too.

Due to circumstances, we’ve only ever really had my parents to call on as babysitters. Which we have done from time to time, and myself and Natalie have had opportunities to go out. I’ve never liked to ask too often though, as there have been stages where Jack has been a real handful. I’m in a better place now, and so is Jack so having a social life is a possibility, which again is more than some people have. Some have to do this all on their own.

Things to be proud of

Being an autism dad might mean you have to move the goalposts of what you hoped for your child, and that’s okay. Maybe you dreamed one day your son would play football for England, but it turns out them just being able to play with a group of other kids. Is something that can bring you just as much pride.

I have so many examples of these sort of things, that are simple everyday happenings for the average person. But mean the absolutely world to us. Things like Jack being able to walk into his school hall. Lily being able to walk into her classroom, with all her classmates. There are loads, but they can be for another post at another time.

Thank you for taking the time to read, and I just hope that it gives people a bit more awareness. Of what it’s like being an autism dad or mum, or autistic person.

Dad Does Autism

Autism and Food

Autism and Food

A subject I see talked about a lot on social media, is autism and food. It seems a lot of autistic people, especially children, have a very limited diet. There are different reasons why this might be the case, and it can go to extremes. A few years ago whilst being shown around a school, myself and Natalie bumped into parents of another autistic child. We had a quick conversation where they told us, their 7 year old son would only eat baby food.

Thankfully we’ve never had a problem with Jack, who I often refer to as the human dustbin. He doesn’t like spicy food, but other than that he eats pretty much anything. Lily on the other hand, is a different story. Before she had her own autism diagnosis, her “fussy” eating was a major concern for us. Now we know she is autistic as well, and that this seems to be fairly common. We have been slowly trying to expand her diet. So I’m going to look at what she eats, and how we are trying to expand her diet.

What Lily Eats

Like most kids she’s more than happy eating sweets, chocolate, cake and crisps. There are limits though, nothing sour, no jelly babies, only homemade icing, and only ready salted and quavers and wotsits.

The one good thing is Lily likes her fruit and veg, she will eat most fruits, other than oranges and other citrus fruit. She loves peas, carrots, broccoli, sweet corn and potato. After that though things get more limited, here’s a quick list of what she will eat.

  • Plain sausages
  • cocktail sausages
  • tinned beans & sausages
  • chicken nuggets (refusing recently)
  • boiled rice
  • plain pasta
  • white bread
  • Cream crackers
  • pepperoni pizza
  • burger (only recently)

She will also eat a few different cereals, until recently the milk had to be in a separate cup. Everything has to be plain, she won’t have sauce on anything, other can ketchup and gravy as long as they are in a separate bowl and not on the plate. Compared to what I’ve heard from others that’s not a bad list. It has taken some time and effort to slowly introduce new foods, or sometimes like recently. Lily randomly asked for a burger when Jack and I were having some.

Autism and food
Lily’s plain pasta meal

How to approach getting them to try new food

The way you approach getting your child to try new foods is very important, and that goes for any child not just an autistic one like Lily. I think we should be well past the days of, eat that or you’ll go hungry, that’ll teach them method. As my dad used to tell me, he was told by his dad. He half threatened that with me and my brother, but never followed it through.

When it comes to autism and food, you have to take the right approach. Just like with everything else with autism. The way we approach it with Lily, is the slow and steady approach. We always offer her everything that the rest of us have, and give her the choice to say yes or no. We get food in for her to try and offer it her. Only once, if she says no, leave it and try again another time. This has worked well with the fruit and vegetables. Keep showing her the foods and wait for her to become interested in them herself.

You never know what they are going to ask to try, I never expected her to ever want a burger. Just keep trying and it will take as long as it takes, Autism and food is not a subject that can be rushed. Getting Lily to learn to cook foods has also been helpful, she really enjoys it and it encourages her to touch different foods. Often it’s not the taste that’s the problem, if they won’t try it, how can it be? It’s the look, the feel and the texture of the food. Until recently I had to pick every last bit of cheese off of her pizza, before Lily would eat it. Now she eats the whole thing, perhaps making her own pizza helped with that? Click to see Lily’s pizza post!

Setbacks

Unfortunately like a lot of things with autistic children, there can be setbacks. Lily has visibly been finding things more difficult, the longer the current “lockdown” situation has gone on. As much as I’ve tried to keep her entertained, she struggles without her routine just like Jack does, and is missing her friends from school.

She has been saying she doesn’t know what she wants to eat a lot, and saying no to a lot of the things she’d normally eat. Thankfully pizza and roast potatoes and vegetables still always get a yes. I hope this is because of the anxiety and uncertainty of the current situation, and she will eventually go back to eating how she was.

We will have to see how that goes, taking the same approach as with new food. Offering it with no pressure, and letting her take her time. Are there any parents of autistic children in the same boat as us? Has the lockdown brought problems like this to the surface? And how have you been dealing with them? I’d love to hear from you in the comments. That’s all from me on autism and food, thanks for reading.

Dad Does Autism

Autism Father’s Day Gift Ideas

Autism Father’s Day Gift Ideas

With Father’s Day approaching, there are plenty of places to find gift ideas. What about Autism Father’s Day gift ideas? I’ve not seen anything specifically aimed at us, especially if you want something “autism themed”. If you are happy with the normal gifts then that’s great, but what is there on offer autism themed?

I’ve had a look about, and found the things I would most like to receive as a gift. I will be honest, though I don’t completely hate the jigsaw piece. It’s not for me, and a lot of the stuff out there has the jigsaw on. I have found some nice bits that don’t though, and here they are. For the record these are just things I personally like, I’m not being paid to advertise them.

My autism Father’s Day gift ideas

Autism parent slogan mug

There a lot of autism themed items over at www.zazzle.co.uk, this mug is my personal favourite. There’s nothing I like better than a cup of tea, so this would be perfect for me, and any other big tea or coffee drinker.

You can get one for £16.55

Dad of an Autistic Jedi t shirt

You can get these t shirts on Etsy, starting at £17.70, and in a variety of colours. Obviously a great gift for any Star Wars fan, and would be very apt for me. Jack likes to tell everyone he is a Jedi!

I.E.P logo

Autism Father’s Day gift ideas

I absolutely love this IEP logo. Over at Red bubble you can get it on numerous things, that are great Father’s Day Gift ideas. Ranging from stickers, prints and canvases, too cups, notebooks and t shirt. Loads of really cool gifts.

They are my favourite Autism Father’s Day gift ideas, like I said they 3 websites all have plenty more to offer is these 3 aren’t for the Dad in your life. Do you have a favourite? Do you know of any other places selling autism related items. I’d love to hear about them in the comments below.

Dad Does Autism

Visiting the Grandparents

Visiting the Grandparents

For those that have been regular readers from the start, you might remember that visiting the grandparents, was a regular Sunday routine before lockdown. We hadn’t been since the middle of March, but with the kids missing them, and especially their dog Mack. We decided we’d go over for a visit, and try and keep the kids to social distance.

It was lovely to get out to somewhere different for a change. My parents live out in the Derbyshire Dales, where it’s picturesque and lovely and quiet. So it’s always nice to go for a visit. When we got there I took a video of the kids seeing Mack, to see how excited they all were. To be fair, Mack is usually more excitable but it was a hot day.

It was nice of Mack to run straight past me, he did at least go to Lily. But his best buddy is undoubtedly Jack. All I’ve heard for the last 8 weeks is, “How do you think Mack is doing?” The kids have been so looking forward to this visit, it was great to finally do it.

A walk to the park

As it was such a lovely day, we decided to go for a walk to the local park. When we got there we had the park completely to ourselves. We played football, which was nice. I’m certainly out of practise, I was exhausted by the time we got back.

It was good to get out there in some fresh country air, on the sunshine. The kids absolutely loved it. I’m not sure when we will all go back again, we will see how things are. It is was really nice visiting the grandparents, and gave us all a boost.

Going out and about again

It’s been clear to see lots of people have been going out and about again, this was our step in that direction. We are all in pretty good health, so we decided it should be okay. I just had to remind the kids we still have to social distance before we went, which they were good at.

We won’t be rushing to the beach though, or any other tourist place that will be packed with people. It’s still too early for that in my opinion, and to be honest I don’t like crowded places anyway. So I’m in no massive rush to join the madness. How are you doing? Have you gone to see family yet? Or started venturing further afield. I’d love to hear how you are taking things, in the comments below.

Dad Does Autism

Lily’s baguette pizza bites

Lily’s baguette pizza bites

Lily always enjoys baking, so I decided to try something different with her. So today we made some baguette pizza bites. A simple thing to make, that I knew she would really enjoy. Pizza is one of the few things that Lily likes to eat, always with pepperoni.

Ingredients

This is a very simple thing to make, which is why it’s always a popular one to make with the kids. All you need is:

  • a baguette
  • tomato sauce (we used a jar of smooth sauce)
  • grated cheese
  • choice of toppings

Making the baguette pizza bites

I cut the the baguette up for Lily, as it was too fiddly, and difficult for her to do. After that it was all Lily, and I just sat back and watched. After putting the sauce and cheese on, she wanted to get the toppings we could find out. So she could make a different one for everyone.

We had quite a few things, including pepperoni (obviously), chorizo, Salami, ham, and peppers. Unfortunately for Jack no pineapple, as he likes his ham & pineapple. For the record Mum also likes her pepperoni, whilst I like everything hah…though if I had to pick a favourite I’d say a “vegetarian” pizza.

Lily made some pepperoni ones, a “meat feast” one, one with just peppers on, and a plain cheese one for Jack. Here’s a picture of a couple before they went in the oven.

Baguette pizza bites
Before cooking

Lily really enjoyed doing this, and I really enjoyed doing what comes next. The eating part! So this is something we will definitely be doing again. Add in a bit of salad and Lily had made tea (dinner, evening meal, whatever you call it where you’re from), and was really proud of herself. Which was really lovely too see. So, now for the finished article.

Cooked baguette pizza bites
after cooking

I had a meat feast and a pepper one, and both were really nice. I loved how apart from the cutting the bread, and putting the trays in the oven, it was all Lily just doing whatever she wanted.

Which leaves me to ask the question, which one of the 4 would you have had? Or what would you have preferred as toppings instead?

Dad Does Autism

Things not to do in a pandemic

Things not to do in a pandemic

It’s been an interesting day. If I was going to advise you of things not to do in a pandemic. Snapping your tooth clean off at the root, would be right at the top of the list. That’s exactly what Lily did today, whilst simply eating a cookie. Normally it wouldn’t be a massive issue. You’d ring up for an emergency dental appointment, and get it looked at.

Of course, these are not ordinary times. Dentists aren’t seeing patients, and it has taken all day. Just to try and sort out getting a prescription for some antibiotics. The dentist have told us they will ring us, as soon as they are seeing patients again. Until then we just have to hope Lily is alright.

Jack struggles to cope

Lily spent most of the morning crying, Jack stayed out of the way and seemed okay. I took him out for our usual walk, and things didn’t go to plan. Jack gets very anxious about flies, bees, wasps etc.. There was a lot about today, and in Lily being upset all morning. Plus the unusual and distressing situation we are all in anyway. It all got to much for him.

He had a full blown meltdown at the side of a busy road, and then got angrier because it was so busy. I don’t know how long it took to calm him down, but it felt like an age. We had a couple of people ask if I needed help, which is a nice thought. In reality it just makes things worse, as it sets Jack off. Eventually he calmed and we walked back calmly.

At home he said he was scared by the traffic. The traffic seemed much busier, than it has been in some time. Perhaps Jack had got used to the roads being so quiet, and couldn’t cope with the change back. Plus the the other stuff happening, it was just too much for him.

A nice evening

This evening I sat with Jack and we matched the movie, Shazam. Which we both loved, so the day finished well. I’m just going to have to think about what we are going to do for a walk, as I don’t fancy risking the same thing happening tomorrow. That won’t be good for either of us.

Things are calm as the day comes to a close, Lily seems okay and so does Jack. Breaking your tooth is definitely up there on the things not to do in a pandemic though.

Dad Does Autism

My 5 favourite autism quotes

My 5 favourite autism quotes

Today I decided to pick my 5 favourite autism quotes, and then using Canva to display them in a image. I’m still fairly new to using Canva, but I think I’ve done alright with these.

1.

My top 5 autism quotes

This one is such an important thing to remember, even with children like our Jack & Lily who are able to talk. They still often communicate in other ways, especially on times of distress.

2.

Quote 2

This really is so true, the things I have learned from Jack and Lily are incredible. I have grown as a person so much because of them.

3.

Quote 3

This one is probably my favourite one, and is the way to look at your autistic child’s learning. It might not be the conventional ways that work, but if you work with them they will find ways to learn.

4.

Quote 4

This is a nice one that gives a simple explanation of what autism can be like.

5.

My 5 favourite autism quotes

This is the one that everybody needs to understand. No one autistic person is that same, the spectrum is so wide and varied. Some have additional diagnosis as well, such as learning disabilities and some don’t. Which is why I always say that I’m no expert when it comes to Autism. I only know my 2 children, Jack and Lily’s needs.

They were my 5 favourite autism quotes. Which one is your favourite? Are there any others that I’ve missed, that are your favourite? Leave a comment below and tell me.

Dad Does Autism

Meet the Family