Episode 53 of my 21andsensory podcast has a very Special Guest on…My Brother!
We chat about his FASD and Autism diagnoses and a bit about his life and growing up (including being adopted). We also chat about his special interests and hobbies.
If you haven’t heard of FASD it stands for Foetal Alcohol Spectrum Disorders. It is a term used to describe the permanent impacts on the brain and body of individuals prenatally exposed to alcohol during pregnancy resulting in a spectrum of physical, emotional, behavioural and neurological characteristics.
Some great FASD resources / Twitter accounts to follow are:
I was also a guest on the @SpotlightonFASD podcast. We chatted about my brother who is adopted and has diagnoses of FASD and is Autistic. I also spoke about my Sensory Processing Disorder and Autism. Listen here: https://youtu.be/TcQNRbq7FdM
My episode with my brother can be heard wherever you usually listen to your podcasts:
Hello everyone I’m here again to share another drawing, this time on masking 🎭. I did one a while back when I first started out sharing my illustrations here on Instagram. I don’t love how it looks so decided to redraw it!
So what actually is masking?
Masking involves trying to hide being autistic so others will accept us. It’s also referred to as camouflaging. This means we act in ways that other people will think we are ‘normal’ and to try and be accepted socially. My drawing includes a few examples of trying to mask.
Over the course of my life I feel I have perfected the art of masking (which isn’t necessarily a good thing). I am extremely good at with-holding my feelings and emotions, bottling them up until I get home. I would cry when I had to go to primary school each morning. Then speed forward a bit in time and I’d come home from secondary school each day very tearful. I even used to cry up in the SENCOs (special needs support) room at break and lunch times because secondary school is quite literally THE most overwhelming place I have ever had to cope in 👀.
But slowly through sixth form and university I began to build up a resilience to the world and although I still get overwhelmed I can always come home, have a bit of a sensory meltdown (and a good cry) then move on with things.
Socialising will always be hard for me and I think I will always cope with the world like this. But that’s okay. I have to actively remind myself that ‘normal’ isn’t real. And I think you should too. Masking is an autistic and sensory way of coping with the everyday and just trying to get by. Now that is brave. To go out in the world and just exist is a huge thing.
Do you have any tips related to masking? Feel free to share below ☺️
Hi everyone – I thought for the next post in my Sensory Series I’d discuss some New Year Autistic and Sensory Struggles…
In my Sensory Series I share text slides on different aspects of Sensory Processing (in between my regular posts of illustrations) so I can share my own outlook on all things sensory related. I thought it would be interesting to share my own experiences, tips and tricks along the way, feel free to scroll back over other posts in this series too over on my Instagram!
Please do share this post and feel free to comment down below how you cope with the New Year and any tips you have!
Image ID below.
Black and white icon of a calendar with a circled tick inside to indicated a day ticked off or countdown to the New Year with text underneath: ‘New year autistic and sensory struggles…’ The a pastel green line with ‘@21andsensory‘ underneath and in the top right hand corner of the post there is a pastel green box that says ‘ SENSORY SERIES’ in to show what series the post is part of.
Pastel green vertical line on left hand side of the image with text next to it: Everything seeming a bit louder, brighter, and just generally more full-on due to desensitising to things over the break. Looking forward to the routine or schedule that your educational or workplace setting gives you when you return again. Worrying more about how your facial expressions and body language are coming across and mimicking other people automatically.
Pastel green vertical line on left hand side of the image with text next to it: The dread of engaging in post- Christmas small talk on return to school, college, uni, work, etc. Not knowing how to word the start of your emails at the beginning of the New Year. (Do you have to ask people how their Christmas / New Year was…is it rude not to…) Having to get back into the practice of maintaining eye contact with people who aren’t your immediate family or friends all over again.
Pastel green vertical line on left hand side of the image with text next to it: Not realising until you are in a safe space that you are masking more in order to cope when you are out and about…and feeling burnt out as a result. Having to get back into tolerating specific clothing again such as formal work wear or school/work uniforms. Panicking about have to be more ‘social’ and switched on. Also the struggle of trying not to zone out of conversations and stay present.
Pastel green vertical line on left hand side of the image with text next to it: Not having to worry about being told or asked to try out new foods and drinks and not stressing about whether you’ll have access to your usual safe comfort foods. Getting back into the rhythm of planning out your downtime to involve special interests, hobbies and things you really love doing. And…No more Fireworks to worry about! (For a little while at least)
21andsensory logo (person holding up a white board with ’21andsensory’ on it. Underneath it says:If you like my work and you are able to, please consider supporting me via my Kofi page (link in bio). Or why not have a listen to my 21andsensory Podcast! With social media icons underneath.
Today I published my 50th 21andsensory Podcast episode! (Available wherever you get your podcasts, Apple Podcasts, Spotify, etc!) It’s a celebratory episode with just me doing an update and catch up so make sure you have a listen (link below this post!)
I started my podcast in August 2017 and it was literally just me talking into my voice memos on my phone. No fancy equipment whatsoever. I just decided to start chatting about my own life and my sensory struggles (little did I know I’d find out I was Autistic in 2019!)
It’s grown massively since then and from episode 17 onwards it wasn’t just me rambling on my own. I have had the pleasure of talking to a huge amount of people from all walks of life who have been so open and honest with me about their own journeys. It’s been an absolute pleasure and a joy to talk to so many people and I am constantly fascinated by what they have achieved. Also: I love nothing more than when my guests info dump about their hobbies and special interests when they come on!
I get a lot of email requests from people asking to ‘speak to my team’ about coming on my podcast and those sorts of emails always make me laugh because…it’s just little old me! I approach potential guests, create a personal podcast outline of questions each time, record, edit and publish the podcast on my own – and I absolutely love doing it. I really do love the audio format (and am a big podcast listener myself) there’s just something that feels really personal about chatting to someone in an informal and chill way.
Anyway! Here’s to more podcast episodes in the future…
(Because why the hell not – they are always handy!)
From garden centres or an online subscription! I had a Barrys Cactus Club subscription for around 9 months which I got for Christmas last year and let me tell you: it is quite literally the gift that keeps on giving! Also Patch Plants do some beautiful plants via delivery.
And that’s it! I hope this gift guide was helpful and gave you some ideas…I hope you all have a lovely Christmas time!
If you have some free time over the festive period why not have a listen to my 21andsensory podcast, there’s over 50 episodes to listen to and I’ve spoken to some amazing guests including some fab Authors, Actors, Influencers, Illustrators, Artists, TikTokers, Educators, Activists, Writers, Speakers, Producers, YouTubers, Podcasters, Sports Teams, Researchers, Scientists and even my own family! Plus many more…
Hi everyone – I thought for the next post in my Sensory Series I’d discuss a few everyday things that are sensory hell…
In my ongoing Sensory Series posts I’ll be sharing text slides on different aspects of Sensory Processing (in between my regular posts of illustrations) so I can share my own outlook on all things sensory. I thought it would be interesting to share my own experiences and tips and tricks along the way. Feel free to scroll back over other posts in this series too over on my Instagram here.
Please do share this post and feel free to comment down below how you cope with change and any tips you have!
Tags and seams in clothing.
Someone brushing up against you as they walk past.
Loud unexpected noise when walking near roads (especially motorbikes and sirens on emergency vehicles).
Electrical appliances that hum, buzz or vibrate.
Forcing yourself to brush your hair and teeth despite hating it.
Socks that won’t stay up or that roll down and come off in your shoe.
Strong distracting smells like air fresheners, scented candles, perfumes, aftershaves, detergents.
Clothing sleeves that get all bunched up and roll up under your coat sleeves.
Someone lightly touching you on the arm when they are talking about you in a conversation.
Bright colourful places like shops, classrooms and workplaces that are visually disorientating and distracting.
Finding holes in the only comfy clothing you have and stressing out about finding the exact replacement.
Anything that flickers or moves too fast like: candles, lights, screens, etc.
Cooking smells and getting your hands messy when preparing food and constantly having to wash them.
Worrying about access to your safe foods constantly when out and about and when you need to stock up at home.
Keeping up a mask and an act of ‘I’m doing okay, I’m managing’ until you can get home, be yourself and stim freely.
Not listening to music and avoiding online videos because songs get stuck in your head for hours on end and this causes overwhelm.
2 years ago on 8th November 2019 I was diagnosed as Autistic aged 25 (I posted this illustration I did above on Instagram on the day…but forgot to post it on my blog!). I can’t believe its been two entire years since then but everyday I am SO grateful to know that little bit more about myself.
Did I walk out of the assessment thinking that the whole world was going to look, feel and just BE different now that I knew this about myself? Yes.
Did it? No…but that’s okay. It’s such a life-altering thing to know about yourself that it’s natural to think like this. But what did happen was a hell of a lot of things slid into place in my mind about all the struggles I’ve gone through and how they are all pretty much down to the fact I had no idea I was Autistic.
Also episode 16 of my 21andsensory Podcast is an entire episode dedicated to just me discussing my entire diagnosis journey if you prefer to listen rather than read. Just search 21andsensory wherever you usually listen to your podcasts!
I thought for the next post in my Sensory Series I’d discuss why I struggle to use make-up & beauty products (and don’t anymore!).
In my Sensory Series I’ll be sharing text slides on different aspects of Sensory Processing (in between my regular posts of illustrations) so I can share my own outlook on all things sensory. I thought it would be interesting to share my own experiences, tips and tricks along the way, feel free to scroll back over other posts in this series too! Please do share this post and feel free to comment down below how you cope with change and any tips you have…