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The Rest Room

The Rest Room

By The Rest Room

The Rest Room is a podcast about living well with chronic illness.

I'm Natasha Lipman, an award-winning chronic illness blogger and journalist from London.

I've been working with experts to bring you evidence-based guides on a whole host of topics like pacing, exercise, and chronic pain.

I'll also be talking to people who live with chronic illness and disability who are doing awesome things and learning how they make it work, as well as digging deep into the businesses and brands that are focussed on accessibility.

Think fashion, theatre, film, work, and play - there's a whole lot coming up to explore. So why don't you get cozy, make yourself a cup of tea, and join me in The Rest Room?
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How to pace without hating it

The Rest RoomFeb 09, 2022

00:00
29:22
How to pace without hating it
Feb 09, 202229:22
What to do when your chronic illness flares up
Jan 10, 202254:26
How accessible is theatre for disabled people?

How accessible is theatre for disabled people?

Many theatres were built hundreds of years ago, without accessibility in mind. It’s true that a lot has changed in recent years, but disabled people still face many barriers both off and on stage.

In this episode, we speak to access consultant and activist Shona Louise about the work she’s doing to drive real change in the industry. We also hear from actor, singer and radio presenter Sandra Gayer about her experience of accessibility as a performer.

So whether you’re a disabled person who wishes trips to the theatre were easier, or you work in the industry and want to know what changes you can make to improve accessibility, this episode is for you.

You can read the transcript here: www.natashalipman.com/theatre-accessibility-disability

Read Shona’s Open Letter here: https://bit.ly/3FyvMw2

Here’s more information about Sandra’s work: www.sandragayer.com

And here’s where you can catch her in the TV series Inside No. 9: https://www.bbc.co.uk/iplayer/episode/m000g1b2/inside-no-9-series-5-5-thinking-out-loud

Thanks to The Old Vic for sponsoring this podcast. You can learn more about their upcoming production of A Christmas Carol and their Access Scheme:

Follow me on Instagram: www.instagram.com/NatashaLipman and Twitter: www.twitter.com/NatashaLipman

If you'd like to dive deeper into any of the research I've highlighted in this episode, check out the links below.

And here’s some access information for theatres in London.

Dec 01, 202145:44
How to make a film about chronic illness

How to make a film about chronic illness

How often do you see chronic illness or disability portrayed on your screens? The answer is, sadly not as often as we should. In fact, disabled people are the most under-represented group in television, both on and off screen.

In this episode, we explore how accessible the industry is as we speak to screenwriter Charlotte Paradise. She’s behind the short film ‘Chronic’ which follows a chronically ill woman as she moves in with her boyfriend for the first time. 

Charlotte herself lives with chronic illness, so we spoke about the highs and lows of the industry, what it's like to tell such a personal story on screen, and how they endeavoured to make this an accessible process from start to finish.

So whether you want to get into the industry, or you simply want to see more representation on your screens, we hope this episode will get the conversation started.

You can read the transcript here: https://bit.ly/rest-room-chronic-film

Learn more about Chronic at: www.instagram.com/ChronicFilm

Thanks to The Old Vic for sponsoring this podcast. You can learn more about their upcoming production of A Christmas Carol and their Access Scheme:

Follow me on Instagram: www.instagram.com/NatashaLipman and Twitter: www.twitter.com/NatashaLipman

If you'd like to dive deeper into any of the research I've highlighted in this episode, check out the links below.

Nov 08, 202143:26
How To Navigate University With Chronic Illness

How To Navigate University With Chronic Illness

Heading to university can be a rollercoaster of emotions – for many, it’s one of the most exciting experiences, but also one of the most overwhelming. And for someone living with a chronic illness, it can be a minefield. 

In today’s episode we aim to take the stress and uncertainty out of the university experience, so you can enjoy the ride. Author, blogger and psychology graduate Pippa Stacey has experienced this all first hand, and shares the lessons she learnt along the way. 

We’re also joined by Dr Melanie Thorley from the student wellbeing service at the University of Greenwich, who shares some great advice, as well as her insights on the impact of the pandemic on the university experience. So, whether you’re returning to uni, or heading off for the first time, this episode has a whole lotta info to help you make the most of it. 

You can read the transcript here: www.natashalipman.com/university-chronic-illness-podcast

If you'd like to dive deeper into any of the research I've highlighted in this episode, check out the links below.

Sep 13, 202143:03
Writing, Chronic Illness & Incidental Diversity with Talia Hibbert
Jun 07, 202140:19
How To Read More When You Live With Chronic Illness

How To Read More When You Live With Chronic Illness

Struggling with reading is something that can be really upsetting to many people, so last year I took to my Instagram Stories to find out what your biggest challenges are when it comes to reading, and what has helped you find a way to make it more accessible.

Helpfully, and perhaps unsurprisingly, most of the reading issues that people shared can be broken down into a handful of categories:

🧠 Concentration and processing
🌩️ Physical issues/pain
😫 Energy
🕰️ Making time

We're going to cover a bunch of tips, tricks, and ways of thinking and approaching reading that I hope will help you!

It’s worth remembering that everybody reads at a different pace. Some people are extremely quick readers and the only things they struggle with are the impact of specific chronic illness symptoms. Others may have bigger challenges on top of that.

I am someone who is naturally an extremely quick reader and writer, and that’s something that I’m eternally grateful for.

This gives me automatic advantages when it comes to tackling these issues because my barrier to entry is already much lower. I’m thankful for everyone across the reading spectrum who has shared their experiences to help widen the scope of this piece of work.

We'll be covering topics like pacing (I know, but it's two different ways of thinking about it!), why reading is reading is reading is reading, different methods of reading, helpful resources, making physical books easier to read, the tracking trap, reflecting on your own experiences, and much more.

I'd love to hear about your relationship with reading: how do you find it, how does your chronic illness impact it, and what tools have you learned that help you?

You can find me on socials:
www.instagram.com/ NatashaLipman
www.twitter.com/NatashaLipman

Cover Art: @MimiButlin

Editing and music: Amit Rai

Blog post: natashalipman.com/how-to-read-more-when-you-live-with-chronic-illness/

Transcript: natashalipman.com/the-rest-room-reading-transcript/
Feb 02, 202132:30
How to learn a language with a chronic illness

How to learn a language with a chronic illness

I’m joined by one of my best friends in the world, Colin Gorrie. Or should I say Dr. Colin Gorrie.

Colin is a linguist and lifelong language learner. These days he works on bringing knowledge of language and linguistics to a wider audience online.

Colin also lives with EDS and experiences a lot of brain fog and fatigue, so I thought it would be a good opportunity to sit down and have a chat about some of the challenges of language learning when your brain doesn’t really retain information in the way that you’d like.

You may know that about a month ago I started learning Yiddish. II honestly don’t think it would be happening or going as well as it is if Colin hadn’t spent hours blowing my mind with how the way we often approach language learning…is not…great.

And that’s exactly what we’ll be discussing:

🌟 How people currently learn languages
🌟 Whether there is a better way (spoiler alert, there is!)
🌟 Figuring out our motivations for language learning and how to get started
🌟 Getting the most bang for your language learning (and energy) buck
🌟 Ways to take some of the pressure off and make language learning fun
🌟 How to think about pacing and retention of information when it comes to language acquisition

As always, language learning may not be something that you're interested in, or you have the ability to do at the moment.

This information is here for people who can make use of it!

-----

BLOG POST:
natashalipman.com/how-to-learn-a-language-with-a-chronic-illness/

TRANSCRIPT: natashalipman.com/how-to-learn-a-language-with-a-chronic-illness-transcript

LINK TO COLIN'S COURSE (10% DISCOUNT): https://hyperlink.academy/discount?discount=02b38cc4-6f47-4d0b-8533-56d2fe92a6f7

Theme music and editing by Amit Rai
Jan 11, 202145:47
How to Start Exercising when Everything Hurts

How to Start Exercising when Everything Hurts

Welcome to Episode 3 of The Rest Room!

In the last episode, we looked at ways to address the barriers that come up when figuring out how to start incorporating movement and exercise into your life.

We learned that we need to throw the whole ‘workout’ mentality in the bin, especially if movement is new to you, but we didn’t cover how to get started in really practical, tangible ways.

Whether you have little confidence in your body’s ability to do the things that you need (and want!) to do day-to-day, or you struggle to find a way to make movement a sustainable part of your life, this episode is for you!

Our aim is to help you find a way to move that feels safe, and that you’re confident you can stick with, even if it needs to be adapted on more challenging days.

There is no doubt that this work is hard. It takes courage, patience and persistence.

I hope this will give you a really tangible place to start thinking about your own movement practice.

Remember, It doesn’t matter how slowly you need to go. If you're consistent, you’ll still be building habits that will hopefully enable you to do what matters in your life.

*One thing I forgot to mention in the episode is that when you're figuring out what your "normal" is, it's important to seek help if something new pops up, even if you have learned coping strategies! I talk about this more in the blog post*

WORKSHEET DOWNLOAD:
bit.ly/movementworksheet

FULL BLOG POST: bit.ly/exercise-chronic-pain

TRANSCRIPT: bit.ly/RRe3transcript

Art: Lucy Dove

Editing and music: Amit Rai
Dec 19, 202035:10
What are your barriers to moving with chronic pain?

What are your barriers to moving with chronic pain?

Changing behaviour can be really hard, even at the best of times.

How many of you have embarked on a new fitness regime to help with your health condition, only to stop within a day, a week, or a month?

That could be because of pain, fatigue, lack of confidence, lack of support, or one of many other reasons.

We often underestimate the difficulties we’ll encounter when we try to break a habit or introduce something new into our lives.

In today's episode we're focussing on all those barriers to movement, specifically:

- The difference between a blip and an actual set back
- How fixed thoughts can stand in our way
- Celebrating small wins and setting realistic goals
- Taking the first step towards building a movement habit
- Understanding why dose matters
- Thinking about movement in the wider context of your life
- Planning for when things don't go to plan

Thinking about movement and exercise can be particularly challenging when you don’t have access to the adequate care that you need.

So, I’ve once again partnered up with the brilliant Claire Campbell from the Physiotherapy Pain Association to share the latest evidence-based information that will help you be able to take some of those first steps by yourself in a safe and sustainable way, and help you to become a more informed and active participant in your care.

Claire also lives with chronic pain, so she “gets this” in more ways than one!

This post still forms part of our introduction - so we may touch on some concepts, tools, and tips that we will be expanding on in the future.

There’s just a bunch of stuff that we think is important for you to keep in mind before you start trying to make any changes.

We hope that this will get you thinking about how your own barriers may be impacting you and your life, and we’ll be sharing some tips for breaking habits that may have formed for very important and legitimate reasons, but may not be helping you anymore.

READ THE BLOG POST:
bit.ly/chronic-pain-movement-barriers
TRANSCRIPT: bit.ly/restroompode2transcript

RESOURCES MENTIONED:

Interview with Dr. Whitney Scott: www.youtube.com/watch?v=moJ38ErQfMU

ACT (Overcoming FEAR): thehappinesstrap.com/upimages/Overcoming_FEAR.pdf

Where to find me: Twitter/Instagram
@natashalipman
www.natashalipman.com

Thank you for taking the time to listen and for your support!
Sep 05, 202031:18
Understanding Movement For Chronic Pain
Aug 23, 202018:25