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Believe in ME with Rhona Barton

Podcast af Rhona Barton

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Videnskab & teknologi

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Læs mere Believe in ME with Rhona Barton

This podcast is all about ME. Each week I’ll bring you short manageable episodes that cover things from living with ME, understanding it, explaining it to others and learning how to love your life with it. As somebody who lived with Myalgic Encephalomyelitis (ME) for almost 10 years, I’m passionate about offering hope and inspiration to others who are experiencing ME. I was bed-bound and wheelchair-bound with ME before finding my feet again and coming through the other side so believe me when I say, I understand what you’re going through. If you are a woman living with ME, or you have recently been diagnosed with ME, then I’m here for you! I’ve been there, done that and I’ve not only got the t-shirt but I’ve worn holes in it too through all my trial and error! So why don’t you join me? You can subscribe now to receive notifications of each episode and Season 1 launches on 16th May 2022 to round off ME Awareness Week. Like, share and subscribe to Believe in ME with Rhona Barton via Apple podcasts, Spotify or wherever you find your podcasts. Website: https://www.rhonabarton.co.uk/

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38 episoder

episode World ME Day 2023 cover

World ME Day 2023

Hello and welcome to Believe in ME with Rhona Barton.  This podcast is about all things Myalgic Encephalomyelitis (ME) related! I'm Rhona and I lived with ME for almost 10 years during which time, I was bed-bound and wheelchair-bound, welcome to my Podcast. Hello and welcome to Believe in ME with Rhona Barton. In this week’s episode, I’m chatting about World ME Day. You can head to www.rhonabarton.co.uk/media [http://www.rhonabarton.co.uk/media] for more information about me and my story. Don’t forget that you can review, share & follow the podcast via Apple Podcasts, Spotify or wherever you’re listening now.  Ok, let’s jump straight in!  World ME Day takes place each year on 12th May. This year, the focus is around the fact that pushing harder with this condition, can make you sicker. The technical name for this feeling is sometimes shorted to PEM which stands for post-exertional malaise.  Post-exertional malaise is something that everyone with ME experiences but what is it? After any physical, emotional, or mental exertion, symptoms get worse. Prior to having ME/CFS or Long Covid, physical, mental or emotional exertion wouldn’t have been an issue, but PEM is a main symptom of ME.  For me, too much noise, too many bright lights or strange and strong smells, could be enough to exhaust me when I was at my worst. And I would feel the impact about 2 days later. Initially it was hard to tell why I felt so bad especially when I hadn’t done anything that day or the day before, but I was, with the help of my family, able to spot the pattern. That then helped with planning things in future, and I knew what to expect when I chose to do more. All of my symptoms, however, would worsen. Things would feel more intense. Lights would feel brighter, noise louder, smells would seem stronger, and my taste buds would change.  This could last for days or weeks and would lead to a crash. Now, knowing this and having explained this to various doctors, you’d think that they would take it on board and realise that I was the expert in my own illness and how it impacted me.  I like this quote from World ME Alliance co-chair and Solve M.E. CEO, Oved Amitay. It’s a reasonably long one but I want to cover it all.  It says, “Post-exertional malaise is a devastating symptom of both ME and Long Covid that is far too often disregarded or incorrectly managed by health care providers. PEM is a varying symptom that is challenging to recognise, and doing so requires intense listening to the person experiencing it. It is vital for health care professionals to identify PEM, as its presence changes the management advice a patient should be given and indicates that a diagnosis of ME should be considered. To avoid prolonging and intensifying the suffering of millions, providers must listen to and believe those who experience PEM.” I can tell you from my own experience that wasn’t the case, and even the supposed expert doctor, would have me trying new things to see if it would help. It was like talking to a brick wall when trying to explain that pushing myself didn’t help me, it made me worse. For people with ME, post-exertional malaise is a reality that can severely impact their daily life as well as the quality of that life. It’s estimated that about half of people with long Covid are experiencing PEM and that means that millions more people are having to deal with and live with this very debilitating symptom.  Before the COVID-19 pandemic, there were between 17 and 30 million people living with M.E. worldwide. But now there are about 65 million people living with long COVID, and half of those individuals are experiencing post-exertional malaise. This means the number of people living with M.E. has likely doubled over the past three years. Unfortunately, there is still no diagnostic test, cure or universally effective treatments for ME and that means that people could be living with this for life. So what can you do to help bring this condition and PEM to the forefront of people’s minds? If you are able, please do share your experience of post-exertional malaise so that others, the public and professionals alike, can learn from you.  Please use the hashtag #LearnFromME when sharing. Signpost your GP, physiotherapist, therapist or other health professional to Action for ME’s recently updated CPD learning module and podcast series as part of their Learn about ME project. Use the World ME Alliance’s online templates and resources to create your own poster and social media content and/or pitch your story to your local newspaper or radio station. If you are over the age of 16 and you are based in the UK, you can take part from home in the DecodeME study. This study hopes to reveal the tiny differences in a person’s DNA that can increase their risk of developing ME/CFS and building a greater understanding of the underlying mechanism of the condition. Please do like, share and subscribe to this podcast and pass it on to your friends, family and healthcare professionals. Let’s help spread education and information and help others #LearnFromME. Let me give you some links for these sites – I’ll also link to them in the show notes below this episode. Ok, first of all, I mentioned Action for ME and you’ll find their website and information about the CPD module at www.actionforme.org.uk [http://www.actionforme.org.uk] Next up is the World ME Alliance and they can be found at www.worldmealliance.org [http://www.worldmealliance.org] You will find more information about the DecodeME study, including the initial questionnaire to see if you meet the required criteria by going to www.decodeme.org.uk [http://www.decodeme.org.uk] And you can find more information about me and my ME story on my website at www.rhonabarton.co.uk [http://www.rhonabarton.co.uk] That’s it for today everybody.   I’d love to hear your thoughts on this and find out what you’re up to, if your able, for World ME Day so feel free to reach out via any of my social media links or my website. You’ll find me on Facebook & Instagram as @RhonaBartonCoaching and on Twitter as @RhonaBCoaching. I’m a proud founding member of the Emmeline podcast network and you can find out more about the Emmeline network by going to www.emmelinenetwork.com [http://www.emmelinenetwork.com] Thank you for listening. Don’t forget that you can review, share & follow the podcast via Apple Podcasts, Spotify or wherever you get your podcasts.  I hope today’s a good day for you. Bye for now.  Don’t forget that you can review, share & follow the podcast via Apple Podcasts, Spotify or wherever you get your podcasts.  You can also sign-up for my mailing list by visiting www.rhonabarton.co.uk [http://www.rhonabarton.co.uk/] or join my Facebook group – Believe in ME Community by following the Facebook page (@rhonabartoncoaching).

9. maj 2023 - 9 min
episode Imperfect ME cover

Imperfect ME

Hello and welcome to Believe in ME with Rhona Barton.  This podcast is about all things Myalgic Encephalomyelitis (ME) related! I'm Rhona and I lived with ME for almost 10 years during which time, I was bed-bound and wheelchair-bound, welcome to my Podcast. Hello and welcome to Believe in ME with Rhona Barton. In this week’s episode, I’m chatting to Jo Bell. Jo is an author, coach and the founder of Write to Thrive and through her group workshops and 1:1 programmes, she’s helped hundreds of people find clarity, confidence and self-compassion. I first came across Jo via Instagram. I’d seen her posting some writing prompts and, as a writer and author, these piqued my interest. As I continued to see her prompts in my news feed, they began to resonate with me and I took to jotting down some thoughts in relation to these. Earlier this year, I saw that Jo was running a 3-day Self-Compassion challenge. This was something that I’d been curious about, so I thought, “what the heck, why not!” and I signed up. In typical Jo style, as I’ve come to learn, she under promised and over-delivered! The 3 days, turned into 4 as she added on a bonus session for us and the private Facebook group for the challenge really got people chatting. I discovered in this short challenge that, although I’m not bad at taking time for myself, I’ve dropped back into old habits of trying to be everything to everyone. I’ve also found out that, when I have my internal monologue running in my mind, I’m not always kind in the way I speak to myself. In fact, I’m quite harsh and it’s something I want to change. So, when the opportunity came up to join Jo’s 8-week Luminous course, I knew I wanted in. I’m thrilled that Jo has agreed to have a chat with me and tell me more about her, her experience and her passion for self-compassion. We jumped on a Zoom call earlier and I hope you enjoy the conversation. You can head to www.rhonabarton.co.uk/media [http://www.rhonabarton.co.uk/media] for more information about me and my story. Don’t forget that you can review, share & follow the podcast via Apple Podcasts, Spotify or wherever you’re listening now.  Ok, let’s jump straight in!  Enjoy the call! I’d love to hear your thoughts on this so feel free to reach out via any of my social media links or my website. You’ll find me on Facebook & Instagram as @RhonaBartonCoaching and on Twitter as @RhonaBCoaching. You can find out more about Jo and the work she does by visiting her Instagram as @writeandthrive, her Facebook as @writethrive and her website at www.joannebell.org [http://www.joannebell.org] and you can sign up to her free newsletter with writing prompts via https://writetothrive.substack.com [https://writetothrive.substack.com] I’m proud to be a founding member of the Emmeline Podcasting Network and you can find out more about the Emmeline network by going to www.emmelinenetwork.com [http://www.emmelinenetwork.com] Thank you for listening. Don’t forget that you can review, share & follow the podcast via Apple Podcasts, Spotify or wherever you get your podcasts.  I hope today’s a good day for you. Bye for now.  Don’t forget that you can review, share & follow the podcast via Apple Podcasts, Spotify or wherever you get your podcasts.  You can also sign-up for my mailing list by visiting www.rhonabarton.co.uk [http://www.rhonabarton.co.uk/] or join my Facebook group – Believe in ME Community by following the Facebook page (@rhonabartoncoaching).

10. apr. 2023 - 28 min
episode International Women’s Day & ME cover

International Women’s Day & ME

Hello and welcome to Believe in ME with Rhona Barton.  This podcast is about all things Myalgic Encephalomyelitis (ME) related! I'm Rhona and I lived with ME for almost 10 years during which time, I was bed-bound and wheelchair-bound, welcome to my Podcast. Hello and welcome to Believe in ME with Rhona Barton. In this week’s episode, I was invited onto the Podcasting for Business podcast with Lynsay Gould. Lynsay is a fellow podcaster, entrepreneur and Founder of the Emmeline podcasting network.  We took some time to chat about this year’s International Women’s Day topic of Equity. You can head to www.rhonabarton.co.uk/media [http://www.rhonabarton.co.uk/media] for more information about me and my story. Don’t forget that you can review, share & follow the podcast via Apple Podcasts, Spotify or wherever you’re listening now.  Ok, let’s jump straight in! Enjoy the recording! That’s it for today everybody.  I hope you enjoyed this episode.  I’d love to hear your thoughts on this so feel free to reach out via any of my social media links or my website. You’ll find me on Facebook [https://www.facebook.com/RhonaBartonCoaching] & Instagram [https://www.instagram.com/rhonabartoncoaching/?hl=en] as @RhonaBartonCoaching and on Twitter [https://twitter.com/RhonaBCoaching] as @RhonaBCoaching. You can find Lynsay’s podcast, Podcasting for Business, on Spotify [https://open.spotify.com/episode/1vjlLyIYQDUoZqYdr7XAej...], Apple Podcasts [https://podcasts.apple.com/.../podcasting.../id1485599658...] or via your usual podcast provider. You can find out more about the Emmeline network by going to www.emmelinenetwork.com [http://www.emmelinenetwork.com] You can get links to each in my show notes also. Thank you for listening. Don’t forget that you can review, share & follow the podcast via Apple Podcasts, Spotify or wherever you get your podcasts.  I hope today’s a good day for you. Bye for now.  Don’t forget that you can review, share & follow the podcast via Apple Podcasts, Spotify or wherever you get your podcasts.  You can also sign-up for my mailing list by visiting www.rhonabarton.co.uk [http://www.rhonabarton.co.uk/] or join my Facebook group – Believe in ME Community by following the Facebook page (@rhonabartoncoaching).

10. mar. 2023 - 20 min
episode ME/CFS & Long Covid Don’t Take Holiday Time cover

ME/CFS & Long Covid Don’t Take Holiday Time

Hello and welcome to Believe in ME with Rhona Barton.  This podcast is about all things Myalgic Encephalomyelitis (ME) related! I'm Rhona and I lived with ME for almost 10 years during which time, I was bed-bound and wheelchair-bound, welcome to my Podcast. Hello and welcome to Believe in ME with Rhona Barton. In this week’s episode, I’m going to be chatting about Holiday time! You can head to www.rhonabarton.co.uk/media [http://www.rhonabarton.co.uk/media] for more information about me and my story. Don’t forget that you can review, share & follow the podcast via Apple Podcasts, Spotify or wherever you’re listening now.  Ok, let’s jump straight in! One of my favourite times of the year is holiday time. I’ve very lucky to be able to take two holiday’s a year including one in our motorhome. That hasn’t always been the case, however. Growing up, we never did foreign holidays. We might take a short break somewhere in the UK but mostly we had time at home and explored our local area. It’s only in the past 15 years or so that I’ve been a position to be able to afford to travel overseas. Sometimes that’s been for a holiday and sometimes it’s been for a work trip.  I love the build-up to a holiday or a break away. Getting out my bag – am I going only hand luggage, or do I need to pack a suitcase? I’ve been away for almost 6 weeks with only hand luggage so selecting a suitcase is a big deal for me! What is the weather likely to be when I’m away? That determines most of my packing choices – I usually end up opting for layers so I can throw more on or take them off as the day unfolds. I’ve never been a girlie girl, so don’t give a whole lot of thought to make-up, dresses, doing more than washing and drying my hair or shoes so I usually get through my packing really quickly. In fact, I’m pretty much a jeans, t-shirt and trainers sort of person and the less time I have to spend picking an outfit, the better it is for all involved! If I can’t get away with a smart-ish top, clean trainers and jeans for going out when on holiday, chances are, I’m not going to be interested in going to wherever it is that’s been suggested. Ultimately, I just want to be comfy, practical and wear what I like. So getting ready for a break away gives me a chance to select my favourite things for wearing and keeping the baggage weight down as much as possible. I gain quite a sense of achievement when I have everything I believe I need in one bag plus whatever I’m using as a day-to-day handbag when we’re away (and that’s, more often than not, a backpack!). But I also love the pre-planning. You know, the thinking about the place you’re going and then planning out some of the activities you’d like to do or places you’d like to visit when there. I also enjoy planning out the books I’ll take with me for reading, the podcasts I’m going to listen to and selecting a new notebook to take with me for the writing bug that’s sure to hit mid-break.  The books that I take with me have changed in recent years. I used to have to limit myself to 2 or 3 for a week away as there just wasn’t room in my bag to take more. However, about 10 years ago, I treated myself to an eBook reader – thank goodness for Christmas sales! And WOW, what a game changer! I will never not love a physical copy of a book but, for travel, I’m hooked on my eBook reader! I’m not limited to the number of books I can take with me now. It’s one of the first items that goes into my backpack – fully charged and with a wide selection of reading options! I’ll also download a couple of audiobooks to go alongside my podcast selections. I really enjoy having something to listen to in the motorhome when we’re driving or, once we’re parked up, listening to something whilst cooking.  I don’t often do that when I’m at home and, certainly during one of our holidays when we meet up with friends and family, I rarely have the chance to listen to podcasts or read, so it’s a treat when I’m away.  It’s something that’s a change from the usual day-to-day life. And it’s lovely to have that complete break from the usual routine.  The reason I mention this is because, whilst it’s lovely to be away from home for a break, the problem with ME/CFS and Long Covid, is that they don’t take a break. They don’t stop to allow us to have time away to join our friends and family for a proper holiday. It doesn’t stop.  For some people, remissions may occur, and their symptoms may lessen to the point that they can have a more “normal” time of things, but these are not predictable and not guaranteed. They are not necessarily within our control. And, unfortunately, it doesn’t happen for everyone. So we don’t get a holiday or a break from ME/CFS or Long Covid but the people who look after us, who care for us, can and should take some time away. We need them to be rested so that we can reach out to them when we need help and support. But for them to take a break, somebody else needs to step in to look after us.  That can bring additional drains on our energy levels and can be a stressful experience which could exacerbate symptoms.  It’s because these conditions don’t discriminate that means that it’s difficult for us to plan and pre-empt how we might be impacted by changes such as this.  What can you do when you’re not the one getting the break away? Well, if you’re able, sit with your family or carer and discuss the plan that needs to be in place for when they’re away. Who is going to be taking care of you? Can you meet them in advance? Can you or your full-time carer talk the new person through your needs and requirements? Can this new person shadow your full-time carer for a few days to learn the routine and get to know you? Or can you consider the likes of respite care if there’s something nearby? Think about the absolutes or the “must have’s” that make up your daily life – if those were the only things taken care of whilst your full-time carer was away, would it be sufficient for you?  And if you are going on a holiday or break away, have a look at things that could make travel a little easier for you.  If you’re going on a plane, can you arrange priority parking, fast track security and boarding? If travelling by train, is there a quiet carriage you can book? Also, do they offer an option to bring food to you to save you having to go to the buffet car?  Would taking noise-cancelling headphones or a neck pillow give you some comfort for the trip? Do you need to think about using a wheelchair or crutches to help you get about in a new environment? Can you break the travel for the trip up to allow for rest time? And, if you’re heading somewhere with sunshine, double check any medications you’re taking with your doctor or pharmacist as some may lead to photosensitivity and you might need to up the SPF in your sunscreen. All of this and then you have your holiday to get through and still get home! It truly is exhausting for healthy people so please go easy on yourself if you find it all too much. Remember, healthy people are likely to need a day or so to recover from travel and deal with getting the house in shape/laundry done/food shop in etc so don’t underestimate the knock-on impact that coming home may have on you too. The good news is there’s absolutely no rush to get back to your home routine. Be kind to yourself and rest when you need to. Let’s think about some key take aways from this episode: 1.    Holidays or breaks away can be a very welcome change from the day-to-day routine. 2.    Unfortunately, ME/CFS and Long Covid don’t care that we want a holiday and they stay with us wherever we go. 3.    If your carer goes on holiday, you may need to make a plan to help the person stepping in to take care of you. 4.    If you are going on holiday, take some time to think about the ways you may be able to make the travel a little easier for yourself. 5.    When you are back home with your full time carer, remember that not everything needs to be done in an instant. Give yourself recovery time. That’s it for today everybody.  I hope you have found this episode helpful and that, if you are planning a break away, it has given you some things to consider.  I’d love to hear about your plans, if you’re making any, so feel free to reach out via any of my social media links or my website. You’ll find me on Facebook & Instagram as @RhonaBartonCoaching and on Twitter as @RhonaBCoaching. You can download your FREE Activity tracker by heading to www.rhonabarton.co.uk/links [http://www.rhonabarton.co.uk/links] Thank you for listening. Don’t forget that you can review, share & follow the podcast via Apple Podcasts, Spotify or wherever you get your podcasts.  I hope today’s a good day for you. Bye for now.  Don’t forget that you can review, share & follow the podcast via Apple Podcasts, Spotify or wherever you get your podcasts.  You can also sign-up for my mailing list by visiting www.rhonabarton.co.uk [http://www.rhonabarton.co.uk/] or join my Facebook group – Believe in ME Community by following the Facebook page (@rhonabartoncoaching).

27. feb. 2023 - 11 min
episode Resetting ME cover

Resetting ME

Hello and welcome to Believe in ME with Rhona Barton.  This podcast is about all things Myalgic Encephalomyelitis (ME) related! I'm Rhona and I lived with ME for almost 10 years during which time, I was bed-bound and wheelchair-bound, welcome to my Podcast. Hello and welcome to Believe in ME with Rhona Barton. In this week’s episode, I’m going to be chatting about how things are going so far in 2023! You can head to www.rhonabarton.co.uk/media [http://www.rhonabarton.co.uk/media] for more information about me and my story. Don’t forget that you can review, share & follow the podcast via Apple Podcasts, Spotify or wherever you’re listening now.  Ok, let’s jump straight in! How are you getting on with your plan for 2023? I’ll be honest, mine went off track a few days into the New Year. I uploaded, via my social media scheduler, a post about goals and motivation and I was jumped on by people in the ME community who thought I was “having a go” at them for not “trying” or not being motivated enough. I was accused of spreading toxic positivity and of trying to take advantage of our community. I was told that I didn’t know what I was talking about and that I clearly didn’t know anything about ME or what it was like to live with.  Now, initially I made the mistake of trying to be rational with the first couple of comments. I considered taking the post down. I thought about editing the post, but I’d pretty much reached the character limit. The notifications for this one Social Media site went crazy! It’s the most interaction I’ve had on a post, and it knocked me for six. What had I done wrong? I began to tailspin, and I read every comment and took them all to heart.  I had a call later that evening with my Podcast coach and our Mastermind group and they received the brunt of my “I’m so over Social Media” rant! They asked me questions and challenged my responses as any good friend, let alone coach, would do. But I was in the middle of the yuckiness of it all and I really didn’t want to be facing what I was being asked. So instead, I listened to what they were saying, and I took some notes so that I could reflect on things when the time felt right for me. But what surprised me from this situation was that I, at 45 years old, was a recipient of cyber bullying. That’s what it was. And I was shocked.  People who didn’t know me, didn’t know my story, felt comfortable to call me all sorts online. All because they disagreed with one hashtag on a post. They didn’t come to listen to the podcast. They didn’t venture to my website to find out more, they just turned into angry keyboard warriors.  I let my social media schedular run the rest of the scheduled posts and I didn’t edit any of them or change their pre-set hashtags. I spent days thinking about and reflecting on what these comments said and trying to weigh up what, if anything, these may have been correct about. I thought about the questions that my Podcast coach and Mastermind group had posed. After all of this, I decided that I needed to take a break from social media. I needed to stop and reset my brain. So I took 4 weeks off and had a holiday. I made a point of not posting anything online and I took the apps off my phone so that if I wanted to lurk on any platforms, I’d have to either download them again or go via the respective website. It was so refreshing! Not only was I able to enjoy time on holiday with friends and family, but I didn’t miss the constant barrage of filtered online ideals. And I learned a few things too! Unlike the people who came after me, if I see a post I don’t agree with, I scroll past it. I know that I don’t believe the same things as the original poster and I know that, even though I think they are wrong, they believe what they are saying is correct. And it makes sense to them based on their experiences. I don’t feel the need to attack them. I know that I can just move past it without having to engage as its online. It’s not in my life and I’m not having to live with that individual. I know that the people who commented on my post are not the people who listen to my podcast. They are not interested in finding out anything about me or my own experiences. I know that they are probably very angry and frustrated that their health isn’t where they would like it to be and that they are searching for answers wherever they can find them. I know I don’t have the answers they are looking for.  I also learned that the reason I felt so attacked from the comments, is because I was going through some self-doubt. I was in the midst of many incomplete things in the run up to Christmas and the New Year and felt very unsettled. Without really knowing it, I’d let things get on top of me. The worry about all of these meant that I wasn’t sleeping well and on top of that, I wasn’t eating properly. It all built up and this was the straw that broke the camel’s back. I knew that I had to take a break. I knew I was beginning to feel overwhelmed with the concern about what I would do in the New Year. So I stopped. I stopped everything that wasn’t just the basics that I needed to make me feel happy and fulfilled. It took a couple of days for things to slow down for me but I began to plan out my days with the “must do” things. This then gave me time back to do some meal planning, shopping and cooking and I began to sleep easier. I reset myself. My holiday gave me time to think about what I want and how I want to carry on with 2023. Let’s think about some key take aways from this episode: 1.    Not everybody sees things the same way we do. 2.    We are all fallible. 3.    Sometimes even when we think we have things figured out, we still need to reset ourselves. 4.    You’re not going to be everybody’s cup of tea. 5.    Social Media isn’t always social! That’s it for today everybody.  I hope you have found this episode helpful and can understand why I have been absent for the past month or so.  I’d love to hear how your year is going, so feel free to reach out and let me know. You’ll find me on Facebook and Instagram as @RhonaBartonCoaching and on Twitter as @RhonaBCoaching. Thank you for listening. Don’t forget that you can review, share & follow the podcast via Apple Podcasts, Spotify or wherever you get your podcasts.  I hope today’s a good day for you. Bye for now.  Don’t forget that you can review, share & follow the podcast via Apple Podcasts, Spotify or wherever you get your podcasts.  You can also sign-up for my mailing list by visiting www.rhonabarton.co.uk [http://www.rhonabarton.co.uk/] or join my Facebook group – Believe in ME Community by following the Facebook page (@rhonabartoncoaching).

13. feb. 2023 - 9 min
En fantastisk app med et enormt stort udvalg af spændende podcasts. Podimo formår virkelig at lave godt indhold, der takler de lidt mere svære emner. At der så også er lydbøger oveni til en billig pris, gør at det er blevet min favorit app.
En fantastisk app med et enormt stort udvalg af spændende podcasts. Podimo formår virkelig at lave godt indhold, der takler de lidt mere svære emner. At der så også er lydbøger oveni til en billig pris, gør at det er blevet min favorit app.
Rigtig god tjeneste med gode eksklusive podcasts og derudover et kæmpe udvalg af podcasts og lydbøger. Kan varmt anbefales, om ikke andet så udelukkende pga Dårligdommerne, Klovn podcast, Hakkedrengene og Han duo 😁 👍
Podimo er blevet uundværlig! Til lange bilture, hverdagen, rengøringen og i det hele taget, når man trænger til lidt adspredelse.

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