The Joel Nelson Podcast

Dr Eleanor Chatburn, Clinical Psychologist, Lecturer, and Ambassador for The British Skin Foundation, joins us at the end of a marathon stream on World Psoriasis Day to discuss the mental health impact and burden of living with a chronic skin condition. We discuss ways of coping, alternative therapies, such as pain management and talking therapies, and the stigma people with skin conditions face. Plus, we get valuable insight into the psychology of living with a skin condition straight from the expert! Follow our GUEST: Instagram: https://instagram.com/dreleanorchatburn Follow the HOST: Instagram: https://instagram.com/joelvsarthritis Facebook: https://www.facebook.com/joelvsarthritis Twitter: https://twitter.com/joelvsarthritis Links: https://linktr.ee/Joelvsarthritis Watch The Chronic Pain Club Talk Show and these interviews LIVE on YouTube and join the conversation! Please remember to leave a review and subscribe wherever you listen to help more people find our peer support community. <3 DISCLAIMER: Please note that the host of this podcast and its producers are in no way medically trained and do not claim to be. On this show, we share the lived experiences of others - their story is their own, and we cannot be held responsible for their views or recommendations. Everyone is unique - what works for one person may not work for another. Always consult your medical professionals.

Eczema and psoriasis are common skin conditions that can cause significant discomfort and disruption to everyday life. This talk show provides practical tips and advice on managing these conditions and living more comfortably from various lived experience perspectives. We talk to experts in the field of skincare, as well as people who have lived with eczema and psoriasis, to get their insights and experiences. We also cover topics such as: How to identify and avoid triggers Alternative treatments and medications How to manage stress and anxiety The emotional and social impact of eczema and psoriasis Tips for living a full and active life Our guests include: Nadav Shraibom, MSc in Traditional Chinese Medicine (TCM), and Scientific founder of Medovie, a skincare company that combines the wisdom of traditional Chinese medicine with advanced scientific research to develop safe, natural, and efficacious skincare and dermatological products. Jo Greenslade, Managing Director of Eczema Clothing, a company that provides super soft, sustainable clothing and sound advice to people with itchy skin and who has personal experience with eczema in her family. The talk show is hosted by Joel Nelson, a father of one and Psoriasis Patient Leader, who has lived with psoriasis since childhood. He shares his story of how he has learned to manage his condition. Follow our GUESTS: Medovie https://www.facebook.com/MedovieOfficial/ https://www.instagram.com/medovieofficial/ https://www.linkedin.com/company/medovie/ https://twitter.com/medovieofficial/ https://www.instagram.com/medovienadav/ Eczema Clothing https://www.facebook.com/EczemaClothing/ https://www.linkedin.com/company/eczema-clothing/ https://www.instagram.com/eczema_clothing/ Follow the HOST: Instagram: https://instagram.com/joelvsarthritis Facebook: https://www.facebook.com/joelvsarthritis Twitter: https://twitter.com/joelvsarthritis Links: https://linktr.ee/Joelvsarthritis Watch The Chronic Pain Club Talk Show and these interviews LIVE on YouTube and join the conversation! Please remember to leave a review and subscribe wherever you listen to help more people find our peer support community. <3 DISCLAIMER: Please note that the host of this podcast and its producers are in no way medically trained and do not claim to be. On this show, we share the lived experiences of others - their story is their own, and we cannot be held responsible for their views or recommendations. Everyone is unique - what works for one person may not work for another. Always consult your medical professionals.

On this episode of the podcast, we are joined by somebody who needs little introduction in the UK access and disability space. Broadcaster, Journalist, Musician and disability advocate Mik Scarlet joins us to talk about his lifelong relationship with pain, the darker side of living with pain and how he uses humour to cope, the amazing work he does for access, disability and inclusion and touches upon his incredible and varied career. Please be aware that this episode contains some language and themes (including suicide and painkiller addiction) that may be unsuitable for younger audiences. If any of the topics discussed in this episode have impacted you, please visit: https://en.wikipedia.org/wiki/List_of_suicide_crisis_lines for signposting to support. Follow our GUEST: Instagram: https://www.instagram.com/mikscarlet Twitter: https://twitter.com/MikScarlet Follow the HOST: Instagram: https://instagram.com/joelvsarthritis Facebook: https://www.facebook.com/joelvsarthritis Twitter: https://twitter.com/joelvsarthritis Links: https://linktr.ee/Joelvsarthritis Watch The Chronic Pain Club Talk Show and these interviews LIVE on YouTube and join the conversation! Please remember to leave a review and subscribe wherever you listen to help more people find our peer support community. <3 DISCLAIMER: Please note that the host of this podcast and its producers are in no way medically trained and do not claim to be. On this show, we share the lived experiences of others - their story is their own, and we cannot be held responsible for their views or recommendations. Everyone is unique - what works for one person may not work for another. Always consult your medical professionals.

In this episode, we are joined by the wonderful Ian Taverner, aka Mr Cookfulness. Ian becomes an instant favourite with our live audience as we talk about adjusting to chronic pain, the mental health impact pain can have and how Ian turned to cooking to cope with his change in circumstances. Following Ian’s incredible journey from the grief of pain and the impact on his family to how he now owns the stage at events like Naidex, this episode is sure to not only inspire you but likely have you reaching for the tissues, as two men talk candidly about their mental health and the burden you can feel with living with a chronic illness. You can find Ian’s book, ‘Cookfulness: A Therapeutic Approach To Cooking’ on Amazon here: https://amzn.eu/d/a5fri3f Follow our GUEST: Instagram: https://instagram.com/cookfulness Twitter: https://twitter.com/cookfulness Follow the HOST: Instagram: https://instagram.com/joelvsarthritis Facebook: https://www.facebook.com/joelvsarthritis Twitter: https://twitter.com/joelvsarthritis Links: https://linktr.ee/Joelvsarthritis Watch The Chronic Pain Club Talk Show and these interviews LIVE on YouTube and join the conversation! Please remember to leave a review and subscribe wherever you listen to help more people find our peer support community. <3 DISCLAIMER: Please note that the host of this podcast and its producers are in no way medically trained and do not claim to be. On this show, we share the lived experiences of others - their story is their own, and we cannot be held responsible for their views or recommendations. Everyone is unique - what works for one person may not work for another. Always consult your medical professionals.

Tracy lived with Antiphospholipid Syndrome for 17 Years, from her first symptom to diagnosis, resulting in internal damage. Over the years, Tracy learned to use art to process and began painting her condition as she saw and experienced it. Now a patient advocate for Antiphospholipid Syndrome, Invisible Disability and Chronic Pain, Tracy joins us on the Chronic Pain Club Talk Show to talk about this often-overlooked autoimmune condition and how, quite brilliantly, she paints it. Follow our GUEST: Instagram: https://www.instagram.com/tjallowart Twitter: https://twitter.com/peculiari01 Follow the HOST: Instagram: https://instagram.com/joelvsarthritis Facebook: https://www.facebook.com/joelvsarthritis Twitter: https://twitter.com/joelvsarthritis Links: https://linktr.ee/Joelvsarthritis Watch The Chronic Pain Club and these interviews LIVE on YouTube and join the conversation! Please remember to leave a review and subscribe wherever you listen to help more people find our peer support community. <3 DISCLAIMER: Please note that the host of this podcast and its producers are in no way medically trained and do not claim to be. On this show, we share the lived experiences of others - their story is their own, and we cannot be held responsible for their views or recommendations. Everyone is unique - what works for one person may not work for another. Always consult your medical professionals.

On this episode, we are joined by Katy Pieris to talk about parenting with Rheumatoid Arthritis, the importance of exercise, why she volunteers and hear her arthritis story. This felt more like two friends chatting at the bus stop than a video call between two people for the first time, and I really hope that mutual respect, candidness and relaxed conversation comes across in the recording. :) Follow our GUEST: Instagram: https://instagram.com/joint.adventure Facebook: https://www.facebook.com/jointadventure.info Twitter: https://twitter.com/KatyPieris Follow the HOST: Instagram: https://instagram.com/joelvsarthritis Facebook: https://www.facebook.com/joelvsarthritis Twitter: https://twitter.com/joelvsarthritis Links: https://linktr.ee/Joelvsarthritis Watch The Chronic Pain Club and these interviews LIVE on YouTube and join the conversation! Please remember to leave a review and subscribe wherever you listen to help more people find our peer support community. <3 DISCLAIMER: Please note that the host of this podcast and its producers are in no way medically trained and do not claim to be. On this show, we share the lived experiences of others - their story is their own, and we cannot be held responsible for their views or recommendations. Everyone is unique - what works for one person may not work for another. Always consult your medical professionals.

We are joined by special guest Russ Cowper - Psoriatic Arthritis Patient Advocate, Charity Trustee and Poet - to hear why they advocate and how writing poetry helps them live with a chronic condition. This one, and the live poetry readings, proved very popular on our YouTube channel at the time of recording. Follow the HOST: @joelvsarthritis (Insta/Twitter/Facebook), or for full links, click here. Watch The Chronic Pain Club and these interviews LIVE on YouTube and join the conversation! Please remember to leave a review and subscribe wherever you listen to help more people find our peer support community. <3 DISCLAIMER: Please note that the host of this podcast and its producers are in no way medically trained and do not claim to be. On this show, we share the lived experiences of others - their story is their own, and we cannot be held responsible for their views or recommendations. Everyone is unique - what works for one person may not work for another. Always consult your medical professionals.

On this episode of The Joel vs Arthritis Podcast, we are joined by inspirational special guest Sukhjeen Kaur. We talk about her path to equality and inclusion advocacy, her founding of Chronically Brown and why Intersectionality is so important. Follow our GUEST: Instagram: @chronicallybrown Facebook: chronicallybrown Twitter: @chronicbrown Website: chronicallybrown.com Follow the HOST: @joelvsarthritis (Insta/Twitter/Facebook) Watch The Chronic Pain Club and these interviews LIVE on YouTube to join the conversation! Please remember to leave a review and subscribe wherever you listen to help more people find our peer support community. <3 DISCLAIMER: Please note that the host of this podcast and its producers are in no way medically trained and do not claim to be. On this show, we share the lived experiences of others - their story is their own, and we cannot be held responsible for their views or recommendations. Everyone is unique - what works for one person may not work for another. Always consult your medical professionals.

I report to you live from EULAR 2023 in Milan in a very special mini-series! Featuring news on what I am working on at the world-famous and largest European Rheumatology conference, I tell you what I see on the ground, in the sessions, the breakthrough research and advances in the rheumatology field through a patient's eyes. Join me every day this week live from EULAR! For live tweeting during sessions, follow me on Twitter: https://twitter.com/joelvsarthritis. For the IFPA Psoriatic Awareness Project: Click here For links to our Twitch and YouTube liveshows: Click here Please remember to leave a review and subscribe wherever you listen to help more people find our peer support community. <3 DISCLAIMER: Please note that the host of this podcast and its producers are in no way medically trained and do not claim to be. On this show, we share the lived experiences of others - their story is their own, and we cannot be held responsible for their views or recommendations. Everyone is unique - what works for one person may not work for another. Always consult your medical professionals.

I report to you live from EULAR 2023 in Milan in a very special mini-series! Featuring news on what I am working on at the world-famous and largest European Rheumatology conference, I tell you what I see on the ground, in the sessions, the breakthrough research and advances in the rheumatology field through a patient's eyes. Join me every day this week live from EULAR! For live tweeting during sessions, follow me on Twitter: https://twitter.com/joelvsarthritis. Please remember to leave a review and subscribe wherever you listen to help more people find our peer support community. <3 DISCLAIMER: Please note that the host of this podcast and its producers are in no way medically trained and do not claim to be. On this show, we share the lived experiences of others - their story is their own, and we cannot be held responsible for their views or recommendations. Everyone is unique - what works for one person may not work for another. Always consult your medical professionals.

I report to you live from EULAR 2023 in Milan in a very special mini-series! Featuring news on what I am working on at the world-famous and largest European Rheumatology conference, I tell you what I see on the ground, in the sessions, the breakthrough research and advances in the rheumatology field through a patient's eyes. Join me every day this week live from EULAR! For live tweeting during sessions, follow me on Twitter: https://twitter.com/joelvsarthritis. Please remember to leave a review and subscribe wherever you listen to help more people find our peer support community. <3 DISCLAIMER: Please note that the host of this podcast and its producers are in no way medically trained and do not claim to be. On this show, we share the lived experiences of others - their story is their own, and we cannot be held responsible for their views or recommendations. Everyone is unique - what works for one person may not work for another. Always consult your medical professionals.

This week, we are joined by special guest Molly Schreiber, Patient and Community Director of Savvy Cooperative, who shares with us their Rheumatoid Arthritis and Type 1 Diabetes lived experience and their work at Savvy Cooperative, helping to amplify patient and caregiver voices. Find our Guest: @mollyeschreiber (Instagram) @mollyschreiber (Twitter) Follow the HOST: @joelvsarthritis (Insta/Twitter/Facebook) Watch The Chronic Pain Club and these interviews LIVE on YouTube to join the conversation! Please remember to leave a review and subscribe wherever you listen to help more people find our peer support community. <3 DISCLAIMER: Please note that the host of this podcast and its producers are in no way medically trained and do not claim to be. On this show, we share the lived experiences of others - their story is their own, and we cannot be held responsible for their views or recommendations. Everyone is unique - what works for one person may not work for another. Always consult your medical professionals.

The Chronic Pain Club returns as Zoë Clark joins us to talk about her Ankylosing Spondylitis journey, how it feels to go through multiple and sometimes incorrect diagnoses, disability identity and how her work as an Allied Health Professional and patient advocate helps her and many others. Find our Guest: @ZoeTheOsteo (Instagram) @ZoeClarkOsteo (Twitter). Follow the HOST: @joelvsarthritis (Insta/Twitter/Facebook) Watch The Chronic Pain Club and these interviews LIVE on YouTube to join the conversation! Please remember to leave a review and subscribe wherever you listen to help more people find our peer support community. <3 DISCLAIMER: Please note that the host of this podcast and its producers are in no way medically trained and do not claim to be. On this show, we share the lived experiences of others - their story is their own, and we cannot be held responsible for their views or recommendations. Everyone is unique - what works for one person may not work for another. Always consult your medical professionals.

The Chronic Pain Club has more real patient stories and chronic illness awareness. This week, we were joined by James Hillery - Ankylosing Spondylitis patient and two-time contestant on the Great British Bake Off. He shares his AS journey candidly, and we get lots of behind-the-curtain insider info on what is happening on the set of The Great British Bake Off! This one was a must-watch/listen! - Watch the Chronic Pain Club live on our YouTube Channel (https://www.youtube.com/@JoelvsArthritis) on Sunday Evenings! You can find our guest on Twitter here: https://twitter.com/Cluckmuckcook and Instagram here: https://www.instagram.com/cluckmuckcook Follow the HOST: @joelvsarthritis (Insta/Twitter/Facebook) Watch The Chronic Pain Club and these interviews LIVE on YouTube to join the conversation! Please remember to leave a review and subscribe wherever you listen to help more people find our peer support community. <3 DISCLAIMER: Please note that the host of this podcast and its producers are in no way medically trained and do not claim to be. On this show, we share the lived experiences of others - their story is their own, and we cannot be held responsible for their views or recommendations. Everyone is unique - what works for one person may not work for another. Always consult your medical professionals.

In this episode, originally recorded in August 2022, we are joined by the inspirational Emma Townley for a Psoriasis Awareness Special, where we discuss Psoriatic Arthritis, its co-morbidities and how it impacts your mental health. We hear Emma's emotional journey from diagnosis to raising awareness to help others. Recorded live on Twitch as part of 'The Chronic Pain Club' weekly talk show - Watch it live and for free at https://www.twitch.tv/joelvsarthritis. SHOW NOTES Connect with our guest: Twitter / Instagram Our new YouTube Channel: https://www.youtube.com/c/joelvsarthritis The video recording of this interview: https://youtu.be/z6VBUdqX-oY If you've enjoyed this podcast, please don't forget to subscribe on whatever platform you are listening to this on, leave a review and send me your comments and feedback via email. It helps massively and allows me to improve future content and episodes. Get in touch with me at: You can find me on Facebook/Twitter/Instagram '@joelvsarthritis' For a full list of links, websites, words, videos and content: https://linktr.ee/Joelvsarthritis Facebook private support groups: Arthritis and Autoimmune Support Group & Chronic Pain Club Join our Discord Server THE PAIN COMPANY This podcast is sponsored by The Pain Company - created to raise awareness of chronic pain and illness. To give a voice to the millions living with daily, relentless pain. DISCLAIMER: Please note that the host of this podcast and its producers are in no way medically trained and do not claim to be. On this show, we share the lived experiences of others - their story is their own, and we cannot be held responsible for their views or recommendations. Everyone is unique - what works for one person may not work for another. Always consult your medical professionals.

Does your invisible illness ever make you feel like a fraud? We have a special guest as the wonderful Amy joins us to talk about her Juvenile Idiopathic Arthritis journey, the awareness she is raising to change future experiences and how it influenced her decision to train as an Occupational Therapist. Part of The Chronic Pain Club weekly chat show - Watch it live at https://www.twitch.tv/joelvsarthritis. SHOW NOTES Connect with our guest: https://twitter.com/amyface91 CCAA UK JIA Charity: https://www.ccaa.org.uk/ Our new YouTube Channel: https://www.youtube.com/channel/UCZrEJm2eWSSpXx8qMTjdgWA The video recording of this interview: https://www.youtube.com/watch?v=Wh7G0-sEIi8 If you've enjoyed this podcast, please don't forget to subscribe on whatever platform you are listening to this on, leave a review and send me your comments and feedback via email. It helps massively and allows me to improve future content and episodes. Follow me on social media for daily news and awareness stories. Get in touch with me at: You can find me on Facebook/Twitter/Instagram '@joelvsarthritis'. For a full list of links, websites, words, videos and content: https://linktr.ee/Joelvsarthritis Facebook private support groups: Arthritis and Autoimmune Support Group & Chronic Pain Club. THE PAIN COMPANY The Pain Company was created to raise awareness of chronic pain and illness. To give a voice to the millions living with daily, relentless pain. Shop here. DISCLAIMER: Please note that the host of this podcast and its producers are in no way medically trained and do not claim to be. On this show, we share the lived experiences of others - their story is their own, and we cannot be held responsible for their views or recommendations. Everyone is unique - what works for one person may not work for another. Always consult your medical professionals.

In this special episode recorded during Mental Health Awareness Week here in the UK, I am honoured to be joined by fellow WEGO Health Award Winner and TEDx speaker Dr Ashley Perkins. In a break from our usual arthritis-based content, Ashley candidly shares her eye-opening journey with anxiety, agoraphobia and OCD and how they significantly impacted her life and career. We learn how an upsetting and dangerous event, along with discrimination in the workplace, started her incredible advocacy journey and how she's making a real difference in the awareness of mental health and illness today. Please note that this episode comes with a Trigger Warning, with suicide, depression, and substance abuse discussed throughout the show due to the nature of this conversation. Please see the links below for support should any of the subjects discussed in this episode affect you. SHOW NOTES Our Guest Dr Ashley on Twitch Dr Ashley on Instagram We Matter Too Inc. Mental Health Support (UK) https://www.rethink.org/ https://www.samaritans.org/ Get help from a mental health charity — NHS (www.nhs.uk) Joel on Twitch (where this episode was recorded in front of a live audience) If you've enjoyed this podcast, please don't forget to subscribe on whatever platform you are listening to this on, leave a review and send me your comments and feedback via email. It helps massively and allows me to improve future content and episodes. Follow me on social media for daily news and awareness stories. Get in touch with me at: Twitter: @joelvsarthritis Facebook: facebook.com/joelvsarthritis Instagram: @joelvsarthritis Twitch: twitch.tv/joelvsarthritis Website: https://joelvsarthritis.co.uk Facebook support groups: Arthritis and Autoimmune Support Group & Chronic Pain Club. Quick Reference Links (Linktree) This episode is sponsored by THE PAIN COMPANY The Pain Company was created to raise awareness of chronic pain and illness. To give a voice to the millions living with daily, relentless pain. Shop here. DISCLAIMER: Please note that the host of this podcast and its producers are in no way medically trained and do not claim to be. On this show, we share the lived experiences of others - their story is their own, and we cannot be held responsible for their views or recommendations. Everyone is unique - what works for one person may not work for another. Always consult your medical professionals.

World yOung Rheumatic Diseases Day (WORD Day) is an annual event on 18th March to raise awareness that children and young people get rheumatic diseases. On Saturday the 19th March, Joel hosted an 8-hour marathon stream on his Twitch Channel to raise awareness of WORD Day 2022 and rheumatic disease in children and raise funds in aid of Juvenile Arthritis Research https://www.jarproject.org. In this second part of three special interviews hosted on the day, Joel talks to JIA patient, parent, volunteer at Juvenile Arthritis Research and all-around inspirational friend Rebecca Beesley about her work and JIA journey as both a patient and a mum. SHOW NOTES Joel on Twitch Donate to WORD Day/JAR Project Fundraiser To request a free support pack (UK only): www.jarproject.org/hope To read more about JIA: www.jarproject.org/myjia Web resources for younger children: www.jarproject.org/kipo Web resources for teens and older children: www.jarproject.org/teen To request a free School Toolkit (UK only, must be requested by the school/educational setting itself): www.jarproject.org/toolkit To find out more about our resources overall: www.jarproject.org/journey And Sophie's story that we mentioned in the interview: www.jarproject.org/stories/sophie If you've enjoyed this podcast, please don't forget to subscribe on whatever platform you are listening to this on, leave a review and send me your comments and feedback via email. It helps massively and allows me to improve future content and episodes. Follow me on social media for daily news and awareness stories. Get in touch with me at: Twitter: @joelvsarthritis Facebook: facebook.com/joelvsarthritis Instagram: @joelvsarthritis Twitch: /joelvsarthritis Website: https://joelvsarthritis.co.uk Facebook private support groups: Arthritis and Autoimmune Support Group & Chronic Pain Club. Quick Reference Links (Linktree) THE PAIN COMPANY The Pain Company was created to raise awareness of chronic pain and illness. To give a voice to the millions living with daily, relentless pain. Shop here. DISCLAIMER: Please note that the host of this podcast and its producers are in no way medically trained and do not claim to be. On this show, we share the lived experiences of others - their story is their own, and we cannot be held responsible for their views or recommendations. Everyone is unique - what works for one person may not work for another. Always consult your medical professionals.

World yOung Rheumatic Diseases Day (WORD Day) is an annual event on 18th March to raise awareness that children and young people get rheumatic diseases. On Saturday the 19th March, Joel hosted an 8-hour marathon stream on his Twitch Channel to raise awareness of WORD Day 2022 and rheumatic disease in children and raise funds in aid of Juvenile Arthritis Research https://www.jarproject.org. In this first part of three special interviews hosted on the day, Joel talks to friend, blogger and advocate Ali Daggett, about her diagnosis journey, the Chronically Connected project and why she shares her story. SHOW NOTES Joel on Twitch Donate to WORD Day/JAR Project Fundraiser Ali Daggett on Instagram Chronically Connected Under Young Skin Blog If you've enjoyed this podcast, please don't forget to subscribe on whatever platform you are listening to this on, leave a review and send me your comments and feedback via email. It helps massively and allows me to improve future content and episodes. Follow me on social media for daily news and awareness stories. Get in touch with me at: Twitter: @joelvsarthritis Facebook: facebook.com/joelvsarthritis Instagram: @joelvsarthritis Twitch: /joelvsarthritis Website: https://joelvsarthritis.co.uk Facebook private support groups: Arthritis and Autoimmune Support Group & Chronic Pain Club. Quick Reference Links (Linktree) THE PAIN COMPANY The Pain Company was created to raise awareness of chronic pain and illness. To give a voice to the millions living with daily, relentless pain. Shop here. DISCLAIMER: Please note that the host of this podcast and its producers are in no way medically trained and do not claim to be. On this show, we share the lived experiences of others - their story is their own, and we cannot be held responsible for their views or recommendations. Everyone is unique - what works for one person may not work for another. Always consult your medical professionals.

Has the Covid pandemic impacted the care we receive for our arthritis or chronic illness? In this 'round table' chat, full of insight, lived experience and heartbreak, we discuss the experiences of Jacyln, Safia and Ashleigh to understand how their 'normal' care has changed over the last two years. From lifelong conditions to the recently diagnosed, we take a sample of stories from across the country to get a snapshot of how treatments and appointments may have been impacted, what shielding was like and how Covid-19 has changed the perception of chronic illness and disability. You can also contribute to this episode by completing a survey HERE to share your experiences during the pandemic. As discussed in the show, we will be using this data to start honest conversations with decision-makers, so your voice makes a difference! SHOW NOTES The Pandemic and your Care Survey Jaclyn Fielden on Instagram (@jaclynleefielden) Safia Awil on Instagram (@snapkrackleandpop) Ashleigh Clarke on Instagram (@ashleighclarke2112) If you've enjoyed this podcast, please don't forget to subscribe on whatever platform you are listening to this on, leave a review and send me your comments and feedback via email. It helps massively and allows me to improve future content and episodes. Follow me on social media for daily news and awareness stories. Get in touch with me at: Twitter: @joelvsarthritis Facebook: facebook.com/joelvsarthritis Instagram: @joelvsarthritis Twitch: /joelvsarthritis Website: https://joelvsarthritis.co.uk Facebook private support groups: Arthritis and Autoimmune Support Group & Chronic Pain Club. Quick Reference Links (Linktree) THE PAIN COMPANY The Pain Company was created to raise awareness of chronic pain and illness. To give a voice to the millions living with daily, relentless pain. Shop here. DISCLAIMER: Please note that the host of this podcast and its producers are in no way medically trained and do not claim to be. On this show, we share the lived experiences of others - their story is their own, and we cannot be held responsible for their views or recommendations. Everyone is unique - what works for one person may not work for another. Always consult your medical professionals.