The Joel Nelson Podcast
![The Joel Nelson Podcast](https://pbcdn1.podbean.com/imglogo/image-logo/13359720/Podcast_Cover_v4_v897ig.jpg)
Your Story Matters. We raise awareness for those living with chronic illness, pain, and associated mental health challenges by providing a platform to share their stories. Their unfiltered reality. Hosted by award-winning Patient Advocate and lived Experience Champion Joel Nelson, weekly on Sunday evenings from 7pm (GMT) in front of a LIVE audience on our YouTube Channel here: https://youtube.com/joelvsarthritis.
Episodes
Episodes
![Day 3 in Vienna | EULAR 2024 Special](https://pbcdn1.podbean.com/imglogo/ep-logo/pbblog13359720/EULAR_Podcast_Cover_v4_33f74d_300x300.jpg)
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Friday Jun 14, 2024
Day 3 in Vienna | EULAR 2024 Special
Friday Jun 14, 2024
Friday Jun 14, 2024
On Day Three of the EULAR Congress in Vienna, we have a bumper episode for you as the podcast series becomes a talking point of the conference!
In this episode, you will hear from:
Raquel Vaz, Scientific Project Leader at IFPA
Paul Studenic, Researcher and Rheumatologist at Medical University of Vienna
Rebecca Beesley, Volunteer at Juvenile Arthritis Research (JAR Project)
Souzi Makri, Past Chair of EULAR PARE and Vice President of the Cyprus League for People with Rheumatism
Katy Antonopoulou, PARE Committee Member and President of Sjogren’s Europe
You can find us all week at Booth O22. Join us and share your great work to be part of this special podcast series recorded live and on location in Vienna.
For more information about the Good Care for PsA project: See here.
Follow the HOST:Instagram: https://instagram.com/joelvsarthritis Facebook: https://www.facebook.com/joelvsarthritis Twitter/X: https://twitter.com/joelvsarthritis Twitch: https://twitch.tv/joelvsarthritis TikTok: https://www.tiktok.com/@joelvsarthritis
Join our Online Peer Support Community and Discord server here: https://discord.com/invite/dUean4vDcX All Links: https://linktr.ee/Joelvsarthritis
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.
Music Credit: Buffon – by Gideon Murray
![Day 2 in Vienna | EULAR 2024 Special](https://pbcdn1.podbean.com/imglogo/ep-logo/pbblog13359720/EULAR_Podcast_Cover_v4_u8pv3u_300x300.jpg)
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Friday Jun 14, 2024
Day 2 in Vienna | EULAR 2024 Special
Friday Jun 14, 2024
Friday Jun 14, 2024
We are putting the patient voice into the EULAR conversation on Day 2 of the Congress as we are joined by Andreas Dam, developer of the RheumaBuddy app, and award-winning patient advocate and Chair-elect of the EULAR PARE Committee, Dr. Simon Stones.
You can find us all week at Booth O22. Join us and share your great work to be part of this special podcast series recorded live and on location in Vienna.
For more information about the Good Care for PsA project: See here.
Follow the HOST:Instagram: https://instagram.com/joelvsarthritis Facebook: https://www.facebook.com/joelvsarthritis Twitter/X: https://twitter.com/joelvsarthritis Twitch: https://twitch.tv/joelvsarthritis TikTok: https://www.tiktok.com/@joelvsarthritis
Join our Online Peer Support Community and Discord server here: https://discord.com/invite/dUean4vDcX All Links: https://linktr.ee/Joelvsarthritis
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.
Music Credit: Buffon – by Gideon Murray
![Day 1 in Vienna | EULAR 2024 Special](https://pbcdn1.podbean.com/imglogo/ep-logo/pbblog13359720/EULAR_Podcast_Cover_v4_75f9c8_300x300.jpg)
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Wednesday Jun 12, 2024
Day 1 in Vienna | EULAR 2024 Special
Wednesday Jun 12, 2024
Wednesday Jun 12, 2024
As we record LIVE from EULAR 2024 on IFPA’s booth to raise awareness of psoriatic disease and the Good Care for PsA project, we speak to some brilliant guests as the Congress heats up.
In this episode, you will hear from Ingvar Ingvarsson, Vice President of IFPA, Zoë Clark, Programme Manager at NASS, and Loreto Carmona, Rheumatologist, Epidemiologist, and EULAR Advocacy Chair. We talk about their hopes, plans, and work at Europe’s largest Rheumatology gathering.
You can find us all week at Booth O22. Join us and share your great work to be part of this special podcast series recorded live and on location in Vienna.
For more information about the Good Care for PsA project: See here.
Follow the HOST:Instagram: https://instagram.com/joelvsarthritis Facebook: https://www.facebook.com/joelvsarthritis Twitter/X: https://twitter.com/joelvsarthritis Twitch: https://twitch.tv/joelvsarthritis TikTok: https://www.tiktok.com/@joelvsarthritis
Join our Online Peer Support Community and Discord server here: https://discord.com/invite/dUean4vDcX All Links: https://linktr.ee/Joelvsarthritis
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.
Music Credit: Buffon – by Gideon Murray
![Raising Awareness of Hidradenitis Suppurativa | HS Awareness Week Special](https://pbcdn1.podbean.com/imglogo/image-logo/13359720/Podcast_Cover_v4_v897ig_300x300.jpg)
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Tuesday Jun 04, 2024
Raising Awareness of Hidradenitis Suppurativa | HS Awareness Week Special
Tuesday Jun 04, 2024
Tuesday Jun 04, 2024
Hidradenitis Suppurativa (HS) affects countless individuals, causing painful abscesses and scarring and impacting every aspect of life. Yet, it often remains shrouded in silence and misunderstanding. Join us for a powerful conversation with Barry McGrath, co-founder of HS Ireland, patient advocate, and former scientific clinical researcher, as we shine a light on this chronic condition.
Barry discusses his own experience with HS and the challenges faced by people with the condition. He also provides advice for people who are newly diagnosed with Hidradenitis Suppurativa, including finding a good medical team, joining a patient support group, and advocating for themselves.
If you enjoyed this episode, please remember to leave a review and subscribe wherever you listen to help more people find our awareness work. <3
Follow our GUEST: Website: http://hsireland.ie Instagram: https://www.instagram.com/hs_ireland Twitter: https://twitter.com/hsireland1 LinkedIn: https://www.linkedin.com/company/hs-ireland YouTube: https://www.youtube.com/@HSIreland
Follow the HOST:Instagram: https://instagram.com/joelvsarthritis Facebook: https://www.facebook.com/joelvsarthritis Twitter/X: https://twitter.com/joelvsarthritis Twitch: https://twitch.tv/joelvsarthritis TikTok: https://www.tiktok.com/@joelvsarthritis
Watch The Chronic Pain Club Talk Show and these interviews LIVE on YouTube and join the conversation!
Join our Online Peer Support Community and Discord server here: https://discord.com/invite/dUean4vDcX All Links: https://linktr.ee/Joelvsarthritis
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.
Music Credit: Buffon – by Gideon Murray
![Lupus Awareness Month | An Occupational Therapist's Journey with Type 1 Diabetes and Lupus](https://pbcdn1.podbean.com/imglogo/image-logo/13359720/Podcast_Cover_v4_v897ig_300x300.jpg)
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Tuesday May 21, 2024
Tuesday May 21, 2024
For Lupus Awareness Month in May, we are joined by Melissa Chieza, an occupational therapist and mental health practitioner who has been living with Type 1 Diabetes and Lupus since she was a child.
In the episode, Melissa discusses her experiences living with Lupus and Type 1 Diabetes since she was a child. She talks about the challenges of managing both conditions, including the emotional toll and the importance of self-care. Melissa also offers advice to others who are living with chronic illnesses, such as finding a support system, advocating for yourself, and learning to say no.
If you enjoyed this episode, please remember to leave a review and subscribe wherever you listen to help more people find our peer support community. <3
Follow our GUEST: Instagram: https://instagram.com/melcee97 Twitter/X: https://twitter.com/@mel_chieza
Follow the HOST:Instagram: https://instagram.com/joelvsarthritis Facebook: https://www.facebook.com/joelvsarthritis Twitter/X: https://twitter.com/joelvsarthritisTwitch: https://twitch.tv/joelvsarthritisTikTok: https://www.tiktok.com/@joelvsarthritis Join our Online Peer Support Community and Discord server here: https://discord.com/invite/dUean4vDcXAll Links: https://linktr.ee/JoelvsarthritisWatch The Chronic Pain Club Talk Show and these interviews LIVE on YouTube and join the conversation!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.Music Credit: Buffon – by Gideon Murray
![The Joel Nelson Podcast Heads to EULAR 2024!](https://pbcdn1.podbean.com/imglogo/image-logo/13359720/Podcast_Cover_v4_v897ig_300x300.jpg)
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Monday May 20, 2024
The Joel Nelson Podcast Heads to EULAR 2024!
Monday May 20, 2024
Monday May 20, 2024
In this brief unscripted update, we bring the exciting news that the Podcast is heading out this summer—and its first stop is the EULAR Congress in Vienna!
Keep an ear out for a special mini-series recorded live at the conference in June and for more announcements about other stops and countries on the tour soon!
If you enjoy this podcast, please remember to leave a review and subscribe wherever you listen to help more people find our peer support community. <3
Follow the HOST:Instagram: https://instagram.com/joelvsarthritis Facebook: https://www.facebook.com/joelvsarthritis Twitter/X: https://twitter.com/joelvsarthritisTwitch: https://twitch.tv/joelvsarthritisTikTok: https://www.tiktok.com/@joelvsarthritis Join our Online Peer Support Community and Discord server here: https://discord.com/invite/dUean4vDcXAll Links: https://linktr.ee/JoelvsarthritisWatch The Chronic Pain Club Talk Show and these interviews LIVE on YouTube and join the conversation!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 Rheum to Thrive Program: A Roadmap to Living Well with Arthritis](https://pbcdn1.podbean.com/imglogo/image-logo/13359720/Podcast_Cover_v4_v897ig_300x300.jpg)
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Tuesday May 14, 2024
The Rheum to Thrive Program: A Roadmap to Living Well with Arthritis
Tuesday May 14, 2024
Tuesday May 14, 2024
Chery Crow has amassed tens of thousands of followers on social media through her informative and energetic videos. She hosts the hugely popular 'Arthritis Life' podcast and website, where she works towards her vision of a world where every patient feels empowered and equipped to participate in meaningful daily activities with more confidence.
Cheryl also shares her Rheumatoid Arthritis story, what made her take to social media to share it, and why she founded the popular 'Rheum to Thrive' self-management and support programs.
Finally, we touch upon Acceptance and Commitment Therapy and why acceptance is not a bad word.
If you enjoyed this episode, please remember to leave a review and subscribe wherever you listen to help more people find our peer support community. <3
Follow our GUEST: Instagram: https://www.instagram.com/arthritis_life_cheryl/ TikTok: https://www.tiktok.com/@arthritislife
Follow the HOST:Instagram: https://instagram.com/joelvsarthritis Facebook: https://www.facebook.com/joelvsarthritis Twitter/X: https://twitter.com/joelvsarthritisTwitch: https://twitch.tv/joelvsarthritisTikTok: https://www.tiktok.com/@joelvsarthritis Join our Online Peer Support Community and Discord server here: https://discord.com/invite/dUean4vDcXAll Links: https://linktr.ee/JoelvsarthritisWatch The Chronic Pain Club Talk Show and these interviews LIVE on YouTube and join the conversation!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.Music Credit: Buffon – by Gideon Murray
![The Second Mountain: Ben's Journey of Self-Discovery with Anxiety and Depression](https://pbcdn1.podbean.com/imglogo/image-logo/13359720/Podcast_Cover_v4_v897ig_300x300.jpg)
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Friday Apr 26, 2024
Friday Apr 26, 2024
Please note that this show contains the following TRIGGER WARNINGS: Suicide, Grief, and Depression - please consider this when deciding how and where you listen.
In this show, my long-time friend, Ben Veal, founder and director of Second Mountain Comms, shares his personal experiences with anxiety and depression and how he managed his mental health during the COVID-19 pandemic. We'll talk about the recent loss of his father and the impact it's had on Ben's self-identity journey.
As fathers, we'll discuss the challenges of raising children today and how Ben is trying to improve his relationships and find purpose in his life, particularly with his work.
Whether you're struggling with your mental health, navigating grief, or figuring out who you are and what you want from life, we hope you'll find something to relate to in this show.
If anything in this episode affected you and you need support, you can find it local to you here: https://findahelpline.com/
If you enjoyed this episode, please remember to leave a review and subscribe wherever you listen to help more people find our peer support community. <3
Follow our GUEST: Instagram: https://instagram.com/secondmountaincommsTikTok: https://www.tiktok.com/@secondmountaincommsLinkedIn: https://www.linkedin.com/company/secondmountaincomms
Follow the HOST:Instagram: https://instagram.com/joelvsarthritis Facebook: https://www.facebook.com/joelvsarthritis Twitter/X: https://twitter.com/joelvsarthritisTwitch: https://twitch.tv/joelvsarthritisTikTok: https://www.tiktok.com/@joelvsarthritis Join our Online Peer Support Community and Discord server here: https://discord.com/invite/dUean4vDcXAll Links: https://linktr.ee/JoelvsarthritisWatch The Chronic Pain Club Talk Show and these interviews LIVE on YouTube and join the conversation!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.Music Credit: Buffon – by Gideon Murray
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Your Host
Joel Nelson is an award-winning patient advocate, published writer and international speaker.
Alongside this Podcast, he hosts a Twitch and YouTube channel where he talks about living with chronic illness and pain.
Joel uses his own experience with chronic illness, pain, and associated mental health challenges to inspire change, educate and reduce stigma while helping others feel less alone.
He has built a growing global community of peer support through his candid, 'no-filter' approach and is known for the creative ways he strives to 'meet patients where they are' and raise awareness.
Joel lives in Norfolk, UK, with his wife and young son.
If you want to learn more about Joel's work or discuss sponsorship opportunities, you can visit joelnelson.uk.