Inflammatory!

Inflammatory Arthritis UK

Inflammatory! We want everyone to understand what life is like living with a chronic fluctuating disease. The founders of Inflammatory Arthritis UK, Debbie and Katy, give a unique insight into their lives covering the realities of living with inflammatory arthritis (IA) in a positive and friendly way. They will discuss popular topics and answer questions with honesty based on their experiences navigating life with IA.  Whether you’re personally affected, supporting a friend or family member, or simply seeking understanding, Inflammatory! is for you.

  1. Jamie Boder: Yoga For AS

    -4 j

    Jamie Boder: Yoga For AS

    Jamie Boder joins Debbie and Katy for a powerful, honest conversation about being diagnosed with Axial Spondyloarthritis (AxSpA) at 18, navigating Crohn’s disease, and learning to care for his whole self through movement, yoga, and mind–body practices. Jamie shares the emotional impact of diagnosis, the challenges of early adulthood with chronic illness, and the tools that helped him reclaim agency, stability, and joy.Key topics: Early autoimmune symptoms and delayed diagnosisEmotional impact of AxSpA at 18Losing identity and social connection through reduced mobilityDual diagnosis: AxSpA + Crohn’s diseaseTreatment limitations (NSAIDs, biologics, care coordination)Microbiome testing and the risks of extreme dietary controlYoga, somatic practices, interoception, and fatigue managementVagus nerve research and nervous system regulationSustainable lifestyle changes vs. “cure culture”Jamie’s recent flare and reassessing medicationBuilding Yoga for AS and supporting the communityKey words: Axial Spondyloarthritis, AxSpA, Ankylosing Spondylitis, Crohn’s Disease, Inflammatory Arthritis, Yoga for AS, Jamie Boder, microbiome, vagus nerve, fatigue management, yoga nidra, somatic practices, autoimmune health, remission, inflammatory bowel disease, IBD, chronic illness support, nervous system regulation. Resources mentioned: The Great Nerve, book exploring vagus nerve and inflammationYoga Nidra (guided deep relaxation for fatigue)Yoga for Arthritis (training organisation)Yoga for AS, Jamie’s organisation supporting AxSpA-friendly movementConnect with Jamie: Instagram: @JamieBoderInstagram: @YogaForAS Connect with IAUK Website: inflammatoryarthritis.orgNewsletter: Sign up for updates and new episodes Social: Facebook, Instagram, BlueSky, LinkedIn YouTube: Watch full episodes, subscribe, and share Disclaimer: Debbie and Katy are not medical professionals. They share personal experiences of living with IA to build connection and community. The podcast is for informational purposes only and is not intended to replace professional medical advice. We talk about our personal health journeys, and the podcast is not intended to provide professional medical advice, diagnosis, or treatment. We are not medical professionals and in no way claim to be medically trained. The podcast does not take responsibility for any losses, damages, or liabilities that may arise from the use of the podcast. The podcast does not assume responsibility for the accuracy of third-party content. For more information, head to https://inflammatoryarthritis.org/

    28 min
  2. Why is Inflammatory Arthritis so Misunderstood?

    26 juin

    Why is Inflammatory Arthritis so Misunderstood?

    This week’s episode brings back a long‑overdue Q&A, complete with a side of chaos. Between sick kids, COVID flashbacks, swollen joints, medication hangovers and the emotional weight of parenting with IA, we still show up with the Inflammatory! honesty and humour you expect. Topics covered: Parenting while managing IA; the guilt, the logistics, the emotional loadCOVID memories, shielding, and how our instincts changedDebbie’s daughter’s JIA flare and the heartbreak of stepping back as a parentMedication hangovers: how we handled them then vs nowTips for remembering injections (and why snoozing reminders is dangerous)Weird symptoms no one warned us aboutFatigue, pacing, and the myth of the “realistic day” with IAHow to avoid falling through NHS cracksHonest conversations with family and why we often don’t have them“The world would be better if…”The dangers of misinformation and preachy “cure” culture onlineCharlie Robards’ Hitting AS for Six and why it’s worth readingKey messages IA affects everyone differently, comparison helps no oneFatigue is under‑discussed and overwhelmingOrganisation helps, but the system is still complexKindness, respect, and active listening make the world betterKey words: Inflammatory arthritis, IA flares, JIA, arthritis fatigue, medication side effects, biologic injections, NHS rheumatology, chronic illness management, pacing, brain fog, and steroid joint injections.Resources: Purchase Charlie Robards Hitting AS for Six (all profits go to NASS) Sign up to our newsletter at inflammatoryarthritis.org Follow Inflammatory Arthritis UK on Facebook, Instagram,Bluesky and LinkedIn Disclaimer: Debbie and Katy are not medical professionals. They share personal experiences of living with IA to build connection and community. The podcast is for informational purposes only and is not intended to replace professional medical advice. We talk about our personal health journeys, and the podcast is not intended to provide professional medical advice, diagnosis, or treatment. We are not medical professionals and in no way claim to be medically trained. The podcast does not take responsibility for any losses, damages, or liabilities that may arise from the use of the podcast. The podcast does not assume responsibility for the accuracy of third-party content. For more information, head to https://inflammatoryarthritis.org/

    29 min
  3. Is it Brain Fog?

    19 juin

    Is it Brain Fog?

    In this warm, funny, and deeply relatable episode, Debbie and Katy dive into the messy reality of living with inflammatory arthritis; from chaotic travel days and brain fog to shooting elbow pain, perimenopause confusion, and the blurred lines between inflammatory arthritis and fibromyalgia. They explore new research finally proving what patients have said for years: weather really does affect pain. They also chat about art therapy, inclusive social activities, bowling with dodgy wrists, and the joy (and chaos) of corporate team‑building games. It’s an episode full of honesty, humour, and the kind of lived experience you only get from people navigating this condition every day. Key words: inflammatory arthritis, brain fog, fibromyalgia, perimenopause, weather and pain, humidity, low atmospheric pressure, patient experience, DMARDs, medication hangover, art therapy, NEIAA audit, remission, chronic illness, lived experience, arthritis research Topics covered: Travel chaos & chronic illnessBrain fog; what is it really?Fibromyalgia vs inflammatory arthritisWeather & pain; new researchWhat do we do with this information?NEIAA audit & the importance of languageClinical vs medicated remissionArt therapy & creative escapesInclusive social activitiesCommunity, local charities & supportResources and mentions: NEIAA – National Early Inflammatory Arthritis Audit (Discussion on terminology and patient engagement)Weather–pain research using smartphone tracking (13,000 participants)Fibromyalgia charities – upcoming guest plannedLocal community charities offering art therapy and support servicesInflammatory Arthritis UK – newsletter & social channelsConnect with usStay up to date with new episodes, resources, and community updates: Website & Newsletter: inflammatoryarthritis.orgSocial: Facebook, Instagram, LinkedIn, BlueSkyYouTube: Watch full episodesTikTok: Coming soon!Disclaimer: Debbie and Katy are not medical professionals. They share personal experiences of living with IA to build connection and community. The podcast is for informational purposes only and is not intended to replace professional medical advice. We talk about our personal health journeys, and the podcast is not intended to provide professional medical advice, diagnosis, or treatment. We are not medical professionals and in no way claim to be medically trained. The podcast does not take responsibility for any losses, damages, or liabilities that may arise from the use of the podcast. The podcast does not assume responsibility for the accuracy of third-party content. For more information, head to https://inflammatoryarthritis.org/

    27 min
  4. EULAR 2026 Insights

    12 juin

    EULAR 2026 Insights

    In this lively catch‑up episode, Debbie and Katy reflect on a chaotic two weeks filled with heatwaves, family events, joint flares, and a whirlwind visit to the EULAR Congress in London. From coping with extreme weather to navigating grief, pacing, and swollen joints, the conversation moves into deeper reflections on patient involvement in research, global collaboration, and the importance of honest conversations in rheumatology clinics. Debbie shares insights from EULAR, including discussions on youth engagement, sex and relationships in chronic illness, and the need for better data—especially for children and young people. The episode closes with excitement about future guests, growing global reach, and the upcoming 60th episode milestone.Key wordsInflammatory arthritis, EULAR, rheumatology, patient involvement, JIA, diagnosis delays, heatwave, pacing, chronic illness, research collaboration, NEIAA, patient voice, global community, sex and relationships in rheumatology, youth engagement.Key topics: Life in a heatwave: coping strategies, sunburn mishaps, heat exhaustion, and how weather impacts joints.Personal updates: family events, grief, operations, and the emotional load of busy weeks.EULAR Congress 2026:The scale of the event and navigating the Excel Centre“United in Motion” theme and reflections on movementFishbowl discussions on youth involvement in researchConversations about sex, relationships, and medication impactsGlobal perspectives on trust, culture, and communicationThe power of patient stories alongside clinical informationThe role of social media in connecting patients, researchers, and clinicians.Charity collaboration: reflections from the PARE roundtable on diagnosis delays, impact, and the realities of limited time and resources.The NEIAA audit: why young people must be included and how missing data limits change.Pacing, burnout, and boundaries when you’re a volunteer or self‑employed.Growing global recognition of the podcast and IAUK’s work.Upcoming guests and the road to episode 60Resources and mentions: EULAR – European Alliance of Associations for RheumatologyPARE – People with Arthritis and Rheumatism in EuropeNEIAA – National Early Inflammatory Arthritis AuditNASS – National Axial Spondyloarthritis SocietyJIA Champions ProgrammePodultery Podcast (episode featuring Debbie & Katy now live)Stay connected: Website: inflammatoryarthritis.orgInstagram & LinkedIn: @inflammatoryarthritisukPodcast: Inflammatory! on all major platformsDisclaimer: Debbie and Katy are not medical professionals. They share personal experiences of living with IA to build connection and community. The podcast is for informational purposes only and is not intended to replaceprofessional medical advice. We talk about our personal health journeys and the podcast is not intended to provide professional medical advice, diagnosis, or treatment. We are not medical professionals and in no way claim to be medicallytrained. The podcast does not take responsibility for any losses, damages, or liabilities that may arise from the use of the podcast. The podcast does not assume responsibility for the accuracy of third-party content. ·       Formore information, head to https://inflammatoryarthritis.org/

    26 min
  5. What's the Human Side of Inflammatory Arthritis?

    22 mai

    What's the Human Side of Inflammatory Arthritis?

    Debbie and Katy sit down after a whirlwind few weeks, including their first ever live podcast event, a national conference, and even a little “pod‑adultery” (appearing on someone else’s podcast). They reflect on the nerves, the joy, and the powerful audience reactions during the live show, where themes like shame, disclosure, grief after diagnosis, and identity came through strongly. The pair also dive into the everyday realities of living with inflammatory arthritis, opening up about the often-invisible challenges behind simple daily tasks like washing and brushing hair, cycling, and managing pain and fatigue. They also discuss concerns around digital-only NHS healthcare pathways, the importance of pacing and rest, and share updates on upcoming IAUK plans, including the return of live Q&As and volunteer opportunities.Key topics: First live podcast experience and audience reactions“Pod‑adultery” — appearing on Mel Brooks’ PSA HQ podcastCommon themes: shame, disclosure, grief after diagnosisEveryday challenges: hair care, cycling, makeup, pain managementNHS App + NHS Online Trust concerns and digital‑only healthcareStress, pacing, grief, and taking time offWeather changes, flares, sun safety on biologicsIAUK updates: live Q&A plans, Volunteers Week, newsletter and socialsKey words: inflammatory arthritis, psoriatic arthritis, chronic illness, live podcast, patient stories, NHS App, NHS Online Trust, digital healthcare, arthritis fatigue, arthritis pain, biologics sun safety, chronic illness grief, disability disclosureResources: PSA HQ Podcast with Mel Brooks — episode coming JuneIAUK Newsletter & Website: inflammatoryarthritis.orgIAUK Socials: Instagram, Facebook, LinkedIn, BlueSkyYouTube Channel: Watch full podcast episodesNational Voices — discussion on NHS Online Trust plansVolunteers Week (June) — opportunities to support IAUKDisclaimer: Debbie and Katy are not medical professionals. They share personal experiences of living with IA to build connection and community. The podcast is for informational purposes only and is not intended to replace professional medical advice. We talk about our personal health journeys and the podcast is not intended to provide professional medical advice, diagnosis, or treatment. We are not medical professionals and in no way claim to be medically trained. The podcast does not take responsibility for any losses, damages, or liabilities that may arise from the use of the podcast. The podcast does not assume responsibility for the accuracy of third-party content.For more information, head to https://inflammatoryarthritis.org/

    25 min
  6. Beyond Awareness Days

    15 mai

    Beyond Awareness Days

    Awareness days come and go, but life with inflammatory arthritis shows up every single day, especially when your hospital appointments disappear into the system. In this episode, Debbie and Katy talk candidly about the reality of being “lost in the system”, from missed biologic reviews and last‑minute phone calls to the emotional and practical fallout when admin goes wrong. Alongside the realities of recovering from surgery, grief, family pressures and the mental load of chronic illness.They also explore the many awareness days and weeks in May, from Axial SpA to mental health, fibromyalgia, auto‑inflammatory conditions, and International Nurses Day and why awareness shouldn’t be limited to a calendar date. Life with IA is every day, and so is the need for understanding, compassion, and community.Key Topics The reality of hospital admin and biologic funding renewals Navigating unexpected appointment changes Surgery recovery, anaesthetic effects, and medication timing Grief, family responsibilities, and emotional load Mental health and long‑term conditions The importance of self‑compassion Awareness days in May: what they mean and why they matter Axial SpA, auto‑inflammatory conditions, fibromyalgia, and arthritis awareness The role of nurses and consultants in IA care Misdiagnosis and overlapping symptoms Why awareness should extend beyond awareness days Keywords inflammatory arthritis, IAUK, biologics, rheumatology, Axial SpA, psoriatic arthritis, fibromyalgia, auto‑inflammatory disease, mental health, chronic illness, grief and illness, patient experience, arthritis awareness month, nurses day, long‑term conditions, self‑compassion, lived experience, inflammatory podcast Awareness Days & Weeks Mentioned Mental Health Awareness Week Axial Spondyloarthritis Awareness Day — 2 May Fibromyalgia Awareness Day — 12 May International Nurses Day — 12 May Auto‑Inflammatory Awareness Day — 20 May Arthritis Awareness Month (US) Mental health support: If you are struggling or need help with your mental health,below is where you can find support: Suicidal thoughts can be distressing, you can find help here:  ·       Samaritans https://www.samaritans.org/ 116 123 always open ·       Mind https://www.mind.org.uk/ 0300 102 1234 Open 9am to 6pm weekdays ·       Shout  https://giveusashout.org/  Text Shout to 85258 open 24/7 Episodes referenced: Episode 5 You are not alone : Mental health discussion Interviews with Rachell Smith, Adam Newton, James Hollens and Charlie Robards Episode 56 with Dr Rosemary Hollick Episode 52 with Andy Kelly good practice of mental health services Connect with us: We love hearing from you — your stories, your experiences, your questions.Follow, like, share and comment to help us reach more people living with inflammatory arthritis. Instagram Facebook LinkedIn Bluesky Newsletter: sign up at inflammatoryarthritis.org If you'd like to share your lived experience, email us at info@inflammatoryarthritis.org. Disclaimer: Debbie and Katy are not medical professionals. They share personal experiences of living with IA to build connection and community. The podcast is for informational purposes only and is not intended to replace professional medical advice. We talk about our personal health journeys and the podcast is not intended to provide professional medical advice, diagnosis, or treatment. We are not medical professionals and in no way claim to be medically trained. The podcast does not take responsibility for any losses, damages, or liabilities that may arise from the use of the podcast. The podcast does not assume responsibility for the accuracy of third-party content. For more information, head to https://inflammatoryarthritis.org/

    24 min
  7. Inflammatory Arthritis Insights with Dr Rosemary Hollick

    7 mai

    Inflammatory Arthritis Insights with Dr Rosemary Hollick

    In this insightful conversation, Debbie and Katy sit down with Dr Rosemary Hollick, a rheumatologist, researcher, and champion of patient‑centred care, to explore the realities of psoriatic arthritis, axial spondyloarthritis, and the evolving landscape of treatment. Rosemary explains how symptoms present, why diagnosis can be so challenging (especially for women), and how biologics have transformed outcomes over the past two decades. The episode also dives into Rosemary’s award‑winning work in health services research and the vital role of Patient and Public Involvement and Engagement (PPIE). She shares how involving patients from the very beginning of research leads to better questions, better care, and better impact. As she says in the transcript, “Just listen to the patient because the patient will tell you the answer.” This is a warm, honest, and empowering discussion for anyone living with inflammatory arthritis or supporting someone who is. Key words: Psoriatic arthritis, Axial spondyloarthritis, Inflammatory arthritis, Rheumatology, Diagnosis delay, Inflammatory back pain, Biologics, Patient‑centred care, PPIE, Health services research, Vasculitis, Uveitis,Spondyloarthropathies, Shared decision‑making Topics covered: Rosemary’s journey into rheumatology and research What psoriatic arthritis is and how it presents Differences between psoriatic arthritis and rheumatoid arthritis How axial spondyloarthritis is diagnosed Why women are often missed or misdiagnosed The difference between inflammatory and mechanical back pain How treatment has changed from 2008 to 2026 The shift from inpatient wards to fast‑track outpatient care Early use of biologics and why it matters The challenge of trial‑and‑error treatment Shared decision‑making and tailoring biologics to lifestyle What meaningful PPIE looks like in practice How patient partners shape research questions, analysis, and impact The importance of trust, respect, and long‑term relationships in research The “you said, we did” approach to accountability IAUK resources: IAUK website: inflammatoryarthritis.org IAUK newsletter sign‑up IAUK social channels: Facebook, Instagram, LinkedIn, BlueSky This episode was funded by UCB how had no involvement in the development of the content or associated materials. Disclaimer: Debbie and Katy are not medical professionals. They share personal experiences of living with IA to build connection and community. The podcast is for informational purposes only and is not intended to replaceprofessional medical advice. We talk about our personal health journeys and the podcast is not intended to provide professional medical advice, diagnosis, or treatment. We are not medical professionals and in no way claim to be medically trained. The podcast does not take responsibility for any losses, damages, or liabilities that may arise from the use of the podcast. The podcast does not assume responsibility for the accuracy of third-party content. ·       Formore information, head to https://inflammatoryarthritis.org/

    26 min
  8. British Society for Rheumatology 2026

    1 mai

    British Society for Rheumatology 2026

    Debbie and Katy return exhausted but energised after three intense days at the British Society for Rheumatology Conference in Glasgow,marking Inflammatory Arthritis UK’s first-ever national conference appearance.In this episode, they unpack what it meant to show up as a young charity, the powerful conversations they had with clinicians, researchers, and other charities, and the surprising innovations they discovered, from robotic ultrasounds to smarter blood monitoring systems. This is an honest, behind‑the‑scenes look at what happens when lived experience meets the wider rheumatology community and how much appetite there is for patient voice, collaboration, and change. “This gives us insights into what happens outside that clinic door and beyond the self‑management side.” Key Topics Our first national conference as a charityMeeting the wider rheumatology communityWhy clinicians are listening to the podcastThe challenge of medication namesThe transition gap for young people (16–18)Admin frustrations & homecare inequalitiesNew technologies on the horizon Research culture is changingPPIE (Public & Patient Involvement and Engagement)Useful Resources & Links Inflammatory Arthritis UK – sign up for the newsletter: inflammatoryarthritis.orgFollow IAUK on Facebook, LinkedIn, Instagram, and BlueSkyPrevious episode on NHS admin challenges (referenced by clinicians at the conference)Upcoming guest: Dr Rosemary Hollick on research, psoriatic arthritis, and axial spondyloarthritisDisclaimer: Debbie and Katy are not medical professionals. They share personal experiences of living with IA to build connection and community. The podcast is for informational purposes only and is not intended to replace professional medical advice. We talk about our personal health journeys and the podcast is not intended to provide professional medical advice, diagnosis, or treatment. We are not medical professionals and in no way claim to be medically trained. The podcast does not take responsibility for any losses, damages, or liabilities that may arise from the use of the podcast. The podcast does not assume responsibility for the accuracy of third-party content. ·      For more information, head to https://inflammatoryarthritis.org/

    18 min

À propos

Inflammatory! We want everyone to understand what life is like living with a chronic fluctuating disease. The founders of Inflammatory Arthritis UK, Debbie and Katy, give a unique insight into their lives covering the realities of living with inflammatory arthritis (IA) in a positive and friendly way. They will discuss popular topics and answer questions with honesty based on their experiences navigating life with IA.  Whether you’re personally affected, supporting a friend or family member, or simply seeking understanding, Inflammatory! is for you.

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