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In this episode, Dr Jess speaks with Lucy Traynor, who was 31 when she first experienced symptoms of multiple sclerosis - a diagnosis that would take three years to confirm. Lucy shares the emotional weight of seeing her brain scan for the first time, the frustration of navigating medical systems not designed with women in mind, and how negative media portrayals of MS fuelled her initial fears about the future. She discusses the challenge of balancing fertility plans with treatment decisions, the isolation of invisible disability, and how panic attacks became worse than physical symptoms. Lucy also reveals what helped her thrive: mindfulness, running marathons, painting, and consciously choosing positivity. Useful links: MS-UK: https://ms-uk.org/ Professor G’s blog: https://ms-selfie.blog/ Subscribe today to join the Wired for hope podcast community and learn with me. Written and hosted by Dr. Jessica Barton Produced by Anthony Zahra Music Credit: SigmaMusicArt DISCLAIMER: This podcast is not intended for use in crisis situations. If you are in immediate danger, experiencing suicidal thoughts, or facing a mental health emergency, please seek immediate help by contacting emergency services or a crisis line. UK Resources Include: • Emergency Services (Police/Ambulance): Call 999 • Samaritans (Free, 24/7 Helpline): Call 116 123 • NHS 111 (Non-Emergency Medical Help): Call 111 • Contact your local Single Point of Access (SPA) for mental health referrals and support — a centralised hub in the UK for accessing local services. • Headway – A UK charity providing resources and support for individuals affected by brain injury and their families. Limitation of Liability While every effort is made to ensure the accuracy and relevance of information shared, the host and contributors to “Wired for Hope” disclaim any liability for any direct, indirect, or consequential loss or damage that may arise from the use of the podcast or reliance on its content.