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Five minutes with... Linseigh Green
Joe interviews theatre actor, Linseigh Green, about the lack of disability representation in the performing arts and the long-term outcomes of her condition, necrotising enterocolitis.
RAREYouth
Feb 13, 2025
Five Minutes with... Dylan Lombard
Joe interviews TikTok sensation Dylan Lombard about MDP syndrome, his love of all things creative and how he overcomes trolls on social media.
RAREYouth
Oct 25, 2024
Grief and rare disease: losing my mum and my ‘life glue’
Joe Rumney, creative designer at RARE Revolution Magazine, writes about the profound effect losing his mum had on his life
RAREYouth
Oct 16, 2024
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