As the festive season arrives, we want to take a moment to thank each and every one of you for your incredible support throughout the year. Your involvement, encouragement, and generosity have been instrumental in…
BY QUINN CLARK Hello folks! Welcome to Pathfinders Research Wrapped: where our Research Team picks their favourite muscle-weakening condition-based research done this year and delivers it to you, broken down simply! I’m Quinn Clark, the…
Our UpLift team member and film fan Connor shares his thoughts on disability representation in the new Wicked film. Despite the musical Wicked premiering on Broadway in 2003, it took 20 years for disabled character…
Pathfinders Neuromuscular Alliance strongly urges MPs to vote against the Second Reading of the *Terminally Ill Adults (End of Life) Bill* and oppose this bill outright. We represent a community living with muscle-weakening conditions with…
Our CEO Jon, a fellow WoW gamer with Duchenne shares his own story after watching The Remarkable Life of Ibelin on Netflix. “We weren’t as rare as you think. WoW was the community I needed…
We have joined forces with Muscular Dystrophy UK and Spinal Muscular Atrophy UK (SMA UK) to raise concerns of people living with muscle wasting and weakening conditions as a result of potential significant changes at…