On the 11th May 2016, a Fibromyalgia Awareness event took place in Parliament, hosted by Andrea Jenkyns MP, and organised by Fibromyalgia Action UK (FMA UK).
The event was well attended by MPs, researchers, healthcare professionals, students and people living with fibromyalgia, their families and carers. There will be some exciting outcomes of this event resulting in greater collaboration of different stakeholders in the fibromyalgia field: patient organisations, healthcare professionals, researchers and policy makers.
During the event Dr Toby Garrood, a consultant from the Guy’s Hospital fibromyalgia clinic, gave an overview of the award-winning and excellent fibromyalgia multidisciplinary service, which can act as a role model to be replicated easily and for low-cost in rheumatology departments of hospitals across the country.…
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I was asked to write a blog to raise the profile of my MSK work supported by the Long-Term Conditions Team and, through the cryptic labyrinth of various schemes and initiatives, share with you my thoughts on how we can support sustainable, cost-effective transformation whilst still championing the more person-centred approach.

by Sarah Marsh, National Policy Lead, Long Term Conditions, NHS England
by Colin Beevor, Matron and Service Manager, Musculoskeletal OPD Services
by Ali Rivett, Director of Clinical Affairs, BSR
by Sarah Wright, Policy and Public Affairs Officer, ARMA
by Professor Anthony Woolf, Chair of ARMA and Chair of the Bone and Joint Decade: A Global Alliance for Musculoskeletal Health