Campaign news
- 21 May 2013
Supporting more people through our advocacy service The Muscular Dystrophy Campaign is this week marking two years since our advocacy service was officially launched. - 17 May 2013
NHS England’s Medical Director commits to speeding up access to rare disease drugs The All Party Parliamentary Group (APPG) on Medical Research marked the launch of the new ‘Vision for research in the NHS’ document today with the Association of Medical Research Charities. - 7 May 2013
Bedroom Tax success could open the door for others The Muscular Dystrophy Campaign is today pleased to announce a recent successful challenge against the 'Bedroom Tax'. - 7 May 2013
Muscular Dystrophy Campaign shortlisted for Charity Awards 2013 The Muscular Dystrophy Campaign has been shortlisted in the Disability category for the 2013 Charity Awards. - 2 May 2013
New Lancashire neuromuscular team launched today We are delighted to announce today the launch of a new paediatric neuromuscular team in Lancashire at an event in Chorley General Hospital. - 1 May 2013
Initial CARE-NMD project findings shared at International Conference Earlier this month the CARE-NMD International Conference, held in Budapest, provided the first opportunity to hear some of the results of the CARE-NMD project on Duchenne muscular dystrophy care and quality of life in Europe. - 30 April 2013
New work experience programme launched with support from London charity The Muscular Dystrophy Campaign is delighted to announce that Trailblazers has received funding from the City Bridge Trust to run an extended work experience scheme in London. - 30 April 2013
Trailblazers victory with expansion of London Underground boarding ramps Trailblazers has welcomed the announcement that 19 additional London Underground stations and 40 additional platforms are to be made accessible from street to train this summer. - 23 April 2013
Families fear gaps in care will stop treatments reaching children Families affected by Duchenne muscular dystrophy gave evidence today to a panel of MPs and peers on their experiences of gaps in specialist care - 19 April 2013
South Wales' families feel 'let down' by NHS care for teenagers Families across South Wales feel teenagers affected by muscle-wasting conditions are being let down as they move from paediatric to adult NHS care.
