Read transcripts of debates in both Houses
Produced by Commons Library, Lords Library and Parliamentary Office Science and Technology
Search for Members by name, postcode, constituency and party
Learn about their experience, knowledge and interests
Celebrating people who have made Parliament a positive, inclusive working environment
Four staff networks for people to discuss and consider issues.
2018 marks 100 years since some women, and all men, could vote. Find out how you can join in
Sign up for the Your Parliament newsletter to find out how you can get involved
Take a tour of Parliament and enjoy a delicious afternoon tea by the River Thames
See some of the sights you’ll encounter on a tour of Parliament
Book a school visit, classroom workshop or teacher-training session
Access videos, worksheets, lesson plans and games
Follow this EDM by:
That this House is aware of the Muscular Dystrophy (MD) Campaign's patient survey, State of the Nation, published in January 2013, which revealed that people suffering from MD continue to experience long delays for a correct diagnosis of their condition and access to a specialist consultant; notes that major reforms led by the NHS Commissioning Board are officially to go live on 1 April 2013, which promises sufferers integrated and effective care for patients at each stage of their treatment; and calls on the Government to ensure that all people with MD or related neuromuscular conditions are supported by multi-disciplinary teams of professionals accessible in their areas and for them to have regular access to specialists able to monitor potentially fatal heart, lung and digestive problems, with regional health boards setting target dates for implementation and establishing accountability criteria if standards are not met.
Total number of signatures: 31
Showing 31 out of 31