"Schools in Northern Ireland work hard to be inclusive for everyone and often contact me for information on muscle-wasting conditions. By completing this survey, you will help us identify areas that will enable you to have a more enjoyable time at school" - Corinna Keaney, Advocacy and Information Officer Northern Ireland.
Ensuring that children with muscle-wasting conditions are supported through education is crucial. If you are living in Northern Ireland please complete this survey to help us identify areas that can be improved. For further information please email firstname.lastname@example.org. >> qoo.ly/akjkh. ... See MoreSee Less
We are proud to announce that our Jake is starting his personal charity journey today. He has been sponsored by two UK companies: SCI-MX and The Fitness Food Co to take on a body transformation, with muscle disease, to raise money for Muscular Dystrophy UK.
As a full-time wheelchair user with limited movement in my arms, I found job-hunting difficult. Applying online or through a recruitment agency was fine, but when it came to the interview stage, often the venue would not be accessible" - Hannah-Lou Blackall, who has congenital muscular dystrophy.
Knowing your rights when looking for employment is crucial, read our new factsheet to find out what help is available to support you in work and when looking for work. >> qoo.ly/ajstr. ... See MoreSee Less