Motion · S2M-05521 · 31 Jan 2007
Duchenne Muscular Dystrophy
The motion
That the Parliament expresses concern that people who suffer from Duchenne Muscular Dystrophy (DMD), a severe and progressive genetic muscle wasting disease predominantly affecting boys and for which there is currently no cure, are dying in Scotland on average 10 years earlier then their counterparts in England; believes that an improvement in the life expectancy and experiences of these young people must be a priority for the Scottish Executive; considers that, in addition to enhanced medical research, better support services, equipment and adapted housing can make a massive difference to the quality of life of people with DMD and can contribute to extending their life expectancy; welcomes the development in 2003 of the Scottish Muscle Network, based at Yorkhill, as a national managed clinical network benefiting patients in Stirling and across Scotland, but believes that more must be done to improve both life quality and life expectancy for people with DMD in Scotland.
Supporters (12)
- Donald Gorrie 1 Feb 2007
- Stewart Stevenson 1 Feb 2007
- Christine Grahame 2 Feb 2007
- Sandra White 2 Feb 2007
- Adam Ingram 5 Feb 2007
- Tricia Marwick 6 Feb 2007
- David McLetchie 6 Feb 2007
- Michael McMahon 6 Feb 2007
- Elaine Smith 6 Feb 2007
- Ken Macintosh 7 Feb 2007
- Mr David Davidson 15 Feb 2007
- Dr Jean Turner 20 Mar 2007
Source: the Scottish Parliament motions and amendments record.