MS is a vile disease (like many chronic diseases). However, the internet and websites such as these can help us share experiences etc and hopefully make us more informed (to the annoyance of the so called experts no doubt). Knowing that others experience the same fears / challenges can help. My thoughts are echoed in a recent piece of research - see below:
http://www.mssociety.org.uk/news_events ... ctive.html
Thanks you Arron and all the people behind this site (I must confess I have yet to donate but will do so soon).