Shift.ms is better if you're logged in

Hello fellow MSers! Do any of you blog about your MS? Or have you come across any blogs about MS that you've found helpful? The background behind the question is: My first clear symptom of MS was optic neuritis. When the hospital consultant diagnosed it, he simply said 'Don't Google it!'. I didn't ask why, but naturally went home and Googled it. From there I read how optic neuritis was often one of the first symptoms of MS, Googled 'Multiple Sclerosis' - I'm fairly certain for one reason or another I added 'video' to my search - and landed on an article and video on the Guardian website about a woman who had progressive MS and had written poetry about it. She had reached a stage where she was almost paralysed, couldn't speak or feed herself. I was devastated. I've since learnt that while at times challenging, having MS is by no means all doom and gloom! For me it's had some incredibly positive impacts on life. I'd like to write about them - to have a blog - so if there's just one new MSer that stumbles on it, being diagnosed isn't quite the same baptism of fire that I went through.