MS is a horrid disease. We have all heard of it but I doubt that everyone knows how it affects the lives of sufferers. This post by Lynne about her daughter is both moving and informative, please have a read.
As Lightly Crunchy pointed out, May is MS Awareness Month. I perhaps should have known this but I and my family are still new to this. Our daughter/sister/niece/cousin/fiance was diagnosed a year ago. I wrote an essay, which I might share at some point, titled “A Helper, A Dreamer and a Radiant Beamer”. It is about my three daughters and Jamie is the Radiant Beamer, and Jamie has MS. We don’t know where this road will take us and unknowns make us fearful and we push them aside.
Jamie is facing this bravely though we know of the fear and the anxiety that lies beneath. I am also still trying to find my way – I want to wave my Mother’s Wand and make it all go away … I should be able to, but I can’t. MS has already affected our family relationships – I do think we are…
View original post 721 more words




























