by Meg | Nov 15, 2013 | Uncategorized
My name is Meg and I have MS. I was diagnosed in 2007, on December 21st (Merry Christmas to me!) One of the most common questions I get is about HOW I KNEW – what were the symptoms that led me to go to a doctor. In 2007 my children were 5,7 and 9 and having finished...
by Meg | Nov 15, 2013 | Uncategorized
Some of you that “know ” me (either for REAL or through other social media outlets) might know that I recently got a NEW badge to hang on my “wall” of things that define me. I was screened and approved to be a Patient Advocate for Biogen Idec...
by Meg | Oct 18, 2013 | Uncategorized
I realize that it has been a while since I gave an update on my experiences with Tecfidera (Biogen Idec’s new MS DMD.) I believe that when we were last together, talking about this…I was in Shawn’s bedroom, in middle of the night, COVERED in shit...
by Meg | Oct 18, 2013 | Uncategorized
I finally did IT! I broke down and bought myself a pack of Depends!!!! It’s NOT as if I have been peeing anymore than “normal” or that I had some terribly embarrassing accident that led me to feeling a great need to find an alternative solution to...
by Meg | Sep 26, 2013 | constipation, disease modidying drug, DMD, embarrassing moments, embarrassing moments, living with a disease, living with MS, MS, Multiple Sclerosis, reasons to laugh and smile, smile & laugh, Tecfidera, Uncategorized
WARNING….The kids and I (and even Shawn) had a bit too much fun coming up with slang terms for some of the topics/content of this post. Would say sorry, but it was just too much fun, and after hearing what happened, you will understand WHY I needed to laugh! I...
