by Meg | Jun 20, 2013 | Uncategorized
I have said that I will continue to update all of you on my experiences with taking Biogen’s newly released disease modifying drug (DMD) for MS, Tecfidera. I believe that this is week four, but I honestly apologize, time just seems to fly and days get clustered...
by Meg | Jun 16, 2013 | dealing with disease, depression, divorce, embarrassing moments, I have fallen and can't get up, inappropriate, living with a disease, living with MS, MS, reasons to laugh and smile, smile & laugh, why me?
AS PROMISED…. My husband (now the EX) had taken the kids out of town for a few days. The weather here was beautiful, clear blue skies, and hot! Heat can be more than slightly problematic for people with MS, enhancing symptoms. I had the house to myself and...
by Meg | Jun 16, 2013 | Biogen, dealing with disease, disease modidying drug, DMD, lesions, living with a disease, living with MS, MRI scan for MS, MS drugs, Multiple Sclerosis, New BETTER, Pain, Tecfidera
An update on the Tecfidera (Biogen). This will be week four (I think, I loose track of time.) It is going well. NO side-effects, and actually don’t REALLY have to take it with food anymore, although I DO try as it provides a GREAT reminder for me to EAT (I...
by Meg | Jun 14, 2013 | dealing with disease, divorce, living with a disease, MS, Multiple Sclerosis, positive attitude, reasons to laugh and smile, smile & laugh, Uncategorized
I have something that I need to get off my chest….to confess to all of you wonderful readers out there. I’m not sure what the reaction to this confession will be, if I will risk loosing some of you, but I can’t NOT say anything, because at the end...
by Meg | Jun 11, 2013 | Biogen, dealing with disease, disease modidying drug, DMD, living with a disease, living with MS, means of mobility, MS, MS doctor, MS drugs, Multiple Sclerosis, Neurologist, positive attitude, segway, Tecfidera, using a cane
I have said that I will keep you updated on what is happening with my latest and greatest med – Biogen’s Tecfidera, and I will, but first wanted to share my story about “OH FUCK.” I was diagnosed with MS in December of 2007, Merry Christmas to...