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 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...
by Meg | Jun 5, 2013 | Biogen, dealing with disease, disease modidying drug, DMD, living with MS, MRI scan for MS, MS, MS drugs, Multiple Sclerosis, positive attitude, smile & laugh, Tecfidera, using a cane
For those of you that may be following my experience with Tecfidera a disease modifying drug (DMD) for the MS, I wanted to give a quick update. I have been taking it for just over a week. I took a half dose for seven days and yesterday bumped up to the full dose. ...
by Meg | May 28, 2013 | Biogen, dealing with disease, disease modifying drug, DMD, MS, MS drugs, Multiple Sclerosis, Pain, segway, smile & laugh, Tecfidera, Uncategorized, weighloss
It’s here…the day that I am finally going to start taking Tecfidea. As I explained in the post about my most recent MRI, it has been three years since I was on a disease modifying drug (DMD) and although I am excited about the prospect slowing future...
