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...
by Meg | May 27, 2013 | MRI scan for MS, MS, reasons to laugh and smile
Writing my earlier post about my most recent MRI scan, brought back memories of my first MRI ever, before I was diagnosed with Multiple Sclerosis, back when I still thought I had Transverse Myletis and believed that I would be “all better” in a year. I...
by Meg | May 23, 2013 | Interferons, MRI scan for MS, MS, MS drugs, Multiple Sclerosis, reducing stress, Rituximab, Tecfidera, Tysabri
One of the things that was explained to me early on in this “journey” was that although there isn’t a cure for Multiple Sclerosis, that there a number of “disease modifying drugs” (DMD) available for those with the disease, and that...
by Meg | May 20, 2013 | Blogging, dealing with disease, living with a disease, living with MS, MS, parenting
I think that just about sums up how I am feeling at this point! I DO NOT think of myself as COMPLETELY tech/computer illiterate, and from EVERYTHING I read and watch (YouTube really is amazing, WHO takes the time to VIDEO tape themselves fixing their broken door...
by Meg | May 16, 2013 | Books about MS, dealing with disease, divorce, living with MS, MS, Multiple Sclerosis, parenting, positive attitude, single parent, smile & laugh
I wrote a book…no REALLY I did (a medical memoir of sorts.) Although I am not sure that means much since it hasn’t been published. BUT that isn’t because I have been told NO over and over again (or even once for that matter.) I’m not sure...
