Today I was diagnosed with MS
Well ok, not really, but in some ways it feels like it. Even though I have had MS since 2007, I have never spent time on-line looking for anything regarding the disease. Not information, not symptoms, not medicine and certainly not others that have MS (or MS-BFFs...
Tecfidera here I come. Thanks Biogen, I think…
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 progression, I...
MRI Scan – A Hole In My Head?!?!?
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 wanted to...
Sad and Lonely
I promised myself, and I guess you (who ever YOU are that might be reading this) that I would do my best to be open and honest, that I would work on putting EVERYTHING out there, because I know that is the only way that this is going to work. It's not fair or...
I Am Not a MeSs….
I had been "advised" to NOT blog a few years ago, not until I moved forward with getting my book published....the thought being that if I put EVERYTHING (all my stories and funny thoughts) out on the internet, people would be a lot less motivated to buy it (why pay...
MRI’s & DMDs (Disease Modifying Drugs)
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 pharmaceutical companies are...