Sunday, October 31, 2010

Is there anyone out there

Is there anyone out there actually reading this? I have nothing new and exciting to report. I still have MS. YEEEEhaw. At least its the one consistant thing in my life. I know everyday when I wake up and everyday when I go to bed that MS my faithful friend will stil be there with me. Although.... if it plans on hanging around for such a long time and attending all my "special" occasions, and butting in at the most inappropriate times, then my good friend MS should at least buy me a Christmas gift!

Wednesday, October 27, 2010

Im too broke to be sick...

Co-Pays. I think there should be an entire class dedicated to people who are sick on Co-pays. There are copays for Drs, regular ones or specialist, there are copays for medications, there are copays for the shrinks that u need to go see to help you deal with the fact that you have this god awful disease... I personally think that being sick should be free! Think about it. You didnt want it, you certainly didnt go out and buy it. So why the hell should you have to pay to take care of it!! Maybe this could be brought up at the prezes next oval room meeting.....

Friday, October 15, 2010

Always something

So this week was full of fun and games in WWMS ( wonderful world of MS). I have been taking Copaxone for close to three years. I had a small stunt with Rebif for a few months that didnt work out so hot. Anywhoo they found two new lesions in the past 4 months and now I have to add IV steriods once per month. Fucking great.

Saturday, October 9, 2010

The Begining

Today is day one of my blog. I have no idea what a blog consists of nor do I know exaclty what im doing. So those of you who actually might read it. Please bear with me. Basically I wanted to start a blog about my life as a person living with Multiple Sclerosis, when I was diagnosed I wished I had more resourses to turn to, so feel free to shout out, yell out, ask out or put out any questions or comments you may have. As I get better at this blogginstuff I will add my " story" of  my MS.