Happy Thanksgiving

As I sit here on the eve of Thanksgiving I am seeing all that I am thankful for. Although I may have MS I have recovered very well from previous episodes and I am fully fuctional. For that I am thankful for everyday...For all of you out there living with whatever cross you may have to bear I wish you  a happy thanksgiving. Remember you never know how many people out there care about you or think of you everyday so if you are feeling alone just remember at some point in time you may have touched someones life and for that I'm sure that THEY are thankful

Have a Happy Health Thanksgiving

Happy Saturday

Made it though another day! This whole being tired thing is really cramping my style. I guess taking my vitamins would help but they dont seem to and I keep forgetting. Do any of you out there have any good suggestions on anti fatigue help? I also take amantadine but I find that it dosnt really help me. On the plus side its almost the holidays and I love to give presents!

New medication on the market

I opened up my email the other day and once again I got yet another email from the MS society. A new medication has been approved by the FDA. The Email was entitled ( eNEWS: FDA approves drug for socially challenging MS symptom)  So now lets get this straight. 1. I have to live with this for the rest of my life. 2. I can cripple me and 3. Now it may make me socially challanged. REALLY!!!
 Aside from the further fun MS fact  that I learned from the email the drug basically helps people who have uncontrollable laughter and or crying from MS. This is what makes us socially challanged. What ever happend to being socially challenged because u are an asshole. Do they have a medication for that?  I personally know quite a few people who could use an anti- asshole drug. Maybe the FDA should look into that.

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!

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.....

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.

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.