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myelinmalarkey: Three years

myelinmalarkey: Three years: " I havent updated my blog for a while as it was the holidays and things got crazy. Here we are already in the month of february and qic..."

Three years

 I havent updated my blog for a while as it was the holidays and things got crazy. Here we are already in the month of february and qickly heading into march,, the time passes so fast I dont know where it goes. This past Wednesday was february 9. Or as I referr to it " my least favorite day of the year. February 9th marks three years to the dat that I was diagnosed with MS.
 Heres the thing... I know that its uncurable, I know that its not going away, but deep down in my heart of hearts I still hope that Ill wake up from this bad dream of Drs visits, MRI's and never ending shots and be able to the live the life that I am suppose to live... the one that was stolen from me.....

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!