Planning The Unpredictable

LIVING with Multiple Sclerosis

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Medical Marijuana

June 5th, 2008 · 2 Comments

Well, those that know me might call me a quaker (Hi Grant!). I don’t really drink and don’t do any drugs. I am pretty boring, I admit. None the less, it was rather interesting to learn this morning that Washington State has a Medical Marijuana law and it specifically allows use for those with multiple sclerosis. Who knew that getting MS might mean I become a fun exciting person! Now I can add something to my list of what MS has given me…

Tom is home from his business trip and now I get to listen to him snort snot because he has horrible allergies. (Another thing MS has given me, no allergies!) He asked me about my MRI report and I promptly responded with “Well, didn’t you read my blog??!” He’s response was priceless as usual… “I shouldn’t have to read my girlfriends blog to get updates!” Oh but yes, you should!

So, I have added a subscribe to the blog via email on the left side. Just add your email and it will email you automatically when I post something new. You can also use one of the many RSS feed readers. My RSS feed link is http://msgirl.org/feed. There are links on the bottom of every post that will allow you to subscribe to my blog with your favorite RSS reader. I like google’s. It is nice and simple.

In other blog news, I have been featured in this week Carnival of MS bloggers. The Carnival of MS Bloggers a bi-weekly compendium of thoughts and experiences shared by those living with multiple sclerosis.

Tomorrow is the big doctors appointment. I might be giving myself shots by next week. Oh goodie.

Tags: Blog · Newly Diagnosed · Treatment

2 responses so far ↓

  • 1 Nadja Tizer // Jun 6, 2008 at 6:11 am

    Colorado has the same laws. Email me and I will tell you what I know. BTW, I recommend lots of research before taking the interferons. Maybe you can do something else…

    [Reply]

    nina reply on June 6th, 2008 7:31 pm

    I agree with the lots of research! I believe the interferons are not for me but I am going to give Copaxone a shot for now. At this point, I am not emotionally able to NOT choose a treatment option. We will see how it goes and maybe I’ll change my mind.

    [Reply]

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