Category Archives: Disability

Don’t get sick and avoid stress!

Those are the two things my neurologist said I must do to try and stop this downward spiral that started in December 2009.

Kinda difficult when you work full-time as an inpatient physical therapist, around ill people most of the day, and you have two young children in 1st grade and daycare that bring home every bug known to man.

Right now I am sick. Like, I have a cold, sick. Feel like a truck ran over me, sick. This stresses me out because I always have an MS flair when I get sick. And there’s my one-two punch. Sickness, one; stress, two. Thus, it’s no wonder that it’s tough to type this post as my left arm isn’t playing nice and my right eye is blurring out my computer screen. I am also limping my way around my house trying to deny the fact that I should just sit my ass down. Just fabulous! *insert oozing sarcasm* One ironically good thing is that I’ve been off work since yesterday because it’s my 7 year wedding anniversary tomorrow. I was supposed to have these few days off to celebrate. Yay, happy anniversary to me… *again with the sarcasm* …my husband will be so thrilled when I give him his present of a hospital-grade cold. So anyway, I have until next Wednesday to feel better before I must return to work.

But more importantly, I am awaiting a couple of things, which is why it is imperative for me to get better and avoid going on steroids for an MS flair:
1. I have an MRI scheduled for Sept. 26th – won’t be able to have it if I have a flair and end up on steroids.
2. I am supposed to start the oral medication Gilenya on Oct. 3rd – won’t be able to do that either if I have to go on steroids.

So, this is where we hope and cross our fingers that I do NOT have an MS flair from being sick, so that everything can go as planned. I really need to start this medication – my optic neuritis (meaning the blurring in my eyes) and old symptoms flair up too often for me to not be on medications. I am still doing better than I was before my CCSVI procedure, but I need to do more as I believe this disease that I have is multifactorial in nature – partially vascular and partially immune system related.

I really need to de-stress. I really need to get well. I really need to get my life back.

Excuse, excuses, and more excuses

I miss blogging. I really do. It’s been so long that I was lucky that my login and password was auto-saved on my laptop, else I may not have made it far enough to even write this post. I used to blog a lot more when my kids were little, I worked only weekends and wasn’t diagnosed with Multiple Sclerosis. I’ll say it – excuses, excuses, excuses.

I miss my mommy blogger friends. I have lost touch with so many, yet I have them all friended on Facebook. I spend way too much lurking around on Facebook in my free time and should try blogging again. Because I really do have a lot to say, and I want to remember a lot things in the future when I look back on posts past.

My boys are now 6 and 4. My poor little Al has “second kid” syndrome when it comes to my external drive full of pictures. I am wondering if he’ll ask me one day if he even was 4 years old. My beautiful Nikon (of which I was so proud of back in the day) is gathering dust and needs to become a more important accessory of mine.

Now I have to figure out and remember how to upgrade WordPress, because I think I am at least 10 updates behind!

Optic Neuritis Again in Full Swing

Well, I just plain feel like crap.

I want to enjoy my 2nd venoplasty, but I can’t shake this ON. Day 4 today for IVSM. I may be off of work for at least another week, because I can barely see out of my right eye. Left eye is a bit better, but it’s tough reading and writing – gives me a headache.

Gonna go rest my eyes now. Will be talking with neuro tomorrow about some additional leave of absence from work.