Browsed by
Tag: neurontin

What’s up

What’s up

I’ve been meaning to post here for the past 2 days, but I have been flaring like crazy.  It’s 1:30 in the morning here and it’s the first time in the past 48 hours that I feel almost normal.  I know that there are so many people who have different autoimmune diseases, and other diseases for that matter, and I don’t know how people do it.  How do you get up in the morning and get ready and go about your day?  I want that back in the most desperate way.  I do realize that this is depression talking, and that things WILL get better, but for now I just can’t see the light at the end of the tunnel.  I still have a month left before I see the neuromuscular doc for my biopsy results.  Has anyone had to wait 2 months for results???  So for now, I just keep taking 2700mg of neurontin a day that does absolutely nothing and wait.

OK, enough with the negative venting!  The Big C and I were talking about getting back into shape.  I’m limited in what I can do in the way of excercise, and neither one of us ‘likes’ to work out…So, we have a WII.  And the kids are always playing games on it, but if we could steal some time on it we want to try out WII fit.  I was reading my fav blogs today and came across this post from Marijke from Help My Hurt and I had to laugh. Check out her blog, she has some really great information for anyone with chronic pain.

And that brings me to National Invisible Chronic Illness Awareness Week.  I wanted to write about this on Monday

, see above, lol.  My bloggin friend Connie will be speaking this week and I sure hope I didn’t miss it.  But if I did, I heard that it will all be archived, so that is cool.  I will be checking it out tomorrow, God willing, I WILL NOT BE FLARING SO HARD!!!  There.  That will work I’m sure.  There was something else I wanted to write but my head is full of mush so I’m signing out.  Peace.

(snail) image:

%d bloggers like this: