The Good the Bad of my Life With Stiff Person Syndrome

What can I say I’m always saying I’m going to do something and I don’t. Meh better late the never I guess! So I’m back you can say or even ask for how long till my next post, but I can’t even tell you, since I promised last time that I would try to do one every week. Well we all see how that worked out. Ha I guess you can say I’m a joke when it comes to blogging especially if I’m trying to talk about my life. SPS is a bitch and not even I can keep up with It sometimes.  Sooo here is here’s a gist of what’s been going on.   As I think I wrote before I had a set back. Last time since last November I felt funny I just didn’t feel myself I felt run down, the pain was going back, and I knew I was having spasms all over. So, when I went to see my endocrinologist I ask to have my GAD level tested. In reality I think I was doing it for shits a giggles to give myself a piece of mind that nothing was going on. Yeah well that didn’t happen the following week when I went to actually see the

Let’s try this again... I’m going to try to do a post each week or month at least. That’s my goal!!! Not going to lie a bit long... Last month I went to the neurologist, and got news that I could be having either be having a flare up or having a relapse. For the past couple of months I had been feeling off with more spasms and pain the usual. I can usually take pain pretty good by now, but there were days I just couldn’t move felt frozen in my own body. So after New Year I had IVIG scheduled for Thursday, Friday, Monday, and Tuesday. Well during the weekend I had a party to attend out of town. Honestly I don’t think I did much during the party but it did run late. Both days I felt fine no problem with IVIG side effects nothing, but then came Monday first of all I had to wake up early to go get blood drawn. When I went in I asked for I don’t know how to explain it. You know when they tell you that you know your body the best I just had this feeling to ask them to run my GAD levels