Poor Kiya, I am so sorry. They wanted me to try lyrica but after my bad experience with some lupus drugs I am very very leery about any new drugs.

I hope you feel better. Have you had a nerve test done? Most neuro doctors can do those in their office and it could hold the answers to whats going on.

Bubbles I am glad you are all moved in. Just don't over due it.

It's been real hot here which makes my lupus worse plus I have had a migraine. Today is better but now my stomach is acting up. I just can't win. So I guess I am throwing myself a pity party. Oh well.

Okarity welcome to PC and welcome to the fibro thread. We have a lot of compassionate people here. I have those patches you talked about and I use them when the pain is really bad. I also try and use a rice pack or a relax wrap that I can heat to help with the pain.

I am feeling like a caged animal. I can't go in the backyard unless someone is with me due to my seizures and almost falling into the pool after a seizure when no one was home. hubby found me in time.

I have promised if I have a seizure I will not drive for 24 hours and if I do not feel well I will stay home. So now I feel like I am in prison. So I think because I have all of these restrictions on me now that I am depressed.

I think I need to start a project and stop feeling sorry for myself.

Ok I am done.

Take care everyone