Hi Shermee, I just wanted to let you know that I'm sorry to hear about your Mirena experience. It makes me sad and very angry to know other women are experiencing the same fears that I did several months ago. I am glad my posts have helped you in some way. That makes me feel better about what I went through. I really don't think your problems are related to MS or lupus. It is the Mirena. But, I know what it's like to have the uncertainty and thoughts in the back of your mind that it could be something more serious. The reason we have to suffer with these thoughts and fears is because these doctors and medical professionals won't admit what Mirena is doing to women. Good luck to you and take care. I will keep an eye out for you and post whenever I think I might be able to help.