Hello my fellow em buddies, I have been diagnosed with em for three years. I have idopathic em and it effects my feet, hands and ears. I have had to give up my job which I loved, and change my lifestyle. I was a very active person, but now I have to adjust to my body. Once I have accepted that my body is now in charge and I co-operate, it is easier to deal with.
I also found that one day a method I will use to ease the flare up, will not work another day, so I find something else. If anything we have a very painful, but interesting disease, and it is so nice to know I am not alone.
Thank you for the opportunity to share my experiences.
Sue xo