I got some useful help from GN last year when I was first diagnosed with PMR and have gone down the route of steroids, which I hate but they are a necessity for me. I am down to between 3-4 mg a day but it is such a slow process.
I need a bit of a boost to keep my spirits up as I have had the illness now for about 14 months and know it can fade in two years to five years but I am getting impatient.
Anyone want to share how they are coping ?
Do you agree with me or parent and child?





