Hello everybody!
I have not been very active on this group but on most days, this is all I have got in terms of support, so thank you so much!
The past year has been tough, it was a nightmare to find a doctor who had heard of Erythromelalgia even though I had self diagonsed myself in the very first month of my symptoms showing out of nowhere. It started with pins and needles and after a couple of months I found my feet getting red hot. Just when I was trying to make significant changes in my lifestyle and coming to terms with the fact that I am going to have to live like this for a long time to come, I got my blood tests yesterday and I have a positive Anti-CCP which from what I have been reading means I am now going to head the Rheumatoid Arthritis way and my EM could be secondary. :(((
This latest finding has made me go in serious depression and I would appreciate any help/suggestions/advice. I have an appointment with a Rheumatologist tomorrow.
Thanks,
Aiyesha