Originally Posted by tammy jo

Hi. i haven't posted before, but ive reading your posts for awhile now. ive found this site to be very helpful and informative.

Ive had cprs for 5 years in march 2015, although i wasnt diagnosed until approx. jan. 2014. its in both of my hands and arms with my left side being the worse. I now fear it has spread to my left hip and ankles. My doctor doesnt feel that it could be cprs in my hip because i have not had a nerve injury there ?

I have actually learned more from this site than anywhere. The medical professionals in my area arent well informed and that leaves me lost.

I feel very alone with this condition. No one seems to know anything about it including medical, friends and family.I dont feel as alone knowing there are others that can identify with me. although i hate meeting you this way, since we are all suffering, but im glad i did.


now in addition to cprs type 2 i have atrophy, high blood pressure, severe depression, anxiety and fear it is spreading.

Any communication would be deeply appreciated.

Best of luck to you all.
Take care of yourselves