I could use more....
 

Hello to all,

My name is Marse, short for Marcella. I was diagnosed with CRPS type II in March of "07". I do my best to get information thru different websites but all seem to say the same thing. I would truely appreciate more information as to how bad this can get and what I am to expect. My neurologist says that I have the type that will never go away. I am learning to deal with this but I must say I am alittle frustrated because there seems to be something new pop up every so often. To say the least I am confused. Please help me try to understand. I forgot to mention that I have cysts in my left wrist and left ankle; does this have anything to do with this syndrom?

Thanks Bunches
Marse

Hi Marse..welcome to NeuroTalk. Here is the link to our CRPS forum..

http://neurotalk.psychcentral.com/forumdisplay.php?f=21

You'll find good support on these forums. :)

Thank you
 

Hello Alffe,

Thank you for replying. I will check these out. :winky:
Hope all is well for you. Take care.

Marse

Marse,

Hello and welcome to NeuroTalk. Great to see you have come to be with us. You will find a great number of caring, supporting members here willing to help each other as they can.

Again welcome, looking forward to seeing you around.

Darlene:hug: