Hello everyone! I am new to this site ---- am not sure if I am 'using' properly! I have CRPS/RSD and am looking for a neurologist in Michigan---any recommendations are greatly appreciated! Thank you!

Hi wonderwoman,

Welcome to NeuroTalk, but I am sorry that you have had to come join us here.

I am from Michigan and have been dealing with CRPS since at least January of 2015, but many of the doctors I have seen think that I may have been dealing with it longer than that. I used to live in the Metro Detroit area but am now living up near Oscoda. All of my doctors are still in Metro Detroit though. Not knowing what area you are in, there is not much I can offer. There are a lot of pain management doctors that claim to have some knowledge about CRPS but I can only remember seeing one neurologist off of the top of my head, Dr Paul Cullis in Roseville. I do not know much about him, so I can not give a recommendation. I do know that the DMC, Henry Ford, UofM Health and some smaller medical centers near Grand Rapids, all supposedly have fairly good programs for patients with CRPS, but I can not say that for certain either. If you live close to the Ohio border, you could also consider going to the Cleveland Clinic as well.

I hope this helps some. Don't give up fighting.

Hi Alaina! Thank you for your response and info :-) I am so sorry you are suffering from CRPS :-( I live in southeast Michigan-wayne county. I am specifically looking for a neurologist to be a part of my CRPS team so looking for someone in my area. Not looking for a program...I have had CRPS since 1-2012 due to injuries from a car accident. It has left me disabled --- had to give up my nursing career which I loved and miss :-( Hoping you are having a low pain day ;-) Never give up fighting!