I saw a neurologist regularly for about the first year -- he kept track of my progress and answered hundreds of questions for me. But after we moved away from the area I didn't seek out a new one because there was really no need for me to -- though still having problems I was on a stable plateau, didn't have a need for new testing, wasn't taking any drugs that needed monitoring. Barbara H. _http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) In a message dated 5/10/2007 12:05:39 PM Eastern Daylight Time, [EMAIL PROTECTED] writes:
Does everyone here on this site have a neurologist? I have only seen the neurologist once since I let the hospital, which was in November 2005. My healthcare is managed by my Physical Medicine and Rehabilitation doctor(Physiatrist). Any problems that I have had since my diagnosis in July 2005, has been handled by my primary care physician or my physiatrist. My neurologist was key in diagnosing my condition, but once I was diagnosed and received plasmapheresis, the only thing that would help me after that was therapy (which I am still trying to get more of). I haven't ran into any issues, where my neurologist was needed. Naomi C-4 quad since July 2, 2005 ************************************** See what's free at http://www.aol.com.
