tag:blogger.com,1999:blog-1808878941229316533.post3274706857061261841..comments2023-04-01T00:48:07.709-07:00Comments on A Piece of Me: Living with Autoimmune Disease and Then Some...: Reflection/OpinionChyvonneBhttp://www.blogger.com/profile/08474864611076145515noreply@blogger.comBlogger2125tag:blogger.com,1999:blog-1808878941229316533.post-60652261753915991622009-06-05T06:32:34.190-07:002009-06-05T06:32:34.190-07:00Response to KeKe,
Thanks for the response! I hop...Response to KeKe,<br /><br />Thanks for the response! I hope you are having more "better" days with the Botox. This is a very tricky disorder, changing from one day to the next.<br /><br />I live in the Midwest. If you get a chance, please send me a comment with the names of your neurologists, regardless of location. I'd like to keep them in my repitoire...just in case. And, ChyvonneBhttps://www.blogger.com/profile/08474864611076145515noreply@blogger.comtag:blogger.com,1999:blog-1808878941229316533.post-20188926729493016422009-06-04T06:40:58.776-07:002009-06-04T06:40:58.776-07:00I relate to your comments above. I too have dysto...I relate to your comments above. I too have dystonia, and I too research everyday. I do not and will not accept Dystonia as a life sentence! I remember prior to being diagnosed, a chiropractor whom I had just started seeing because I thought I just had a "stiff neck", told me at that point, with my neck twisting off my shoulders that I would just have to "accept" that this Kekehttps://www.blogger.com/profile/10158364152862185708noreply@blogger.com