thanks alot. there's actually a doctor not too far from me that has alot of positive comments atleast now if something does show up i have an idea of who i can contact.
thanks again. I'm really glad i found this forum!
HI yes we do have a thread where members can add to the list and I have the names added to the Health Pages top right of this screen...here is the link-
http://www.medhelp.org/health_pages/Neurological-Disorders/DOCTORS-LIST-FOR-CHIARI-SYRINGOMYELIA/show/1062?cid=186
As I have mentioned in the other threads, this is not a referral, the list is to help u start researching Drs...all names r of drs that members here have used, and liked...it is not all inclusive.
"selma"
I keep seeing reference to a list of doctors................is there some where to look for a list of doctors that may bo in my area?
U r deff not alone and I hope u post an update of ur results.....I am interested to hear how u do and what ur drs say is going on.
I was told I need more surgery and am putting it off as long as possible too, no one wants to have multiple surgeries.
I pray u get answers soon
"selma"
Thanks for the input. I'm sure it will be nothing and I'm just over reacting. I'm usually a cup half full kind of person, it's just the thought of having the surgery scares me to death. Thanks alot for the response. It's nice to know I'm not alone in the world. :-)
HI and welcome to the Chiari forum.
I am also at the same point post op as u..I had my surgery in May '09.....
It is possible to develop scar tissue and that can cause a CSF obstruction, the other issues could be tethered cord, ICP....or a bulging disk.
I continued t o have some issues, but do have tethered cord, and a bulging disk along with Ehlers-danlos...so I know it is not surgery related.
I pray u get answers from ur MRI...and I would suggest u request copies of the MRI's and the report so u could get a 2nd opinion if u feel u want one depending on the results.
Good luck
"selma"