Parosysmal Dyskinesia as diagnosis
Posted: Sat Jul 25, 2009 3:08 pm
Hi JL,
Thanks for your post. I have now been to 3 neurologists, seen 3 or 4 Physicians, had 2 MRI's and a lumber puncture, an EEG a video Telemetry (an EEG with video recording over 2.5days including nights) god only knows how many bloods, etc. etc. Anyhow we finally have got a tentative diagnosis based on the evidence. The last Neuro believes it to be Paroxysmal Dyskinesia with some episodes of Dystonia. From what i can gather people with MS that have tremors, numbness and balance problems and even the MS Hug actually have PD as a secondary to their MS so that explains why i was drawn to TIMS but have not been showing on the MRI's (YET). I am hoping like hell that i only have the PD and not MS, we are just so glad to be finally close to a diagnosis. anyhow thanks for the links i will have a look at them, i am sure there will be some useful information.
Cheers Scotty.
Thanks for your post. I have now been to 3 neurologists, seen 3 or 4 Physicians, had 2 MRI's and a lumber puncture, an EEG a video Telemetry (an EEG with video recording over 2.5days including nights) god only knows how many bloods, etc. etc. Anyhow we finally have got a tentative diagnosis based on the evidence. The last Neuro believes it to be Paroxysmal Dyskinesia with some episodes of Dystonia. From what i can gather people with MS that have tremors, numbness and balance problems and even the MS Hug actually have PD as a secondary to their MS so that explains why i was drawn to TIMS but have not been showing on the MRI's (YET). I am hoping like hell that i only have the PD and not MS, we are just so glad to be finally close to a diagnosis. anyhow thanks for the links i will have a look at them, i am sure there will be some useful information.
Cheers Scotty.