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Old 01-30-2016, 02:03 AM
cesar cesar is offline
Junior Member
 
Join Date: Jun 2007
Posts: 22
15 yr Member
cesar cesar is offline
Junior Member
 
Join Date: Jun 2007
Posts: 22
15 yr Member
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Quote:
Originally Posted by Pyr2 View Post
So, I am in a sticky situation. I have had undiagnosed symptoms for 2.5 yrs which are basically coming down to first cervical dystonia and then throat dystonia. I don't have any tortion or flexing with either, just the cramps, but Im told its dystonia, what do I know. No other real P symptoms.

Anyway, here is where it gets scary. I have also developed mild sleep apnea (although sleep dr says it was probably there for years before) and now urinary issues. I am super concerned about Multiple System atrophy and am going to a movement disorder specialist in February. I read that head/neck dystonia is a red flag for MSA.

However, it strikes me as odd that I would develop a motor symptom of MSA, for 2.5 years, yet not any of the other motor symptoms, i.e., Parkinson symptoms. I would imagine that all motor Parkinsons would have shown already. I do get some sleep onset twitching and myoclonus but I think thats normal in the general population.

Just wondering if your dystonia developed before, after or at same time as your Parkinsons. Also, anyone with urinary issues? Again, did you develop them before, after or with P?

Sorry for so many questions. I am 47 and have been on this merry go round for 2.5 yrs. I have 3 children, 2 of whom are very very young, and Im very very scared. With MSA on the table, Parkinsons sounds acceptable to me.
Dear PYR2,
I think you are too much worried about your situation. You have mild sleep apnea. Has the doctor proposed any treatment such as first staying in sleep laboratory for two nights 1st night normally and 2nd night with a CPAP (Mask).
So do not worry about that. 2.5 years in many cases is too short to develop any PD symptoms such as tremor or rigidity and slowness. As to MSA your neurologist would catch that if you really had it. As to urinary issues there are many cases between two extremes. Either you have it at the beginning which paves the way for the PD diagnosis or you have it after 20 years of PD as an additional symptom certifying that you have PD by your urologist.
Just enjoy life today and do not think about tomorrow. Any other questions just feel free to post them.
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