Guest guest Posted July 20, 2002 Report Share Posted July 20, 2002 Hi folks. Is there anyone who has striato nigral degeneration to contend with? I see lots of info about Shy Drager, some about OPCA but not a lot specific to SND. I would love to be in touch with the SND folks out there. Thanks Pat in N.S. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 20, 2002 Report Share Posted July 20, 2002 That's what my husband has, what would you like to know? Ginger looking for folks with experience with striato nigral degeneration > Hi folks. Is there anyone who has striato nigral degeneration to > contend with? I see lots of info about Shy Drager, some about OPCA > but not a lot specific to SND. I would love to be in touch with the > SND folks out there. Thanks > Pat in N.S. > > > If you do not wish to belong to shydrager, you may > unsubscribe by sending a blank email to > > shydrager-unsubscribe > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 20, 2002 Report Share Posted July 20, 2002 My father's symptoms were primarily those of SND. The way I understand it, they are the symptoms most closely related to PD...tremors, rigidity, etc. My dad had the cervical dystonia (neck flex) which is common in folks with SND. I'm not sure I can be of a lot of help, but I'd be happy to try to answer any questions if I can. in OK --- bluenose123ca pjd@...> wrote: > Hi folks. Is there anyone who has striato nigral > degeneration to > contend with? I see lots of info about Shy Drager, > some about OPCA > but not a lot specific to SND. I would love to be > in touch with the > SND folks out there. Thanks > Pat in N.S. > > > If you do not wish to belong to shydrager, you may > unsubscribe by sending a blank email to > > shydrager-unsubscribe > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 21, 2002 Report Share Posted July 21, 2002 Hi Pat, My name is Annette and my husband has SND. his symptoms began about eight years ago. I don't do a lot of posting, I've found that there are many here that can say about what I have to say and much better but if you would like to send me an email the address is Jwmop@...- I'm in the Yahoo chat room now and will be in the MSA chat around 2:00 central time. -- In shydrager@y..., " bluenose123ca " wrote: > Hi folks. Is there anyone who has striato nigral degeneration to > contend with? I see lots of info about Shy Drager, some about OPCA > but not a lot specific to SND. I would love to be in touch with the > SND folks out there. Thanks > Pat in N.S. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 21, 2002 Report Share Posted July 21, 2002 Pat, My mother Joyce (71, died 11/5/00 from complications) had SND. She was originally diagnosed with PD, but that changed to SND within about 1-1/2 years later. I would be happy to communicate with you. You may email me privately or on the list. Debbie Quote Link to comment Share on other sites More sharing options...
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