Thread: Dyskinesia?
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Old 12-29-2010, 07:28 PM
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reverett123 reverett123 is offline
In Remembrance
 
Join Date: Aug 2006
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15 yr Member
reverett123 reverett123 is offline
In Remembrance
reverett123's Avatar
 
Join Date: Aug 2006
Posts: 3,772
15 yr Member
Default Like everything else, it varies

I have 10 years of meds in me and am just now beginning to think of dyskinesia. Others have reached this point in months.

Don't assume that sinemet is the danger. It looks like the agonists are the greater problem.

You might want to take advantage of being in the first stages to investigate ways that might slow the process. In particular, search the archives for mucuna pruriens and dextromethorphan. Good luck.


Quote:
Originally Posted by YogaLife View Post
My husband is delaying getting on Sinemet until his PD worsens to a point where he needs it to mantain a good quality of life. This is due to what we have heard about dyskinesia. We are both wondering something about this. I understand it causes dyskinesia, but when? At the first dose? After 6 months? 5 years? Nothing online really explains how this side effect mainifests and how bad it gets. Does it just keep getting worse until you cannot take Sinemet anymore?

What is your personal experience with SInemet and dyskinesia?
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Born in 1953, 1st symptoms and misdiagnosed as essential tremor in 1992. Dx with PD in 2000.
Currently (2011) taking 200/50 Sinemet CR 8 times a day + 10/100 Sinemet 3 times a day. Functional 90% of waking day but fragile. Failure at exercise but still trying. Constantly experimenting. Beta blocker and ACE inhibitor at present. Currently (01/2013) taking ldopa/carbadopa 200/50 CR six times a day + 10/100 form 3 times daily. Functional 90% of day. Update 04/2013: L/C 200/50 8x; Beta Blocker; ACE Inhib; Ginger; Turmeric; Creatine; Magnesium; Potassium. Doing well.
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