Michel, Your description of the what madopar does to you is not the same it does to any other PWP's. However your reactions on the dopamine might be the same as is on different ways described below. If that is true you belong to a minority among the PWP's who suffer from wearing off symptoms, who have the so called DID reaction on dopamine. You say after a time of doing its work fine, you get the feeling it's influence is disturbing. You did not write exactly how it disturbs you.The fenomenon of DID and wearing of med's dyskinesia are recently ample discussed and it is clear that the fenomenon gets not much attention. I have gathered some relevant passages from recent postings about this matter. I hope that by reading them your confusion about what is happening will be dimished. Ida Kamphuis 52\12 Holland By David Langridge: There is however a fly in the ointment because the effecftiveness of each dose of sinemet is curtailed because mainly at the end of a dose when it's effect is beginning to wear off I experience an unpleasant drug induced state akin to dyskinesia but not in it's wild form- I can best describe it as a sort of mainly internal writhing with incipient neck movements and body swaying all reasonably controllable although an outside observer might guess that I was having a bad go of indigestion!Also more often than not my left leg goes rigid and I find it harder to walk than if I had not taken Sinemet.So here is a drug induced problem which seems to more or less fit the term diphasic dyskinesia which I first came upon in the 'Algorithm for Parkinsons' By Rosemary Paul: After being diagnosed with PD about 8 years ago this symptom started for me a year ago - and at times drives me batty (g). I had always thought dyskinesia happened when there was too much dopamine was released in your brain but this definitely happens at the end of dose time.My muscles get rigid from trying to stop moving and I ache all over.This dykinesia does not seem to noticed by others but I feel I am going to squirm out of my chair. >From the archives: Choreodystonic dyskinesias are also seen in a second distinct pattern, in which these adventitious movements occur just at the beginning and again at the end of the levodopa response cycle. This has beentermed "diphasic dyskinesia" or D-I-D response, a shorthand for"dyskinesia-impro- vement-dyskinesia").[124] This pattern is much less common than peak-dose dyskinesia and is often difficult to diagnose because the pattern may not he obvious, either to the patient or the clinician, The end-of-dose period of dyskinesias is typically more prolonged and troublesome than the initial dyskinetic period of the levodopa cycle. >From myself: The confusing thing was that I felt fine when the med's were high and bad when they were low. It seemed to make sense to take more. I did and the results were more end of the meds dyskinesia and losing part of my "good times". My neuro said I should not take more but less leva dopa. The impulses to move were caused by l-dopa and were always worse with higher intake. I could hardly believe him, but had to try anyhow. I had no alternative. So I gave it the benefit of the doubt. And the result showed my neuro was right. So the symptoms were caused by a too high dosis but were manifest after the dosis had diminished. A sort of abstinence phenome- non. On my next visit my neuro said the exact causes was unknown, but it indeed seemed to be the same phenomenon that addicts suffer from (cold turkey) and that unfortunately it is not easy to treat.