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Karen - My husband had a similar reaction to Sinemet. He had more dystonia (very painful) than dyskinesia, but wasn't able to tolerate enough Sinemet to relieve his PD symptoms. He had DBS (short for deep brain stimulation), specifically pallidal stimulation, bilaterally three years ago, and that worked wonders. He has also had tremendous success with Mirapex. He was able to cut his Sinemet intake in half once he started Mirapex, and got good relief from many of his remaining symptoms. He was able to get more dopamine into his system and bypass the nasty side effects of Sinemet. Is there a good movement disorder specialist in your area? Or a PD specialist? That would be beneficial. You might ask your neuro/doctor about trying Mirapex. It seems to me that you'd be a good candidate for the kind of benefits Dick got from it. BTW, Dick's age of onset was 37, and he was diagnosed at age 38. He has had PD now for 17 years. You'll find a lot of young-onset Parkinsonians on this list, plus a tremendous amount of help and support. I think our children were about 11 and 13 when Dick was diagnosed. I don't have any good advice for helping your daughter deal with your diagnosis and your symptoms, but I do know that teenagers are notoriously easily embarrassed by their parents, and any hint of "differentness" can be very difficult for them to deal with. Your daughter will be able to cope with it better when she's a few years older. Meanwhile, if Mirapex or another med would help decrease your symptoms, that will help her cope for now. I also think it's pretty frightening to teenagers deep down inside when their parents prove vulnerable to disease. Our children are adults now, and are extremely supportive of Dick. Wishing you the best. Margie Swindler, cg for Dick, 54/17