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Welcome, Layla--I'm sure you can be a big help to your parents. Glad you are finding the PD list useful--in the info got got when you joined you were told about the archives,available through the www. There's a wealth of info there, too , from past discussions. Layla wrote: >I subscribed to this list just a few days ago for my father. He was >diagnosed with Type A PD in 1991.Since than he has been taking med. >and trying to adjust the amount which is very difficult. We were told >that if he takes a little bit more or a little bit less, it shows >similar signs. I wonder if it is true. > SNIPPED Camilla Flintermann, CG for Peter 79/8 Oxford, OH [log in to unmask] * * * * * * * * * * * * * * * * * * Ask me about the CARE list for* * Parkinson's caregivers ! * * * * * * * * * * * * * * * * * *