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Dear Mrs. Schmidt: Yes, this list can be very helpful but please don't forget to contact each of the three national organizations for PD (Parkinson's Disease Foundation, American Parkinson's Disease Association and the National Parkinson's Foundation) - we all publish educational materials on all aspects of the disorder. Also, have you thought about joining a local support group for PWPs and their families? These can be very helpful as well. Jeanne Lee-Rosner Parkinson's Disease Foundation Chicago [log in to unmask] ----- Original Message ----- From: Susan Schmidt <[log in to unmask]> To: <[log in to unmask]> Sent: Wednesday, December 15, 1999 10:42 PM Subject: The List > Last night I could not sleep. My husband often wakes me up because he > either cannot sleep himself or he is kicking me every few seconds until > I am totally awake. I decided to search for a place where I could get > some kind of info on this disease called Parkinsons. I am the care > giver so I cannot begin to imagin what my > husband is going thru, but I have to try. I need all the information > and feedback from people who are going thru the same things he is so I > will be better able to help him. So after much searching I found this > list. I admit I did not expect much so when I came home from work and > saw 22 messages on my machine I thought Mercy, what have I gotten into? > I have read all 22 messages plus and I want to tell you that I > appreceiate the information contained in each of them. I feel better > now that I have some source that I can refer to when things get too > confusing . I think belonging to this list will help me to > understand my husbands situation much better. Thank you all. > Susan Schmidt >