At 06:01 PM 10/30/98 -0500, you wrote: >Barbara Mallut wrote: >> I'd like to see all newly diagnosed PWPs be contacted by another >> Parkie who will act as a contact person ...a tactful one... with >> answers to the myriads of questions the newby Parkie may have, and >> suggestions and hints on how best to adapt to the disease and to ease >> newly diagnosed into a support group sooner, rather than later. > > When a newly diagnosed young onset contacts the Parkinson office here, >they are invited to join our support group. If they are interested, they >are told that they will be called by one of the leaders. Then, either >Joe (co-leader) or I (whichever) call the new person and invite them to >meet us at our home. > This past summer we had two new couples here with the four of us - Joe >and his wife, Donna, and Al and myself. We have found that small >meetings like this make new PWP more comfortable prior to meeting the >whole group. > Sometimes they are not ready to join the group, but prefer to meet and >talk to someone one on one. In that case, Joe or I will be contacted to >set up a meeting. Joe has even met new PWP in a coffee shop - sort of >neutral territory. > There are contact people available to talk to older newly diagnosed PWP >and/or their spouses, too. > >> I suspect my experience was an extreme because of that one man, but >> it haunted me the whole time that I spent working up to going to the >> group again. > >I had a similar experience which is one of the reasons I like to invite >newbies here. > >Judith >-- >Judith Richards, London, Ontario, Canada ><[log in to unmask]> > ^^^ > \ / > \ | / Today’s Research > \\ | // ...Tomorrow’s Cure > \ | / > \|/ > ``````` > JUDITH you see my nero had me working one on one and our group. as now i got 2 i am working on. one is driving me up the wall. even on his love live. how can an old good looking talk to a some one a bout sex lo lo? yesterday on phone about 1 hour. gaing slowly just let you know its a good idea. i did try to tell list how to get up if they don't have a lift chairm and use a cane to get up. but no respose from any body. you and AL know some of the things to help PWP'S (i have). C U I.Y.Q. DON & VIVIAN