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Herb welcome. Perhaps it could be circulation???Did u ask ur neuro or GP ?? OR What I do is I wear istoner type gloves or leather gloves with slightly loose insulted gloves over the leather ones. open and close ur hand maybe ?? Do u use a cane with that hand?? ok sorry i have to add this in. really weird. BUT while I was tying this reply the doorbell rang. FED EX. No answer , so I did the worse thing and opened the door by myself. MY big brother fedexed a pizza from LOU MALANATI'S PIZZERIA (WWW.LOUTOGO.COM) U see he has spoken to me in years. After our parents died he could not stand illness. Maybe this is a ssign that he is accepting the neurodegenerative illness. and i guess I can always rely on my big brother after all. I would email this to him but ont know his email, just that he is at the Marriot on michigan in chgo.Boy I am lucky. Yesterday I couldn't take the PDand the added symptoms. MY aid quit for the umpteenth time, I cried on the senior van, jada jada So herb how's this fit into ur question?? How can we have humor on this list and laugh at oneself even on the crapiest moments. ??? ok the pizzia was packed in dry ice and I have delayed reaction to touching the ice. I grabbed the pie box out of excitement and ouch my finger tips on my fight hand sortof hurt. For a split sec the dry ice was cold:) nancy m. Herb wrote: > > Hi. > > Herb here, PWP, 38 years old, 1 year after diagnois. > > Regarding the "what is this list" controversy, I think it's probably a > mistake to try to change what an email list is after it has existed for > some time. It's not fair to those that started it and have participated, > and it's not practical. I am on several email lists - each has a different > style: some are closely moderated, some are free-for-alls. But a list is > what it is... > > However, there is nothing that prevents starting new lists, sub lists, > whatever, to meet different needs. They may even alread exist and we just > need to know about them. It may seem sad because some will leave, but we > each have our own interests and needs, and we deserve to try to meet them. > There is nothing wrong with that. > > I'm relatively new to the list, and I have found it informative, but I > frankly can't keep up because of the sheer quantity of postings. (This is > not a critique or a request for change, just an observation!) I am mostly > interested in the so-called "hard" stuff. I'm also more interested in the > issues that face those of us who have the "young" onset version of PD. I'd > rather not start my own list... so: does anyone know of another list that > might address my needs more closely? > > AND ON A DIFFERENT TOPIC -- > My right (bad) hand is very often cold - much colder than the other hand. > Does anyone have any experience with this problem? > > Thanks, > Herb