Just a brief introduction. My name is Jane. But it is my husband who has Parkinson's. We lost his Mom a few years ago, then three, almost four years ago he was diagnosed, he has tremors on his left side, the PD mask, drools, ans shuffles. He has a lot of pain and I dislike his neuro..never available, never calls back...but we live in the boonies, more than a half hour in either direction, so we don't have many choices. I hope this finds you well. Jane

Hi Jane and Welcome, Thank you for introducing you and your husband to us. I'm usually on the crps/rsd forum, but noticed your post. I recently met a lady with Parkinsons-I'm glad there is more 'public' information regarding the diagnosis. Sounds like your you and your husband have a lot to handle. Wish his neuro was more attentive. I've had three-one especially good in every way.
Wish that were no the norm. Especially with a disorder like his and mine, we need attention whenever that occurs even a 'call back'
Glad you posted and hope you continue. I've found enormous comfort here.
Take care- loretta

Jane,

It is great to have you come and be with us. You will fine a great number of dear friends to listen when you are in need of ears. You will find out we are supportive and relaxing place.

Sad to hear about you DH, I have listed the PD forum below just click on it and it will carry you to the forum. There are a great amount of friends to assist you on many things, including doctor questions.

http://neurotalk.psychcentral.com/forum34.html

Please keep us up to date on your situation. Again welcome, looking forward to seeing you around. My thoughts and prayers are with you.