Thanks, Elaine, for taking this on. It is certainly worthwhile. I have obtained some helpful information from this site.
Now, a question to all the social workers out there..........does anyone offer a support group for DBS patients? I have facilitated a DBS Support Group since January, 2007. I am curious to hear about other such groups, especially in Canada.
Subscribe to:
Post Comments (Atom)
Elaine, I agree. Thanks so much for taking this on.
ReplyDeleteI know that Sally at the Parkinson Resources of Oregon runs a monthly DBS support group. It is open to all; people considering DBS, people who have had DBS, spouses, adn others.
I hope everyone is well.
Jason
My husband was diagnosed with early onset Parkinson's disease at 57.his symptoms were shuffling of feet,slurred speech, low volume speech, degradation of hand writing, horrible driving skills, right arm held at 45 degree angle, things were tough for me, but now he finally free from the disease with the help of total cure ultimate health home, he now walks properly and all symptoms has reversed, he had trouble with balance especially at night, getting into the shower and exiting it is difficult,getting into bed is also another thing he finds impossible.we had to find a better solution for his condition which has really helped him a lot,the biggest helped we had was ultimatehealthhome they walked us through the proper steps,am highly recommended this ultimatehealthhome@gmail.com to anyone who needs help.
ReplyDelete