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Parkinson Disease - My experience as a Parkinson Disease sufferer.
Small Website About Parkinsons Disease
Shake, Rattle and Roll: An insider's view of PD
From the Advisors' Desk
Parkinson's Disease Update
MOZART MOVEMENT

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From the Advisors' Desk
Posted by: jwongcpg
ADDED: 6/22/2007 6:43:14 PM

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jwongcpg Posted Jun 25 2007 10:01PM	How the PDBN works
Dirty Butter Posted Jul 16 2007 3:00AM	Please stop by my blog and post about any early undiagnosed symptoms you had. http://parkinsons.dirtybutter.com/blog/2007/07/earliest-undiagnosed-symptoms-of.html
jwongcpg Posted Jul 31 2007 4:50PM	There are a few different ways to respond and comment via this Network. This Network page is best suited to post information about the network itself. Comments here should be directed at the network functions, such as the rating system or the new Resources page. In the blog that is linked to this network page, I intend to post news of major Parkinson’s developments, and readers can reply to that blog. Lastly, I am seeing replies posted (often from newly-diagnosed people) that are basically unrelated to the blog subject. I strongly recommend that those people start their own blogs and register them on this Network; that should give you the best chance of getting answers to your questions. There are knowledgeable people who write excellent blogs and also constantly seek out new Parkinson’s posts, who will find and help you. We will highlight one of these top-rated bloggers each month.
jwongcpg Posted Oct 1 2007 3:42PM	In browsing this site, I see that there are many people seeking help and information in posts scattered as comments about various blogs. These posts are not being seen by other bloggers, and these people are not answered. I will set up three new blogs where these first-time posts can be gathered for greater visibility. The most frequent types of questions appear to be from people Just diagnosed with PD, Care-givers of those just diagnosed, and about meds, so I will start with those three areas. I hope this improves our utility by allowing direct replies .
jlandis81 Posted Oct 21 2008 7:14AM	I am new to this blog, but need some friends. I have been diagnosised with Essential Tremors in my head, Parkinson's in my body, Anxiety Disorder and Seizures (either Epilisy or associated with the Movement Disorders) basically everytime I go in the is something different the change or thing I may have. I have tremors in my throat now that cuts of my breathing when I have a seizure. I am afraid and really no one gets it, my sister and son are finally beginning to understand some of how I feel, but that is after many hospital stays, being placed in a mental hospital, threating to take all my rights away, etc. My mom has Alzheimer's so my dad is a care giver to 2 with very trying diseases. I have no were to go, my mom accuses me of everything. I'm only 48 and should be living life and enjoying my 1st grandbaby but I can't even do that without hurting for days after. Is this the way my life is going to be from here on out? No one will give me a straight answer.
clpopeo Posted Jul 19 2009 7:44PM	I am looking for information about late state Parkinsons. What can we expect of the final stage with our mother? We are looking for details.
CLINICALPARKINSON Posted Aug 3 2010 3:44PM	There is a Parkinson Clinical Study in San Diego, CA. For more information oneangeliclady@yahoo.com. Patient Stipend Payment for time and travel.
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