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parkinsonsforum.org | parkinsonsforum.blogspot.com Reviews

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1

parkinsonsforum.org: I'm a doctor, I can cope !!

http://parkinsonsforum.blogspot.com/2009/05/im-doctor-i-can-cope.html

Monday, 4 May 2009. I'm a doctor, I can cope! I have read the other blogs and can identify with much of what has been written. Where my story differs is that I knew what was wrong but tried over many months to ignore it as being the usual vivid imagination of a medic. At the age of 42 I had been qualified as a doctor for 20 years and had been a GP for major part of that time. I was used to getting on with things by myself and not needing outside help, not letting my guard down, I was the helper, supporte...

2

parkinsonsforum.org: February 2009

http://parkinsonsforum.blogspot.com/2009_02_01_archive.html

Saturday, 28 February 2009. My Other Family by Jane. My life was good. I was part of a very supportive and loving family who have always been there for me. Then I began to become aware that my handwriting was getting smaller, I seemed to be slowing down, I developed a limp when I was tired and I was struggling to keep going. I was exhausted. In February 2002, at the age of 46, I was diagnosed with PD. I can remember being partly relieved because I had imagined something far worse. It was like being part ...

3

parkinsonsforum.org: An Optimistic View by Annie

http://parkinsonsforum.blogspot.com/2009/04/optimistic-view-by-annie.html

Saturday, 25 April 2009. An Optimistic View by Annie. Winston Churchill said “I am an optimist - it does not seem to be much use being anything else. ” Which is very much how I feel in relation to Parkinson's. There is no point in being anything else, there is nothing I can do about it. There is no point in fighting it. There is no point in railing against it. Why me? Becomes, Why not me? Was it always thus? No, it wasn't. It has taken nearly four years to reach this plateau. Without the medication I was...

4

parkinsonsforum.org: April 2009

http://parkinsonsforum.blogspot.com/2009_04_01_archive.html

Saturday, 25 April 2009. An Optimistic View by Annie. Winston Churchill said “I am an optimist - it does not seem to be much use being anything else. ” Which is very much how I feel in relation to Parkinson's. There is no point in being anything else, there is nothing I can do about it. There is no point in fighting it. There is no point in railing against it. Why me? Becomes, Why not me? Was it always thus? No, it wasn't. It has taken nearly four years to reach this plateau. Without the medication I was...

5

parkinsonsforum.org: My Story

http://parkinsonsforum.blogspot.com/2009/06/my-story.html

Friday, 19 June 2009. I retreated into myself, did only the bare minimum to keep my kids going to school. None of us understood it. After a diagnosis and medication I improved somewhat although briefly. After my first neurologist told me that I would never get better and that I should get used to the idea that I would become disabled down the road about 10 years. I didn't take these words very easily. 19 November 2010 at 18:31. Pls contact me at chandran1621@yahoo.com or. A place where they can talk.

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Parkinson's Focus Today

Welcome to my PD journey of discovery, progress and stops along the way. Read comments for more information, add a comment to join in the discussion. Select from the topics. click Older Posts to read all. Use Contact Us to do just that. Subscribe in the box below Search this Blog. Friday, January 12, 2018. An Act Relative to Parkinson's Disease, Disability and Death in Firefighters. Please click on this link, read the petition and do what you can do by lending your voice. Share this petition with friends...

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Friday, 19 June 2009. I retreated into myself, did only the bare minimum to keep my kids going to school. None of us understood it. After a diagnosis and medication I improved somewhat although briefly. After my first neurologist told me that I would never get better and that I should get used to the idea that I would become disabled down the road about 10 years. I didn't take these words very easily. Tuesday, 2 June 2009. Two 6 monthly visits later we finally plucked up the courage to corner the special...

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Parkinson’s Foundation

The National Parkinson Foundation and the Parkinson’s Disease Foundation have joined forces to become the Parkinson’s Foundation. John Kozyak, Esq. Constance Woodruff Atwell, Ph.D. J Gordon Beckham, Jr. Marshall Burack, Esq. Karen Elizabeth Burke, M.D., Ph.D. Alessandro Di Rocco, M.D. G Pennington Egbert III. Stanley Fahn, M.D. Guido Goldman, Ph.D. Michael S. Okun, M.D. Timothy A. Pedley, M.D. Daniel Novak, Ph.D. People with Parkinson’s Advisory Council. HELPLINE: (800) 4PD-INFO (473-4636).

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Parkinson's Straight from the Horse's Mouth

Parkinson's Straight from the Horse's Mouth. Welcome to the blog of Barbara Waters. Experience my personal up's and down's in this new cycle of becoming a Parkinsonian. All is not doom and gloom! Join me on this adventure within and without. Sunday, October 15, 2006. Off With Their Heads! In a way I'll be glad to be rid of them. If PD doesn't finish you off, sooner or later fighting the Medical System will. Posted by Parkinson's Straight from the Horse's Mouth @ 7:36 PM. Saturday, September 30, 2006.

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Yellow Birds for Parkinson's

Yellow Birds for Parkinson's. Saturday, July 11, 2009. News from Mike's Studio. After more than 20 years of living well with Parkinson’s disease I must now sort out my shop and hang up my welder. For three years I created the Yellow Bird garden sculptures to raise not only my own hopes but to contribute money to Parkinson’s foundations working to improve quality of life and finance research. Every bird flying has helped toward those goals. Maintaining her traditional French cooking techniques, Anne has c...

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