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i have 2 eye problems. one is slow accommodation eg by the time i focus on the street sign ahead we are already half a block beyond it! the other is double vision, which occurs either when i am tired or when i  am ready for my next dose of medication. but i find i am so used to seeing double that i hardly notice it any more!

i went to see a neuro ophthalmologist, who after five hours of testing and examination came to the conclusion that what was wrong with my eyes was parkinsons disease!!!   she said there is not much treatment available but i could try taking neurontin. i have heard enuff stories of this drug not to want to take it unless absolutely  necessary, so i remain seeing double and  not knowing what street we're on.

hilary blue



________________________________
 From: Bob Allison <[log in to unmask]>
To: [log in to unmask] 
Sent: Friday, April 20, 2012 5:10 PM
Subject: Re: April Tip of the Month from American Parkinson Disease Association
 
Different eye problem:  I have developed double vision due to PD, Ithink, My movement specialist says it is possible.  It is like  super dry eyes that stick while trying to focus.  Prism glassess have been mentioned.  Any thoughts  Bob
----- Original Message ----- From: "Rayilyn Brown" <[log in to unmask]>
To: <[log in to unmask]>
Sent: Thursday, April 19, 2012 2:48 PM
Subject: Fw: April Tip of the Month from American Parkinson Disease Association


> From: American Parkinson Disease Association
> Sent: Thursday, April 19, 2012 6:33 AM
> To: [log in to unmask]
> Subject: April Tip of the Month from American Parkinson Disease Association
> 
> 
> 
>            Home | Donate | News & Updates
> 
> 
> 
>            It’s springtime, and in this Tip of the Month email, American Parkinson Disease Association supporters like you share some helpful tips on getting out and about while living with Parkinson’s disease. We hope you find them useful!
> 
>              a.. While my father was alive, I was continually thinking of ways to assist him so that he could assist himself.  One idea was to purchase “diabetic socks.” They were soft and non-restrictive, so they were easy [for one] to pull on by oneself (requiring no special apparatus or device), and they were even easy for me to put on my father when he was no longer able to reach and balance to put them on.  They were so elpful.  –Claudia from Virginia
>              b.. Carefully consider footwear, especially out-of-doors. In my observation of my PD care-receiver, the softer, more flexible and form-fitting, the better. Long laces, Velcro tabs that extend, etc. become very likely tripper-uppers. These things are double hazards if the PD-er has lost manual dexterity to do them up properly.  –Dorothy from USA
>              c.. I walk very well now; however, when I was first diagnosed with PD, the only way I could walk by myself was to look at someone else walking and then my feet seemed to know what to do. When I'd get out of the car either at work or at the shopping center, I would look for someone going my way and just watch their feet.  –Larae from California
>              d.. When I am walking with my husband, who is in the last stages of PD, I find if I put my foot in front of his foot, he will step over my foot and start walking a few steps. I repeat this action until my husband gets to where he was going.  –Kay from USA
>              e.. Without a doubt, keep exercising. My man has had the disease for 10 years and he keeps going. Nothing makes you keep going like keeping going. He has a sparkle in his eyes after a bike ride or walk that is never quite there without. I am absolutely convinced of the value of exercise.  –Frances from USA
> 
>            Would you like more information? Check out APDA's National Resource Center for Rehabilitation!
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>            Do you have a tip that you would like to share with us? Click the button below to share your healthy tip!
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>            Or e-mail your tip to [log in to unmask], and be sure to let us know if you'd like us to use your name and/or tip on our website or in one of our healthy tip of the month e-mails.
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>                 Copyright © 2012 | American Parkinson Disease Association | All Rights Reserved | Privacy Policy 135 Parkinson Avenue | Staten Island, NY 10305 | Tel. (800) 223-2732 | www.apdaparkinson.org If you prefer not to receive APDA e-mail correspondence, please unsubscribe here.
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>     The American Parkinson Disease Association, Inc. was founded in 1961 to "Ease the Burden - Find the Cure" for Parkinson's disease. Headquartered in New York, the organization focuses its energies on research, patient support, education and raising public awareness of Parkinson's disease.
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