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The blog below is fantastic!i sure enjoyed reading the two entries. I tried to post a comment but don't think it saved it, not really sure how to do it?  Any suggestions would be wonderful. Please keep it up,  thank you, 

Fondly sent to you from: Patti 

On Mar 10, 2014, at 2:19 PM, [log in to unmask] wrote:

> MY HUSBAND AT 92 SUFFERING FROM ALL THE SAME THINGS----BUT---  THERE IS 
> LOTS OF  HELP THRU THE PARKINSON ASSOCIATION AND NOW TELEHEALTH  PROGRAMS.  
> LOOK FOR ALL THE INFORMATION REGARDING  PARKINSON ON  BOTH THE VETERAN 
> ADMINSTRATION AND MEDICARE WEB  SITES.   IT'S THERE---SO DO NOT GIVE UP UNTIL YOU 
> FIND IT AND  ENROLL.
> 
> MARGARET (HIS WIFE)
> 
> 
> 
> 
> In a message dated 3/10/2014 2:28:20 A.M. Pacific Daylight Time,  
> [log in to unmask] writes:
> 
> Unable  to communicate ?
> From  the woman who (along with the others in the  list) saved my sanity 
> (possibly stopped me suiciding) when first  diagnosed.
> Amanda
>> Date: Sun, 9 Mar 2014 19:41:13 -0700
>> From: [log in to unmask]
>> Subject: Re: Blog
>> To:  [log in to unmask]
>> 
>> Sharon
>> 
>> Your  family will never understand because it is impossible to describe
> it.
>> 
>> my first 5 years were great and even after  DBS in 2003  I  could do
> things. 
>> Now going on year 18 I'm in real trouble.  I  never knew talking,
> writing, 
>> doing anything  could be so  painful.  Communication is so hard, it
> affects 
>> my whole  body.   I mean everybody can talk, right?  I once said that  PD
>> is like rigor  mortis without benefit of death, and I stand by  that.
>> 
>> But I look good, people say, so what could be  wrong?  At 78 I'm in good 
>> shape for the shape I'm in.
>> 
>> -----Original Message----- 
>> From: Sharon
>> Sent:  Saturday, March 08, 2014 11:00 AM
>> To:  [log in to unmask]
>> Subject: Re: Blog
>> 
>> I'm  glad to join in. Have had PD for a while although I'm still
> reasonably  
>> we'll. however, I need somewhere to air my feeling as my family  doesn't
> seem 
>> to understand how I look at my possible future. I  deserve this because
> my 
>> Father lived with PD for 20+ years and I  never really understood what he
> was 
>> experiencing. I thought it was  just aging and resented him because he
> never 
>> tried to do anything to  help himself. Didn't know about abulia (the lack
> of 
>> motivation that  was part of his longstanding depression). As you surely
> know 
>> its  impossible to foresee the future and some of us will stay
> relavitively  
>> well, others will go on a never ending downhill journey that is not  
> pretty. 
>> I think they want me to stay positive but I am being  realistic in my
> fears, 
>> I believe. Thet don't seem to want to  understand when I am experiencing 
>> something that I know is part of  the disease and they think I am 
>> overreacting. They scoff at my double  vision, crazy dreams, soft hoarse 
>> voice, shaky  illegible  handwriting, etc.
>> 
>> Sent from my iPad
>> 
>>> On  Mar 7, 2014, at 6:44 PM, A Phillips <[log in to unmask]>  
>>> wrote:
>>> 
>>> I've started a blog; if anyone  is interested it's at 
>>> http://phillips-writes.blogspot.co.uk/
>>> Not much on it yet but am  working on it.
>>> The blog will probably just be about whatever I  happen to feel like 
>>> writing about.
>>> 
>>> Amanda Phillips
>>> 
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