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Thanks. Sorry about the problems with the comments; I hadn't turned them on - learning as I go.
 
> Date: Thu, 13 Mar 2014 17:15:05 -0400
> From: [log in to unmask]
> Subject: Re: Blog
> To: [log in to unmask]
> 
> APhillips, I just read your blog. Nice work. I am looking forward to reading
> more of your clear writing style. Thanks
> Rick M
> 
> -----Original Message-----
> From: Parkinson's Information Exchange Network
> [mailto:[log in to unmask]] On Behalf Of Patti Zapf
> Sent: Thursday, March 13, 2014 3:59 AM
> To: [log in to unmask]
> Subject: Re: Blog
> 
> 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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