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Caregivingly Yours

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July 2008
Wednesday, July 23, 2008

caregiving: what is it like to live with Multiple Sclerosis?

Succinctness is important in caregiving journaling. Time is precious for readers.

 

I target no more than a minute or two of a reader’s time with a word count cap of 350 words.

 

“International average reading speed is accepted to be about 250 words per minute” Turbo Read Speed Reading

 

Bea, of AOL Journal, “Wanderer” (until a more suitable name presents itself) recently raised the bar pointing out how gifted writers can tell a story in only 6 words.

 

Did you know that in speaking English people average about 100-120 words per minute? Try timing and reading your entry out loud to yourself, is anyone still listening? <grin>

 

Over on YouTube the average video is 2 minutes. In this 21st Century as harried people turn to view information, this may ‘say’ more than words.

 

With all this said, I am going to make an about face exception and embed this following 8 minute YouTube video by Kristie Salerno Kent.

 

It is not only creative but an excellent attempt to demonstrate Multiple Sclerosis symptoms and what it is like to have MS.

 

Not the chronic progressive type like Patti, but there was a time that Patti too went through these more common remitting remissive symptoms of MS.

 

[Time Alert] Stick with it, after the first two and a half minutes she visits a mall and the video becomes genuinely extraordinary.

http://www.youtube.com/watch?v=6oraM8IF2Gc

 

Caregivingly Yours, J Patrick Leer 

musings:  www.lairofcachalot.blogspot.com

website: www.CaregivinglyYours.com

videos: http://www.youtube.com/daddyleer

 

(also available in Blogger edition, Caregiver Blog: "Caregivingly Yours")



daddyleer at 12:49:00 AM EDT Blog about this entry
This entry has 8 comments: (Add your own)
  • #8 Comment from motoxmom72 
    8/2/08 10:27 AM Permalink
    WOW WOW WOW.  Thank yo so much for sharing that video.  Quite impressive.  I agree with Kristie......I TOO hope she can come back in a few years with a video that says.....MS Cure.
    Hugs to you my friend,
    Gina
  • #7 Comment from motoxmom72 
    8/2/08 10:27 AM Permalink
    WOW WOW WOW.  Thank yo so much for sharing that video.  Quite impressive.  I agree with Kristie......I to hope she can come back in a few years with a video that says.....MS Cure.
    Hugs to you my friend,
    Gina
  • #6 Comment from hugsdoodlewacky 
    7/23/08 8:27 PM Permalink
    ((((((((((((((((((((((HUGSTOYOU))))))))))))))))Thank you for sharing the video with me.Have a nice night.
  • #5 Comment from paula933 
    7/23/08 6:44 PM Permalink
    Wow, what a great video.    Hubby (MSer) had me pass link to friends and family because that is such a great demonstration of MS!  He has tried for years to tell them what the symptoms feel like and that video says it perfectly.  Thanks for sharing!
    Paula
  • #4 Comment from midwestvintage 
    7/23/08 3:49 PM Permalink
     I really enjoyed the video.  What a great way to get how it feels across.

                 Julie
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