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The Show Must Go On


A film by Kristie Salerno Kent about living with MS.

Channel: People & Blogs
Uploaded: November 30, 1999 at 12:00 am
Author: sheamssociety

Length: 08:23
Rating: 4.85
Views: 27202

Tags: Festival  Film  Forward  Moving  MS  National  Society  The  

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Video Comments

singer85 (November 30, 1999 at 12:00 am)
I have MS and as a singer it is so hard to sing in flippers and may Godd bless this lady for her courage i was waiting to Die until now Thank you Kelly
v3rnondotcom (November 30, 1999 at 12:00 am)
Any chance that this and the other videos will have open captioned versions posted so that the Deaf can watch it??
tinacontino (November 30, 1999 at 12:00 am)
Gosh, The first time we saw this was at the Tour of Champions event, our daughter Ashley was diagnosed at the age of 15 (she is now 17) and this would be great to show all her teammates from her volleyball team along with her high school,,,,any chance of a copy being able to be sent to us??? It would be greatly appreciated. Tina
sajosiebird (November 30, 1999 at 12:00 am)
Bravo. If only more people could understand how we feel. I think I am going to use this to help my kids understand how I feel. Thank You
ytammam08 (November 30, 1999 at 12:00 am)
Wow, loved it..!!! I have MS and one problem I definetly have is that ppl never understand what's going on..!
blake7xx (November 30, 1999 at 12:00 am)
MS SUCKS!
hnoelles99 (November 30, 1999 at 12:00 am)
Awesome video, it shows other people just a part of what we go through on a daily basis. I saw this at my MS Support Group meeting a few months ago and it made me cry. I plan to post this on my myspace and show all my friends as well. Thank you to Kristie and the MS Society for making this!
mbethdavis (November 30, 1999 at 12:00 am)
I saw this today @ the National MS Women against MS luncheon in D.C...loved it ! and Kristie! I will send it to everyone I know! a fellow MSer
raclmtsu (November 30, 1999 at 12:00 am)
I first saw this at the M.S. Society's tour of champions in Jan. Most of us watching had M.S. We laughed (esp. at "you look so good") and cried. I used this link on my M.S. Walk fundraising emails. I've had M.S. for 18 years but my husband and my son had no idea just what it felt like for me until they watched your video. Thank you Kristy!
kocickasmom (November 30, 1999 at 12:00 am)
Very well done! That is the best I've seen since the print ad showing the barbed wire wrapped around the feet.

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