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karenking94 (August 12, 2008 at 3:22 pm)
Thank you for a great video. we would love to use for teaching purposes only (would ref/show video link)and would gladly acknowledge owner/youtube. Do you know how we would go about getting permission?
makezmuzic (April 23, 2008 at 1:49 am)
I have my o2 concentrater on my walker. I can tell by the way people look at me that I look pretty wacked. LOL But I don't care. I wish I had the money to have PR though. It's different with a group.My intercostal wall is inflamed from the plaque on my lungs from asbestos exposure. So breathing is very painful. Especially when I'm breathless. But if I take enough pain meds, I've been able to walk for 20 minutes now. Fortunately, I only have to drive 3 blocks to get to flat ground.
makezmuzic (April 23, 2008 at 1:45 am)
Thank you so much for this video. People don't know what it's like for us. The fear of becoming housebound. Unfortunately I live in the US. I'm a medicaid patient. I'm of no value to our society so getting a Pulmo to help me get PR as a big Black woman is pretty much out of the question. I demanded it when I had an HMO. I friend told me about it, not my pulmo. It was great.The few sunny days we've gotten here in the NW have made it possible for me to walk on my own.
realtamedia (September 26, 2007 at 5:35 pm)
thank you for your feedbackmuch appreciated
mriser (September 26, 2007 at 5:19 pm)
Excellent! Just the type of video needed to get the word out. You have done the world a great favor. My hat is off to the writers and producers and I salute the people with COPD who participated in this video series. Thanks to everyone involved!
drkennyg (September 4, 2007 at 11:31 pm)
a great study and help for those of us with COPD - a lot of hope
drkennyg (September 4, 2007 at 10:58 pm)
Both of these videos are very encouraging to those of us that have COPD |
