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Post by John on Feb 28, 2011 16:28:29 GMT -5
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Post by susanny on Feb 28, 2011 23:46:43 GMT -5
Uploaded with ImageShack.ushappy to have you join us, and thank you for sharing your experience with the Daxas. I'll be waiting to hear more about how you're doing with it.
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Post by Blossom/Jackie W. on Mar 1, 2011 13:06:18 GMT -5
Welcome hour! (bit of a play on words there)
It's nice to have you join us.
There's a great deal of info here and a lot of learned, shared, knowledge and experience. You'll find the members here supportive, caring and sharing. If they don't know something, they'll at least point you in the right direction.
I see you've already jumped in....... WTG! And; we're looking forward to your on-going input; including you Daxas/Roflumilast experiences.
My name is Jackie aka Blossom. I look forward to getting to know you better!
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Post by virginia on Mar 1, 2011 14:02:32 GMT -5
Hourlibourli, to our group, lots of helpful people here...
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Post by hourlibourli on Mar 1, 2011 20:29:03 GMT -5
Thanks for the Welcome. So: I live in Laval, a suburb of Montreal. I have been diagnosed with COPD in 1996. Then I had an FEV1 of 45%. Now I'm down to %. But still going strong....well somewhat strong. On oxygen only at effort. My sat remains around 95% at rest but falls to 84-85% if I don't use O2. So I use it! I use a portable concentrator: Invacare XPO2. I'm now a 78 years old youngster! I use Ventolin, Atrovent, Symbicort and now Daxas for the last 6 days. I hope it works! :-) I am glad to have found this message board!
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