colosrc.org
Respiratory Programs Archive - Colorado Society for Respiratory Care
https://colosrc.org/respiratory-programs
Become a Corporate Partner. Concorde Career College, Aurora, Colorado AS in Respiratory Care. 111 N Havana Street. Aurora, CO 80010. Shane Pearson, BS, RRT. Pickens Technical College, Aurora, Colorado AS in Respiratory Care. Aurora, CO 80011-9307. 303-326-2000 ext. 27781/27782. Jamie Sahli, BS, RRT. Jlsahli@aps.k12.co.us. Director of Clinical Education. Jackie Holland BS, RRT. Jaholland@aps.k12.co.us. 303) 344-4910 ext 27781. PIMA Medical Institute, Denver, Colorado AS in Respiratory Care.
66roses.blogspot.com
66 roses: October 2014
http://66roses.blogspot.com/2014_10_01_archive.html
Tuesday, October 28, 2014. At least we have a plan! So what do we do? Posted by Erin Moore. Monday, October 20, 2014. I hadn't opened my computer once since Thursday afternoon until last night, and even then, it was only briefly. So when this morning rolled around and our nanny knocked on the door at 9am, I had plans to find a quite place to sit and get back to business. But my calendar was free! I am going to schedule a day off from time to time, and I'm going to appreciate how it refreshes me. Show us ...
66roses.blogspot.com
66 roses: I admit it, I'm tired
http://66roses.blogspot.com/2013/09/i-admit-it-i-tired.html
Thursday, September 5, 2013. I admit it, Im tired. I've gotta be honest, i'm exhausted. This whole back to school thing is kicking my butt. It's not just the back to school, it's also the extra hour and a half of treatments that we now need to find time for in a day, and the swim lessons, and the dance lessons, and our upcoming fundrasier (which will be awesome). This is how yesterday went:. I finally get to bed a little after 11pm, but, SURPRISE! The day isn't over yet! Posted by Erin Moore. Cystic fibr...
66roses.blogspot.com
66 roses: Rare Disease Day 2015
http://66roses.blogspot.com/2015/02/rare-disease-day-2015.html
Saturday, February 28, 2015. Rare Disease Day 2015. A few years ago, I wrote this post. About what a typical day looks like for us. What I wasn't able to. Articulate at that time, whether it was because I was so deep in the motions of everyday life or the true burden of this disease hadn't yet full sunk in, was how it makes me feel. So today, on Rare Disease Day, I want to share what a day really feels like for me. I wonder if I’m keeping too much from them? I think his mental and emotional well being ar...
66roses.blogspot.com
66 roses: December 2014
http://66roses.blogspot.com/2014_12_01_archive.html
Wednesday, December 10, 2014. I read this fantastic article the other day called Why We Are Getting Patient Engagement Backwards. And it is so spot on I can't stand it. If you haven't read it yet, go read it now, I'll wait. .waiting. Now I will quote:. Our healthcare system inadvertently, yet potently, discourages engagement. It ignores the fact that the patient is already the most engaged person in healthcare." ". The reality is that patients have no choice but to be engaged. I'd like to share with you ...
66roses.blogspot.com
66 roses: April 2015
http://66roses.blogspot.com/2015_04_01_archive.html
Thursday, April 16, 2015. It has been a whirlwind month for us! As I mentioned in my last post. This is the really hard thing about CF, for me anyway. It's never really being sure if we're out of the woods, in the clear, well. Is this slightly changed baseline his new baseline? Does the benefit of trying more medications and other treatments to try to get rid of symptoms outweigh the risks of those harsh drugs and the time that it takes us to implement? Posted by Erin Moore. Subscribe to: Posts (Atom).
66roses.blogspot.com
66 roses: March 2015
http://66roses.blogspot.com/2015_03_01_archive.html
Tuesday, March 31, 2015. Not tomorrow. Probably not this year or next or the year after. Hopefully, dear God hopefully, he will be with us forever. Everyone tells me we will cross that bridge when we come to it, but in the meantime I'm searching desperately for anything that might offer a new hope. I cannot wait until we get to that bridge to figure out how we will cross it. You may have seen something that was recently shared on Twitter about a day that I spent partnered with Susannah Fox. Saturday, Mar...
66roses.blogspot.com
66 roses: August 2014
http://66roses.blogspot.com/2014_08_01_archive.html
Saturday, August 23, 2014. A Book of Hope. About a year ago, a learned about a project that another parent advocate in a different disease community had been working on. He had asked the question of some of his peers, "If you could, what advice would you give to someone who was newly diagnosed? The response he got was overwhelming, and he created a Book of Hope. For the IBD Community. Posted by Erin Moore. Thursday, August 21, 2014. Our Story in US News and World Report! Unfortunately I don't have an ele...
66roses.blogspot.com
66 roses: #CFEveryday
http://66roses.blogspot.com/2015/04/cfeveryday.html
Thursday, April 16, 2015. It has been a whirlwind month for us! As I mentioned in my last post. This is the really hard thing about CF, for me anyway. It's never really being sure if we're out of the woods, in the clear, well. Is this slightly changed baseline his new baseline? Does the benefit of trying more medications and other treatments to try to get rid of symptoms outweigh the risks of those harsh drugs and the time that it takes us to implement? Posted by Erin Moore. April 26, 2015 at 12:05 AM.
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