Happy Monday Folks… Here’s a nice video to show you how (I think) all of us are feeling on the final Monday before the holidays…
Just trying to go to this store and than this happens pic.twitter.com/5aymAQEvhl
— Tyler Bisson (@BissonTyler) December 16, 2018
Revolutionary Study Proves Talking to Patients is Helpful
You can make this up, folks. From STAT:
A new study suggests a simple idea could go a long way toward curbing dangerous medical errors: looping in patients and families about what’s happening with their care…[the intervention] starts with heading to a patient’s bedside and right off the bat, asking if the patient or family has any questions or concerns. Then, health care providers are supposed to give updates and go over the treatment plan in a way that minimizes medical jargon and makes everything clear.
The fact that someone had to spend money to prove communication with patients and families improves patient safety is beyond me. The above article almost reads as a satirical story. This is seems like the most basic of stuff, folks. What we’re really talking about here is the lunacy of the medical profession – the “I’m better than you attitude” that gets people killed. It goes without saying that there’s a culture in the clinic that looks down on patients. You’ve felt it, I’ve felt it…hell we’ve all felt it.
Trust the doctor who introduces himself with his first name. Leave the doctor who introduces himself as “doctor __________”
I still can’t believe she is gone, it’s like a horrible nightmare that I can’t wake up from. The past few days have been terribly difficult to get through, but I really do appreciate all the messages of support. I am finding comfort in knowing just how many people she was able to touch, and I think you should, too! Her reach was far beyond what she ever knew and that speaks volumes to her character.
We have a massive infectious disease problem in cystic fibrosis, and it sort of feels like we keep brushing it under the rug. I live with it, and Lea lived with it. We’re going to change that. It’s time to demand new options to treat chronic infection, and I mean NOW. Tell your local Cystic Fibrosis Foundation chapter, call national Cystic Fibrosis Foundation, talk to your cystic fibrosis center, educate your government representative, and yell it from the top of your lungs… we deserve new options. Not in 2 years, not in 5 years…. NOW. Pour the pressure on the organizations representing us… Lea would want that for all of us.
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“You changed my life without even trying, and I don’t think I could ever tell you how much you mean to me. I can’t imagine what my life would be like if I hadn’t have met you.”💜 — Lea got her angel wings…💜 — Lea, 1/2 of Salty Cysters, my best friend was my rock. She knew how to brighten my day with a single text message. Lea brought me a bond that I will never have with anyone else. My life has been forever changed by Lea and I’m so honored to say she was my best friend. From the day she slid into my DMs to tell me I had helped her, I knew this friendship was going to be a special one. Not only did we have CF in common, we were literally the same person. We liked the same things, got annoyed by other things. We had sassy pets who were basically the same as well. Our love for each other grew to something that could not be explained. We started Salty Cysters because we both had one goal; help the CF and chronic community using our own experiences. Doing so, we’ve gained so many new friends. Please know I got all of your thoughtful messages, posts, and stories, this just shows me what I already knew…she was such an inspiration and loved by so many. I will continue Salty Cysters and make sure Lea is with us always. I will never stop talking about her and reliving our special memories. — Lea, You made the world a better place, and although we would do anything to have you back here with us, it also brings relief to know you are up there and breathing easy. I know you are having a fun dance party with a bunch of sloths, eating cheese, and being the sassy, fun best friend I love so much. — Thank you for being my biggest supporter, the best friend I could’ve ever asked for, and my Salty Cyster. I love you, Lea…💜 Until we meet again.. 💜 — ❌⭕️❌⭕️ Tiff — #saltycysters #CF #cysticfibrosis #curecf