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NFT不仅仅是收藏，更是数字身份的象征。加入我们，和全球藏家一起见证未来！ 探索NFT的无限可能！每一枚数字藏品都讲述着独特的故事，加入我们的社区，开启你的元宇宙之旅吧！
💐 💐 🌹 🌸 👍 💐 💎 🍂 🌂 🚀 for instead of quitting his hold on the flap in his hand
Sharing a personal memory. Today would have been my oldest daughters 34th birthday. We lost her 11 years ago to Cystic Fibrosis, awaiting a lung transplant. My youngest daughter presented this quilt to me today made from Lauren's clothes. #ILoveYouLauren #CureCF #RIP
“There were moments where I was so tired that I didn't think I was going to be able to keep going, but there's so many reasons to keep fighting.” -@travisflores, an adult with #cysticfibrosis who recently received his third double-lung transplant on.cff.org/37VKM7I
nbcnews.com
Meet Travis Flores, a survivor of a rare third lung transplant
Flores, who has cystic fibrosis, said being able to hold his partner again provided motivation for him to keep fighting.
Airway clearance techniques (ACTs) loosen thick, sticky mucus so it can be cleared from the lungs by coughing or huffing. Here's what you need to know about how clearing the airways may help decrease lung infections and improve lung function. on.cff.org/2VkJMVG
Last week, nearly 200 teens from the #cysticfibrosis community joined us virtually for our 12th annual Teen Advocacy Day to ask their members of Congress to support expanded paid family and medical leave during the #COVID19 pandemic. #CFadvocacy on.cff.org/31usCsK
1. CF is just like asthma. No, it isn't. It isn't like asthma at all and although asthma can be a debilitating disease, CF and asthma progress completely differently. on.cff.org/3ibMo1X
We applaud the critical #preex protections in the Patient Protection and Affordable Care Enhancement Act. We thank the House of Representatives for passing these important protections and urge the Senate to take up the legislation swiftly. #CFadvocacy on.cff.org/31xsYPm
"I've always thought that humor is the best medicine for my cystic fibrosis. My CF isn't a genetic disease, it is a genetic mutation that makes me a part of an elite community of superhumans." on.cff.org/3ijWfmo
“Every summer I got more used to -- and more confident about -- explaining that I had cystic fibrosis. I believe that because I had so much practice telling other kids what CF is and showing them my treatments, I'm more open about my CF now.” on.cff.org/2ZCTc08
Do you provide chest physical therapy (CPT) to a child with #cysticfibrosis? Learn simple tips to ensure you're doing it comfortably and carefully. on.cff.org/3iEsrRH
“Living with cystic fibrosis means, at least for me, that I have to actively refute the idea that I could live every day as if it was my last." on.cff.org/3eaCyKx
If I had to guess how long coronavirus panic will last, if Biden wins it’ll be done by November 4th but if Trump wins it’ll be right around January 2025.
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