Viewing 2 reply threads
  • Author
    Posts
    • #18379

      KC White’ feels she is alive today because of the generosity of others.

      When KC was diagnosed in the early 1980s, CF was a disease of little hope, but because of advances in research during her lifetime, she is now a wife, mom, graduate student, and coach. KC is also about to embark on a new adventure as chair of the Cystic Fibrosis Foundation’s board of trustees.

      ‘I am more motivated than ever to find the answers for every person with CF.”

      KC, it’s people like you who get us closer to a cure! We are so grateful you exist.

      Now back to our CF Community: How does talking about a possible cure make you feel?

      To read the rest of KC’s story, and learn more about her life with CF, click here.

      Our #31DaysOfCF initiative is running for the entire month of May. Each day, we are featuring a different story, and a different view of life with CF. To read all of the stories, visit our website.

    • #18399
      Paul met Debbie
      Participant

      Congratulations to ms. White with her election as chair of the CFF!

      Talking about a cure for CF is as old as CF. I am from 1963, my brother who died in 1959 was 7 years old. A cure for CF was a recurrent subject in our family, understandably.

      Talking about a cure gives hope, but should not lead us away too much into the future. People with CF are living NOW and having CF is also conducive for increasing awareness and presence for what Is.

      I remember when being young, I quickly became tired of talking about a cure in the future, and in stead concentrated on being-here-now. This liberated me from feeling trapped in the body and time, and it reduced the illusions of my mind to a point that they disappeared.

      Having said this, of course it is great to have new medication like Trikafta, and lots of research into new medication for those of us still not being helped by improvements like this. All these researchers and the people of the CFF of course envision and imagine and use their lucid brains to find a cure or solution, but they are not dealing with it in the future, but right here and now. Presence is what makes them tick best.

      So, remember: The real cure for CF is being found NOW, not “One Day”.

    • #18412
      Jenny Livingston
      Keymaster

      While I am fully supportive of continued research, fundraising, and discussion about finding a cure, I also think it is incredibly important to talk about how so many people with CF are living beautiful, fulling, passionate lives right now. For many of us, that is in great part due to the dedication of those who came before us and “the generosity of others” as KC says. If a cure is found in my lifetime, that will definitely be celebrated! Until then, I’ll continue to be grateful for every step and milestone reached along the way.

Viewing 2 reply threads
  • You must be logged in to reply to this topic.

©2022 KLEO Template a premium and multipurpose theme from Seventh Queen

CONTACT US

We're not around right now. But you can send us an email and we'll get back to you, asap.

Sending

Log in with your credentials

or    

Forgot your details?

Create Account