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Living Well

A HAPPY ENDING Let’s Do It!

Casey and John were married on an idyllic beach in South Carolina. You would never know from these snapshots that John suffers from Cystic Fibrosis. You probably would also never know that he is lucky to be alive…at 30.

casey & john beach wedding bouquet

casey & john beach wedding details

casey & john beach wedding groomsmen

casey & john beach wedding bridal party

Today I’m dedicating this post to a cause that’s dear to someone dear to me: finding a cure for Cystic Fibrosis. Tamra of ever swoon recently enlightened me on the devastating reality of this degenerative disease that affects her best friends, Casey and John. I think like most of us, I had heard of it, but really didn’t know anything about it.

THE FACTS:

Cystic fibrosis is an inherited chronic disease that affects the lungs and digestive system of about 30,000 children and adults in the United States (70,000 worldwide). A defective gene and its protein product cause the body to produce unusually thick, sticky mucus that clogs the lungs and leads to life-threatening lung infections, and obstructs the pancreas and stops natural enzymes from helping the body break down and absorb food.

  • About 1,000 new cases of cystic fibrosis are diagnosed each year.
  • More than 70% of patients are diagnosed by age two.
  • More than 45% of the CF patient population is age 18 or older.
  • In the 1950s, few children with cystic fibrosis lived to attend elementary school.
  • Today, the predicted median age of survival for a person with CF is in the late 30s.

WHAT YOU CAN DO…NOW

Support Tamra and “Team Sparkle” in the GREAT STRIDES Walk happening this Sunday by contributing to their fundraising goal! It’s not too late, and any amount you can spare is appreciated!

I’ve asked a lot of you this week, I know. But clearly this trumps asking you to read a guest post or repin an image. It ain’t pretty; it’s real.

Let’s leave our bubble for a day and help Casey and John grow old together.

Much much gratitude,

Images via ever swoon
For more information on Cystic Fibrosis, please visit CFF.org

Erika Brechtel

Erika's passion for guiding women to "Style Your Biz, Your Home, Your Self, Your Life" led her create 'The E List' (formerly the Small Shop blog) in 2010. Since, she's expanded globally into speaking, mentoring, course offerings, angel investing, and social entrepreneurship through the Élanoura Collective for women founders.

Reader Interactions

The Comments

  1. Tamra {ever swoon} says

    June 1, 2012 at 7:13 am

    Thank you so much Erika for sharing my friends story and spreading awareness about our fight against CF! xo

  2. Mandy Riggar says

    June 1, 2012 at 9:26 am

    Beautifully written Erika! It’s so easy to stay in our daily bubbles when in actuality there is so much we can do to help others.

  3. Julia says

    June 1, 2012 at 9:35 am

    What a sweet sweet story. Such a great cause!

  4. Lonely Wife Project says

    June 1, 2012 at 9:44 am

    You are so kind and so is Tamra! I heart you both!

  5. Albertina says

    June 1, 2012 at 12:31 pm

    So proud of you shedding light into this terrible disease. A lot of people read your blog so it is sure to have great reach. I help with raising awareness about neurological diseases and how difficult it is because its not really attractive but its “real” as you put it. Well said.

  6. Taylor Presson says

    June 1, 2012 at 12:55 pm

    Thank you so much for sharing with us and reminding us of what is really important in this world. Love.

  7. elizabeth says

    June 1, 2012 at 12:58 pm

    They are a truly beautiful couple – thanks for sharing. Love love love.
    xoxo -e (modern24seven)

  8. Andi of My Beautiful Adventures says

    June 1, 2012 at 4:54 pm

    Amaaaaaaazing!!!!!!!!! Love love love!

  9. Mae Badiyan says

    June 1, 2012 at 6:00 pm

    Thank you for educating me about this! Love to both you and Tamra! And Casey and John! Such a great cause

  10. A Reader says

    June 2, 2012 at 9:20 am

    What a beautiful couple! Thank you for sharing their story.
    (Would love it if you posted the name of their photographer. Those pictures are wonderful.)

  11. Samantha Penner says

    June 4, 2012 at 5:00 pm

    I had a grade school friend that suffers from the disease as well. So glad to see you are telling more about it! Go Erika and Tamra!

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