Happy CF Awareness Month Ya’ll!! Please take a moment to check out some of my favorite CF things happening around the world!

Nothing to say except the CF Foundation is the reason that I am alive today. I owe them everything! Please visit the site to learn everything about CF and also donate to my Great Stides Team!! I LOVE you!

Check out Somer’s Love to Breathe site: “Love to Breathe was created so we could give hope to families with newly diagnosed children. I believe it is important to educate and raise awareness about CF whenever I can.” Read her blog, by some LTB jewelry and find some HOPE!
Just Let Me Breathe by Somer Love

My buddy Josh “Moterin” Mogren is the boss of this site! Fun blogs about life and also video’s with his new BFF Moganko. Want to laugh? Go HERE!

Stay connected with CF patients all over the map at Cystic Life. CL was created by my buddy Ronnie and his finace’ Mandi. Bringing us all together for support and fun! Register today and be in the now!

Breathe 4 Tomorrow was founded by thee Sarah Morris Pearson, an adult CF patient who wants to help the CF patients that are living!! Power of 1 Person.

Newly diagnosed CF family? I’ve got just the place for you! Head over to the Blooming Rose Foundation and check out what Kat, a CF mom, has going on. She can set you up to talk with CF patients and families all over the world on how to raise a CF child and how to thrive and fight on.

I’ll end with one of my absolute most favorite CF sites, CFVoice.com. CF Voice allows you to immerse yourself in the most positive, amazing, stories, videos and podcasts. Kids can play games with Zude, teens can get advice, adults can watch other adults talk about how they’re rocking and parents have a much needed resource for staying strong.

Please check out the BREATHE song event at CFVoice.com. It features my mermaid friend Rosie and Josh from Welcome To Joshland. Tess, a CF teen shows her pipes too!

Love to all of you and thank you for the continued support in my quest to rock cystic fibrosis so hard that CF WILL on day stand for Cure Found..we are close my friends, very close. Unfortunately we have lost some absolutely incredible CF friends this year. Very inspirational people who have changed lives for the good. Please continue to do what you are doing and take this month to tell others about cystic fibrosis.

Rock CF,

Em