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Breathe Easy! Help me donate to CF by buying these stickers at my Tidewater Comic Con booth in Virginia Beach May 18-19. Any profits from the stickers will be donated to the Cystic Fibrosis foundation in honor of my two cousins with cystic fibrosis (one of which is currently in recovery from a recent double lung and liver transplant), and my nephew who also has CF.
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As most of you probably know, my cousin Jenni died in 2002 because of Cystic Fibrosis. December 15, 2002. She was only 19. It’s been sixte
As most of you probably know, my cousin Jenni died in 2002 because of Cystic Fibrosis. December 15, 2002. She was only 19. It’s been sixteen years without her. Her death left a void in her family’s hearts. I love and miss her everyday.
So I’m asking all of my friends to please donate to the Cystic Fibrosis Foundation for my birthday so they can help other CF patients. It would mean the world to me.
Thank you,
Rebecca Tollingworth
To Understand My Mom
To Understand My Mom
That morning I ordered waffles, which I almost never do. Funny I can recall the waffles with such clarity (syrup-soaked, dense) and next the walk home along a Chicago street bordered by pudgy brownstones. It was a sunlit April day, the bitterness of Midwest winter finally releasing its grasp. My phone rang — “book the next flight, come home” — and what happened after I only know as disconnected…
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Little coughs, little panic, please go away
http://wp.me/p2Y9Wt-3FZ
“Laila, is he breathing? What’s Eli doing?”
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Yesterday I was nominated by a friend of mine to do the Saltwater Challenge for the CF Foundation (Cystic Fibrosis). This video is of me on my Facebook page completing the challenge in order to raise awareness of Cystic Fibrosis. I'm sharing this video here on Tumblr because I want others to be aware of Cystic Fibrosis and to know for those looking for ways to raise awareness or to do something for a good cause, completing this challenge is one way you can do that. I also haven't seen anything on Tumblr about this challenge either so I wanted to see if anyone else knows about this challenge at all or not.
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In pictures: A little boy's experience at the cystic fibrosis clinic
In pictures: A little boy’s experience at the cystic fibrosis clinic
Today marked Eli’s appointment at the cystic fibrosis clinic. He sees his pulmonologist every three months.
Eli has developed strong opinions on just about everything. He says just a few words these days, but I’ll let the pictures show what one little boy had to say about his experience at the doctor’s office:
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Join the Village Cycle Center team and #fightcf as we participate in the Cystic Fibrosis Foundation's Cycle for Life ride. Not only will we have a team of riders, we are mechanically supporting the ride. Whether you have been personally touched by this life threatening disease, or just want to ride for a good cause, join us for a 30 or 65 mile ride through beautiful Geneva, Illinois. Register here > http://goo.gl/1hAqHV and help us give people with CF more tomorrows.
