Hi All,
Here is a link to CF Tube where I was interviewed by the wonderful Sarah at cysticfibrosis.com
This was an interview we did at the recent CFRI Conference in California.
Can you say motor mouth?? :)
The folks at CFRI and cysticfibrosis.com are wonderful. A sincere thank you to everyone at both organizations!!!
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We are workng to raise Organ Donation Awareness. PLEASE PASS ALONG TO EVERYONE YOU KNOW!
We are competing for a $1.5 million dollar grant from American Express to promote organ donation awareness. With your support,
"Second Chances: Mobile Organ Donation Awareness" project could save countless lives.
http://www.membersproject.com/project/view/UZHKO0
THE STORY TO PASS ALONG: My niece, Melissa, who has been fighting an unrelenting battle with Cystic Fibrosis (CF) for 18
years was blessed to receive two double lung transplants in her short life of 18 years. Melissa is well-aware that for many others
this is not the case, as she has watched 7 friends with CF pass on while awaiting organs.
WHAT WE NEED FROM YOU:
Melissa is competing for $1.5 million dollars from American Express to promote organ donation awareness. With your support,
her "Second Chances: Mobile Organ Donation Awareness" project could save countless lives.
THE DEADLINE:
Please nominate Melissa's project by clicking on the link below and please forward this email to as many people as possible. Our
goal is 5000 nominations! The Nomination deadline is September 1, 2008!
http://www.membersproject.com/project/view/UZHKO0
WE THANK YOU FOR SUPPORTING THIS IMPORTANT CAUSE! PLEASE PASS ALONG TO EVERYONE YOU KNOW.
Gabby? Yes. Articulate and passionate? Yes!
You did great !!!!
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