Michael, Ariya and I are going to walk in the CF Great Strides event on May 19, 2012 and we would like you to help support us. For those who don't know, Michael and I are both carriers of CF which means that any kids we have will have a 25% chance of having the disease and a 50% chance of being a carrier. We just found out that Ariya does not have the disease but that does not change our decision to continue to support the cause. This is something that is very close to both of our hearts! If you notice the name of our team is "Born to Breathe"! Michael and I believe that every child should be born to breathe and the only way to make that happen is to find a cure for CF! Please support us and donate! Also, if you would like to join our team and walk with us, please contact me and I can get you all set up!
Here is some more info about Cystic Fibrosis!
Cystic fibrosis (CF) is a devastating genetic disease that affects tens of thousands of children and young adults in the United States. Research and care supported by the Cystic Fibrosis Foundation is making a huge difference in extending the quality of life for those with CF. However, we continue to lose precious lives to CF every day. That's why your help is needed now more than ever to ensure that a cure is found sooner - rather than later.
We would love to have you or anyone you know join our team or at least make a donation! Remember, even $5 helps! Share this with friends, coworkers, family members, ANYONE! Also, if you work for a company that matches donations, that is great too! Share this blog with anyone you know and make a donation... Or join us for the walk!
Thank you in advance for your help!
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