I can’t believe I’m a mother without…
Life has been twisted and turned upside down. As a mother, I had both the wonderful privilege of holding my sweet son as I brought him into this world…and the horrible chore of holding him as he took his last breaths and left this world, at only 7 years old. June 24, 2010 he earned his angel wings, passing away after an inspiring but brief fight against Cystic Fibrosis. Now I live, solely focusing on living a life to get to be with him again in heaven, and to raise awareness for Cystic Fibrosis research. I am dedicated to a cure, not only for my sweet sons legacy but so that other CF families never experience the greatest loss of their lives that we are now facing. My mother’s arms are missing Connerman, yet he still inspires me daily to leave a mark of LOVE on this world…so for you my sweet prince, mommy will try!
Love Love Love
Always Always Always
After a lot of tears, I was able to register Conner’s Angels team to this years Great Strides walk for Cystic Fibrosis. I ask that you take a moment to donate (any amount it all adds up!), forward to all your contacts, join our team, or even create a Conner’s Angels team where you live. Let his legacy of LOVE shine on..
Love Love Love
http://www.cff.org/Great_Strides/dsp_DonationPage.cfm?walkid=7136&idUser=134723
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:
Go to http://www.cff.org/ for more information
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