tag:blogger.com,1999:blog-8196325701492314396.post6423877581458561784..comments2024-03-27T19:44:04.418-07:00Comments on Sassy Sites!: CFSassy Sites!http://www.blogger.com/profile/04072674620737572638noreply@blogger.comBlogger5125tag:blogger.com,1999:blog-8196325701492314396.post-72172249221790824622011-08-27T10:41:59.428-07:002011-08-27T10:41:59.428-07:00One of my dear friends has a 2 year old girl (only...One of my dear friends has a 2 year old girl (only 6 months older than my little girl) and a newborn son who both have CF. It's not fun, and more people need to know about it.I am lucky enough to have both of these mini people in my life, and thanks to the large amount of medicine they will always have to take I will get to see them both grow up. Thanks for the post, I have been looking for more information so I can be more aware when I am with my friend and her family.TaraD'Lainhttps://www.blogger.com/profile/05176036585277407095noreply@blogger.comtag:blogger.com,1999:blog-8196325701492314396.post-25984346130839633682011-08-27T09:15:16.991-07:002011-08-27T09:15:16.991-07:00So great!! Keep us posted on things we can do to ...So great!! Keep us posted on things we can do to help! You are wonderful!Shayhttps://www.blogger.com/profile/06508049690680505497noreply@blogger.comtag:blogger.com,1999:blog-8196325701492314396.post-25795778268807270342011-08-26T22:25:17.644-07:002011-08-26T22:25:17.644-07:00I am new to following your blog.
As a heart transp...I am new to following your blog.<br />As a heart transplant recipiant...I know the importance of educating those around us.<br />Thank you so much for sharing so much about CF.Janiecehttps://www.blogger.com/profile/07719395047651079234noreply@blogger.comtag:blogger.com,1999:blog-8196325701492314396.post-21124257069785682142011-08-26T20:19:39.130-07:002011-08-26T20:19:39.130-07:00This is wonderful news. And thank you for wanting ...This is wonderful news. And thank you for wanting to get involved with the CF Foundation. My little girl as CF as well and are part of a Team Called "Team Audre". We do fundraisers all year around raising money for the foundation. Its so wonderful the amount of people that give up there time and/or money to help support in finding a Cure. I believe one day there will be a cure. And on that day were throwing a huge party :) Please feel free to follow http://sylloh.blogspot.comAnonymousnoreply@blogger.comtag:blogger.com,1999:blog-8196325701492314396.post-14353263829120727402011-08-26T18:20:41.985-07:002011-08-26T18:20:41.985-07:00Great post! Thank you!
xo SusanGreat post! Thank you! <br />xo SusanHomeroadhttps://www.blogger.com/profile/17466121382989231017noreply@blogger.com