tag:blogger.com,1999:blog-8121963203914214070.post7652309697233507927..comments2023-12-26T03:00:35.586-07:00Comments on Run, Sickboy, Run - Cystic Fibrosis and Exercise: Cystic Fibrosis Doesn't Define MeAnonymoushttp://www.blogger.com/profile/06849674714471543078noreply@blogger.comBlogger2125tag:blogger.com,1999:blog-8121963203914214070.post-39398978225840480062010-01-11T13:40:50.752-07:002010-01-11T13:40:50.752-07:00I love this.... it inspires me so much. I have a 3...I love this.... it inspires me so much. I have a 3yr old son who has CF. I try so hard to just make it feel like all the treatments are just part of our life but sometimes it is hard. I just want to the best by William. your blog makes me feel better about not being so ,up tight about things and just letting stuff go because something has come up... (his dad gets so upset if i dont make sure Brenda Coffeynoreply@blogger.comtag:blogger.com,1999:blog-8121963203914214070.post-48855161951914187342009-04-14T14:19:00.000-07:002009-04-14T14:19:00.000-07:00I ♥ this post.
Michael & I sometimes laugh wh...I ♥ this post. <br />Michael & I sometimes laugh when he starts coughing or when he really wants to skip a treatment and one of us will say <br />"Oh yea I forgot about this CF thing"<br />We always say the hospital is the only reason we remember he has CF...just 1 of those goofy things we do..kinda funny and this post made me think of it.<br /><br />Oh and thanks for the awesomly Kelleehttps://www.blogger.com/profile/18375802334017681242noreply@blogger.com