tag:blogger.com,1999:blog-7869955268765485323.post1671812880932792090..comments2024-03-25T05:31:05.321-04:00Comments on Living My Dreams With CF: CF Community Interview - Megan Lee Mobley (Cyster)Johnhttp://www.blogger.com/profile/06866357988143268043noreply@blogger.comBlogger2125tag:blogger.com,1999:blog-7869955268765485323.post-91867009222139556012014-04-11T07:41:02.230-04:002014-04-11T07:41:02.230-04:00Thanks so much for reading this interview!! I wish...Thanks so much for reading this interview!! I wish you and your little girl all the success life has to offer. Johnhttps://www.blogger.com/profile/06866357988143268043noreply@blogger.comtag:blogger.com,1999:blog-7869955268765485323.post-6579388397496765082014-04-10T12:17:21.136-04:002014-04-10T12:17:21.136-04:00I am the mother of the 4 year old little girl that...I am the mother of the 4 year old little girl that Megan spoke about and I can tell you this...Without this young woman helping me when my baby girl was diagnosed...I would have lost my mind! We spent many a late night on Facebook having conversations that to this day, are very special to me! Although we have never met face to face, not only is Megan a friend...she is, and forever will be, family to me! We will be meeting soon...face to face...on her wedding day and I cannot wait! She is so special to me!!! She paid it forward to me and I try to live in that model and pay it forward now to other parents of newly diagnosed children!! I owe it to Megan, and to her donor and donor's family!!! I hope I can make as much of an impact on someone as she did for me!Anonymoushttps://www.blogger.com/profile/10162162345677713102noreply@blogger.com