Jamie at 'Walk for Strides" To find a cure for Cystic Fibrosis. She loved raising awareness about how her illness. For the last five years Jamie and her JamieBug team would raise money every year with yard sales, raffles and with the help of local business that would do cash donations. She raised close to $8,000.00 in those years that she fought for her friends suffering with her disease. CF is a illness that you are born with most patients only live into their twenties. Jamie's upbeat love for life has helped her live past her normal life expectancy but with a double lung transplant, she could live even longer. Help us fight for her and her chance for a new, deep breath of fresh air!
1 comment:
Hi Jamie! My name is Jamie Lynn Norman. I just found out that I am going to have a transplant and that I should've been on the list 6 years ago before I left the care of LeBonheur Childrens Hospital in Memphis, TN. I have Burkholderia in my lungs and am so afraid that noone will do the transplant. But I just wanted to let u know how much u inspire me n that with God all things are possible. FAITH is my favorite word. I have watched several of my CF friends die w/cf the past three years waiting on lungs and it scares me. I have a 3 year old sweet baby girl who needs me n I need her. So i hope n pray to just be able to watch that sweet little face grow into a beautiful woman. U have given me faith. I saw your page and I got the feeling that maybe everything will be alright in the end. U definitely have God on your side n I pray 4 u. U can c my sweet baby Bailey on my myspace my sister made 4 me. www.breathlessjamie@myspace.com or my facebook- www.jamienorman@facebook I think thats how u find me. Please feel free to email me at jlnorman92@yahoo.com too. I thank u for inspiring me. And giving me (my other favorite word)HOPE! Thank u thank u thank u. Love, Jamie Lynn Norman
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