Kayli's Lung Transplant
Donation protected
About my Kayli-Bug:
She has Cystic Fibrosis but that is not what defines her and you would never know by just looking at her.
She is 15 yrs old, loves to listen to music. Run around shopping(dollar tree), movies, ride her 4wheeler. All when she actually feels good enough to do it.
Her heart her HEART is something special. You give her 100 dollars she will spend 5 of it on Taco Bell or McDonalds (she is obsessed with those and really thats all she can stomach CF kids are super picky with what they can eat) and use the rest of her money buying things for her family. She is something special. She gets so tickled she loses her breath (which isnt hard right now it doesnt take much) we like to laugh alot! She hopes to get this lung transplant and start being able to do some normal things that other kids her age do without having to stop multiple time or being limited. She doesnt go to school because of all the sickness she is exposed to and its a little much for her to make it through a whole day of school. My Kayli-Bug is a fiesty little firecracker but has a heart of gold! I love her personality and for what all she has to go through in and out of hospital, all the medicine, limits, stress, tiredness, pain, shots, feeding tube, back beating, breathing treatments! She SMILES (laughs through it all) and is happy and thankful! Im so proud of her and how she handles it all so well!
Why we are making the go fund me: Recently my little Kayli Bug has drastically went down in lung function she is currrently in the hospital now with lung funtion of 22/3.. that is not good at all they are doing everything they can to get her numbers up. She also recently went to Ohio to be tested to see if she is a good candidate for new lungs and she is (thank you jesus) so now she is on the list for a transplant! Which we are very thankful for! She also has been approved by insurance for her lungs to be covered! (Blessings) .. As soon as the perfect lungs for her little body come available she has to be back in surgery within 90 minutes of them receiving the new lungs for her. With it being this way her and her mom are going to have to move to Ohio to live so that they can be there within that time frame plus minimum 3 months of recovery once she has her new lungs. So their expenses will add up very fast and everything before the procedure will come out of their pocket! 6 months minimum will be spent in Ohio. Thats not including the 4 kids that will still be at home and step-dad works away 4 days a week. We are asking for donations to help with living, food, gas and everything else that will be included in this whole process it will add up very fast. Having financial stress added to the stress of it all in the first place is what we are hoping to avoid. Please help and share with as many people you can! Anything small or large iz appreciated we just hope and pray for this to be as smooth as we can make it. Most of all we ask for prayers!
ALL IN GODS HANDS
Thank you from the bottom of our hearts
--Kayli & Kayli's Family ❤
She has Cystic Fibrosis but that is not what defines her and you would never know by just looking at her.
She is 15 yrs old, loves to listen to music. Run around shopping(dollar tree), movies, ride her 4wheeler. All when she actually feels good enough to do it.
Her heart her HEART is something special. You give her 100 dollars she will spend 5 of it on Taco Bell or McDonalds (she is obsessed with those and really thats all she can stomach CF kids are super picky with what they can eat) and use the rest of her money buying things for her family. She is something special. She gets so tickled she loses her breath (which isnt hard right now it doesnt take much) we like to laugh alot! She hopes to get this lung transplant and start being able to do some normal things that other kids her age do without having to stop multiple time or being limited. She doesnt go to school because of all the sickness she is exposed to and its a little much for her to make it through a whole day of school. My Kayli-Bug is a fiesty little firecracker but has a heart of gold! I love her personality and for what all she has to go through in and out of hospital, all the medicine, limits, stress, tiredness, pain, shots, feeding tube, back beating, breathing treatments! She SMILES (laughs through it all) and is happy and thankful! Im so proud of her and how she handles it all so well!
Why we are making the go fund me: Recently my little Kayli Bug has drastically went down in lung function she is currrently in the hospital now with lung funtion of 22/3.. that is not good at all they are doing everything they can to get her numbers up. She also recently went to Ohio to be tested to see if she is a good candidate for new lungs and she is (thank you jesus) so now she is on the list for a transplant! Which we are very thankful for! She also has been approved by insurance for her lungs to be covered! (Blessings) .. As soon as the perfect lungs for her little body come available she has to be back in surgery within 90 minutes of them receiving the new lungs for her. With it being this way her and her mom are going to have to move to Ohio to live so that they can be there within that time frame plus minimum 3 months of recovery once she has her new lungs. So their expenses will add up very fast and everything before the procedure will come out of their pocket! 6 months minimum will be spent in Ohio. Thats not including the 4 kids that will still be at home and step-dad works away 4 days a week. We are asking for donations to help with living, food, gas and everything else that will be included in this whole process it will add up very fast. Having financial stress added to the stress of it all in the first place is what we are hoping to avoid. Please help and share with as many people you can! Anything small or large iz appreciated we just hope and pray for this to be as smooth as we can make it. Most of all we ask for prayers!
ALL IN GODS HANDS
Thank you from the bottom of our hearts
--Kayli & Kayli's Family ❤
Organizer
SaVannah Kay Templeton
Organizer
Knoxville, TN
