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my coaches would do that to me too. but once i showed them i was fine, they now just ask the "how do u feel". just keeping saying im fine to head starts. and ask your coach if he could throw a little harder.

my coaches would do that to me too. but once i showed them i was fine, they now just ask the "how do u feel". just keeping saying im fine to head starts. and ask your coach if he could throw a little harder.

my coaches would do that to me too. but once i showed them i was fine, they now just ask the "how do u feel". just keeping saying im fine to head starts. and ask your coach if he could throw a little harder.

my coaches would do that to me too. but once i showed them i was fine, they now just ask the "how do u feel". just keeping saying im fine to head starts. and ask your coach if he could throw a little harder.

my coaches would do that to me too. but once i showed them i was fine, they now just ask the "how do u feel". just keeping saying im fine to head starts. and ask your coach if he could throw a little harder.

im really sorry. when my father found out i had cf he started crying. i was only five, and told me his back hurt. I know Kayla is strong. I have a friend with cf and when she was born she needed an operation on her heart too. Im proud to say she in 2nd grade now. At first its hard to get used to...

im really sorry. when my father found out i had cf he started crying. i was only five, and told me his back hurt. I know Kayla is strong. I have a friend with cf and when she was born she needed an operation on her heart too. Im proud to say she in 2nd grade now. At first its hard to get used to...

im really sorry. when my father found out i had cf he started crying. i was only five, and told me his back hurt. I know Kayla is strong. I have a friend with cf and when she was born she needed an operation on her heart too. Im proud to say she in 2nd grade now. At first its hard to get used to...

im really sorry. when my father found out i had cf he started crying. i was only five, and told me his back hurt. I know Kayla is strong. I have a friend with cf and when she was born she needed an operation on her heart too. Im proud to say she in 2nd grade now. At first its hard to get used to...

im really sorry. when my father found out i had cf he started crying. i was only five, and told me his back hurt. I know Kayla is strong. I have a friend with cf and when she was born she needed an operation on her heart too. Im proud to say she in 2nd grade now. At first its hard to get used to...

i know how u feel. my friends say how i can eat alot and dont gain anything. i know there no close but explain to them in more detail. i tell my friends if i dont eat enough i get a g-tube. your health is very important so if u need to find new lunch buddies go ahead. that dosent mean not to be...

i know how u feel. my friends say how i can eat alot and dont gain anything. i know there no close but explain to them in more detail. i tell my friends if i dont eat enough i get a g-tube. your health is very important so if u need to find new lunch buddies go ahead. that dosent mean not to be...

i know how u feel. my friends say how i can eat alot and dont gain anything. i know there no close but explain to them in more detail. i tell my friends if i dont eat enough i get a g-tube. your health is very important so if u need to find new lunch buddies go ahead. that dosent mean not to be...

i know how u feel. my friends say how i can eat alot and dont gain anything. i know there no close but explain to them in more detail. i tell my friends if i dont eat enough i get a g-tube. your health is very important so if u need to find new lunch buddies go ahead. that dosent mean not to be...

i know how u feel. my friends say how i can eat alot and dont gain anything. i know there no close but explain to them in more detail. i tell my friends if i dont eat enough i get a g-tube. your health is very important so if u need to find new lunch buddies go ahead. that dosent mean not to be...

CF is a rare diease that effects the lungs, stomache, and nose. CF is life changing, we have take many medications and treatments. You also have to explain what CF is to everyone CF does effect me, but i try not to let it. I dream big. Many kids ask what i take medicine for, why i cough so...

CF is a rare diease that effects the lungs, stomache, and nose. CF is life changing, we have take many medications and treatments. You also have to explain what CF is to everyone CF does effect me, but i try not to let it. I dream big. Many kids ask what i take medicine for, why i cough so...

CF is a rare diease that effects the lungs, stomache, and nose. CF is life changing, we have take many medications and treatments. You also have to explain what CF is to everyone CF does effect me, but i try not to let it. I dream big. Many kids ask what i take medicine for, why i cough so...

CF is a rare diease that effects the lungs, stomache, and nose. CF is life changing, we have take many medications and treatments. You also have to explain what CF is to everyone CF does effect me, but i try not to let it. I dream big. Many kids ask what i take medicine for, why i cough so...

CF is a rare diease that effects the lungs, stomache, and nose. CF is life changing, we have take many medications and treatments. You also have to explain what CF is to everyone CF does effect me, but i try not to let it. I dream big. Many kids ask what i take medicine for, why i cough so...