want to know things about cf!

P

pixelperfect12

Guest
<img src="i/expressions/face-icon-small-blush.gif" border="0"><img src="i/expressions/face-icon-small-happy.gif" border="0">My bestest freind ever has cystic fibrosis!<img src="i/expressions/rose.gif" border="0">
I want to help her when she is sick.<img src="i/expressions/brokenheart.gif" border="0">
So please tell me more about it!
<img src="i/expressions/face-icon-small-cool.gif" border="0">,thanks
It's princess95




-------------------------------
Taylor Thomas 12 years old<img src="i/expressions/lips.gif" border="0">
God is good!God is great!
Let him bless these kids today!<img src="i/expressions/face-icon-small-happy.gif" border="0">
 
P

pixelperfect12

Guest
<img src="i/expressions/face-icon-small-blush.gif" border="0"><img src="i/expressions/face-icon-small-happy.gif" border="0">My bestest freind ever has cystic fibrosis!<img src="i/expressions/rose.gif" border="0">
I want to help her when she is sick.<img src="i/expressions/brokenheart.gif" border="0">
So please tell me more about it!
<img src="i/expressions/face-icon-small-cool.gif" border="0">,thanks
It's princess95




-------------------------------
Taylor Thomas 12 years old<img src="i/expressions/lips.gif" border="0">
God is good!God is great!
Let him bless these kids today!<img src="i/expressions/face-icon-small-happy.gif" border="0">
 
P

pixelperfect12

Guest
<img src="i/expressions/face-icon-small-blush.gif" border="0"><img src="i/expressions/face-icon-small-happy.gif" border="0">My bestest freind ever has cystic fibrosis!<img src="i/expressions/rose.gif" border="0">
I want to help her when she is sick.<img src="i/expressions/brokenheart.gif" border="0">
So please tell me more about it!
<img src="i/expressions/face-icon-small-cool.gif" border="0">,thanks
It's princess95




-------------------------------
Taylor Thomas 12 years old<img src="i/expressions/lips.gif" border="0">
God is good!God is great!
Let him bless these kids today!<img src="i/expressions/face-icon-small-happy.gif" border="0">
 
P

princess95

New member
<img src="i/expressions/face-icon-small-smile.gif" border="0"><img src="i/expressions/face-icon-small-happy.gif" border="0"><img src="i/expressions/rose.gif" border="0">Hey tay tay cf is a lung and intstinol problem!


----------------------------
Emily Fritz 12 years old
the lord has blessed me and you!
 
P

princess95

New member
<img src="i/expressions/face-icon-small-smile.gif" border="0"><img src="i/expressions/face-icon-small-happy.gif" border="0"><img src="i/expressions/rose.gif" border="0">Hey tay tay cf is a lung and intstinol problem!


----------------------------
Emily Fritz 12 years old
the lord has blessed me and you!
 
P

princess95

New member
<img src="i/expressions/face-icon-small-smile.gif" border="0"><img src="i/expressions/face-icon-small-happy.gif" border="0"><img src="i/expressions/rose.gif" border="0">Hey tay tay cf is a lung and intstinol problem!


----------------------------
Emily Fritz 12 years old
the lord has blessed me and you!
 
A

Audz

New member
Hey, every case of cf is different so I couldn't really say exactly how severe your friends case is. Basically cf is a genetic disorder which effects mostly the lungs. The lungs produce thick mucous and daily physiotherapy and nebulisers are needed to help cough the mucous out. The digestive system is also affected as the pancreas is blocked and can't secrete enzymes properly so you have to take enzyme supplements with each meal. Also the body finds it hard to absorb nutrients which explains why some cfers are a lot smaller than other people their age.
There are a lot more complications to cf which would take a year to write, So I hope that helped <img src="i/expressions/face-icon-small-smile.gif" border="0">... You could always ask your friend as well if she doesn't feel to sensitive talking about it.
 
A

Audz

New member
Hey, every case of cf is different so I couldn't really say exactly how severe your friends case is. Basically cf is a genetic disorder which effects mostly the lungs. The lungs produce thick mucous and daily physiotherapy and nebulisers are needed to help cough the mucous out. The digestive system is also affected as the pancreas is blocked and can't secrete enzymes properly so you have to take enzyme supplements with each meal. Also the body finds it hard to absorb nutrients which explains why some cfers are a lot smaller than other people their age.
There are a lot more complications to cf which would take a year to write, So I hope that helped <img src="i/expressions/face-icon-small-smile.gif" border="0">... You could always ask your friend as well if she doesn't feel to sensitive talking about it.
 
A

Audz

New member
Hey, every case of cf is different so I couldn't really say exactly how severe your friends case is. Basically cf is a genetic disorder which effects mostly the lungs. The lungs produce thick mucous and daily physiotherapy and nebulisers are needed to help cough the mucous out. The digestive system is also affected as the pancreas is blocked and can't secrete enzymes properly so you have to take enzyme supplements with each meal. Also the body finds it hard to absorb nutrients which explains why some cfers are a lot smaller than other people their age.
There are a lot more complications to cf which would take a year to write, So I hope that helped <img src="i/expressions/face-icon-small-smile.gif" border="0">... You could always ask your friend as well if she doesn't feel to sensitive talking about it.
 
G

GB91361

New member
Dear Audrey

I'm the mother of a son 15 yrs. old. He has C.F. and his older brother who is 17 also has it. I would really like it if you could correspond with my 15 yr. old. I truly admire your input and feel you to be a friend he could relate to. e-mail address is countryboi91@aol.com

Thanks,
From a mom,
Gloria Butler<img src="i/expressions/face-icon-small-confused.gif" border="0">
 
G

GB91361

New member
Dear Audrey

I'm the mother of a son 15 yrs. old. He has C.F. and his older brother who is 17 also has it. I would really like it if you could correspond with my 15 yr. old. I truly admire your input and feel you to be a friend he could relate to. e-mail address is countryboi91@aol.com

Thanks,
From a mom,
Gloria Butler<img src="i/expressions/face-icon-small-confused.gif" border="0">
 
G

GB91361

New member
Dear Audrey

I'm the mother of a son 15 yrs. old. He has C.F. and his older brother who is 17 also has it. I would really like it if you could correspond with my 15 yr. old. I truly admire your input and feel you to be a friend he could relate to. e-mail address is countryboi91@aol.com

Thanks,
From a mom,
Gloria Butler<img src="i/expressions/face-icon-small-confused.gif" border="0">
 
M

minichic

New member
hi,Taylor my name is Ashley i am 12 w/cf if your friend need's to talk to her doctor about a portacath it is the best thing ever no more needle sticks in the vains tell her to e-mail me if possible minichic_2006@rr.com thnx Ashley
 
M

minichic

New member
hi,Taylor my name is Ashley i am 12 w/cf if your friend need's to talk to her doctor about a portacath it is the best thing ever no more needle sticks in the vains tell her to e-mail me if possible minichic_2006@rr.com thnx Ashley
 
M

minichic

New member
hi,Taylor my name is Ashley i am 12 w/cf if your friend need's to talk to her doctor about a portacath it is the best thing ever no more needle sticks in the vains tell her to e-mail me if possible minichic_2006@rr.com thnx Ashley
 
M

minichic

New member
hi,Taylor my name is Ashley i am 12 w/cf if your friend need's to talk to her doctor about a portacath it is the best thing ever no more needle sticks in the vains tell her to e-mail me if possible minichic_2006@rr.com thnx Ashley
 
M

minichic

New member
hi,Taylor my name is Ashley i am 12 w/cf if your friend need's to talk to her doctor about a portacath it is the best thing ever no more needle sticks in the vains tell her to e-mail me if possible minichic_2006@rr.com thnx Ashley
 
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