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Blogs by children with a CF parent

cfbites

New member
Hi,

Does anyone know of a blog or blogs by children who have a CF parent?

I have an 8-year-old daughter and was hoping to get some insight into what to expect as she becomes more aware of my CF.

Please let me know if you have any blogs. Much appreciated.

Thank you.
 

cfbites

New member
Hi,

Does anyone know of a blog or blogs by children who have a CF parent?

I have an 8-year-old daughter and was hoping to get some insight into what to expect as she becomes more aware of my CF.

Please let me know if you have any blogs. Much appreciated.

Thank you.
 

cfbites

New member
Hi,

Does anyone know of a blog or blogs by children who have a CF parent?

I have an 8-year-old daughter and was hoping to get some insight into what to expect as she becomes more aware of my CF.

Please let me know if you have any blogs. Much appreciated.

Thank you.
 

cfbites

New member
Hi,

Does anyone know of a blog or blogs by children who have a CF parent?

I have an 8-year-old daughter and was hoping to get some insight into what to expect as she becomes more aware of my CF.

Please let me know if you have any blogs. Much appreciated.

Thank you.
 

cfbites

New member
Hi,
<br />
<br />Does anyone know of a blog or blogs by children who have a CF parent?
<br />
<br />I have an 8-year-old daughter and was hoping to get some insight into what to expect as she becomes more aware of my CF.
<br />
<br />Please let me know if you have any blogs. Much appreciated.
<br />
<br />Thank you.
 

LouLou

New member
I haven't seen any blogs by kids of cfers but I think it's a great idea. In fact, as soon as my child can write I think I'll let him start a blog. He already is aware of cf in our family. I would think by 8 yrs old he'll be much more than just aware but have feelings and thoughts about it. Sounds like a great summer project. And journaling is a therapeutic! Please let us know if you find any or decide to start one with your daughter. My son and I would definitely follow it.
 

LouLou

New member
I haven't seen any blogs by kids of cfers but I think it's a great idea. In fact, as soon as my child can write I think I'll let him start a blog. He already is aware of cf in our family. I would think by 8 yrs old he'll be much more than just aware but have feelings and thoughts about it. Sounds like a great summer project. And journaling is a therapeutic! Please let us know if you find any or decide to start one with your daughter. My son and I would definitely follow it.
 

LouLou

New member
I haven't seen any blogs by kids of cfers but I think it's a great idea. In fact, as soon as my child can write I think I'll let him start a blog. He already is aware of cf in our family. I would think by 8 yrs old he'll be much more than just aware but have feelings and thoughts about it. Sounds like a great summer project. And journaling is a therapeutic! Please let us know if you find any or decide to start one with your daughter. My son and I would definitely follow it.
 

LouLou

New member
I haven't seen any blogs by kids of cfers but I think it's a great idea. In fact, as soon as my child can write I think I'll let him start a blog. He already is aware of cf in our family. I would think by 8 yrs old he'll be much more than just aware but have feelings and thoughts about it. Sounds like a great summer project. And journaling is a therapeutic! Please let us know if you find any or decide to start one with your daughter. My son and I would definitely follow it.
 

LouLou

New member
I haven't seen any blogs by kids of cfers but I think it's a great idea. In fact, as soon as my child can write I think I'll let him start a blog. He already is aware of cf in our family. I would think by 8 yrs old he'll be much more than just aware but have feelings and thoughts about it. Sounds like a great summer project. And journaling is a therapeutic! Please let us know if you find any or decide to start one with your daughter. My son and I would definitely follow it.
 
T

TonyaH

Guest
Hi there,
Most people here know me as a mom with a CF son. However, I also lost my mother to CF two days before Andrew was born. Well, I should clarify that she was undiagnosed, but when my son was diagnosed all of the puzzle pieces fell into place and her doctor finally had his answer. (He had been trying to diagnose her for years before genotying was common, and also treated her as a CF patient most of her life.) My mom was ill all of my life. I knew frequent hospitalizations, hemoptysis in the middle of the night, picc lines and visiting nurses from the time I was very young. I have often thought of starting a blog about my experiences growing up,,in hopes that it may help other children. The illness of a parent requires kids to grow up must faster and mature very quickly. I have a special place in my heart for children and young adults dealing with this. At any time if you would like to talk to me, please don't hestitate to contact me. I would benefit just as much as hopefully you and your family would!
 
T

TonyaH

Guest
Hi there,
Most people here know me as a mom with a CF son. However, I also lost my mother to CF two days before Andrew was born. Well, I should clarify that she was undiagnosed, but when my son was diagnosed all of the puzzle pieces fell into place and her doctor finally had his answer. (He had been trying to diagnose her for years before genotying was common, and also treated her as a CF patient most of her life.) My mom was ill all of my life. I knew frequent hospitalizations, hemoptysis in the middle of the night, picc lines and visiting nurses from the time I was very young. I have often thought of starting a blog about my experiences growing up,,in hopes that it may help other children. The illness of a parent requires kids to grow up must faster and mature very quickly. I have a special place in my heart for children and young adults dealing with this. At any time if you would like to talk to me, please don't hestitate to contact me. I would benefit just as much as hopefully you and your family would!
 
T

TonyaH

Guest
Hi there,
Most people here know me as a mom with a CF son. However, I also lost my mother to CF two days before Andrew was born. Well, I should clarify that she was undiagnosed, but when my son was diagnosed all of the puzzle pieces fell into place and her doctor finally had his answer. (He had been trying to diagnose her for years before genotying was common, and also treated her as a CF patient most of her life.) My mom was ill all of my life. I knew frequent hospitalizations, hemoptysis in the middle of the night, picc lines and visiting nurses from the time I was very young. I have often thought of starting a blog about my experiences growing up,,in hopes that it may help other children. The illness of a parent requires kids to grow up must faster and mature very quickly. I have a special place in my heart for children and young adults dealing with this. At any time if you would like to talk to me, please don't hestitate to contact me. I would benefit just as much as hopefully you and your family would!
 
T

TonyaH

Guest
Hi there,
Most people here know me as a mom with a CF son. However, I also lost my mother to CF two days before Andrew was born. Well, I should clarify that she was undiagnosed, but when my son was diagnosed all of the puzzle pieces fell into place and her doctor finally had his answer. (He had been trying to diagnose her for years before genotying was common, and also treated her as a CF patient most of her life.) My mom was ill all of my life. I knew frequent hospitalizations, hemoptysis in the middle of the night, picc lines and visiting nurses from the time I was very young. I have often thought of starting a blog about my experiences growing up,,in hopes that it may help other children. The illness of a parent requires kids to grow up must faster and mature very quickly. I have a special place in my heart for children and young adults dealing with this. At any time if you would like to talk to me, please don't hestitate to contact me. I would benefit just as much as hopefully you and your family would!
 
T

TonyaH

Guest
Hi there,
<br />Most people here know me as a mom with a CF son. However, I also lost my mother to CF two days before Andrew was born. Well, I should clarify that she was undiagnosed, but when my son was diagnosed all of the puzzle pieces fell into place and her doctor finally had his answer. (He had been trying to diagnose her for years before genotying was common, and also treated her as a CF patient most of her life.) My mom was ill all of my life. I knew frequent hospitalizations, hemoptysis in the middle of the night, picc lines and visiting nurses from the time I was very young. I have often thought of starting a blog about my experiences growing up,,in hopes that it may help other children. The illness of a parent requires kids to grow up must faster and mature very quickly. I have a special place in my heart for children and young adults dealing with this. At any time if you would like to talk to me, please don't hestitate to contact me. I would benefit just as much as hopefully you and your family would!
 

amysue78

New member
That is an awesome idea. I bet my 12 year old would love to do something like that.

Amy Long
32 wcf, mother to Monique, 12 years old (almost) noCF; Elijah 8 nocf and Samuel 7 nocf
 

amysue78

New member
That is an awesome idea. I bet my 12 year old would love to do something like that.

Amy Long
32 wcf, mother to Monique, 12 years old (almost) noCF; Elijah 8 nocf and Samuel 7 nocf
 

amysue78

New member
That is an awesome idea. I bet my 12 year old would love to do something like that.

Amy Long
32 wcf, mother to Monique, 12 years old (almost) noCF; Elijah 8 nocf and Samuel 7 nocf
 

amysue78

New member
That is an awesome idea. I bet my 12 year old would love to do something like that.

Amy Long
32 wcf, mother to Monique, 12 years old (almost) noCF; Elijah 8 nocf and Samuel 7 nocf
 

amysue78

New member
That is an awesome idea. I bet my 12 year old would love to do something like that.
<br />
<br />Amy Long
<br />32 wcf, mother to Monique, 12 years old (almost) noCF; Elijah 8 nocf and Samuel 7 nocf
 
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