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How do you keep your hope alive?

chrissyd

New member
"Another tip from a CFer (although I know many like to disregard what the adult CFer's have to say) is research."

I research everything! When I was first diagnosed I didn't know this site existed...I didn't find it until a few years ago. I wish I had found it back then...maybe I would have taken better care of myself. Coming to the site really opened my eyes. And I was ready for them to be opened.
I totally second research! It's your best friend when dealing with the unknown (not just CF), heck it's you best friend when dealing with stuff you think you know...

<img src="i/expressions/rose.gif" border="0">
 

chrissyd

New member
"Another tip from a CFer (although I know many like to disregard what the adult CFer's have to say) is research."

I research everything! When I was first diagnosed I didn't know this site existed...I didn't find it until a few years ago. I wish I had found it back then...maybe I would have taken better care of myself. Coming to the site really opened my eyes. And I was ready for them to be opened.
I totally second research! It's your best friend when dealing with the unknown (not just CF), heck it's you best friend when dealing with stuff you think you know...

<img src="i/expressions/rose.gif" border="0">
 

chrissyd

New member
"Another tip from a CFer (although I know many like to disregard what the adult CFer's have to say) is research."

I research everything! When I was first diagnosed I didn't know this site existed...I didn't find it until a few years ago. I wish I had found it back then...maybe I would have taken better care of myself. Coming to the site really opened my eyes. And I was ready for them to be opened.
I totally second research! It's your best friend when dealing with the unknown (not just CF), heck it's you best friend when dealing with stuff you think you know...

<img src="i/expressions/rose.gif" border="0">
 

chrissyd

New member
"Another tip from a CFer (although I know many like to disregard what the adult CFer's have to say) is research."

I research everything! When I was first diagnosed I didn't know this site existed...I didn't find it until a few years ago. I wish I had found it back then...maybe I would have taken better care of myself. Coming to the site really opened my eyes. And I was ready for them to be opened.
I totally second research! It's your best friend when dealing with the unknown (not just CF), heck it's you best friend when dealing with stuff you think you know...

<img src="i/expressions/rose.gif" border="0">
 

chrissyd

New member
"Another tip from a CFer (although I know many like to disregard what the adult CFer's have to say) is research."
<br />
<br />I research everything! When I was first diagnosed I didn't know this site existed...I didn't find it until a few years ago. I wish I had found it back then...maybe I would have taken better care of myself. Coming to the site really opened my eyes. And I was ready for them to be opened.
<br />I totally second research! It's your best friend when dealing with the unknown (not just CF), heck it's you best friend when dealing with stuff you think you know...
<br />
<br /><img src="i/expressions/rose.gif" border="0">
 
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