What's new
Cystic Fibrosis Forum (EXP)

This is a sample guest message. Register a free account today to become a member! Once signed in, you'll be able to participate on this site by adding your own topics and posts, as well as connect with other members through your own private inbox!

TAKING A SURVEY

JazzysMom

New member
Do you come to this forum MORE for:

1) CF Info & Serious inquiries

2) Having a connection to other CF families ~ serious exchange or
not

3) Both because you cant decide LOL
 

JazzysMom

New member
Do you come to this forum MORE for:

1) CF Info & Serious inquiries

2) Having a connection to other CF families ~ serious exchange or
not

3) Both because you cant decide LOL
 

JazzysMom

New member
Do you come to this forum MORE for:

1) CF Info & Serious inquiries

2) Having a connection to other CF families ~ serious exchange or
not

3) Both because you cant decide LOL
 

JazzysMom

New member
Do you come to this forum MORE for:

1) CF Info & Serious inquiries

2) Having a connection to other CF families ~ serious exchange or
not

3) Both because you cant decide LOL
 

JazzysMom

New member
<br />Do you come to this forum MORE for:
<br />
<br />1) CF Info & Serious inquiries
<br />
<br />2) Having a connection to other CF families ~ serious exchange or
<br />not
<br />
<br />3) Both because you cant decide LOL
<br />
<br />
 

izemmom

New member
3

It really is a combination. We are lucky to be at a point where everything is good, so I don't need new information. I will someday, soon, I"m sure. So, now I come here to check in on everyone, see if I can help anyone with info or just a ((((hug))))).

And, I'n naturally indecisive, so I'd pick 3, anyway.
 

izemmom

New member
3

It really is a combination. We are lucky to be at a point where everything is good, so I don't need new information. I will someday, soon, I"m sure. So, now I come here to check in on everyone, see if I can help anyone with info or just a ((((hug))))).

And, I'n naturally indecisive, so I'd pick 3, anyway.
 

izemmom

New member
3

It really is a combination. We are lucky to be at a point where everything is good, so I don't need new information. I will someday, soon, I"m sure. So, now I come here to check in on everyone, see if I can help anyone with info or just a ((((hug))))).

And, I'n naturally indecisive, so I'd pick 3, anyway.
 

izemmom

New member
3

It really is a combination. We are lucky to be at a point where everything is good, so I don't need new information. I will someday, soon, I"m sure. So, now I come here to check in on everyone, see if I can help anyone with info or just a ((((hug))))).

And, I'n naturally indecisive, so I'd pick 3, anyway.
 

izemmom

New member
3
<br />
<br />It really is a combination. We are lucky to be at a point where everything is good, so I don't need new information. I will someday, soon, I"m sure. So, now I come here to check in on everyone, see if I can help anyone with info or just a ((((hug))))).
<br />
<br />And, I'n naturally indecisive, so I'd pick 3, anyway.
 
B

brewz2

Guest
All of the above - not b/c I can't decide - <img src="i/expressions/face-icon-small-smile.gif" border="0">
 
B

brewz2

Guest
All of the above - not b/c I can't decide - <img src="i/expressions/face-icon-small-smile.gif" border="0">
 
B

brewz2

Guest
All of the above - not b/c I can't decide - <img src="i/expressions/face-icon-small-smile.gif" border="0">
 
B

brewz2

Guest
All of the above - not b/c I can't decide - <img src="i/expressions/face-icon-small-smile.gif" border="0">
 
B

brewz2

Guest
All of the above - not b/c I can't decide - <img src="i/expressions/face-icon-small-smile.gif" border="0">
 

Alyssa

New member
4.) I made up my own answer :)

I come here because I want to stay informed about CF and hear what others are experiencing or talking about - it keeps me better informed. I also come here because I feel I have something to contribute, especially to those who are questioning if they or their child has CF. I tend to watch the newly diagnosed board for those people posting who have been led to believe that a normal sweat test and mild symptoms or no digestive issues means they do not have CF. This is precisely how our daughter was misdiagnosed for 8 years. So I come to share our story with other, in the hopes of educating them so they can pursue more testing or a different doctor when trying to figure out if they are in fact dealing with CF.
 

Alyssa

New member
4.) I made up my own answer :)

I come here because I want to stay informed about CF and hear what others are experiencing or talking about - it keeps me better informed. I also come here because I feel I have something to contribute, especially to those who are questioning if they or their child has CF. I tend to watch the newly diagnosed board for those people posting who have been led to believe that a normal sweat test and mild symptoms or no digestive issues means they do not have CF. This is precisely how our daughter was misdiagnosed for 8 years. So I come to share our story with other, in the hopes of educating them so they can pursue more testing or a different doctor when trying to figure out if they are in fact dealing with CF.
 

Alyssa

New member
4.) I made up my own answer :)

I come here because I want to stay informed about CF and hear what others are experiencing or talking about - it keeps me better informed. I also come here because I feel I have something to contribute, especially to those who are questioning if they or their child has CF. I tend to watch the newly diagnosed board for those people posting who have been led to believe that a normal sweat test and mild symptoms or no digestive issues means they do not have CF. This is precisely how our daughter was misdiagnosed for 8 years. So I come to share our story with other, in the hopes of educating them so they can pursue more testing or a different doctor when trying to figure out if they are in fact dealing with CF.
 

Alyssa

New member
4.) I made up my own answer :)

I come here because I want to stay informed about CF and hear what others are experiencing or talking about - it keeps me better informed. I also come here because I feel I have something to contribute, especially to those who are questioning if they or their child has CF. I tend to watch the newly diagnosed board for those people posting who have been led to believe that a normal sweat test and mild symptoms or no digestive issues means they do not have CF. This is precisely how our daughter was misdiagnosed for 8 years. So I come to share our story with other, in the hopes of educating them so they can pursue more testing or a different doctor when trying to figure out if they are in fact dealing with CF.
 

Alyssa

New member
4.) I made up my own answer :)
<br />
<br />I come here because I want to stay informed about CF and hear what others are experiencing or talking about - it keeps me better informed. I also come here because I feel I have something to contribute, especially to those who are questioning if they or their child has CF. I tend to watch the newly diagnosed board for those people posting who have been led to believe that a normal sweat test and mild symptoms or no digestive issues means they do not have CF. This is precisely how our daughter was misdiagnosed for 8 years. So I come to share our story with other, in the hopes of educating them so they can pursue more testing or a different doctor when trying to figure out if they are in fact dealing with CF.
 
Top