We are Family...

kayleesgrandma

New member
The one thing I always loved about this place was how we were like a "family", and--as Light once said--a "community". Jeanne has carefully set up the site so that we would all feel welcome, and that we could come here for any problem we have. I think what this site means to each of us is a many and varied concept. Some come here ONLY for CF info. Some come here for fellowship. Some come here because of a spouse, child, family member having CF. Some come here BECAUSE they have CF. THIS IS NOT A SITE ABOUT CF ONLY!!!

Everyone should feel welcome to ask whatever question they have, be it CF-related or not. Because we are family, we will answer, or not, whatever. If you don't like the question don't answer it. No question is trivial, be it about a wart or an IV. Each of us is a member here, be they a CFR or not. Each has a right to ask questions--CF-related or not


<b>I am PROUD that this is the first place many of us think to come to with a problem or question! This is the "home" that Jeanne has tried to build. Let us be respectful of each of us and the problems they bring to us. </b>
 

kayleesgrandma

New member
The one thing I always loved about this place was how we were like a "family", and--as Light once said--a "community". Jeanne has carefully set up the site so that we would all feel welcome, and that we could come here for any problem we have. I think what this site means to each of us is a many and varied concept. Some come here ONLY for CF info. Some come here for fellowship. Some come here because of a spouse, child, family member having CF. Some come here BECAUSE they have CF. THIS IS NOT A SITE ABOUT CF ONLY!!!

Everyone should feel welcome to ask whatever question they have, be it CF-related or not. Because we are family, we will answer, or not, whatever. If you don't like the question don't answer it. No question is trivial, be it about a wart or an IV. Each of us is a member here, be they a CFR or not. Each has a right to ask questions--CF-related or not


<b>I am PROUD that this is the first place many of us think to come to with a problem or question! This is the "home" that Jeanne has tried to build. Let us be respectful of each of us and the problems they bring to us. </b>
 

kayleesgrandma

New member
The one thing I always loved about this place was how we were like a "family", and--as Light once said--a "community". Jeanne has carefully set up the site so that we would all feel welcome, and that we could come here for any problem we have. I think what this site means to each of us is a many and varied concept. Some come here ONLY for CF info. Some come here for fellowship. Some come here because of a spouse, child, family member having CF. Some come here BECAUSE they have CF. THIS IS NOT A SITE ABOUT CF ONLY!!!

Everyone should feel welcome to ask whatever question they have, be it CF-related or not. Because we are family, we will answer, or not, whatever. If you don't like the question don't answer it. No question is trivial, be it about a wart or an IV. Each of us is a member here, be they a CFR or not. Each has a right to ask questions--CF-related or not


<b>I am PROUD that this is the first place many of us think to come to with a problem or question! This is the "home" that Jeanne has tried to build. Let us be respectful of each of us and the problems they bring to us. </b>
 

kayleesgrandma

New member
The one thing I always loved about this place was how we were like a "family", and--as Light once said--a "community". Jeanne has carefully set up the site so that we would all feel welcome, and that we could come here for any problem we have. I think what this site means to each of us is a many and varied concept. Some come here ONLY for CF info. Some come here for fellowship. Some come here because of a spouse, child, family member having CF. Some come here BECAUSE they have CF. THIS IS NOT A SITE ABOUT CF ONLY!!!

Everyone should feel welcome to ask whatever question they have, be it CF-related or not. Because we are family, we will answer, or not, whatever. If you don't like the question don't answer it. No question is trivial, be it about a wart or an IV. Each of us is a member here, be they a CFR or not. Each has a right to ask questions--CF-related or not


<b>I am PROUD that this is the first place many of us think to come to with a problem or question! This is the "home" that Jeanne has tried to build. Let us be respectful of each of us and the problems they bring to us. </b>
 

kayleesgrandma

New member
The one thing I always loved about this place was how we were like a "family", and--as Light once said--a "community". Jeanne has carefully set up the site so that we would all feel welcome, and that we could come here for any problem we have. I think what this site means to each of us is a many and varied concept. Some come here ONLY for CF info. Some come here for fellowship. Some come here because of a spouse, child, family member having CF. Some come here BECAUSE they have CF. THIS IS NOT A SITE ABOUT CF ONLY!!!

Everyone should feel welcome to ask whatever question they have, be it CF-related or not. Because we are family, we will answer, or not, whatever. If you don't like the question don't answer it. No question is trivial, be it about a wart or an IV. Each of us is a member here, be they a CFR or not. Each has a right to ask questions--CF-related or not


<b>I am PROUD that this is the first place many of us think to come to with a problem or question! This is the "home" that Jeanne has tried to build. Let us be respectful of each of us and the problems they bring to us. </b>
 

Imogene

Administrator
I've been giving little lessons about

e-Patients

in my <a target=_blank class=ftalternatingbarlinklarge href="http://blogs.cysticfibrosis.com/blogpost.cfm?threadid=24470&catid=175#comments">blog</a>

We are all e patients

We are not just the patients themselves.

We are the caregivers and the family members. (Certainly this group needs to be strong to take care of the patients!) We want to help them too!

I think we learn so much here because we're all included!!

I am so touched every day by the hospitality exhibited here.

Thank you!

Jeanne Barnett owner of cysticfibrosis.com
established in 1996
 

Imogene

Administrator
I've been giving little lessons about

e-Patients

in my <a target=_blank class=ftalternatingbarlinklarge href="http://blogs.cysticfibrosis.com/blogpost.cfm?threadid=24470&catid=175#comments">blog</a>

We are all e patients

We are not just the patients themselves.

We are the caregivers and the family members. (Certainly this group needs to be strong to take care of the patients!) We want to help them too!

I think we learn so much here because we're all included!!

I am so touched every day by the hospitality exhibited here.

Thank you!

Jeanne Barnett owner of cysticfibrosis.com
established in 1996
 

Imogene

Administrator
I've been giving little lessons about

e-Patients

in my <a target=_blank class=ftalternatingbarlinklarge href="http://blogs.cysticfibrosis.com/blogpost.cfm?threadid=24470&catid=175#comments">blog</a>

We are all e patients

We are not just the patients themselves.

We are the caregivers and the family members. (Certainly this group needs to be strong to take care of the patients!) We want to help them too!

I think we learn so much here because we're all included!!

I am so touched every day by the hospitality exhibited here.

Thank you!

Jeanne Barnett owner of cysticfibrosis.com
established in 1996
 

Imogene

Administrator
I've been giving little lessons about

e-Patients

in my <a target=_blank class=ftalternatingbarlinklarge href="http://blogs.cysticfibrosis.com/blogpost.cfm?threadid=24470&catid=175#comments">blog</a>

We are all e patients

We are not just the patients themselves.

We are the caregivers and the family members. (Certainly this group needs to be strong to take care of the patients!) We want to help them too!

I think we learn so much here because we're all included!!

I am so touched every day by the hospitality exhibited here.

Thank you!

Jeanne Barnett owner of cysticfibrosis.com
established in 1996
 

Imogene

Administrator
I've been giving little lessons about

e-Patients

in my <a target=_blank class=ftalternatingbarlinklarge href="http://blogs.cysticfibrosis.com/blogpost.cfm?threadid=24470&catid=175#comments">blog</a>

We are all e patients

We are not just the patients themselves.

We are the caregivers and the family members. (Certainly this group needs to be strong to take care of the patients!) We want to help them too!

I think we learn so much here because we're all included!!

I am so touched every day by the hospitality exhibited here.

Thank you!

Jeanne Barnett owner of cysticfibrosis.com
established in 1996
 

Ratatosk

Administrator
Staff member
Of course, like most families... We probably aren't all going to get along 100% of the time either <img src="i/expressions/face-icon-small-smile.gif" border="0">
 

Ratatosk

Administrator
Staff member
Of course, like most families... We probably aren't all going to get along 100% of the time either <img src="i/expressions/face-icon-small-smile.gif" border="0">
 

Ratatosk

Administrator
Staff member
Of course, like most families... We probably aren't all going to get along 100% of the time either <img src="i/expressions/face-icon-small-smile.gif" border="0">
 

Ratatosk

Administrator
Staff member
Of course, like most families... We probably aren't all going to get along 100% of the time either <img src="i/expressions/face-icon-small-smile.gif" border="0">
 

Ratatosk

Administrator
Staff member
Of course, like most families... We probably aren't all going to get along 100% of the time either <img src="i/expressions/face-icon-small-smile.gif" border="0">
 
Top