new to the website

[anonymous]

hello everyone, my name is tom and i've finally decided to join this club after checking this site out for a few months. i'm 29 yrs old dx at 3months.

 

[onlyoneloveinmylife]

oops that was me for got to log on><img src="i/expressions/face-icon-small-smile.gif" border="0">

 

[mellimoo91]

Hi Tom!!! I'm Melissa, 15 years old with cf, diagnosed at birth.
  i'm fairly new here too, welcome to the site!!!! it is
very addictive LOL...and a great place to learn a lot and share
your experiences as well as meeting some great people so i hope you
enjoy!!!!! feel free to ask me anything or talk about yourself; i
love hearing other people's stories!!<br>
          Mel

 

[EnergyGal]

Hi Tom and Melissa. Welcome aboard<img src=""> I had a double lung transplant and I am doing well.

 

[Jane]

Hi Tom and Melissa,

Welcome to the family!

Melissa, I have a son who is 15 too, but he doesn't come on the site. I wish he would talk to other kids with CF.

 

[JazzysMom]

Welcome, welcome, welcome. My signatures tell you about me!

 

[Scarlett81]

Welcome! Glad you are joining. You'll find lots of friends here and learn loads of info. It's a big help. Look forward to hearing more about you.

 

[Diane]

Welcome Tom and Melissa ~~ *waves*
enjoy the site, there is so much to offer on here and good friends to be made <img src="i/expressions/face-icon-small-smile.gif" border="0">

 

[NoExcuses]

Welcome! Glad you decided to join! Where do you live?

 

[thelizardqueen]

Welcome to the site!

 

[Hughett]

Good to meet you!

 

[julie]

Hi Tom and Melissa, welcome to the site. It's always so nice to have new "faces" <img src="i/expressions/face-icon-small-smile.gif" border="0"> around here!!!!

 

[randford]

<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>anonymous</b></i> hello everyone, my
name is tom and i've finally decided to join this club after
checking this site out for a few months. i'm 29 yrs old dx at
3months.</end quote></div><br>
<br>
<b>Tom,<br>
</b><br>
Welcome to the family. I've been here of a few months. I was
diagnosed back in April. You'll find that all the people here are
really wonderful, friendly and informative. I've learned a lot.
Remember, you're not alone. We're all here to fight the battle
together.<br>
<br>
<b>Randford,</b> 43/CF/Ostio

 

[onlyoneloveinmylife]

i live in baker city oregon, i go to OHSU hospital for my checkups
, anyone else ever go there?

 

[littlemisssilly]

Hello and welcome to you both!! Always nice to see new people joining <img src="i/expressions/face-icon-small-happy.gif" border="0">