Erin's Website

[ErinsMommy]

Hey Everybody... Erin is doing great, she's getting big and she'll be off her tobi for a little while in 3 more days.
I made her a website and feel free to check it out!!
It has pictures of her, updates, and other stuff... here it is...

<a target=new class=ftalternatingbarlinklarge href="http://www.geocities.com/erinsmommy05/ErinElizabeth.html
">http://www.geocities.com/erinsmommy05/ErinElizabeth.html
</a>
Enjoy !!

xoxoxo

 

[anonymous]

I visited your website. Just wanted to let you know that I live I live in Maine as well. My daughter Maggie was born ar Eastern Maine Medical Center in Bangor almost 3 years ago with CF. She also had a meconium ileus at birth requiring surgery. She had a tough time this summer and was hospitalized for a resp infection but now she's been home and doing ok. We go to a CF clinic in Bangor as well as one in Massachusetts.

Rebecca(mom to Sammy 7 no CF and Maggie almost 3 with CF)

 

[anonymous]

Yay!! another mainer!! hahaha



Melissa mom to dylan 7 no cf and caleb 4 wcf- caleb goes to the cf clinic in portland!

 

[teknogeek1300]

Dang, Geocities limits you to a certain bandwidth per month. Wish I could have seen it <img src="i/expressions/face-icon-small-sad.gif" border="0">.

 

[julie]

Cute websites, I really enjoyed the photos of her! Thanks for sharing!!!!

 

[cfgirl2008]

nice website. she so cute!


tiffany 15 w/cf

 

[imondeck]

She is precious. The picture with her gloworm is absolutely adorable!

 

[anonymous]

I have an Erin Elizabeth, who we also call our little princess <img src="i/expressions/face-icon-small-smile.gif" border="0">. She just turned 4 last month and she also has CF. Your website is adorable and she is just beautiful.

Erin's Mommy <img src="i/expressions/face-icon-small-smile.gif" border="0">

You can see a picture of her at our fundraising page:

www.justgiving.com/pfp/cure4erin