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suepettit

New member
Hi everyone! I am Sue Pettit, my daughter is Valerie. She is 13 and has CF. Currently, she is in the hospital and has been for the past 11 days.
I just wanted to say hi, I am sure I will have more to say later. If you want to learn more about Valerie, please visit our web site, www.curecf4valerie.com.
Thanks,
Sue Pettit<a target=new class=ftalternatingbarlinklarge href="http://www.curecf4valerie.com">Valerie's story</a><img src="i/expressions/rose.gif" border="0"><img src="i/expressions/face-icon-small-sad.gif" border="0"><img src="i/expressions/rose.gif" border="0">
 

anonymous

New member
Hi Sue, I loved your website! I have question though, in one of the pictures, your daughters wearing a mask, does your cf centre make all cfers wear masks or is it cas she cultered something? I'm just really curious to see how other centres operate! Shamrock, x
 
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