im new here

dippydi

New member
Hello im Diane, i live in the north west of England, my son Jordan aged 5 had CF.

Jordan was born with meconium ileus(blocked bowel) and had surgery to correct this at 9 hours old. We had no idea that my partner & i were carriers of this gene and having Jordan born with this was a complete shock.
I usually post on our CF forum in England and recentley came across this forum and decided to have a look and introduce myself.
Jordan is a very active and very well little boy, he hasnt had any chest infections and any coughs and colds have been treated with oral anitiotics (thankfully)
I have also got another little boy Nathan who doesnt have CF he is 16 months old.

I probably wont be posting too often due to the time difference between me and you there in the USA, but i just wanted to say hello and hopefully sometime join in

Hopefully chat soon
Diane <img src="i/expressions/face-icon-small-smile.gif" border="0">
 

lflatford

New member
Welcome. Don't worry about the time difference we have many people on this forum who post late at night and even early in the morning. I look forward to hearing from you.
 

julie

New member
Welcome to the site. Don't feel bad about the posting times. Sometimes I am still up at 3am on a weekend typing away on this place. Hope you find it useful and informative!
 

mt004h0873

New member
Welcome to the forum Diane.
I'm Sarah pretty new also. I also live in the UK with my daughter who's 2 1/2 with cf.
Hope you find the group useful. Feel free to email at mt004h0873@yahoo.co.uk
I'll be happy to help wherever possible
 
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