Cystic Fibrosis Forum (EXP)

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  1. H

    Need to know more!!!!

    Hi both parents have to be carriers of the CF gene, you then have a 1 in 4 chance of having a child with CF, but if one parent is just a carrier and the other not then no there's no chance. Hope this helps Emma mum to Chelsie 5 w/cf from the UK
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    Average cost of CF Center visit

    <blockquote>Quote<br><hr><i>Originally posted by: <b>Anonymous</b></i><br>mother of 7yr old with cf from uk. i am always shocked that americans have to pay for medical treatment in such a wealthy country! people here moan about having to wait for hosp. appts. but no one has to worry about...
  3. H

    When/how was your child diagnosed?

    Sorry forgot to sign in that's me above. Emma.xx
  4. H

    Pics of our kids

    Trying to attach pic's hope i can do it soon. Emma.xx mom to Chelsie 5 w/cf
  5. H

    CF Recipes, Pretty Please!

    <blockquote>Quote <hr><i>Originally posted by: <b>cfgirl2008</b></i> I got a milky way cake recipe which is good for cfers.I'll bring it tomorrow. Hi i see that you say you have a milky way cake recipe please can you either put it in here or send it to me via email hope2cf@yahoo.co.uk. Thank...
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    If anyone will talk to me, I'd appreciate it (2nd termination mentioned inside)

    Hi sorry i havent been logged in before. Lilth Hi i'm glad i hadn't offended you, and that your comments weren't against me. Emma.x
  7. H

    If anyone will talk to me, I'd appreciate it (2nd termination mentioned inside)

    I agree with the last few posts on here. Some people have said they wouldn't be able to cope with another child with CF, i know i wouldn't.
  8. H

    If anyone will talk to me, I'd appreciate it (2nd termination mentioned inside)

    Well there sure has been some different views here. I have a daughter with CF who is now 5, we have had to deal with alot, i have said when i get pregnant again and was a CFer i would have a termination BECAUSE, i wouldnt want another child to go through what my daughter has already, and us as...
  9. H

    infections in daycare

    My daughter was diagnosed at 8 months old, (now 5 & 1/2) i had gone back to work when she was 6 months old, and Chelsie was with a childminder, but when she was diagnosed i left work, i left work because i felt i wanted to spend all my time with her once we knew what cf was, BUT she was so well...
  10. H

    medications for psuedomonas

    My daughter is on Colomycin inhaled and is now on antibiotics for staphylococcus which is for 3 months
  11. H

    Any idea where to get a vest?

    Thanks very much i'll have a look,xx
  12. H

    Any idea where to get a vest?

    Hi i live in UK but cant really find anything on the vest, does anyone know where or how to get one thanks.x
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