Babies: 0 - 3 Months

Cystic Fibrosis

This is a repost from special needs...Does anyone have a child diagnosed with CF?

Re: Cystic Fibrosis

  • I don't, but I'm an RN and took care of adults with CF for 3 years, so I know quite a bit about it.  Does your LO have that diagnosis?
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  • Our 12 and 13 yr old nieces both have it.
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  • Yes. We are going to a specialist this week. I was just wondering if there was anyone else out there. Apparently only 850-1000 babies are born with it each year. I was looking for a good parents of kids with cf website. Everything on the internet seems scary and overwhelming. There has to be something better.
  • We do not but I have a friend who was faced with all the scary facts who is 30 years old and living an amazing life (and raising awareness and $$$ for the cause). Wait to go to the dr. to get your facts and ask him/her for resources.
    "Normal day, let me be aware of the treasured day you are. Let me learn from you, love you, bless you before you depart...let me hold you while I may."

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    TTC #1- unexplained...lost left ovary 4/07 IUI #1 2/10/09-BFN IUI #2 3/5/09-BFN IVF # 1-BFP

    TTC#2- FET 4/7/11 BFP, Natural mc 5/5/11 IVF#2 ER 9/13/11, ET 9/16/11, Beta #1 9/27/11 BFP 254 Beta #2 9/30/11 793 -Twins!

  • I would imagine that it's incredibly overwhelming.  Each person with CF is different, though.  So like a PP said, wait to see what the MD says before you worry yourself sick.  Best of luck to you.  If worse comes to worse, you can alway PM me with worries/concerns.  I will try to help you as best as I can.
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