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  1. M

    I salute you all

    Thanks so much for this post, Skye. Yes, it's always hard when your kid is sick, no matter what it is. With CF care it never stops, though. That's one of the hardest parts, isn't it? Your message was wonderful. Ktsmom, Leila screams "I hate you" at me occasionally too. Last time she did...
  2. M

    I salute you all

    Thanks so much for this post, Skye. Yes, it's always hard when your kid is sick, no matter what it is. With CF care it never stops, though. That's one of the hardest parts, isn't it? Your message was wonderful. Ktsmom, Leila screams "I hate you" at me occasionally too. Last time she did...
  3. M

    I salute you all

    Thanks so much for this post, Skye. Yes, it's always hard when your kid is sick, no matter what it is. With CF care it never stops, though. That's one of the hardest parts, isn't it? Your message was wonderful. Ktsmom, Leila screams "I hate you" at me occasionally too. Last time she did...
  4. M

    I salute you all

    Thanks so much for this post, Skye. Yes, it's always hard when your kid is sick, no matter what it is. With CF care it never stops, though. That's one of the hardest parts, isn't it? Your message was wonderful. Ktsmom, Leila screams "I hate you" at me occasionally too. Last time she did...
  5. M

    I salute you all

    Thanks so much for this post, Skye. Yes, it's always hard when your kid is sick, no matter what it is. With CF care it never stops, though. That's one of the hardest parts, isn't it? Your message was wonderful. Ktsmom, Leila screams "I hate you" at me occasionally too. Last time she did...
  6. M

    A question for all you parents of CFers

    First and foremost, I am sad for my daughter. When she says things now like "I'm going to be the best mommy!" as she cradles a doll, I feel that pang of knowing that someday she will know she can't (or shouldn't) carry a biological child and that it may make her very sad. We've started talking...
  7. M

    A question for all you parents of CFers

    First and foremost, I am sad for my daughter. When she says things now like "I'm going to be the best mommy!" as she cradles a doll, I feel that pang of knowing that someday she will know she can't (or shouldn't) carry a biological child and that it may make her very sad. We've started talking...
  8. M

    A question for all you parents of CFers

    First and foremost, I am sad for my daughter. When she says things now like "I'm going to be the best mommy!" as she cradles a doll, I feel that pang of knowing that someday she will know she can't (or shouldn't) carry a biological child and that it may make her very sad. We've started talking...
  9. M

    A question for all you parents of CFers

    First and foremost, I am sad for my daughter. When she says things now like "I'm going to be the best mommy!" as she cradles a doll, I feel that pang of knowing that someday she will know she can't (or shouldn't) carry a biological child and that it may make her very sad. We've started talking...
  10. M

    A question for all you parents of CFers

    First and foremost, I am sad for my daughter. When she says things now like "I'm going to be the best mommy!" as she cradles a doll, I feel that pang of knowing that someday she will know she can't (or shouldn't) carry a biological child and that it may make her very sad. We've started talking...
  11. M

    New here and question to cf'ers (or parents of)

    Welcome, Jessica! We also live in Jacksonville, FL. I assume you see the docs at Nemours? Please consider attending our parent support group meetings. We have a great time! We meet once a month, usually the third Monday, from 6-7:30pm. Different speakers come about topics relating to CF...
  12. M

    New here and question to cf'ers (or parents of)

    Welcome, Jessica! We also live in Jacksonville, FL. I assume you see the docs at Nemours? Please consider attending our parent support group meetings. We have a great time! We meet once a month, usually the third Monday, from 6-7:30pm. Different speakers come about topics relating to CF...
  13. M

    New here and question to cf'ers (or parents of)

    Welcome, Jessica! We also live in Jacksonville, FL. I assume you see the docs at Nemours? Please consider attending our parent support group meetings. We have a great time! We meet once a month, usually the third Monday, from 6-7:30pm. Different speakers come about topics relating to CF...
  14. M

    New here and question to cf'ers (or parents of)

    Welcome, Jessica! We also live in Jacksonville, FL. I assume you see the docs at Nemours? Please consider attending our parent support group meetings. We have a great time! We meet once a month, usually the third Monday, from 6-7:30pm. Different speakers come about topics relating to CF...
  15. M

    New here and question to cf'ers (or parents of)

    Welcome, Jessica! We also live in Jacksonville, FL. I assume you see the docs at Nemours? Please consider attending our parent support group meetings. We have a great time! We meet once a month, usually the third Monday, from 6-7:30pm. Different speakers come about topics relating to CF...
  16. M

    New here and question to cf'ers (or parents of)

    Welcome, Jessica! We also live in Jacksonville, FL. I assume you see the docs at Nemours? Please consider attending our parent support group meetings. We have a great time! We meet once a month, usually the third Monday, from 6-7:30pm. Different speakers come about topics relating to CF...
  17. M

    Lindsey update - 5/11/07, 1:00 pm

    Hi all - I know everyone is looking for an update. We hoped Lindsey would be posting her own update today. Things are still going very well, just a little bump in the road. Lindsey needed a small tube placed in her chest cavity to get rid of some air docs saw on x-ray. This is normal in...
  18. M

    Lindsey update - 5/11/07, 1:00 pm

    Hi all - I know everyone is looking for an update. We hoped Lindsey would be posting her own update today. Things are still going very well, just a little bump in the road. Lindsey needed a small tube placed in her chest cavity to get rid of some air docs saw on x-ray. This is normal in...
  19. M

    Lindsey update - 5/11/07, 1:00 pm

    Hi all - I know everyone is looking for an update. We hoped Lindsey would be posting her own update today. Things are still going very well, just a little bump in the road. Lindsey needed a small tube placed in her chest cavity to get rid of some air docs saw on x-ray. This is normal in...
  20. M

    Zoe4life

    Yea Zoe!!! Jada, I'm so glad you and your sweetie are going home. She must have been stir crazy in that little room. I hope IV's at home go smoothly. Call me anytime! <img src="i/expressions/face-icon-small-smile.gif" border="0"><img src="i/expressions/face-icon-small-smile.gif"...
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