Cystic Fibrosis Forum (EXP)

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  1. P

    df508 on one gene and 5T variant on the other

    Heather: I began to become PI when I was in my late 20's but remember that I wasn't dx until I was 47. Up until I was 47, I had never been treated for mucus (much less CF). Had I been treated, the mucus would not have been free to flow and collect on my pancreas. My feeling is that had I...
  2. P

    df508 on one gene and 5T variant on the other

    Heather: I began to become PI when I was in my late 20's but remember that I wasn't dx until I was 47. Up until I was 47, I had never been treated for mucus (much less CF). Had I been treated, the mucus would not have been free to flow and collect on my pancreas. My feeling is that had I...
  3. P

    df508 on one gene and 5T variant on the other

    Heather: I began to become PI when I was in my late 20's but remember that I wasn't dx until I was 47. Up until I was 47, I had never been treated for mucus (much less CF). Had I been treated, the mucus would not have been free to flow and collect on my pancreas. My feeling is that had I...
  4. P

    df508 on one gene and 5T variant on the other

    I have DF508 and V562I and the T5 variant. Part of the INTERPREATION of the FULL CF GENE SEQUENCE reads ad follows: This analysis identified one copy of c. 1521_1523delCTT (p. F508del). a clinically significant sequence change, one copy of c. [1684G>A; c.3017C>A] (p. [V5621; A1006E]), and...
  5. P

    df508 on one gene and 5T variant on the other

    I have DF508 and V562I and the T5 variant. Part of the INTERPREATION of the FULL CF GENE SEQUENCE reads ad follows: This analysis identified one copy of c. 1521_1523delCTT (p. F508del). a clinically significant sequence change, one copy of c. [1684G>A; c.3017C>A] (p. [V5621; A1006E]), and...
  6. P

    df508 on one gene and 5T variant on the other

    I have DF508 and V562I and the T5 variant. Part of the INTERPREATION of the FULL CF GENE SEQUENCE reads ad follows: This analysis identified one copy of c. 1521_1523delCTT (p. F508del). a clinically significant sequence change, one copy of c. [1684G>A; c.3017C>A] (p. [V5621; A1006E]), and...
  7. P

    8 yr old son with missing vas deferens

    Mary, you are correct but may I add that the Genetic Screening should be a FULL SEQUENCE. Bill
  8. P

    8 yr old son with missing vas deferens

    Mary, you are correct but may I add that the Genetic Screening should be a FULL SEQUENCE. Bill
  9. P

    8 yr old son with missing vas deferens

    Mary, you are correct but may I add that the Genetic Screening should be a FULL SEQUENCE. Bill
  10. P

    8 yr old son with missing vas deferens

    Your son certainly shows classic CF symptoms but waiting until March is too long. Call your local APPROVED CF CENTER, tell them your story and ask for an appointment. In the mean time that can arrange for a sweat test. Don't wait. Bill
  11. P

    8 yr old son with missing vas deferens

    Your son certainly shows classic CF symptoms but waiting until March is too long. Call your local APPROVED CF CENTER, tell them your story and ask for an appointment. In the mean time that can arrange for a sweat test. Don't wait. Bill
  12. P

    8 yr old son with missing vas deferens

    Your son certainly shows classic CF symptoms but waiting until March is too long. Call your local APPROVED CF CENTER, tell them your story and ask for an appointment. In the mean time that can arrange for a sweat test. Don't wait. Bill
  13. P

    newborn daughter just diagnosed

    PLEASE. Move your daughter to an APPROVED CF CLINIC at the earliest possible opportunity. Bill
  14. P

    newborn daughter just diagnosed

    PLEASE. Move your daughter to an APPROVED CF CLINIC at the earliest possible opportunity. Bill
  15. P

    newborn daughter just diagnosed

    PLEASE. Move your daughter to an APPROVED CF CLINIC at the earliest possible opportunity. Bill
  16. P

    How do we CFers die?

    mea6195 and others: I was born in January of 1940. At that time there were two names for CF, Celiac Syndrome (a disease of the pancrease) and in the late 1930's it was given the name Cystic Fibrosis. Cystic Fibrosis, at that time, was "caused by a deficiency of Vitamin A". There were NO...
  17. P

    How do we CFers die?

    mea6195 and others: I was born in January of 1940. At that time there were two names for CF, Celiac Syndrome (a disease of the pancrease) and in the late 1930's it was given the name Cystic Fibrosis. Cystic Fibrosis, at that time, was "caused by a deficiency of Vitamin A". There were NO...
  18. P

    How do we CFers die?

    mea6195 and others: I was born in January of 1940. At that time there were two names for CF, Celiac Syndrome (a disease of the pancrease) and in the late 1930's it was given the name Cystic Fibrosis. Cystic Fibrosis, at that time, was "caused by a deficiency of Vitamin A". There were NO...
  19. P

    How do we CFers die?

    My wife says I'm still scarcastic and angry. Lucie, I appreciate your kind words. I seem to get in trouble, out here, alot. Bill
  20. P

    How do we CFers die?

    My wife says I'm still scarcastic and angry. Lucie, I appreciate your kind words. I seem to get in trouble, out here, alot. Bill
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