Cystic Fibrosis Forum (EXP)

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  1. S

    Baby who needs your prayers

    Bengi and your family is in my prayers............... Stay encouraged and strong.
  2. S

    Baby who needs your prayers

    Bengi and your family is in my prayers............... Stay encouraged and strong.
  3. S

    Baby who needs your prayers

    Bengi and your family is in my prayers............... Stay encouraged and strong.
  4. S

    soooo SCARED DEATH not sure where to go from here

    Just keep the faith and everything will be o.k. I was new to it as well with my family being African American it is very rare for us and when they told me what the disease was I 'd never heard of it befor in my life. I looked through medical books to see exactly what it was and if the books...
  5. S

    soooo SCARED DEATH not sure where to go from here

    Just keep the faith and everything will be o.k. I was new to it as well with my family being African American it is very rare for us and when they told me what the disease was I 'd never heard of it befor in my life. I looked through medical books to see exactly what it was and if the books...
  6. S

    soooo SCARED DEATH not sure where to go from here

    Just keep the faith and everything will be o.k. I was new to it as well with my family being African American it is very rare for us and when they told me what the disease was I 'd never heard of it befor in my life. I looked through medical books to see exactly what it was and if the books...
  7. S

    Message of Hope

    I guess looking at my name you assume that I would be a gentleman but my name is short for Seanette, I am actually his mother. Thank you for all of your responses. Sean
  8. S

    Message of Hope

    I guess looking at my name you assume that I would be a gentleman but my name is short for Seanette, I am actually his mother. Thank you for all of your responses. Sean
  9. S

    Message of Hope

    I guess looking at my name you assume that I would be a gentleman but my name is short for Seanette, I am actually his mother. Thank you for all of your responses. Sean
  10. S

    Message of Hope

    I just wanted to give everyone a message of hope. My son is 10 years old and was diagnosed with cystic fibrosis when he was 5 months old. After diagnosis he hemmoraged on his brain due to lack of vitamin k from cf at 7 months. we had lots of hospitalizations for pneumonia and respiratory...
  11. S

    Message of Hope

    I just wanted to give everyone a message of hope. My son is 10 years old and was diagnosed with cystic fibrosis when he was 5 months old. After diagnosis he hemmoraged on his brain due to lack of vitamin k from cf at 7 months. we had lots of hospitalizations for pneumonia and respiratory...
  12. S

    Message of Hope

    I just wanted to give everyone a message of hope. My son is 10 years old and was diagnosed with cystic fibrosis when he was 5 months old. After diagnosis he hemmoraged on his brain due to lack of vitamin k from cf at 7 months. we had lots of hospitalizations for pneumonia and respiratory...
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