hi all,
i'm Patrick and my son, joshua (5 months old) has just been diagnosed with cf.
We are from malaysia and according to statistics there have only been 16 cases of cf reported as of last year. this makes it a rare disease in our country.
still reeling from the shock. joshua's started on vits adek and creone. he is currently undergoing physio after using the nebulizer (around 4 times a day).
just hope that some of you will share some stories and provide advice on what to expect.
thanks
i'm Patrick and my son, joshua (5 months old) has just been diagnosed with cf.
We are from malaysia and according to statistics there have only been 16 cases of cf reported as of last year. this makes it a rare disease in our country.
still reeling from the shock. joshua's started on vits adek and creone. he is currently undergoing physio after using the nebulizer (around 4 times a day).
just hope that some of you will share some stories and provide advice on what to expect.
thanks