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hi all, thanks for the adv. it is really appreciated. even though cf is not common in malaysia, the docs at the hospital (university medical centre) are quite experienced. they suspected it and provided tratment quite fast. the hospital has so far given us a lot of help and advise. the docs are...

hi all, thanks for the adv. it is really appreciated. even though cf is not common in malaysia, the docs at the hospital (university medical centre) are quite experienced. they suspected it and provided tratment quite fast. the hospital has so far given us a lot of help and advise. the docs are...

hi all, thanks for the adv. it is really appreciated. even though cf is not common in malaysia, the docs at the hospital (university medical centre) are quite experienced. they suspected it and provided tratment quite fast. the hospital has so far given us a lot of help and advise. the docs are...

hi all, my name is patrick. my son joshua was diagnosed with cf a couple of weeks ago. he is 5 months old. we are from malaysia and this is a rare diasease here as only about 16 people have been diagnosed with cf till last year. the hospital we are at is treating 3 kids (various ages) for cf...

hi all, my name is patrick. my son joshua was diagnosed with cf a couple of weeks ago. he is 5 months old. we are from malaysia and this is a rare diasease here as only about 16 people have been diagnosed with cf till last year. the hospital we are at is treating 3 kids (various ages) for cf...

hi all, my name is patrick. my son joshua was diagnosed with cf a couple of weeks ago. he is 5 months old. we are from malaysia and this is a rare diasease here as only about 16 people have been diagnosed with cf till last year. the hospital we are at is treating 3 kids (various ages) for cf...

thanks guys. it means a lot to hear from you all. there is no support group of any kind in malaysia. even trying to meet parents of the other kids to see how they are coping is difficult. i left my contact details with the hospital in hope that they might be able to set up a meeting. only...

thanks guys. it means a lot to hear from you all. there is no support group of any kind in malaysia. even trying to meet parents of the other kids to see how they are coping is difficult. i left my contact details with the hospital in hope that they might be able to set up a meeting. only...

thanks guys. it means a lot to hear from you all. there is no support group of any kind in malaysia. even trying to meet parents of the other kids to see how they are coping is difficult. i left my contact details with the hospital in hope that they might be able to set up a meeting. only...

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...

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...

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...