Parents with cystic fibrosis/bronchiectasis

[madhairday]

We used to have a thread going but it's disappeared into the ether so I thought I'd start up a new thread to see if any of you are still around or if there are any more CF/bronchi parents around that want to talk at all? Would be good to share advice/tips/rants etc.

Hope to hear from you :)

hiya just replying to ur post....are u still about??

hiya i am a mummy of a 2 year old son wcf if anyone wants to talk :) xx

hi zoelouise87, i strarted a new thread as this one seemed quiet, ive not been on for a while to see if any replies but im going to check now. we've just got back from manchester after being in for a few days, luckily we didnt have to stay for IV's....how is your son getting on?

this is the link to the other thread, a couple of people have joined in on there :-)
www.mumsnet.com/Talk/life_limiting_illness/1494714-Cystic-Fibrosis-any-threads

this is the link to the other thread, a couple of people have joined in on there :-)
www.mumsnet.com/Talk/life_limiting_illness/1494714-Cystic-Fibrosis-any-threads