Our newsletter is one of the key ways we are able to link our widespread community. Cross-infection issues mean that it is difficult for people with Cystic Fibrosis to mix together in the way other groups can. Please make use of the newsletter and this website. If there is anything you would like to share with the rest of the community, simply get in touch by email or phone.

We aim to produce our colour newsletter 3 times per year, usually around March (after our February AGM), July and October/November.

Occasionally we mail "flyers" to members advertising social events. If a matter is urgent or simply cannot wait until our next newsletter, our Chairperson will email members. If your email or address details are incorrect or change, please send an email to the branch so that we can update our records.

We are very grateful to Wellington Council's Publication & Design Department which prints, folds and staples our newsletter at cost, for around $1.20 per copy. We print around 120 copies, which are sent to our CF adults and families of children with CF, supporters and extended family who are on our mailing list, medical contacts such as paediatricians and physios and other branches. We usually reserve a few copies to accompany grant applications.