What We Do

Breath4CF was established within the Cystic Fibrosis Association of NZ, after discussions with medical specialists who unanimously agreed that (aside from medications) physical exercise is the best way for a person with CF to preserve their own quality of life, lung function and longevity. However it was identified that families affected by CF struggle to meet the cost of these extras as well as the ongoing substantial medical and nutritional costs of this condition. Therefore under the Breath4CF grant fund, financial assistance is given to every person in NZ with CF so that there is no barrier to participating in life preserving exercise or activity. Assistance is by way of gym memberships, entry fees, lessons, sports equipment etc infact Breath4CF will help towards any physical activity, for a person with CF, that would produce a health benefit. Assistance is by way of reimbursement for activity costs.

OUR MISSION

To help increase the quality of life and longevity of people with Cystic Fibrosis by encouraging people them to participate in physical activity and sport.

To educate the public about Cystic Fibrosis and its impact on those affected and their families.

To raise sufficient funds to allow these two things to happen.

OUR VISION

• That all people with Cystic Fibrosis participate in physical activity as part of their regular daily life.

• That the cost of such activity is not a barrier to participation.

OUR VALUES

• We believe that physical activity is integral to quality of life.

• We believe that people’s choices and the ability to participate should not be affected by their financial status.

• We believe that physical activity is possible for everyone regardless of health, finances or ability.