Part one of three from this full length documentary.
Part two of three from this full length documentary.
Part three of three from this full length documentary.
The credits for this documentary.
There’s a constant level of worry and a long-term grief.– Andrea Hitchings (Sarah’s mother)
We want a cure within her lifetime. But still, it’s an abbreviated life.– Andrea Hitchings (Sarah’s mother)
Congratulations on capturing what is a very moving tribute to a very special girl. I strongly believe through this work once again the arts community has shown what an important place it has in bringing awareness and providing insights to issues faced within the community.– Dr Faten Zaibak, The Stem Cell Research Laboratory, Department of Pathology, University of Melbourne
I found the documentary truly captivating and especially Hitchings. It showed her warts and all – a lovely beautiful young woman, but also one with temper tantrums, frustrations, family stresses and of course her struggle to cope with cystic fibrosis. The producers have done a superb job of letting it speak for itself without over dramatising it.– David Farrar on Kiwiblog