19/08/2026
Meet beautiful Princess Arayah. 🤍✨
At just 2 years old, Arayah lives with Prader-Willi Syndrome (PWS) — a rare genetic condition that affects many areas of the body, often including muscle tone, growth, feeding, and development. Children with PWS may require lifelong support and personalised care to help them reach their full potential.
Arayah is unable to sit independently or fully support her head, so this session was carefully tailored around her needs, comfort, and abilities. Instead of a traditional studio session, we brought the experience to her home — her safe and familiar environment where she could feel relaxed and comfortable.
This beautiful princess had her session through The Butterfly Wishes Network , an incredible charity I am honoured to volunteer for, providing photography memories for families of children with life-limiting or serious medical conditions.
And Arayah did absolutely amazingly… even sending a few precious smiles to Auntie Aga. 🥹🤍
A little note about the images: on a few photographs, Arayah’s feeding tube has been edited out at mum’s request. Mum has received both versions of the images — with the tube and without the tube. The tube was not removed for the session; it is a medical necessity and an important part of Arayah’s everyday life. It is also part of her journey, and we respect and honour every part of her story. 🤍
Thank you, Arayah, for letting me capture your beautiful smile and the incredible love that surrounds you.
