Help our brave boy Noah, who lives with permanent lung damage, breathe easier by creating a warm, dry, healthy home where he can thrive.
Flaxmere, Hastings
Anyone who's met Noah knows he's a cheeky, smiley little boy who lights up every room. But behind that beautiful smile is a three-year-old who's spent much of his life fighting to stay healthy.
Since six months old, Noah has battled persistent chest infections, eventually being diagnosed with bronchiectasis – permanent damage to his airways that makes him vulnerable to recurring infections.
The past year has been especially tough. While welcoming his baby sister Billie, we've faced three hospitalisations, weeks of IV antibiotics and countless procedures. After three PICC lines, Noah may now need surgery for a permanent IV port.
Through it all, he keeps smiling.
Meanwhile, our home desperately needs repairs. Black mould grows rapidly in our unventilated bathroom, our kitchen is rotting, and our draughty, single-glazed windows have deteriorated so badly that my fist went through a rotten frame while attempting repairs!
With hospital stays lasting 2–4 weeks, we've exhausted our leave and lost income. Bills keep piling up, and essential home repairs are constantly pushed aside.
We're not asking for a fancy home. We're asking for a warm, dry, healthy place where Noah's vulnerable lungs have the best possible chance.
We can't change his diagnosis, but with your help, we can change his environment.
Every donation or share brings us closer to giving our brave little boy the childhood he deserves. 💙
We are Noah's Parents, and we raising funds to give my little boy a healthier, safer home to support his ongoing battle with bronchiectasis.
Funds will help create a warm, dry, healthier home for Noah by repairing mould, poor ventilation, rotten windows and kitchen damage, while helping cover mortgage payments and essential family expenses when hospital stays prevent us from working.
Uncharted territory 28 October 2026
Noahs sister Billie who has just turned 1! is now waiting on a CT scan and more blood testing and is starting long antibiotics for diagnostic work up to find out if she too has the same thing or something else entirely. How unlucky to have siblings present the same way... is it genetics? Is it the home? Or is it a factor of everything, I tried to push harder and earlier for Billie so I wonder if this earlier intervention will have a different outlook for her.
Her paediatrician is amazing and is always so honest and is looking at all the right channels and pathways. Bless her sweet sweet soul i hope
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