In loving memory of Noah Harrison Wilson · 26.08.25 — 01.10.25

Noah may no longer be among us, but he can still make a difference.

Noah's Gift Foundation raises awareness of Titinopathy — a rare muscular and respiratory condition — and empowers expectant mothers to insist on the tests that can save lives.

100%
of profits to awareness
Addenbrookes
NICU supported
A tiny newborn's feet held in gentle adult hands
Together we can make a difference
Awareness · Support · Early Testing
Raising Titinopathy Awareness
Supporting Families
Early Testing Awareness
Preventing Child Loss
A single candle glowing in memory of Noah
In Memory Of
Noah Harrison Wilson
26 August 2025 — 1 October 2025
Noah's Story

A little fighter who gave everything he had.

Noah Harrison Wilson was born on 26 August 2025. From his first breath he struggled to breathe on his own and was transferred to Addenbrookes NICU. After many tests, scans and an MRI, doctors found he had a rare muscular and respiratory disease called Titinopathy — he could not manage to breathe or feed on his own and relied on machines for every moment.

Noah gave everything he had, but could not overcome his fight. He sadly lost his battle on 1 October 2025.

Throughout her pregnancy, Noah's mother told the hospital and doctors that something was wrong — that she was worried about Noah's lack of movement in the womb. She was told repeatedly that everything was fine, and was sent home. We started this foundation because Titinopathy can be detected early — and families deserve to be heard.

“Together we can make a difference. #StrengthUnited”
About Titinopathy

A condition many have never heard of — and that's exactly the problem.

We're working to change that. Awareness leads to action — and action saves lives.

What it is

Titinopathy is a rare muscular and respiratory condition that can prevent newborns from breathing or feeding on their own.

Why testing matters

It can often be detected during pregnancy. Early identification gives parents time to understand, prepare and make informed choices.

Trust your instincts

If something feels wrong — reduced movement, or your gut tells you so — you can and should insist on the tests. Your voice matters.

An expectant mother in soft daylight
For Expectant Mothers

You know your baby best.

If you feel something is wrong — if your baby isn't moving or responding as they should — you can insist on tests. Ask questions. Ask again. You are your baby's first advocate.

Get awareness resources
Events & Campaigns

G.U.B.P events that build strength — and fund awareness.

All profits from future G.U.B.P bodybuilding and sports events support Titinopathy Awareness and Addenbrookes NICU through Noah's Gift Foundation.

Follow @gubp_uk & @gubp_world
Compete in upcoming events
Spectate and support
Purchase merchandise
Hashtag
#StrengthUnited

Everything and anything will be greatly appreciated. Whether you train, spectate, share or donate — every act keeps Noah's gift moving forward.

Share your story.

Other families can post their stories here, too. Together we build a community of support, awareness, and remembrance.

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Contact

Get in touch.

We'd love to hear from you — for support, partnerships, awareness, or simply to share Noah's message further.

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