Experience London in a different light, walk by the Capital’s landmarks as darkness falls and the moon rises.

Select “Sign up for a listed charity” and select Mikaere Foundation in the Registration form


Minimum age

8+ for a 10km/10 mile distances.

About the Thames Moonlight 10 walk

Take on a spirited 10km or an energetic 10 mile looped route through the heart of London as darkness falls, passing famous landmarks – including St Paul’s, Westminster Abbey, Tower Bridge, the London Eye and more. A lively finish awaits – with a glass of fizz & a special Moon medal – followed by some welcome hot food & drink.

You can choose from 10km or 10 mile options, and walk as an individual or a team.

Once you escape, there are ghostly looped routes, with zombie rest stops, and if you manage to get back in one piece there’s a macabre medal, a glass of the Devil’s fizz, some horrific hot food and drink – and a souvenir bobble hat to ward off the spirits as you head off home.

You’ll start at the dungeon, near the Oval Cricket Ground in Kennington, London.
10 km start times – 5.30 – 6.30 pm
10 mile start times 4.30 – 5.30 pm
The whole route is signposted with clearly marked arrows.

What support will I get?

You’ll get:

  • Fully signed route and pick up support
  • Souvenir neck buff and glow-stick
  • Medal and glass of fizz at finish
  • Hot food at the finish


The Mikaere Foundation also offers all our walkers a fantastic support package, including:

  • Loads of training and fundraising advice, with regular email updates
  • A Mikaere Foundation t-shirt
  • A dedicated event coordinator to give you information and support in the run-up to your event

Why we need you

The Mikaere Foundation needs your support more than ever. By fundraising, you’ll help fund:

  • Groundbreaking research into effective treatment and gene therapy therapy for Nonketotic Hyperglycinemia (NKH) – drastically changing the outcome for children born with NKH.
  • Support services for children and families living with NKH. With NKH comes seizures, dystonia, pain and developmental delay.
  • Outreach to newly diagnosed families, so they have support in their corner, right when they need it.
  • Getting NKH specific information to families, nurses, therapists, carers and doctors.

could fund special restriction enzymes, used in NKH Research. These work like molecular scissors to cut up the long strands of DNA in our cells. This is vital in helping us learn more about the genetic mutations of NKH.

could fund a months worth of outreach, providing NKH information to newly diagnosed families right when they need it most.

could fund a week of a post doc researcher, analysing sample assays, which tell us if NKH gene therapy is working in our models, getting us closer to a cure.

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