Walk off the festive celebrations and kick start the New Year with an invigorating winter jaunt!

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


Minimum age

12+ for the Half Marathon distance and 8+ for a 10km/10 mile distances.

About the London Winter walk

A great event to walk off the Christmas and New Year celebrations, and maybe kick start the new with a bang! All distances start and finish at The Oval Cricket Ground, and take in highlights of the Thames, its historic bridges, and many of the Capital’s landmarks.

You can choose from 42km, 25km and 10km options, and a NEW family fun 5K on Sunday (that’s accessible!) Walk as an individual or a team.

10km CHALLENGE

What support will I get?

You’ll get:

  • Free Coffee, tea and biscuits at the start
  • Rest stops en-route, with a range of snacks & drinks (for full & half marathon distances)
  • Hot food at the finish for everyone!
  • Medal and certificate for finishers


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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