Run London Landmarks Half Marathon with the Mikaere Foundation in April 2025

Run the LLHM and make a difference! One in three children born with NKH won’t see their first birthday. With your help, we e can change this outcome! Conquer this stunning closed road, central London run – the only half marathon to go through both the City of London and City of Westminster. This scenic run is great for first-time runners or regular runners wanting to hit their PB.

Date: Sunday 6 April 2025
Registration fee: £30
Location: Pall Mall, London, ‎SW1
Minimum sponsorship: £395 (excluding gift aid)

Registration and payment close date: 19th January 2025.

    Charity Place

    Apply for a charity place with the Mikaere Foundation today!

    Registration Fee: £30
    Fundraising Target: £395
    Date: Sunday 6 April 2025

    Already have a place?

    If you have a ballot place on the 2025 London Landmark Half Marathon, we’d love to have you on the team!

    Join for free, with no minimum fundraising target. We just ask that you raise what you can, so we can keep pushing for a future for children with NKH.

      I have questions

      The Course

      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.

      Scroll to Top