Team MikaereTeam Mikaere
  • Posts
  • Events
  • About NKH
  • Donate
Tag

Data

Mar 23
3075

Forest Path

By Ellly | Food for thought | 2 Comments

Even the all-powerful Pointing has no control about the blind texts it is an almost

Read More

About Mikaere

Our son Mikaere was born in October 2016 with Nonketotic Hyperglycinemia (NKH). It's a rubbish, horrid disorder. This is our story.

Recent Posts

  • What we’re up to… December 04, 2024 at 06:00PM
  • What we’re up to… December 03, 2024 at 07:13PM
  • What we’re up to… December 02, 2024 at 04:39PM
  • What we’re up to… December 02, 2024 at 04:26PM
  • What we’re up to… November 30, 2024 at 10:00AM

Site Map

– Home
– Blog
– Donate
– Events
– Mikaere Foundation

About

Team Mikaere is for those following the journey of Sam, Elly and Mikaere - a baby boy with Nonketotic Hyperglycinemia. We've partnered with Joseph's Goal to raise funds for the NKH Research done by Dr Nick Greene as part of UCL. He's currently the world leader in NKH research.

We're so hopeful that better treatment options will be found for kids with NKH. It's so rare, less than 500 kids worldwide are diagnosed with it. Every pound we raise has a direct and profound effect on the research that can be done.

Fundraise with us

Help us raise money for NKH Research. Help us help give Kai future. It sounds so cheesy, but holds a sobering amount of truth for us. NKH is terminal, without treatment Kai may not have a future.

Please help us raise money for NKH Research.

  • Posts
  • Events
  • About NKH
  • Donate