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LPUK representatives had a great time at the Grand Arcade in Cambridgeshire on Sunday raising awareness of dwarfism, and also fundraising, whilst supporting the Grand Arcade's Christmas lights switch on, which was undertaken by LPUK President Warwick Davis. 

We met lots of people, speaking to them about dwarfism and raising awareness and it was fantastic to help educate people about the many forms of dwarfism, correct terminology and helping them see that people with dwarfism are just like everyone else. 

A huge thank you to the Grand Arcade and BBC Cambridgeshire's Jeremy Sallis, who also interviewed Warwick on his show. 


Gareth Jenkins

Our daughter, Freya, was born in June 2019 and she has a condition called Achondroplasia, which is a form of dwarfism. 

Very little is known about the condition (the chances are about 1 in 25,000 of having a baby who will have the condition) and most people think it is just a case of having shorter arms and legs. But there are so many more health complications that can be attached to the condition. When Freya was 2 weeks and then 5 weeks old she stopped breathing, resulting in lenghty hospital stays and multiple tests. But we are now home and she is doing really well. She will always have to have routine check ups throughout her life.

I am running the following events in order to raise money and awareness. If anyone would like to come and join me or support me on any of them then please feel free.

  • 6th October 2019 - Bournemouth Marathon
  • 10th November 2019 - New Forest Half Marathon 
  • 22nd December 2019 - Portsmouth Marathon
  • 26th January 2020 - Farnborough Half Marathon
  • 1st March 2020 - Vitality Big Half Marathon (London)
  • 19th April 2020 - Brighton Marathon
  • 16th May 2020 - Jurassic Coast Ultra Marathon 

If you would like to support, please visit JustGiving

Check out Gareth's fantastic interview on BBC Radio 5 Live where he talks about having a child with Achondroplasia and Little People UK.

'Small Steps to Great Things’ A Monthly LPUK News Update


We firstly want to offer our congratulations to everyone who has started school, transferred to secondary school, prepared for University and also anyone who has taken on a new challenge in September. Well done!

September was also a new experience for LPUK, where we attended our first Rare Disease Summit in Cambridgeshire. We met a great number of people from medical professionals, charity partners and Public Health England to name a few, all are great connections to help LPUK move forward and continue to support our members.

Raise Funds to Raise Awareness

just giving

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