Exploring the fascinating kaleidoscope that is Down syndrome, and its community. 

Our great friends that help us pull it all together

Rachel Mewes

Rachel is mother to Betsy, who has Down Syndrome. Rachel’s background is in teaching, support and care of people with learning disabilities and she seeks to use her experience to advocate for people with Down Syndrome in every arena. By becoming involved with Making Chromosomes Count, Rachel aims to raise the voices of people who need to be heard and tackle issues relevant to equality of human rights for all. (Photos by Simon Greener and Martin Bishop)

Denise Humberstone

Denise is a mother of 3 and an advocate for people with disabilities in general and Down Syndrome in particular, as she has a 21 year old daughter with the condition. She has spoken at the United Nations in Geneva. Having lived around the world, Denise has a broad experience of life with Down Syndrome in a range of countries. She sees Making Chromosomes Count as an ideal platform and opportunity to bring to the fore and share the incredible realities of Down Syndrome in the 21st Century.

Sarah Mayes

Sarah is Mum to Tilly and Izzy. Izzy is two years old, has Down Syndrome and is an Ambassador for Wouldn’t Change A Thing.. Sarah has been an active member of Wouldn’t Change A Thing and the family have featured in several projects. Sarah joined Making Chromosomes Count in order to spread awareness of Down Syndrome. Izzy has some complex medical needs and Sarah is passionate that a rounded view of Down Syndrome should be made available to new or future parents, as well as medical professionals.

Jemma Baker

Jemma is a proud Auntie to a little boy named Evan, who has Down Syndrome. She became involved with running Making Chromosomes Count after yearning to be more active with the Down Syndrome community. She aims to share the reality of the positive and inspirational individuals from within the community and make sure that everyone’s voice matters.

Julie Helen Williams

Julie is mother to Evan, who has Down Syndrome and two older daughters. Julie was proud to be Mum number 50 in the original Wouldn’t Change A Thing video and is currently Management Admin in the successful support group that followed. Now part of the team at Making Chromosomes Count, Julie aims to continue spreading awareness about the reality of life with Down Syndrome.

Claire-May Minett

Claire-May, 41, Independent woman, Self advocate for the International Mosaic Down Syndrome Association. Passionate about spreading awareness for Mosaic. Freelance Film Maker/Editor producing documentary based shorts. Love Stephen King and playing Ukulele.

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