About us
The journey to establishing Keeping Independence Together (KIT) began with a deeply personal and inspiring experience. When our son, Kit, was diagnosed with Duchenne Muscular Dystrophy (DMD), we were faced with numerous challenges, both emotional and financial. One of the significant hurdles was securing a power chair for Kit, an essential tool for his independence and quality of life.
In response to this need, we set up a crowd funding page. The outpouring of support we received was overwhelming and humbling. Friends, family, colleagues, strangers, and even a charity came together to help us achieve our goal. This collective effort provided Kit with the power chair he needed and filled our hearts with gratitude and hope.
We realised how incredibly fortunate we were to have such a strong support network. However, it also became clear to us that many other children with DMD and their families might not have access to the same level of support. Every child with DMD deserves the same opportunities for independence and quality of life that Kit has, and they shouldn't have to face these challenges alone.
This realisation inspired us to create KIT. We want to extend the generosity and compassion we experienced to other families facing similar struggles. By providing financial assistance, resources, and support, KIT aims to help children with DMD achieve greater independence and enjoy a better quality of life.
Our mission is to ensure that no family feels isolated or overwhelmed by the obstacles that come with a DMD diagnosis. Through KIT, we hope to foster a community where every child with DMD receives the support they need, just as Kit did. Together, we can make a difference, one child at a time.
Who is Kit?
Kit Brown
The Inspiration
Kit is a bright and spirited little boy with an infectious smile and an unyielding sense of humor. Despite facing the challenges of Duchenne Muscular Dystrophy (DMD), Kit never complains. He tackles each day with remarkable mental strength and a positive attitude that inspires everyone around him.
Kit's adventurous spirit and love for exploration are evident in everything he does. Whether he's playing with his toys, spending time with friends, or simply enjoying the outdoors, Kit's joy and enthusiasm shine through. His resilience and determination to make the most of every moment are truly awe-inspiring.
Despite the physical impairments that come with DMD, Kit’s mental fortitude remains unshaken. He embodies the essence of courage and perseverance, showing us all the true meaning of strength.
Our Vision
We envision a future where those with Duchenne in Dorset have access to the tools and resources they need to lead independent and fulfilling lives. We are committed to making this vision a reality through community support and dedicated fundraising efforts.
How do we get there?
As a newly established charity, we are committed to creating impactful programs that support those with Duchenne muscular dystrophy in the Dorset area. Our programs are designed to provide financial assistance for essential technology, equipment, and fully accessible holiday experiences. Although we are in the early stages of our journey, we are dedicated to turning our vision into reality with the support of our community.
To ensure transparency and foster trust, we invite you to review our Business Plan and Governing Document. These documents outline our mission, goals, and operational strategies, providing a detailed overview of how we plan to achieve our objectives.
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