Eve Rushmer is a valued and important member of our operations support team. Eve lives with a rare chromosomal disorder in which all or part of the short arm (p) of chromosome 18 is deleted. People living without this part of their Chromosome 18 have disabilities that make the world more difficult to navigate. Despite this, Eve has been very successful and has even found ways to help others.
She recently appeared on the C18 Podcast where she discussed both life and work whilst living with the disorder. She tells a remarkable story of resilience and determination to succeed at school, learn to drive, and get a good job. On top of that, Eve has completed a number of daring and demanding activities to raise money for Chromosome 18 Europe.
Eve very much lives her life by pushing herself to do the things she loves the most. Her condition doesn’t stop her from dancing, exercising, and even learning how to drive! Her story of overcoming these challenges throughout life are an inspiration to anyone facing difficulties.
“I would like to say to any parent out there (with a child that has C18 disorder) that it is okay to give your child the support they need to thrive in life. I know it is going to be hard, but you will get there. Look at me now. I drive a car, I have passed my driving test. I’ve even got a job in London and it is the best feeling”
Listen to the podcast below:
