We raise funds to support individuals and families affected by genetic disorders.
There are around 6,000 life-altering genetic disorders.
Some genetic disorders are apparent at birth while others are diagnosed at different stages throughout childhood, adolescence and sometimes into adulthood, having a devastating impact on individuals and their families.
The Jeans for Genes campaign raises awareness of the daily challenges faced by those living with a genetic disorder and raises money to fund projects that make a tangible difference to the lives of those affected.
Most importantly, the campaign:
brings together the genetic disorder community in order to make a loud noise about the issues that matter to them,
shines a light on the organisations that work tirelessly to improve the lives of affected individuals; and
celebrates the achievements of those living with a genetic disorder.
Please take a look below to learn more about the lasting impact your Jeans for Genes donations make.
A multi-sensory wonderland
Monies raised on Jeans for Genes Day funded Oily Cart, a theatre company, to visit special schools with a production that involved tactile and multi-sensory activities.
Specialist nursing care
Helen is the Clinical Nurse Specialist for chronic granulomatous disorder at Great Ormond Street Hospital. Her role is funded through monies raised on Jeans for Genes Day.
Summer fun for young carers
Jeans for Genes Day funded a summer camp for the Scottish Huntington's Association for young people affected by Huntington's disease.
Pioneering Medical Research
Rhys Evans hit the headlines in 2002 as the ‘bubble baby’, a child with no immune system, whose life was saved by pioneering gene therapy partly funded by monies raised through Jeans for Genes. Rhys is now 19 and has been able to live a full and active life.
New vital patient groups
Seven year old Josh has Norrie disease, a genetic disorder that has caused him to be blind from birth as well as him currently losing his hearing
2020 Jeans for Genes Grant Charities
This year, because of your Jeans for Genes donations, we were able to fund 23 charities providing vital support to those living with a genetic disorder in the UK during the coronavirus pandemic.
Five-year-old Dominic has Ohtahara Syndrome, a rare genetic disorder which causes epilepsy. Dominic has complex needs: He is not able to move independently and can’t hold his head up. He can’t talk or communicate. He has an unsafe swallow and is ‘peg fed’ which means he receives nutrition through a tube in his abdomen. He has severe visual impairment and he has a catheter fitted. Many children with Dominic’s condition do not reach their tenth birthday.
Four year old Henry was born with the rare genetic condition, Diamond Blackfan Anaemia. His condition meant that he was unable to make his own red blood cells, which carry oxygen around the body and so he required blood transfusions every 3 – 4 weeks to keep him alive.
Ellie and Hayden's story
Ellie shares what it’s like to have a little brother like Hayden who has the genetic disorder Duchenne Muscular Dystrophy, a progressive and life-limiting muscular degenerative disease.
It is estimated that one in 25 children is affected by a genetic disorder. 30,000 babies and children are newly diagnosed in the UK each year. Meet just some of the amazing children who you can help when you support Jeans for Genes.
Francesca, aged 4, has Acrodysostosis. A rare genetic disorder which affects many parts of her body. She has skeletal problems, can’t walk any distance, is fed through a tube, has global developmental delay, hearing loss, serious neurological problems and has had brain surgery, plus suspected heart issues.
Cameron is 5 years old. He was born with the genetic disorder Norrie Disease. This means he is blind. He is also deaf in his right ear and may lose his hearing completely as he grows older. He has autism, learning difficulties and hasn’t learned to speak yet.
Freddie is 15 months old and has an extremely rare genetic disorder called Trichothiodystrophy (TTD) which affects one child in a million. He was born very prematurely at 28 weeks, weighing just 2lb 5oz. He has many complex health problems.
Faith, 11, has Kleefstra syndrome, a rare genetic disorder which means she has epilepsy, delayed physical and intellectual development. She will need lifelong support.
Ashley has Treacher Collins syndrome meaning he was born without a jaw, cheekbones and ears.
Tamilore has sickle cell anaemia and often experiences debilitating pain. His limited physical health has a knock on effect on his education, hobbies and acceptance by others.