One Mum’s story
Mel & Charlie have three children, Tom, Harry and Rosie. Whole Genome Sequencing identified that both Tom & Rosie have the same ultra rare DHDDS gene mutation. These mutations cause […]
genetic testing
I’m proud of my epilepsy. It’s made me who I am.
Millie has just turned 30. She had her first epileptic seizure when she was just 11 months old and was then diagnosed with the rare genetic condition, Tuberous Sclerosis Complex
I’m proud of my epilepsy. It’s made me who I am. Read More »
I would never have known that I carry the BRCA gene if it wasn’t for my daughter
Lisa first heard about genomics thanks to her daughter, Emily. Emily has a rare form of cerebral palsy called Worcester Syndrome and it was suggested to the family that they
I would never have known that I carry the BRCA gene if it wasn’t for my daughter Read More »
Discovering our children have a rare genetic mutation has opened new doors for the future
Mel & Charlie have three children, Tom, Harry and Rosie. When they were born, both Tom and Rosie didn’t learn to speak quite as quickly as their friends, and both
Current trends in the management of the infertile couple
This RSM webinar will address the recent developments in the field of infertility. The key learning objectives will be as follows: To better understand current fertility investigation and treatment. Assess the
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A day in the life of a Genetic Counsellor
A day in the life of a Genetic Counsellor Eshika Haque, a genetic counsellor at Guy’s Hospital, speaks to us about how she provides support, information and advice for patients
A day in the life of a Genetic Counsellor Read More »