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Helene Cederroth: Solving the unsolvable – A revolutionary new model for diagnosing rare diseases

Interview by Emma Bishop, RARE Revolution insider, featuring Helene Cederroth, founder and CEO,Wilhelm Foundation

“Genome sequencing can provide answers for 40% of people living with an undiagnosed disease. That means 60% don’t receive a diagnosis and we need to change that. We need to focus on the 60% that we can’t solve.” Helene

Interview by Emma Bishop, RARE Revolution insider, featuring Helene Cederroth, founder and CEO, Wilhelm Foundation

“We need to include the families to show everybody that these are not just cases, they are people.” – understanding the human impact on the diagnosis process


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