Just over 20 years ago our first child, Ivan, was born with a rare disease that would ultimately take his life. Since then, genomics has developed at such a rate that we are now able to talk about the possibility of treatments, even cures. That’s why I’m joining the
@OHRareDisease Centre – with an ambitious mission to develop 40 new treatments for rare diseases in the next decade and give hope to families like my own.
thetimes.com/uk/politics/art…