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So that was a mixed experience. I think that's a problem. We've ended up travelling the country
going to Birmingham to find an endocrinologist and psychiatrists with relevant experience
are fairly few and far between. So it seems to me that to actually provide a single assessment
locally is going to be difficult for a syndrome like the one that Hannah has. So probably
you'd need to have a sort of national assessment centre or perhaps a regional one, maybe a
few dotted around the country, that might work. So I think the concept is good, but
making it work in practice is going to be challenging locally, because of the availability
of the right people with the right skills and experience.