The BBC documentary department is planning to produce a documentary on Kallmann syndrome.

While still at the idea stage they are after any input from any interested people with KS or HH who wishes to take part in person or just provide ideas for background information or content.

A previous documentary did not fully explore a lot of the aspects of having KS. In an attempt to avoid the same thing happening again they are keen to hear from as many people as possible to get a good general idea.

I have already mentioned any potential programme has to be more
comprehensive and include women with KS, late diagnosis by GP's and
the psychological impacts of delayed / absent puberty.

It is only a idea at this stage, I think they are still at the
initial research stage and are after views from people with KS or HH.

The contact details if anybody is interested in taking part or just
giving their views, whether positive or negative:

Sara Kandasamy

Associate Producer
BBC Documentaries
Media Centre | 201 Wood Lane| London | W12 7TQ
Tel: (+44 (0)20 8008 4925

Email: sara.kandasamy@bbc.co.uk