
As Tamsin Coates explains, to parents whose children are not deaf, this decision seems like a no-brainer. But it’s not. In fact implants are hugely controversial within the deaf community. It is after all surgery to the head, with attendant risks and possible side-effects such as facial nerve damage. Then there’s the whole question of identity for the child and the dangers of seeing a deaf child as a “damaged” child rather than a different one. To add to the pressure for parents, that’s a decision that (for medical reasons) cannot be left until later.
Meanwhile I Keep Dancing not only discusses both points of view but also sets out the facts and relates the personal reasoning processes which she went through and the many setbacks and challenges that she and other parents of deaf children went through. There’s plenty of practical information (the dangers for small children of hearing aid batteries, for example) and examples of useful routines around school showers, swimming and so on. There’s an important lesson in one example of a friend’s family, where hearing problems were mistaken for and mis-categorised as autistic spectrum difficulties.
Meanwhile I Keep Dancing contains a number of photographs of the boys at different stages, showing both their implants and their hearing aids while they are enjoying various ordinary activities. There’s a separate chapter towards the end of the book, packed with factual information, charts and diagrams for those who want more detail. But the bigger value of the book, as I see it, is in how the writer’s own optimism and determination shine through. The emphasis is on compassion – not pity. For me, the spirit of the book is encapsulated in a comment the author makes early on: on receiving a diagnosis of deafness in a child we need to “relax and appreciate these new surroundings, and we have to enjoy every silly moment we can with our children.”
PWT rating:♥♥♥♥♥
Meanwhile I Keep Dancing