We set up as a community group
about 18 years ago by a group of parents after the
birth of their first
D/deaf child. It was a daunting experience because we felt isolated and under pressure, making lots of decisions and
dealing with so many different
professionals. Without
support from people with similar experiences it is difficult.
but having a need to know how to deal others people in similar situations were managing to cope, a couple of families established this group offering support to each other and extending that support to families of newly diagnosed deaf children