Patient Public Involvement

The work of the HCC is steered by the Public and Patient Voice group. The group meets once a month normally on the last Thursday night of the month, but the timing of this is may to change. The group discusses the work of the HCC and how the resources of the HCC can be used to improve patient outcomes and which areas should be worked on as a priority. If you would like to attend the meetings please contact Ralph Brown and Eni Kuseju by clicking here



The group is chaired by Patrick Ojeer a knowledgeable campaigner on the improvement of Sickle cell services.