Has anyone had social services appoint an advocate to help with general medical care? What are your experiences? How did you manage to get an advocate and were they there when you needed them?
My sensory issues combine with my medical phobias to produce melt down or shut down in medical situations. At times in the past this has meant that I temporarily do not have mental capacity. It often means I am not taking in a word and leaves me in high anxiety states.
My GP referred to social services but social services are refusing.
At present I simply cannot access any health care.
