This is a new group led by Kate Weston and Marisa Robertson, both of whom have personal experience of PSPA and are active PSPA members The group is for people affected by PSP or CBD, their families, friends and carers to meet, give support and have the opportunity to chat informally, make new friends and enjoy and cup of tea or coffee. Volunteers who would like to give their time and any healthcare professionals who have an interest in PSP or would like to find out more about this condition are very welcome. Please come along and give your support at this first meeting. If you would like to attend please contact firstname.lastname@example.org or telephone 01327 322410 for more details. (Map link; goo.gl/qCex1)
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