Hastings and Rother Lymphoedema and Lipoedema Support Group

We hold social meet ups for people who have Lymphodema or Lipoedema who live locally.  A chance to meet up with people dealing with similar issues, make connections and support each other.

We meet roughly every 2 months in accessible venues for a tea/coffee and a natter.

Get in touch if you would like to find out more and for details of our next meeting.

We also have a Facebook group.