splick 03/04/18
Last reply 2 weeks ago
Introducing a new support group…

Welcome to Many Scars. We are based in Norfolk but will speak/text/FaceTime/Skype to anyone in the UK coming to terms with a new diagnosis or just simply needing some support.

Four of us run the group. Three of us have varying degrees of ms and the forth member of the team is the mother of one if us. She us excellent at arranging family support meet ups.

If you feel as though you need some support either locally or nationally, any one of us can be contacted using the methods below.

We will shortly be releasing a programme of events for 2018, a little later than planned, as the weather has been so depressing. Be sure to check our website or follow us on Facebook. *Many Scars Norfolk*

Contact one of the Team:

Kate Sanchez – Mother of 2, diagnosed 2008 with Highly Active RRMS, founder of Many Scars- [email protected]

Nick Jarvis – Partner of Kate Sanchez, diagnosed 2011 with PPMS, founder of Many Scars – [email protected]

Vicky Rapley – Diagnosed 2008 with Highly Active RRMS, very good friend of Kate.
[email protected]

Lynne Sanchez, Mother of Kate. Lynne organises events for family and friends of those affected by MS.
[email protected]

http://www.manyscars.co.uk

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ammatime
2 weeks ago

Thanks for all the information. Do you do any London groups?

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