Hi there - are there any group meet ups in person please?

[RachelSPforGL]

I am supporting someone who has FND and she would really like to meet other people who have this condition. I am just doing some investigating on her behalf.

[LEEJUNFAN]

Hi there,

My wife has FND and we live in Manchester and wish that there was some support group, but unfortunately isn't.

It's best to contact your GP and maybe he or she could point you in the right direction.

I think there's one in Kent.

It's all about funding unfortunately.

I send information leaflets to our local GPs to spread the awareness for FND.

We wish you all the very best as it would be nice for a support group to visit.

Best wishes!

Tony and Kim 👍

[Shimmyaway]

Hello

The Brain and Spine charity run online support groups for those with neuro problems,.. not specifically FND. Due to mobility problems and /or other issues some FND patients might find getting to a F2F group difficult .,,hope your friend can manage it if you find one for him/her.

[FND-wife]

Where are you located?

[RachelSPforGL]

Thank you. I am based in Worthing. Kent is a little way away sadly but thank yuo for the Brain and Spine Charity Suggestion