Want to be a Community Ambassador for... - Myalgic Encephalo...

Myalgic Encephalomyelitis Community

2,020 members633 posts

Want to be a Community Ambassador for Myalgic Encephalomyelitis Community?

SaskiaHU profile image
SaskiaHUHealthUnlocked
1 Reply

What we are looking for

We accept all applications, but ideal candidates are members that have been active in the community for at least 6 months.

Why you should apply

The community ambassador makes sure the community stays active, positive and helpful place to be by keeping members informed, encouraged, and happy.

Are you passionate about supporting your peers?

Do you have ideas about how to make the community stronger or more engaged?

Do you feel strongly about improving or maintaining the community atmosphere?

Your community needs you!

How to apply

If you think you would be a good ambassador please fill out the application on this page: blog.healthunlocked.com/201...

We look forward to hearing from you!

Written by
SaskiaHU profile image
SaskiaHU
HealthUnlocked
To view profiles and participate in discussions please or .
1 Reply

Hi SaskiaHU, I was wondering what sort of time commitments does this require?

As you may know sometimes, on occasions, in some people, M.E. may cause a little tiredness :) and people may sporadically be 'down' and unable to keep a consistent presence - what about those situations.

I'd be happy to try a few of my stand up routines on here - it will be great since Frankie Boyle is too disgusted with me to listen any more :)

You may also like...

Advice wanted - relatively new here

The Effect of COVID on ME/CFS

articles on how COVID affects people who already have ME/CFS before contracting COVID? I'm looking...

Canary in a Coal Mine

cripple or heal you? How would you fill your life, and what would you toss aside, if you only had...

Living with ME/CFS - as a partner.

and I can see how that's an extra load for him. I'm really looking for ideas and help on how we...

CFS in every day living

Hello I am new to your community and hope you are all ok? I was diagnosed with CFS 3 years a go, it...