Jump to content
The MS PEOPLE UK Forum
Support, help, advice and information for Multiple Sclerosis. Ask questions and share experiences with people affected by MS.
Marina

Additional New Moderators

3 posts in this topic Last Reply

Recommended Posts

Sluggish
Marina

I'm delighted to announce that we have two new moderators in addition to Chris and myself. Given that we all have MS, I felt it useful to have several of us in the event that one or more of us should be having an "off" time and not be up to it or not be around for a while. This way, there should always be at least one us around for any help etc that might be needed.

 

I'd like to welcome on board the team of moderators:

Dawn who kindly applied for it

and

Ron who didn't apply for it but whom I had to cajole into it ;-)

 

Between Chris, Dawn and Ron, I think we now have a great team of moderators to help me, and I'm grateful to them all for being there - thank you both :howdy:


Marina

(belated DX in June '05, SPMS)

Share this post


Link to post
ddgorgeous

Marina,

 

A big thankyou, I will do what I can to assist anyone.

 

Take care and best wishes,

 

Ron :howdy:


ppms, dx 2001

Share this post


Link to post
dawney-t

Hi Marina, Hi Ron

 

Thank you too, Marina, for allowing me to help out as a moderator. I will do whatever I can to help out at any time.

 

Best wishes to all

 

:howdy: Dawn


MS diagnosed May 2004, PPMS diagnosed July 2004

Share this post


Link to post

About Us

Founded in 2004, MS People UK is a community website and discussion forum by and for people with Multiple Sclerosis as well as for friends, families, supporters and those interested in this disabling condition.

If you’re newly diagnosed or want to ask about possible first symptoms, or if you’ve had Relapse Remit, Secondary or Primary Progressive MS for some time, a welcoming group of fellow MS sufferers is here to chat with you about MS symptoms, diagnosis and treatments.

The atmosphere is friendly whilst being compassionate, supportive and caring. Members also post about a variety of subjects not related to MS, as well as share jokes, talk about their hobbies, have fun, and more.


The MS People Forum is not responsible for advice or information supplied by members. We suggest you seek medical advice before trying anything.
×