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Are you diagnosed with CIS?

 

Hi

I originally became a member of this forum when my sister was diagnosed with MS and I needed more info from real people:-). But I work in documentaries and I am currently making films about people living with different kinds of MS and thought this forum would be a good way to spread the word.

Some of you might have already had private messages from me but I thought I would write a post as well. 

I work as an assistant producer for a company called Minnow films
http://www.minnowfilms.co.uk/
They are currently making 4 films about MS for a big international doctors conference happening in Pars later this year. As we are wanting to show how people live with different kinds of MS at different stages, I have been looking for someone who has been diagnosed with CIS. The films are NOT going in-depth on people's medical histories but more so about the emotional and personal journey people have experienced.

My email is salma@minnowfilms.co.uk in you would like some more info. 

Look forward hearing back from you.
Thanks
Salma