Seeing the thread for the research group in Columbia, I was wondering if and where there is a research group for MM?  I have had many people approach me wanting to do a fundraiser for MM research in Arianna's memory.  I would love to do this, but for whom and where would I send the proceeds?

Anyone know anything about this?

Sorry if this is posted somewhere, I cannot find it.

I wish I could help, but I don't know anything either. I think that would be a wonderful idea though. Maybe you could contact some of the hospitals that have mm specialists. Maybe they know of something or could atleast point you in the right direction. Good luck and keep us posted on what you find out.