Forming a Non-profit organization for EC research

Hey guys I'm new here. I hate having Exfoliative Cheilitis and I'm so glad there are forums like this where we can all input ideas to go about curing this condition eventually. Many of you are much more knowledgeable than me. Keep up the good work/research! I will try to contribute when I can.

This may sound crazy but sometimes I think of forming a non-profit organization/foundation that is dedicated to finding a cure for EC or even broader like for Dermatillomania, or Compulsive Skin Picking (CSP). An organization that can be branched out in our respective regions where we can meet and discuss on progress and solutions. Maybe such an organization already exists. I still need to do research.

I just want to add that you two should really not fight. You are here to help one another after all.