Keratoconus - Rebecca's Journey

Our daughter has been diagnoised with a degenerative eye disease called Keratoconus.  Although not uncommon in adults, it is very uncommon in children.  The younger the child the more progressive the disease.  However there is hope. . . the procedure Rebecca needs is not yet approved in the US by the FDA and will not be until maybe December of 2014 (maybe).  Rebecca can't wait.  Again, the younger the child the more progressive the disease.   The procedure is being performed in Europe and other countries.  We have even been in contact with a doctor who is willing to waive his fees to perform the sugery via a foundation called Lightforsight.org.  Are you asking what can you do?  We need to be able to pay the hospital fee in Switzerland, airfare to get there, a hotel for at least a week and any pop up expenses.    Anything you can do would be appreciated.  Please help in Rebecca's Journey. . .  Thank you for your time and God Bless.