you also might remember that aliza was diagnosed with a rare terminal disease known as san filipo syndrome type "a" but you also might remember there is hope in the form of gene therapy that can be tested in clinical trials. right now they're lacking the government funding that they need. aliza's parents glen and cara want to do everything they possibly can. glen had this idea to enlist a viral video creator, and ben von wong says i think i can do this. wis actually spoke to him. >> they need to raise money, they need a viral video and they need it now. >> this video you're seeing here is a preview of the viral video and the goal is to get the video out there. also get information out there about the go fund me pay. they are hoping to raise $1 million by june of 2014. and we wanted to know more about how the family is doing in the processed of raising money, so "right this minute" from columbia, south carolina, we have glen, kara and little aliza via skype. welcome back to the show, you guys. >> hi. >> thank you. >> thanks so much for having us again. >> how are things going right now for