I too would like to add my thanks to ALL of you that come here routinely to help others. OCF works hard in ways that most people do not hear much about, I am in the halls of the NIH and the NCI with regularity lobbying for various important trials to get funding, arguing with members of Congress and the Senate to see that funding for NIH/NCI does not get cut further, after several years of cutbacks, and the thankless task of working with for profit insurance companies to try to get more coverage of restorations that they do not wish to pay for. I sit on two NCI oversight committees, one in the very exciting area of immuotheraputics in head and neck cancers. I have been asked to sit on a third, which I will have to say yes or no to this coming week, which is a very early funding approval committee, that decides what moves forward with funding in head and neck and what does not. Because of the huge extra workload these impose on me, and my already stretched time for OCF other obligations, I am still weighing adding another thing to my workload. But it is a privilege to be asked, and it says something about OCF's reputation as much as my own. There is also the writing of tons of articles for the public, and as a being a respected source of vetted information which is often quoted in articles, and proofing many journalists writings from public media for accuracy before they put them out in the world. We don't hoop and holler much about this work, but it is a huge and necessary part of OCF's mission and obligation to the community of people we serve, let alone the American public that gets far too much bad information about HPV and our disease.

But when you look at OCF and what it has become over the years, the crown jewel in the organization is this support group. Over 15 years it has seen many come and go with 11,000 registered members. But literally hundreds of thousands have visited and read the boards without signing up and are not reflected in that number. You can see them in the wings at any time by looking at the "whose on line" link, and view all the people at any given moment from around the world that are reading your writings, your stories of hope and pain, and loss for sure; but also the stories of success, healing and love. We have had many come and go, some drift away as they wish to put this disease experience out of their minds and get on with life� but others, a very special few, have been here for years to see the path of those behind them made just a bit easier. That a fear is appeased, that an uncertainty is put to rest. There are many, but without a doubt Christine - who diligently each day cleans off the spammers, and rides herd on those that might be less than polite, is always there to welcome the new, and with her many years of learning about the disease, aid those in trouble. That you all call her out for her dedication pleases me, she certainly deserves it.

But newbie or old timer, you are all OCF family. We share each others pain or happiness at the end of a journey. We all understand what bonds us to each other in a way that outsiders cannot understand or experience. I just wanted to thank you all for giving of yourselves to make this a community that is safe, knowledgable, caring, and gives without conditions for that concern for others. You are all so remarkable.

To give you an idea what you have created, last month the head and neck staff at Johns Hopkins designated the OCF support group the only one that they would recommend to all their patients. While they have once a month meetings at the clinic, they recognize the need for additional support, and after review of many years of postings, they feel comfortable that OCF is a venue that they can trust to be free from misinformation, and because of its anonymous nature, safe for their patients and their families. Congratulations. You all built this.