Thanks for your asinine comment on this post that is really important to me. First of all, this kind of hopeless depressed attitude about the future for DPD is not doing anyone any good. It may be true that a "cure" won't come out of the IDS group, but at least it is an effort, which is a hell of a lot better than nothing. Secondly, the people who care about researching DPD aren't all gone. The Kings College DPD unit still exists, and Anthony David is still doing research on TMS for DPD. Jeff Abugel seems to have some kind of vision with this IDS group and I say we all support it with our best effort. He talks of groundbreaking conferences in the U.K. and the U.S. that will happen when enough money is raised. I heard someone say there are 33,000 members on here? If everyone donated $5 it would raise enough money. Right now it says 38 people have raised $1,900. Imagine if it changed to 5,000 people raising $25,000. It would show there is demand for research for our neglected condition. Which is so true. And people in the future are gonna just keep getting DPD and suffer until someone figures this out. Also I want to add that the research done in the past (even though it isn't much) has made a difference. 10 years ago the nuerobiology of DPD was far less understood. Through studies we got some more clues into the mystery of DPD, like an overactive prefrontal cortex dampening the insula, tempero-parietal dysfunction, abnormal glutamate avtivity, and some potential treatment options like lamictal paired with an SSRI and kappa opiate receptor antagonists. So studies do move things along and I think you are wrong in saying that money isn't the right motivator. What else would it be? We need to donate to this guys, it is an effort to benefit us all. You don't have $5 to spare?