Hi, Let me offer some thoughts along side yours, if you will. I have no wish to start an argument but I would love to start an exploration of these statements... ... that ... is not in fact true we will be better prepared to deal with that reality. ... I offer the following thougts ## The cure is coming soon: Of course it depends on how you define 'soon' [snip] * they are still at the basic research stage with the most lines of investigation - no-one has yet got past the 'this looks very promising' stage. As the lead time from E Day (Eureka Day) to C Day (Cured Day) is anything from 5 to 10 years we have that period of time still in front of us AS A MINIMUM. It could well be very much longer. [Dr. Fischback of the National Institutes of Neurological Diseases and Stroke, which does most of the PD research, and grants most of the dollars in the U.S., says that with enough funding it may be able to be done in less than 5 years. [snip] what they are saying is, to speed up a cure takes money, so that research ... must not be put off for the lack of funds, because that will lead to decades of delays. We want to see various research approaches on repairing and replacing brain cells to go forward simultaneously, not sequentially--that will take too long. There is brain cell replacement going on in humans already. Conclusion: There is a realistic, authentic, educated reason to pushing the legislators to fund vital, research for a cure, AND for improved therapies that last.] * I would suggest that the medical establishment anticipates that the cure will be some while yet. A strong indicator of this is the proliferation of centres performing PD surgery and the numbers of doctors learning the techniques. You don't invest that much time money and infrastructure unless you anticipate a return on your investment over a reasonable period. [You must realize that this is the U.S. and competition is the name of the game--everyone doing and promoting their own thing; it not controlled and coordinated by government. Just because there are new developments in Fiber Optics, ...and digital cable doesn't mean that everyone is suddenly going to give up the Modem business at 56K---alot has been invested in current therapies already, and the possibility of being outdone or replaced is something that coexists with innovation in the global economy daily, and certainly very strongly in the US, where there is little government control over industry.] ## The cure will be found Again it depends on exactly how you define cure. If we are talking about eradicating a disease so that it no longer exists then we are really going up against the odds. I tried to think of how many and which diseases medical science had eradicated and there aren't many - and most of those were 'cured' by preventing people getting them in the first place. If the 'cure' for Pd falls into that category it will only occur after they find the cause and wonderful as that will be it won't be of much help to those of us already afflicted. As any cure of this nature is only likely to occur after a cause has been found I would think it is a long way off yet. [ Let's define prevention as eradicating the incidence of PD, and therefore, in future, no cure needed. And let's define cure, as a way to reverse/repair virtually all damage, and halt progress of disease that already exists, and very nearly a cure, virtual cure, for therapies that make an outstanding improvement by repairing the brain and greatly slowing progression and/or protecting the brain from further degeneration: * Agreed--Prevention will take a long, long, time--it's not going to be eradicated in time for us, but maybe for our children who are at risk of inheriting it. Again, I agree, it will require what the causes are to do this. * Since they are already making real progress in repairing human brain tissue, and there is some research for strategies in slowing progression, there is a REALISTIC expectation for a Cure or Virtual Cure in 5 to 10 years or less. I don't agree that it requires solving the causes of PD to cure it, but it would be helpful in halting the progression. Let me give you a real-life story, my son's story, to try to make my point: He had Acute Lymphocytic Leukemia when he was 4 years old and had a 55% chance of survival and what they called Virtual Cure, since the children who were survivors had not yet lived out their lives at that time. They did not know then, and still do not know why children get leukemia OR why the protocol of chemotherapy and radiation works. But I'm HAPPY TO TELL YOU and MY SON'S HERE TO TELL YOU THAT IT DOES! He's 28 years old and has never relapsed along with, the other 45%, before him and since his experience. Some are in their forties, married and have children. I repeat, there is a realistic REASON (as in reasoned) why we can expect far better therapies, and a cure.] Any cure which will benefit those of us who already have PD will, by definition, be one that cures the individual but does not remove PD from the earth. Which means that the often expressed wish - for the day to come when we are cured and PD is no more - is meaningless unless we are talking about two different days and two different cures. [Yup, two different days two different things--eradication and cure are two entirely different things in my view.] ## The cure will benefit everyone This, as already discussed, will depend on what form it takes. A preventative helps only those who don't yet have PD, an inhibitor is better for those in the early stages than for those in the later, and so on. [All of aspects of what you say here are being addressed---is there a guarantee that all will be helped in the PD community? No. But I believe that the advocates who say, all will be helped are talking about the funding for research, which will help all the other diseases' research progress.] ## the cure should be the paramount consideration of the PD community I believe that it is far from certain that the cure is imminent and also that we do not know that it will be of equal benefit to all of us. [And?] Consequently I believe that research into managing the disease should have at least equal priority. [Agreed, but there again it has a far higher priority as things exist today, i.e., the drug companies!] This type of research has the added advantage that benefits flow from it continually as opposed to us all waiting on a cure that will be some years yet and may be a great many years yet. [True, but better therapies, maintenance, and intervention are needed, and has always been dominant; but without a way to stop and reverse the disease process, I will end up as my mother did, choking to death on her own saliva, unable to move or speak, during the night in a nursing home alone. Morris Udall, for which the Udall Act was named here in the US (he was a Congressman from Colorado) died in 1998 just like my mother did.] ## time is running out - we must have the cure now [we're in a hurry BECAUSE of the very things you say; advocates want to put the pressure on to speed things up because we don't want another 30 years to pass between when my mother died in 1972 five years after she was in the L-Dopa trials at Columbia Presbyterian, and when they develop really life-saving therapies. Not because it has to be for us, but because it won't happen unless we advocate for it.] I too would like to see a cure in my lifetime (preferably one I can benefit from), but I have never quite worked out why so may of us seem to think that it MUST happen in time to save THIS generation - what's so special about us? [And why shouldn't we want to be rescued, and make sure that are children won't have to face the threat of PD. We're as special as any other generation.] ## anyone who disputes any of these is thinking negatively. [If the situation is truly negative and virtually hopeless, then I would agree that a reasoned understanding of a poor outlook is realistic; but IMHO yours is not a reasonable outlook to have; I think there is a realistic reason to expect major improvements in the management, reversal, and slowing the progression of PD for many of if not all of us.] It is not negative to see things as they are. [ This presents the question of how you think things are.] A positive attitude which exists by ignoring the realities is really denial [Agreed; that is why I am so positive about a reasonable expectation for a major improvement and/or cure. It's doable, no guarantee, but since it is already happening, why not have a realistic, reasonable, positive perspective to move the process forward?] [What do you say? Comments, Dennis or anyone? A debate, not an argument?] [Charlotte} Dennis. +++++++++++++++++++++++++++ Dennis Greene 49/dx 37/ onset 32 There's nothing wrong with me that a cure for PD won't fix! email - [log in to unmask] Website - http://members.networx.net.au/~dennisg/ -- Charlotte Mancuso *************************************************** For advocacy, medical, and other PD-related material, go to: http://www.onelist.com/subscribe/CurePD-NorCal