^^^^^^ WARM GREETINGS FROM ^^^^^^^^^^^^ :-) Ivan Suzman 49/39/36 [log in to unmask] :-) Portland, Maine land of lighthouses 50 partly cloudy deg. F :-) ******************************************************************** Alastair Wyse wrote this rather provocative commentary at the end of his reply to my original paper on the possiblility of a VIRAL origin of Parkinson's Disease. In re-reading it, I found many issues worth re-visiting by those on the List interested in action strategies which will PUSH towards finding the CURE. I feel that there has to be a combination of research dollars in Foundations (like today's list from Robin Elliot of the PDF of $600,000.00 in grants just distributed) and VISIBILITY-pressure from PWP's, artfully using the media to get attention. With PD awareness Month (April) just about here, we have a BIG chance to get somewhere. Thank you, Alastair. Ivan S. I have for the last year or so been taking all sorts of things to see what works . My investigations have been seriously hampered by the government/medical establishment which does not allow this activity . I am researching methylprednislone and human growth hormone in low doses .( I had to go to Mexico to get around these control freaks ). I was hoping that this list would be a forum for exchange of information on PD . This would be far more effective research than done by the medico/government complex . I have had to read countless wingeing about the non spending by the goverment ( delete all the obvious ones but some getthrough from bad subject heading ) . The gay community( good for them ) managed to get effective funding for HIV research by being a public nuisance . they were helped by the fact that HIV is a very new problem and there were no entrenched ideas/ people . How do you get an expert in position of power to agree to to research that will prove that what he has been saying for the last 30 years is wrong and that he got a very fat salary for misleading people ? What if this expert is part of a gang in positions of power ? A PWPs approach togetting reseach done will be one of the following . 1) do it himself on a suck it and see policy 2) organise public nuisances with other PWPs to force the government to do something . Sending letters is a complete waste of time as it makes the recipient think he is important . Camping outside his front door will be more effective than any number of well reasoned letters . 3)wait for a private company to do the researchand find a cure . The problem is that they will charge a high price which you may not be able afford . People in the UK are being denied treament because of the high cost . My research priority it researching the possibility that my PD is caused by a viralbrain inflammation that can be treated by anti inflammatory drugs . peace Alastair ( [log in to unmask] )