If you want to support CCSVI research, you can do many things, you could make a record and donate proceeds to the "Brave Dreams Trial"......that's your choice.....Alternatively, you could give it to your local MS Societies, so that the work on the subject is properly peer reviewed, competitively tendered and independently undertaken to get a meaningful answer. It will help offset the millions that MS Societies around the World have spent on this aspect, such that it limits their ability to fund other MS research.
The only conspiracy here is in people's heads (we all want effective safe treatments), If it works great, but let's examine it properly.
CoI. We have recieved research funds from MS Charities............ and proudly so!