Have you guys heard anything about CCSVI + CHRONIC CEREBROSPINAL INSUFFICIENCY? There is much talk of it helping people with MS, but England do not do this procedure, and Scotland do, but you can not get an appointment as they are so busy. As I understand it, in people with MS many of them can have thickening of the arteries in the neck. If that is the case when they are tested they insert balloons in the arteries, which helps with the blood flow and toxins etc., so much so that it really can help with their symptoms, and brain fog. So it MIGHT help TM'ers too???????????????????????? I have looked quite extensively on the internet including the MS site, but there is conflicting info on there, so I am now trying to "ask around" because I often feel that, to save money the UK policy to everything, is to remain sceptical? When I had breast cancer I became more aware of what they did not tell in terms of treatment and options, and what perhaps worked in other countries but that was still not acceptable in the UK! So if any of you have come across this, and have information or comments........they would be most welcome! Also Rob Pall, I have lost your e-mail address. Please e-mail me at work. Ta! Many thanks Sally in the UK. (whose husband Roger has TM)
