Guest guest Posted August 1, 2011 Report Share Posted August 1, 2011 I've been a group member for two+ years and I had no idea this was an " LDN support group " ....I've always viewed it as an " alternative therepy MS support group " . If anything, the BBD is promoted more widely. Some members are more transparent about promoting LDN than others. I think at one time or another most of us have been misunderstood or misinterpreted in here. Having said that I think one thing is pivotal to keep in mind. Dialogue, productive or not is absoluteley necessary to usher in change. Common sence and tact when exercised the right way should keep the wheel turning smoothly. Right? -M Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 4, 2011 Report Share Posted August 4, 2011 My husbands vision did not improve until 2 months after his third procedure for CCSVI. The doctor who treated him the third time around seemed to be much more detailed and my husband thinks he did a much better job dilating the veins. Hopefully this procedure will last longer than the first 2 did. That is why we don't know if it truly helped his vision or if the LDN he had recently started made the improvements. I asked about being checked and treated for CCSVI because I have thoracic outlet syndrome which has been shown to be correlated with CCSVI also and the doctor declined. He only wants to address it in MS patients at this time. Good thought though. Take care Amy Quote Link to comment Share on other sites More sharing options...
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