Guest guest Posted June 18, 2004 Report Share Posted June 18, 2004 Hello everyone this is my 1st posting since diagnosis last year. I've an amswe to a question, hich has been posted on here~ i've been told by a Dr Lawrence here in the UK that LDN isn't that ood for MS people in wheelchairs & who can't walk. So i'm under the inprection that Dr Bihari told him that and that is the rule of thumb. Hey babes i've no idea what to believe but can someone tell Dr Bihari to contact the UK MS Society as they seem hell bent on not being able to talk of this drug i've noticed on their site. Maybe if anyone is seeing Dr Bihari soon they should tell him to contact them/those nim wits. They are so 1800 as they seem to look backward in looking forward. Dan Quote Link to comment Share on other sites More sharing options...
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