Guest guest Posted July 11, 2003 Report Share Posted July 11, 2003 Just thought I would share this with you from a letter I received from my neuro here in the UK: "Dr X has had other patients who have raised this issue (LDN) before. He has found no evidence of it's benefit when he has done a previous literature search and as such, he cannot recommend this treatment to patients. Also, we do not have any experience of patients using the treatment." Looks like I had better just sit here and let my primary progressive MS get worse then, until I finish up permanently in a wheelchair and eventually rot away like an old cabbage. (No ABC drugs available here for PPMS) LIKE HELL !!! These people don't realise that we are a determined lot. It's called survival. We will fight this thing as long as we draw breath. Keep up the good work. God bless. Moyra Quote Link to comment Share on other sites More sharing options...
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