Guest guest Posted January 1, 2010 Report Share Posted January 1, 2010 Bill, Having a disease related to ALS and running a group similar to this one for people in Australia and New Zealand with ALS and other motor neurone diseases I know of quite a few people who've tried LDN for ALS and PLS (what I have). For ALS there has been somewhat mixed success, with some reporting no effect (although possibly they had candida or other issues which prevented it from working), but many reporting positive effects such as slowing of progression, dramatic increase in mucus problems etc.. It's such a terrible and in some cases rapidly progressing disease that there can be no promises, but LDN IS MOST DEFINITELY WORTH TRYING!! Apparently is has also been discussed positively on www.patientslikeme.com in relation to ALS, but I spend so much time on this and my own group(s) that I hardly ever get on PLM. Cheers, Bill Zader wrote: Hello Friends--does anyone have experience with NALTREXONE and ALS? I have a friend that has been diagnosed with this terrible disease. Thanks, Bill Quote Link to comment Share on other sites More sharing options...
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