I want to hear or rather see how everyone who is taking LDN doing on the drug.....how has it helped...how has it not helped...have you seen a change....do you feel better or worse....have you had a neuro do an MRI on you recently and see anything different in the brain....this message is purely out of curiosity AND also to share the info with others who may be considering taking LDN....I think that this is what DS is all about..communication...if we all share what is working and what is not working it may help the next person...for me .... LDN is working....it is NOT an overnight magic pill to make MS go away but with POSITIVE thinking and a healthy environment to help combat MS I feel like LDN is doing "something" for the better for me...I can walk, talk and have a little more energy but my short term memory is horrible (missed doc appt yesterday) ....be blessed all...be blessed!!!
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Seems very quiet here on this forum, since I was on the RA/Hypothyroidism forums, would start something up here also. I have been taking LDN almost 3 months now, so still a newbie, for my RA. Dropped Embrel and Methotrexate, and hope with a little help from prednisone ( 2.5mg twice a day) to make it to that 6 - 9 month period.Would be interested in how others have done on LDN longterm,