My first Crohns experience was having an obstruction in 1990 which resulted in a night at the hospital. They did not diagnose me at that time, I had NO symptoms prior to that obstruction, and had no symptoms untill 14 years later, then out of the blue I got my second obstruction which again landed me in the hospital, and again noone managed giving me a diagnose. No scopes, no bloodtests, just telling me to relax.
From that second hospital landing I wasn't able to relax at all ;-)....too much pain and discomfort, too often...and a lot of what I later learned was partial obstructions...and full blown obstructions...
At last, in 2007, I got my diagnose. I had no medication between 2004 and 2007. When they finally looked at my small intestines, in 2007, they found 4 narrowed areas. I have been using LDN, since 2007, and on occations prednisone (pred for just for a few weeks each time) and have to do a resection within a year from now according to my GI. He has expected me to get much sicker much earlier, so he has sharpened his knives since the fall 2007.
Have been without symptoms from 2007 when I started using LDN, and still am, so LDN is keeping my disease at bay, I am convinced that my disease would have developed dramatically without Low Dose Naltrexone. For me, this medication was heaven sent. /Bee
Post Edited (BeeSting) : 12/11/2010 1:41:20 PM (GMT-7)