In my last post subject 'nausea', I stated that my doctor was checking my inflammation markers to see how high they were, we have yet to get the results as the pathology lab messed up and only took a CBC.. which I'm not sure what that is exactly.. but that's what the nurse said. So I'm still waiting for the results.
Although, I can tell them with out even knowing that my inflammation markers are going to be higher than normal.. I'm getting joint pains again, stomach pains, intestinal pains, I woke up three times last night to use the bathroom.. which I know for some of you, only three times would be a dream.. I typically can sleep the whole night with not bathroom trips.
I suppose I'll wait it out for that call back on Monday.. I most definitely do not want to end up in the hospital again.
Just thought I'd vent a little!
26 years old
Diagnosed 9/06 with Pancolitis. The diagnosis was changed 9/20/07 to Crohn's disease.
I've had flares in my mouth, stomach, large intestine, and the duodenum.
I currently take Humira 40mg bi-weekly, prdnisone 8mg (oh so close!!), methotrexate as a weekly shot, prevacid, celebrex, foilica acid, and.. I think that's it. myspace.com/kandice789