Well hello everyone..
I'm a 41 year old guy living in the Boston area. I was diagnosed with Crohns about eight years ago, after I suffered a bowel perforation in the Sigmoid. Was a mess, ended up taking Sigmoid, most of transverse colon and anastamosis (re-joining) of the ends of the bowel that was removed.
The majority of my CD issues are Ileum, with some small bowel involvement. Through legal wrangling, my employer at the time (a major multinational firm) terminated me, revoked all of my benefits, including long-term disability. In Mass, as I was to find out, this is completely legal and leaves you with no recourse. Soon after, I applied for Social Security Disability, and was approved on the first pass, after only two weeks... from what I understand, that is simply unheard of. For what it is worth, I was not the only person terminated in this way, in fact, employees who had what was to be considered chronic disease were specifically targeted for "Layoff". In Mass, it's very easy for a company to make an end run around the law... and yes I consulted several attorneys, who all arrived at the same conclusion- I have no reasonable recourse against what they did. The stress of all this of course only made my disease worse. After a time, it just made no sense to persue it further as the impact on my health was too great.
I have become a stay-at-home dad for my two children, due to the frequency of my illness I am simply not employable. I've spent a lot of time learning ways to relax and not let the world get to me, which as any crohnie knows is critical in keeping the disease managable.
To this point, Immune modulators have been off the table, as I have the kids in public schools..which means they bring home every germ on the planet. Shutting down the immune system has been deemed to be a last resort for me. I got no relief from Cipro/Metro, 5-ASA's, and pretty much all the other standard therapies. When I have had severe flares, Prednisone has worked, but at a tremendous cost-- I am a poster child for Roid Rage.. can't sleep, and just plain pissed off at everything and everybody any time I am on it.
about six weeks ago I began having severe lower back pain, which I originally thought might be a pulled muscle or strain from exercise. Instead of getting better with time however, it has been getting worse.. and at the moment, I'm now waiting to hear back the results of spinal xrays, the concern being possible Ankylosing Spondylitis (fairly common with CD), a kind of arthritis frequently associated with other autoimmune disorders. At this point, I am capping maximum safe dosages of Tramadol (Ultram) to help with the pain, but at 400mg a day and more, it barely is taking the edge off.. I'm no stranger to pain and have passed 5mm kidney stones (also crohns related) with only Tramadol.. a fact which my pain specialist was blown away by.
So... hello all, I've got a lot of experience with the disease as well as a pretty solid medical background. I'm happy to help folks out if I can, don't be shy-- experience has taught me some tricks in dealing with this thing as well as the almost mandatory Depression that comes with chronic illness and pain.
Nice to meet you all!