Hi all,
This is my first time posting on a forum, but alas, my symptoms bring me here. I am hoping to learn, educate myself, help others if I can, and ultimately make the wisest choices for my healthcare.
I was diagnosed with IBS 10 years ago. It started out rather mild with the usual bouts of stomach cramps and diarrhea and locating every bathroom wherever I went (sound familiar?)
The last couple of years I have experienced more "episodes" to the point that I would be off work three or four days recuperating. I would place myself on a diet of juice, soups, and jello.
This past year caused me to go to my human resources department (after speaking with a lawyer) and getting what's called an intermittent leave of absence. When I take the days off for IBS, mu work cannot hold those days against me, (which they had been causing me more stress).
A couple of weeks ago, I was told by my G.P. to see a G.I. specialist , who has ordered a colonoscopy and upper endoscopy for me next week. This last week I experienced the worst pain I had ever had along with a new symptom of bloody stools. I almost went to the E.R. I am feeling a little better , but a little more frightened.
I have been under a lot of stress and pressure at work with my boss. (no compassion there). And wondered if this stress has an affect on my health. Our office acquired a new manager this past year, making life difficult for everyone at work, particularly me. And it seems my health has worsened this past year. Wondered if it was coincidental.
Has anyone ever had to go on disability with this? I would love to keep working, (evil boss withstanding), but I have missed a lot of work this past year due to worsening symptoms. What has been your experiences with working when having IBS?