just a thought...

So when looking for a job and applying and interviewing, do you tell them about your IBD?

Personally, it depends on the job. For instance there is one that I just interviewed for and they asked me if I would have any trouble traveling. I said not really and then I explained my situation with UC and Remicade and how it’s something I can work around. I’m nervous though. I don’t know if employers believe me when I saw that I can handle it if I have a flare up. I mean I’ve had the disease for almost six years and I feel like I can understand it. But I don’t know how to convince employers that I’m okay! This is one of the reasons why I want to switch to Humeria. I’m tired of planning my life around my UC.

Also on applications, I don’t know what to say when they ask: Do you have a disability?

Yes, I do have one, but it’s not the kind that you’re thinking of. And why does having a disability come with such a struggling connotation?  I’m no struggling. My disability does not define the kind of work I can do.

I wonder if it helps or hinders me from a job. I mean I know they can’t not hire me becasue of it, but do you think it effects the decision?

Usually I wait till I’m hired but I hate lying and then having that conversation. Especially when an employer asks you if you have any medical conditions where you would need a hospital overseas.

What would you do?