Posted 2/14/2012 5:37 PM (GMT 0)
Wow, I am so sorry to hear that that is happening with you. I know that I have trouble with people understanding the debilitating effects that this condition has on me and the life that I lead. There are a great many things I can no longer do because of this illness and like you, I never asked for it.
Unfortunately there are alot of people out there who think that because what we have is not widely known, then it must be something that is either fictitious or we MUST be exaggerating. I have been forced to get Dr's notes relating to my need to have to hit the bathroom for extended periods of time during a flare..... and the reason was because once I had that on file then that could not be used against me at some point as some kind of "attendance" or "availability" issue.
It sounds as if this is recent. Have you spoken with your GP or Specialist about it? They may have something they either know about or can recommend you for that you might not otherwise have been able to access. Never underestimate the kind of information that your professionals have access to.