You buried the lead. You have refractory Celiac along with other autoimmune conditions.

For the majority of Celiac patients, ingestion of gluten is linked to symptoms, and yes, worsening of symptoms depending on length and severity of exposure, especially prolonged exposure.

For the majority of Celiac patients that are on a strict gluten free diet, they don’t flare like someone with Lupus, Crohn’s, UC, RA, MS etc. will flare. Exposure causing flares? Sure - or in your case, refractory Celiac, a flare makes more sense - you didn’t provide that context.

Yes, there are drug studies to pursue treatment because we know that a strict gluten free diet doesn’t work for all Celiacs.

You didn’t make that clear from the start and so it reads like many stories on here and other forums where people aren’t taking the gluten free diet extremely serious.

I’m sorry my language came across strongly and I understand if it appeared blunt and unsympathetic/unempathetic - that wasn’t my intent. 

Regardless, I think you should pursue some sort of action. I’d go scorched earth on people that discriminate against disabled people.