I think there is a need for advocacy and activism for people with MCS. Many doctors do not recognize that MCS exists. Even Andrew Weil, who I have found helpful, does not recognize that MCS exists.

The problem I have run into is that i have chronic stomach pain, possibly a stomach ulcer, and am allergic to a lot of the medicine that is available for stomach ulcers. I have had chronic stomach pain for almost 4 years now. It is hard to go to work everyday with such significant stomach pain.

Does anyone have any information that might be helpful?

someone told me he fixed this with broccoli, not for dinner but capsules if I remember correctly

and I'd expected more of Andrew ;(

Interesting, broccilli supposedly has an effect on tests for H.Pylori, which suggests that HP may have been the prob there, worth getting an HP test. Also look at MCAS. Both MCS and MCAS now have WHO accreditation & ICD10 codes. Doctors have to take them seriously.

en.wikipedia.org/wiki/Mast_cell_activation_syndrome