Yeah, don’t beat yourself up about it!! I have Fibro, too, as well as MCAS & Lyme, plus co-infections, so this happens to me all the time! But, I saw (& commented on) your other post, & I think it’s probably bad for you right now because you are unintentionally triggering yourself by ingesting things (and/or using topical products) that you are sensitive 2… :/ Hope you can isolate/identify & eliminate your triggers to minimize symptoms!!! <3 P.S. Have you ever been tested for Lyme? Btw, u are more likely to get a false negative than false positive for Lyme test, & not definitive, or totally reliable & accurate, since, after the acute/initial phase of infection, bacteria (& any co-infections, which can include viruses, parasites & fungi) can form biofilm cysts and hide throughout your body. This is why it will oftentimes not show up on test because they are not circulating in your bloodstream…But, still recommend that anyone with MCAS get tested for Lyme because it is a very common comorbidity & it is what triggered my MCAS. Good luck 2 U!!! <3

Hi,I get memory fog a lot and have noticed it’s from MCAS

Not really

I definitely do. It has a lot to do with the underlying causes of your MCAS though. If it’s gut related then it will definitely do that. If not, then maybe not so much.

Yes, my short term is damaged I also can become non verbal during reactions or attack episodes. 😔

Brain Fog is a real thing. LDN has helped me along with a new binder that has helped me with histamine as that is the mediator I have the most issue with.