CIRS Question - Does Anyone Else Get Worsening Symptoms After Eating?

Just as the title states, does anyone get worsening symptoms after eating? Just minutes after ingesting food (I eat very healthy and tried avoiding histamines, foods high in glutamate, high sugar, etc. I only eat 100% organic 1 ingredient real food), I get extreme anxiety, enhanced vertigo (MdDS), things around me look less real than they even did before, etc.

It sucks.

Does anyone relate?

I think I really need to treat this stuff soon but it's getting my docs on board to do it in a way that makes me tolerate it a bit better. I feel maxed out lately. Just today a foot bath with Epsom salt sent me into a panic. I am so shaky right now, and everything is moving. It's so uncomfortable. It worries me that maybe this isn't all I have. Or maybe I am just really bad. Maybe my brain is just pressing hard on all of the wrong buttons. Maybe it's the untreated Babesia, I don't know. Bleh!

I have wondered if that is my cause, but at the same time, I don't understand it. Now, when I say I am suffering, it is 24/7. 30+ symptoms interchanging all of the time, but this vertigo and anxiety are the worst. I honestly wonder how people don't... you know... let it all go. I am not that kind of person and I need to be alive for many reasons, but I just don't get it. I get to the point of going near insane. I am feeling that way often. It's like my symptoms are alway on overdrive. I wonder if maybe my infection(s) are getting deep. I may need to treat this all sooner than later, but I don't know what the next move really is. My doc wants me to do the Babesia next, but like I said, I am really bad. One more push over the line and I don't think I will make it to be honest. I am already bedridden and I often can't even look at the lights around the house without getting a huge increase in symptoms. I am fortunate that compared to when this started, at least I can watch TV again, but it's still tough.

Maybe I need to speak with my doc about MCAS and treating the overall inflammation. I have yet to do tests for CIRS too, so I need to do those. My doc has no doubt that I have it. I'm only on B12, D3 and Turmeric. I also do take a Binder but it's mainly Chlorella and Probiotic based, which is good, but I think I need more rotation. darn, I just don't know. Even my docs make me feel somewhat alone on this. Here I am, searching the internet on what to do and get all of the info I can possible. I have Babesia, Gilotoxin, and Ttrichothecene group (mixed). These are all confirmed. But we don't know everything, and without doing the tests for CIRS, I don't know what pieces are missing. I believe it's important. I do like my docs, but I feel kinda pushed into treating the Babesia and I am extremely sensitive. I even reacted to an anti-anxiety nervine tincture. Ugh.

Sorry, I am just everywhere with this. Where to go from here, I really don't know. I do wish you the best of luck!