Does anyone suffer from CIRS (Chronic Inflammatory Response Syndrome)?

@marshasanger I hope the following site will be of some help to you.
https://moldfreemenu.com/35-safe-foods-when-recovering-from-mold-exposure-and-five-to-avoid-completely/
It has a list of foods that are safe for you to eat and ones to avoid.
Do you live in a town that’s near to a hospital?

Where do I find a reply? Just keeps spinning me around.

Sorry,
I haven't read the full thread yet, as I have only just made an account to comment.

Just wanted to let you know that after a lot of self diagnosis due to useless doctors, and weighing up what symptoms could be due to long covid. After nearly three years i've finally managed to find the correct diagnosis of CIRS.

It's been the worst three years of my life, and I am only just starting to be able to make some headway toward getting back to normal after nearly 6 months of sleeping in a makeshift isolation bedroom.

I haven't gotten much further than being able to think slightly more clearly, and some steps toward getting my mobility back, but it still sucks.

Being in Australia, there aren't even any labs capable of running the complete screening blood tests that can indicate whether or not it's likely that you have it.

So I'm at an impasse medically.
I have a decent GP now, but the infrastructure doesn't exist to test for it.
The only way is to have one of two doctors in the country, who both happen to work on the other side of the country; send off the blood samples to a singular lab in Brisbane capable of running the first round of testing. Then send the blood-work in dry ice, to one lab in the US.

There is no pathway for actual medicinal treatment, due to the strict guidelines around prescribing the applicable medications.

So attempting to get better is very slow going at the moment

Does anyone know of doctors that treat CIRS in the Chicagoland area? I am in the north suburbs. I have CRPS and it was looking forward to a treatment two weeks after moving to a new apartment and the treatment can you possibly put me back to work part time for the first time in eight years. I moved into my new apartment and became incredibly sick at the time I woke up the first morning. Bottom line is the place was filled with mold, the entire building was but my unit was the worst how am I all they did was lie about it and didn’t care, because I’m disabled and low income I had waited five years to live there and my small emotional support pet is now dying after never being sick a day in his life and I am getting worse very quickly. I live there from August, 2019 until October, 2020 as it was very difficult trying to find a place but I did. I’m 59 years old and feel like getting better is hopeless at this point.

I’ve never had a doctor call me back that is certified in detox and my understanding is that none of them take insurance anyway.

I will take any suggestions. Running back-and-forth to a bunch of different places for tests and things is not possible either. Very desperate!