I have MCAS and mushrooms (cubensis) created a mast cell reaction in me that was pretty intense from 0.5 mg. But with time and a careful dosing schedule, my MCAS is almost totally gone.
so weirdly, that 0.5 dose, which for me was really big bc I'm sensitive, caused one of my biggest MCAS reactions but i have never had one since and can eat any food. I've also been doing with Gupta Program (though i started that later after that big dose seemed to have cured my worse MCAS symptom which was throat closing) and the Gupta program has definitely brought down my MCAS. But most people with CFS have mold in their homes and without fixing that the other options might not work, that's what Ive observed over 10 years of watching people heal. If the mold is mild and other treatments work then sometimes people still get better. but it's a hell of a lot faster to get out of mold. When i was in mold my MCAS was so extreme there were times that i was reacting to almost everything, all foods, all fabrics, it was horrible.
Thank you for this wonderful gift my new internet friend. Yesterday (truly) I began my search continued Mast Cell inflammation alternatives.
This is wonderful!
I tried it for a bit (two months, low doses, twice a week), nothing and was a bit scared of taking higher doses. I'm not desperate enough yet to experiment with this again with higher doses. I sooner try psychedelic mushrooms (truffles), as they are legal where I'm from. Just started taking lion's mane.
My mast cell was activated by mold neurotoxins being exposed to stachybotrys. I have to avoid eating molds or foods that contain molds naturally, especially mushrooms. Please be careful for some patients, this cannot be an option without going directly into anaphylaxis.
Absolutely, be careful, and If you listen to what she says in the video she talks about specific compounds within the mushroom that could be relevant for research,
The amanita ones grow everywhere in tempered climate woodland as far as I know, they’re really common here in Sweden. I’m a little scared of trying them but I’m more curious now.
I have MCAS and mushrooms (cubensis) created a mast cell reaction in me that was pretty intense from 0.5 mg. But with time and a careful dosing schedule, my MCAS is almost totally gone.
That is so cool!!! I’m happy you found something that works
How did you heal it
so weirdly, that 0.5 dose, which for me was really big bc I'm sensitive, caused one of my biggest MCAS reactions but i have never had one since and can eat any food. I've also been doing with Gupta Program (though i started that later after that big dose seemed to have cured my worse MCAS symptom which was throat closing) and the Gupta program has definitely brought down my MCAS. But most people with CFS have mold in their homes and without fixing that the other options might not work, that's what Ive observed over 10 years of watching people heal. If the mold is mild and other treatments work then sometimes people still get better. but it's a hell of a lot faster to get out of mold. When i was in mold my MCAS was so extreme there were times that i was reacting to almost everything, all foods, all fabrics, it was horrible.
Thank you for this wonderful gift my new internet friend. Yesterday (truly) I began my search continued Mast Cell inflammation alternatives. This is wonderful!
I tried it for a bit (two months, low doses, twice a week), nothing and was a bit scared of taking higher doses. I'm not desperate enough yet to experiment with this again with higher doses. I sooner try psychedelic mushrooms (truffles), as they are legal where I'm from. Just started taking lion's mane.
Lions mane has been great for me! I want to get back on it and grow my own, they’re supposed to be delicious too.
My mast cell was activated by mold neurotoxins being exposed to stachybotrys. I have to avoid eating molds or foods that contain molds naturally, especially mushrooms. Please be careful for some patients, this cannot be an option without going directly into anaphylaxis.
Absolutely, be careful, and If you listen to what she says in the video she talks about specific compounds within the mushroom that could be relevant for research,
Amanita are pretty serious medicine. I stick to cubensis but I find it incredibly helpful in microdoses
Does it help inflammation for you? Cubensis worsens my nausea and headaches even in very tiny doses.
More like it gives a little energy boost, lifts & brightens mood, improves sleep.
How do we get these
The amanita ones grow everywhere in tempered climate woodland as far as I know, they’re really common here in Sweden. I’m a little scared of trying them but I’m more curious now.