Asdis, is there any chance you could get hold of pesticide-free fruit and veggies, so either somebody else's homegrown or organic, especially from small farms or small market gardens where you can trust that they are actually organic? I know that's a long shot but thought I'd suggest it. No need to justify yourself if not feasible because I can imagine all sorts of hindrances.
Before I knew I had cptsd I worked on my own ED both inpatient and outpatient. I remember back then I was a little underweight tho I didn't believe that, I was often exhausted, i had a lot of stomach pain and digestive trouble plus on the advice of my doctor at the time I was avoiding this food and that food and everything was getting worse rather than better... I saw a different doctor who did the 'right' tests the way dollyvee probably means and he really listened and I found out later that in his opinion I couldn't digest anything anymore in a figurative way. In my first inpatient stay in the ED group that's the kind of thing they said too, or rather they'd ask certain patients: What else can't you digest? Who else/What else are you allergic to? I had a nut allergy when I was admitted and based on various of my emotional reactions I'd say now that there was a lot of fear behind the allergy. In fact towards the end of that super-long inpatient stay, I tried out nuts and I had no reaction. In the intervening years whether or not I have a real reaction to nuts that I mistakenly consume depends on how emotionally stable I am. I never reacted again with the intensity of the pre-inpatient stay, and even if I had a minor itch, I could sometimes talk myself out of it. This isn't to say that allergies don't exist, because they do! But there could be an emotional component too. If it doesn't resonate in any way, just ignore all that. It's going to be harder with DID anyway. It would be wonderful if all your docs and therapists etc could work together to tease it all apart.
Anyway I hope you can feel a little lighter even with just writing it out here and feeling understood or semi-understood.
Before I knew I had cptsd I worked on my own ED both inpatient and outpatient. I remember back then I was a little underweight tho I didn't believe that, I was often exhausted, i had a lot of stomach pain and digestive trouble plus on the advice of my doctor at the time I was avoiding this food and that food and everything was getting worse rather than better... I saw a different doctor who did the 'right' tests the way dollyvee probably means and he really listened and I found out later that in his opinion I couldn't digest anything anymore in a figurative way. In my first inpatient stay in the ED group that's the kind of thing they said too, or rather they'd ask certain patients: What else can't you digest? Who else/What else are you allergic to? I had a nut allergy when I was admitted and based on various of my emotional reactions I'd say now that there was a lot of fear behind the allergy. In fact towards the end of that super-long inpatient stay, I tried out nuts and I had no reaction. In the intervening years whether or not I have a real reaction to nuts that I mistakenly consume depends on how emotionally stable I am. I never reacted again with the intensity of the pre-inpatient stay, and even if I had a minor itch, I could sometimes talk myself out of it. This isn't to say that allergies don't exist, because they do! But there could be an emotional component too. If it doesn't resonate in any way, just ignore all that. It's going to be harder with DID anyway. It would be wonderful if all your docs and therapists etc could work together to tease it all apart.
Anyway I hope you can feel a little lighter even with just writing it out here and feeling understood or semi-understood.
to you
I assumed that if you 'have trauma' to the degree that your nervous system is consistently dysregulated, then you're likely to have ptsd or cptsd.
