Hey Opu girl. Shabichick and Nan777 I addressed you as well below.
I already take those herbs. I have for a year and they are what knocked out all body, bone, joint, nerve pain, and face, bone, nerve pain and brought down alot of eyeball and surrounding tissue and extra orbital bone pain, and lot's of brain inflammation.
They have literally knocked out body stuff. But I am
....very extreme to support my body. Strict, boring diet. Absolutely no carbs or sugar thru breads, or fruit or veg. Being exfitness this was easy for me. Plus home colonics to rid dieoff and sauna detox. hard to do with my physical head symptoms but pulled it off.
Unfortunately due to my primary being brain encephilitus which has rendered me non functional, and eyeballs (lot's of edema from die off around top of lids from Stephania), which does no render me nonfunctional, due to me being hit harder in head than many it's obvious I need some antibiotic help. It's very hard to talk with the extreme of my head stuff. I was hit hard in head. Non of it is emotional based. It's simply pathogen based.
I do appreciate your kindness. I'll add what I am currently so all of you members can see it.
this is what I am already on. I am on 6 whole herb form antibiotics I buy in bulk. No powder. It's strong. I herx. I make decoctions daily and made huge amounts of homeade tincture for all. I take both forms daily.
Sida Acuta for babs bart.
Houttunyia for bart
Stephania for lyme bart
Cat's Claw for lyme
Japanese Knotweek lyme bart
Artminisin Nutricology (The only bottle extract of herb I take.)
Serrapeptese for biofilm. GSE for Cysts.
Hi Shabi Chick,
Thanks for that! My ND and I are going to add it, so I will be taking along with my whole plants, Rifampin, Azithromycin, and Tindimax to break cysts. I hope this brings the head under control so I can begin to be daily functional to treat the remaining.
Hi Nan777, I'm not new to this but I don't post often. Yes, toxins are one of the factors. I am familiar with that Jernigan Product and tried it but it doesn't touch my deal. I probably........
...........have the MTHFR gene mutation so can't rid my body of toxins. I'm going to try the supplements for that but I'm not counting on it. All of these things really do not seem to
........target my severity to really be of symptom reduction benefit. That said, the things that do help me are pathogen load decrease, sauna, and homeade colonics. They are not making me comfortable per se but I feel a bit of toxic load off. Just not enough to make me comfortable.
The more pathogen load I get down and manage the toxin aspect daily helping my body, that is the only way I feel I'll get out of chronic.
As for adrenals. I do not have any cortisol problems or adrenal issues. I know what that is, and I do not have excess cortisol. It's hard for some to understand a particular brain function interference couple with brain inflammation that we feel, that some of us get.
Many are familiar with body stuff, and cognitive problems arising from it but haven't experience the actual physicality of feeling your brain infected and swollen and inflammed inside your head. Not headachey, but swollen, inflammed with the neuropathy running thru tissue of grey matter. But the neuropathy, head pressure frontal lobe and top of head, it took almost a year but I knocked it out.
I've literally not been able to talk to people or look at them because of how I hit. Not looking for sympathy. Just being specific so people understand how completely different our primary symptoms can be.........
yet we're hit by the same bugs. Really whacked this deal isn't it guys? Traveller knows me. She's been unreal. Love you Trav. xo
It's simply as you said a combo of toxins, and cytokine activity that causes the inflammation unfortunately make the neurotransmitter overactive and cause the signals to fly everywhere making for rapid thoughts and add buzzing, whooshing, vibrating and that all is a good recipe for lyme rage.
So the rapid thoughts, are completely unrelated to cortisol. It's all toxin and pathogen cause and affect. Hopefully, the pharma with my plants will take it down a few notches to bring me out of chronic.
Very unfortunately unlike many, I was hit so hard in brain, I can PHYSICALLY FEEL the infection behind forehead and under scalp bone. But that said, the site used to cover the whole area, now it's much much smaller and more on left side under scalp and behind left eyeball and behind left side of forehead plate.
I'm too tired to spell check. Thankyou all very much for your suggestions, insight, and generosity sharing your time with me. xo
Post Edited (1runner) : 3/16/2013 2:54:58 PM (GMT-6)