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Terrifying ayahuasca PTSD - advice please

LemonzLinez

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Jun 1, 2016
Messages
4
Hi, all. I will try to make this brief.

I have a serious case of advanced Lyme disease. Currently, I am recovering pretty well but for many years there was no explanation for what was happening to me and as my health was declining to the point of disability, I was absolutely hopeless. In a desperate act, after about 18 months of researching ayahuasca, I tried it. I did this because I felt like I was probably going to die (from the then-unknown illness that took my ability to function and often even to think), and I had read that ayahuasca had proven beneficial for anxiety and depression.

Well, it changed my life. It took time for me to incorporate what I experienced (no visuals) into my life experience, but despite the difficulty of a couple of ayahuasca experiences, the whole thing was overwhelmingly positive and life affirming. I believe it actually set me on a path of hope and healing that ultimately led me to a diagnosis and treatment for Lyme, as well, so that's an undeniable benefit.

However, my father had a major surgery a couple of months ago and I was really, really worried about his ability to come through. Prior to my first ayahuasca experience, I had never been a spiritual person--but although I couldn't define exactly what it was, ayahuasca made me feel connected to "the other side" or another side. So before my dad had his surgery a couple of months ago, I took ayahuasca to help cope with the real possibility that he might not make it and to try to find solace and come to peace with it. Obviously, my "set" was anxious, and I am sure this colored the experience.

Unlike years ago when I was sure I was in a slow dying process and had accepted it, I now have absolutely no wish to die. I want to live.

Well, this most recent ayahuasca experience kicked my ass to say the very least. It was...well, hell. And death. I had never before in my life had open-eyed hallucinations. What I saw was visually and mentally overwhelming to a degree that still gives me anxiety to think about. I knew I shouldn't resist what was coming on, but I did and it was the fight of my life. During the experience of that night, I lost the fight. I am tempted to write "I thought I died," but I actually still carry the experience with me and I feel like I did, in fact, die. It was horrific. The sensory overload of the experience was too much to handle and it pounded me for what seemed like an unending amount of time. I was absolutely devastated when I realized that I was dying and that I had no power to ward it off. I was given a clear message: sorry, game over. It wasn't nefarious, just matter of fact: You messed up. That happens. There's no turning back. All I could think of was my family finding me dead of some kind of drug overdose and that part was torture. I couldn't let go. I begged for what felt like weeks or months and then eventually I accepted that I had died and would not return, and I absolutely hated myself for it. I got so much information about the nature of existence in a very cold, cut-and-dry way that was devoid of any emotion--that was totally contrary to all my previous experiences with ayahuasca. Those felt like I was under the care of a nurturing mother figure; this felt like an emotionless masculine force showing me, against my will, things that I have asked to know all my life. Before I reached the point of encountering "him," which I would equate with an omniscient being, there were really terrifying visions and feelings coming at me at breakneck pace. The only way I can describe it that makes sense to me is black magic or voodoo. I just kept thinking oh no, oh no, oh no, I've fallen for something truly evil and I'm lost forever.

NONE of this way of thinking is anything that was within my conscious mind prior to this experience. I had no religious faith of any sort, and certainly no fear of demons or black magic or anything like that. None at all.

Well, you cannot imagine my disbelief when I woke up the next morning. My first thought was that it was a cruel joke--a "flashback" to when I was alive. But I had no choice other than to go with it and hope it wasn't. I went to work and wondered as I walked there whether other people could see me. I wondered if I was in some sort of a computer program. At a certain point during the day I confessed all this to a coworker-friend who assured me that, yes, I am alive and I had a bad trip.

OK, I can accept that that is what happened, even though it was SO real.

My life has changed remarkably, mostly for the better since that time. But that was two months ago and I still feel a recurring panic that it might all fall away from under my feet for me to discover that I am not really here, or that the world is simulated or something. I feel like a fool for writing any of this. And I am terrified to know that I feel this way. It's a literally psychotic feeling, not knowing what is real and what is not real, and it scares me. I really don't know what to do.

I have moments at home when I am alone, and even in my office on occasion, during which I feel like I am about to leave my body and it sends me into a panic. I suppose it's some kind of post-traumatic stress flashback from the experience. Besides being just plain scary, it's also so disappointing because my previous experiences with ayahuasca were all comforting even though they were difficult. This one has me terrified both of being alive and terrified to die, which isn't really anything I ever experienced before.

I've gotten a lot of positive lessons out of it: I have a fierce will to live, which was waning for a long time. That will to live came from my first few ayahuasca experiences, but since I am now terrified to die and be back in that place of absolute darkness and information overload, I'm also highly motivated to be alive. I do appreciate day to day life a lot more. Every moment, actually. I even appreciate and love being grounded by gravity now, which again isn't even something that ever would have occurred to me.

But is there anything I can do? I am pretty sure I will never take another mind-altering substance because the anxiety from this one still reverberates through me. I'm on edge all the time and I feel like I may have set myself up for a really bad life.

Any advice? Will I ever get over this, or did I royally f*** up my mind and lose it to this thing?
 
Did you take it alone? Or did you go to a country where you can legally take it in a religious ceremony with a guide/teacher?

I don't think that you lost it; but for the mean time you should avoid taking all drugs including cannabis and alcohol, and talk to a therapist about what happened. Stay safe.
 
Hi LemonzLinez-

It is VERY serendipitous for me to have read this post at this time. I'll tell you why:

I *also* have a very serious case of advanced lyme. Well, that's what I'm calling it for now. (Yes, I did get tested positive for it, albeit years ago). It manifests as severe rheumatoid arthritis in all the large joints (and then some) and mental/emotional numbness/fuckery. One could call it a lot of things: Just plain ol' rheumatoid arthritis (that started in an 18 y/o male, huh, strange), a "shamanic" disease with psychospiritual origins, and/or, advanced lyme disease.

My first ayahuasca trip, which was about 2 years into the disease, was HORRIFIC. It was like being stuck in an eternal place of cold cosmic information, and yet forgetting that I had even took ayahuasca--I felt like I was eternally in a mental ward / spiritual torture chamber. Yeah. I can relate. Though i didn't think I was dying, I felt very much in touch with death, and saw myself as a walking skeleton at one point.

However, recently, I've been dosing ayahuasca made by *myself* (acacia confusa and B. caapi) and it's MUCH better. It guides me toward healing. In fact, I believe it guided me to the right herbs for my condition which I am taking currently. It's a bit early to tell if they are really working, but feel free to bug me a few weeks down the line and ask me.

Do your PTSD/HPPD/shell-shock symptoms relate at all to your Lyme symptoms?

It sounds like you just need to be *grounded.* There are many ways to do this. In my arsenal:

Sex/love
Bone broth/animal protein
peppermint
Liver tonic herbs
Physical activity
Therapy with a GOOD psychotherapist
Meditation, especially in nature (like by a stream)
Progressive relaxation techniques

Maybe I'll think of more, but there are ways to help you feel balanced. Don't despair! You're faced with a problem and there are ways to deal with it.

Keep in touch,
RS
 
I find it very interesting, and not surprising at all, that your life-affirming trips happened after you accepted your own mortality, and that your death-trip happened once you decided you wanted to live.

Ayahuasca is teaching you a hard lesson about fear of death. As Laughing Bull in Cowboy Bebop says, "Do not fear death. Death is always at our side. When we show fear, it jumps at us faster than light, but if we do not show fear, it casts its eye upon us gently and then guides us into infinity."


Anyway, I've had some horrific trips on ayahuasca and DMT. I know what it's like. You'll bounce back eventually.
 
To me it seems that this experience has a lot to do with your family. Maybe you should share those feelings you have, or have had, about for instance the state your father was in. I think that just sharing these feelings with your family may help a great deal.
 
Hey, is it alright if I ask some more questions of you (the OP)?

What were your symptoms of lyme?

How did you find out that you had it?

What were the protocols you did to help it?

Do you feel like your past lyme treatment affected your ayahuasca experience at all?
 
My life has changed remarkably, mostly for the better since that time. But that was two months ago and I still feel a recurring panic that it might all fall away from under my feet for me to discover that I am not really here, or that the world is simulated or something. I feel like a fool for writing any of this. And I am terrified to know that I feel this way. It's a literally psychotic feeling, not knowing what is real and what is not real, and it scares me. I really don't know what to do.

If things are better, why worry if it is real or not? Go with it.
I'm not being a smart ass, for a change, I am serious.
I have read others posts as well as having some of these same feelings from time to time, usually after some heavy DMT sessions and then thought, "WTF do I care if it is real or not? I'm here "life" is good, so enjoy it". And I am/do.
I truly hope you get back to where you want to be though...my GF was ready to end it all if she had stayed in the DP/DR state for good, but she didn't...end it all OR stay that way.
You'll be back.
You may wake up one day and wish you were dead again.
 
Hi RS,

It sure is serendipitous. (I've been using that word a lot myself over the past couple of weeks.) See below for some responses/reactions to your questions and comments...

Hi LemonzLinez-

It is VERY serendipitous for me to have read this post at this time. I'll tell you why:

I *also* have a very serious case of advanced lyme. Well, that's what I'm calling it for now. (Yes, I did get tested positive for it, albeit years ago). It manifests as severe rheumatoid arthritis in all the large joints (and then some) and mental/emotional numbness/fuckery. One could call it a lot of things: Just plain ol' rheumatoid arthritis (that started in an 18 y/o male, huh, strange), a "shamanic" disease with psychospiritual origins, and/or, advanced lyme disease

I'm really sorry you're going through this. My Lyme story is a long one, but it boils down to this timeline:
Age 18/19: Diagnosed w/ Lyme based on rash.
Early 20s: Weird health issues that never made much sense: recurring pinkeye, fluctuating hearing loss, poor memory, "air hunger" (although I didn't know this term then...I went to a doctor and asked if I could have asthma and she put me on Zoloft without even checking my breathing--said it was anxiety)
Mid-20s: Significant cognitive problems, scary night vision, some nerve issues in my feet and legs, mild dizzy spells, stretch marks appeared on my shoulders and arms
Late 20s: Severe peripheral neuropathies to the extent I stopped driving, severe joint pain in elbows, tremors when I got overheated/after working out
30s: Rapid progression of (first) severe nerve pain throughout body, fasciculations, sudden onset of various types of rashes, unexplained fevers, balance and coordination problems, total lack of recall and occasional spatial disorientation, paralyzing panic attacks in all social settings, obsessive suicidal thoughts, severe joint pain in all joints, including hips, stretch marks all over my chest, flanks (sides), hips, legs, even my knees, epsiodes of double vision, 50 percent hearing loss in one ear, cluster headaches (also called suicide headaches--supposedly much more severe pain than migraines), vertigo attacks, fatigue--that's just some of it. Doctors thought at first that it might be ALS or MS, did a zillion tests, found some abnormalities, but couldn't conclude anything and so they dismissed me.
36: My mother found a photocopy of my Rx from when I was diagnosed with Lyme and it was only 10 days of docycycline, 200mg/day, which we learned is insufficient to treat Lyme. Found a Lyme specialist, was tested, and discovered I have not only Lyme disease but a very, very severe bartonella infection, which is what has caused the shoulder-to-knees stretch marks.

My first ayahuasca trip, which was about 2 years into the disease, was HORRIFIC. It was like being stuck in an eternal place of cold cosmic information, and yet forgetting that I had even took ayahuasca--I felt like I was eternally in a mental ward / spiritual torture chamber. Yeah. I can relate. Though i didn't think I was dying, I felt very much in touch with death, and saw myself as a walking skeleton at one point.

That is similar to the "scary" initial part of mine, which was hellish in a way I never could have imagined. But then it went far beyond that to a place of, let's say, "intelligent design," and it was just so mechanical and cold and emotionless and meaningless, and that was what has really shaken me up to this day.

However, recently, I've been dosing ayahuasca made by *myself* (acacia confusa and B. caapi) and it's MUCH better. It guides me toward healing. In fact, I believe it guided me to the right herbs for my condition which I am taking currently. It's a bit early to tell if they are really working, but feel free to bug me a few weeks down the line and ask me.

I have only ever made my own, with banisteriopsis caapi and psychotria viridis. This time, I made a huge mistake and added in a tiny bit of mimosa, which I had never experienced before. I've never had much in the way of visions and I always felt like I was somehow not "breaking through" fully--although my visionless ayahuasca experiences have been soul stirring and affirming--and so I added that in. Worst experience of my entire life. Just...sheer terror.

To the herb point. Let's talk about serendipity. I actually credit ayahuasca for having saved my life in a completely real way. I took it at my bleakest and sickest point as a desperate effort to cope with life. It was transformative and made me a spiritual person. It also made me look at plants in an entirely different way than I ever would have before. I see them now as highly intelligent, sentient creatures on another level of being. And I understand to some extent the medicine they can offer. Had I never taken ayahuasca, I never, ever would have had any faith in plant medicines. As I said, my mother found my Rx from 1997 and we saw that I was undertreated for Lyme way back then. I was still skeptical about going to another doctor because I had seen SO MANY already and they were all useless to me. All of them. But I read about herbal protocols and about the Herxheimer reaction, and so I ordered some herbs to "test" my body and see if my symptoms would flare up. I didn't know if the Herx thing was real when I took them. I had a strong reaction from the herbal tinctures and went straight to a Lyme specialist and confirmed what was wrong. After all those years. So in a real way, the ayahuasca sent me to the plants, and the plants sent me to the doctor. I am on antibiotics now, but also tons of supplements, and if I phase out either one, I get sick again. So far, both are necessary and helping me recover.

Do your PTSD/HPPD/shell-shock symptoms relate at all to your Lyme symptoms?

Not in any way that I can discern consciously, no. My shell shock is purely from the nightmarishness, sensory overload, and then the bleakness and almost computer-programminess of the last ayahuasca experience.

It sounds like you just need to be *grounded.* There are many ways to do this. In my arsenal:

Sex/love
Bone broth/animal protein
peppermint
Liver tonic herbs
Physical activity
Therapy with a GOOD psychotherapist
Meditation, especially in nature (like by a stream)
Progressive relaxation techniques

I do indeed. I have some difficulties with some of these, though. My body is scarred all over, as discussed, and the scars burn like severe burns when they are inflamed. This is typical of bad bartonella infections. It's repulsive to look at, and it hurts to be touched, so physical intimacy doesn't have a place in my life right now. I am gay, and every gay man I've known has been 98 percent physical with respect to other gay men. You're expected to look great before any kind of intimacy--including intimate conversation. So that's unlikely. I see a therapist I love and have seen her every month for six years. She had me on four psych meds including an antipsychotic early on because of the severity of my anxiety and depression. Since I've been treated for Lyme, my symptoms have more or less gone away and I am now on none of those medications. I actually asked her today if she thinks I should be based on this recent experience and she said no, after six years, she's confident that I'm physically ill and that I don't have a pathological mental illness. My Lyme doctor has told me Zoloft can be useful for Lyme because it actually reduces brain inflammation, and my psychiatrist confirmed that it does, so I consider sometimes going back on it to quell symptoms. But this "PTSD" anxiety is a marketly different feeling than the social anxiety and panic attacks I had for years. It's not at all the same.

Maybe I'll think of more, but there are ways to help you feel balanced. Don't despair! You're faced with a problem and there are ways to deal with it.

Thank you!
 
Yes, your point has occurred to me and is sort of my default, go-to explanation to myself. I do hope the shell shock wears off, but I know ayahuasca is supposed to "give you what you need, not what you want," and I'm praying that was a good thing and I didn't make some huge, life-altering mistake.
 
Hey, is it alright if I ask some more questions of you (the OP)?

What were your symptoms of lyme?

How did you find out that you had it?

What were the protocols you did to help it?

Do you feel like your past lyme treatment affected your ayahuasca experience at all?

Hi...please see above for my symptoms of Lyme. They've run the gamut of severe neurological, neuropsychiatic, arthritic and dermatologic problems. Also cognitive and fatigue (adrenal?). I was originally diagnosed when I was 18 and didn't realize I still have Lyme + bartonella until I was 37, so I have been living with it for at least half of my life. That's a long time for the infection to affect just about every system of my body--and in doing so, the symptoms are so complex and pervasive that it really does seem like too much to be happening to one person, and so it seems the default medical diagnosis is "this isn't possible." When I first went to doctors around age 33-34 because of double vision, partial paralysis, cluster headaches, imbalance, vertigo, etc., their first thoughts were to test for ALS and multiple sclerosis, brain tumors, etc.

A lot of people who have Lyme go through what I did, and because Lyme tests are so insensitive (inaccurate), they often test negative and after other tests are negative, doctors tend to dismiss us and suggest that we are either hypersensitive to normal aging patterns, we are overly imaginative or attention seeking, or that we have a mental illness that results in psychogenic or psychosomatic health problems. My curse is also a blessing in a sense in my case, to the question of how I found out I have it. My skin is severely scarred with what look like stretch marks, all over my body. I am male and I've always been thin; at almost 6' tall, my waist has never been larger than 31" and I think at my heaviest I was about 173 (presently about 165). So being a thin male covered in stretch marks doesn't make much sense; yet, every doctor I've ever seen has asked about them (appearing to be repulsed, which I understand, but it really is poor bedside manner IMO to make a patient feel so embarrassed about a physical problem that isn't his or her fault) and determined that I "must have been very overweight" at some point. No, I've said, I was never overweight or obese. And they just kind of stare at me, obviously assuming I am lying.

As soon as I saw my Lyme specialist, she was my skin and was floored. She immediately recognized my "stretch marks" to be rashes (or lesions) from a bartonella infection, and she said it's one of the worst cases she has ever seen. Unlike usual stretch marks, mine "flare up" and become inflamed at times, usually for weeks at a time, and they burn like they're on fire. It is a curse, to be sure.

So while a lot of Lyme patients don't get any farther than doctors concluding that because labs show nothing, they must be physically well, in my case I have such severe skin scarring of a particular type that it was actually enough for a clinical diagnosis of bartonella. One type of bartonella causes "cat scratch disease," which can be caused by a cat scratching a person, and which leaves scratch-like rashes/scars on the skin. It can also be transmitted by fleas, biting flies, possibly mosquitoes...and ticks. More and more people are finding out that they have bartonella *and* Lyme disease (the term is "coinfections"), and that those of us who do tend to be really sick because the two bacterial infections seem to somehow help one another out in evading the immune system. Not to get too technical, but the Lyme bacterium (Borrelia burgdorferi) needs an anaerobic environment without oxygen, so as soon as it gets in the body from a tick bite, it spreads across the skin (which is what causes the rash) and then "dives" into the bloodsteam. Blood is oxygen rich, and that's a toxic environment for Borrelia, and so the Borrelia bacteria go for a quick ride in the blood stream and then get out of it ASAP and make their homes in various parts of the body. Their favorite places seem to be brain tissue, which is fatty and is a feast for them, and the synovial fluid in joints. And so as a result, the primary symptoms of Lyme disease are neurological (because it's a brain infection) and arthritic (joint infection and inflammation). Bartonella, on the other hand, is an intracellular infection. The bacteria get inside of our red blood cells and, like Lyme but in a different way, Bartonella causes very severe brain inflammation and neurological dysfunction. Primary symptoms of bartonella infection include: 1) neurological pain, numbness, and dysfunction (for example, one of my legs became temporarily paralyzed several years ago); 2) "stretch marks" or other types of skin rashes and scars that sometimes appear and then disappear with no exapanation, usually on the arms, shoulders, flanks, hips, abdomen, back, and thighs. In my case, it even includes my knees. (Stretch marks on knees! Knees don't get fat...); and 3) severe pressure pain in the soles/undersides of one or both feet and sometimes the palms of the hands. All these are typical of bartonella infections. Years ago, I went to a specialist to ask why it felt like I was walking on a jagged rock under my right foot when I went barefoot, especially first thing in the morning. As far as I could tell, she didn't even listen to my question. She had absolutely no interest in addressing the foot pain or even acknowledging it, even though it was causing mobility problems for me. Had she known anything about bartonella, she would have recognized that as a primary symptom and once she saw my skin, she would have known to test me and also to diagnose me clinically. But she just simply didn't think it was important and sent me away with a clean bill of health. She could have saved me years of progressive illness.

What protocols have I taken?

Well, as discussed above (sorry about my clumsy quoting and replying here...this is a brand new forum for me), my first protocol was herbal. I'm not sure which one I used, but I think I ordered a bunch of Nutramedix herbs recommended by Buhner. I took those for 2-3 weeks and experienced a moderate Herxheimer reaction--moderate being severe for most people, as it was painful and uncomfortable, but it wasn't as severe as certain Lyme-related symptoms have been in the past.

So after the Herx reaction I went to a Lyme specialist. She put me on several antibiotics, including minocycline, biaxin and bactrim. She took me off a couple of the supplements I had been taking and said I should continue with most of them. (For the record, she has never attempted to sell me anything at all; she explains what supplements may be useful, gives me copies of medical journal articles that explain how and why, and I buy them on my own. I'm stating this because there's a pervasive rumor promoted by the IDSA that Lyme doctors are "snake-oil salesmen" who mark up various supplements and sell them to vulnerable patients at an exorbitant cost. In my experience, that's not only false, but my Lyme doctor has been the only doctor I've ever seen besides my psychiatrist who actually seems to regard me as a human being--she's certainly not taking advantage of me.) Sorry, tangent. Here's a summary of the protocols with brief notes:

Phase 1: Minocycline, Biaxin, Bactrim (antibiotics); various herbal supplements including but not limited to burbur (for detoxing), cat's claw, Japanese knotweed, astragalus, vitamin C, magnesium, and more. I was taking serrapeptase when I first saw my doctor and she told me not to take it--that it was too soon in the treatment process.

Problem: I had a very severe reaction to minocycline, which presented as a severe rash and inflammation all over my body and particularly in my genital region. My Lyme doctor said to monitor it carefully, but she hoped I could tolerate it because minocycline can cross the blood-brain barrier better than most antibiotics and therefore is best at addressing the brain infection aspect of Lyme. I saw my dermatologist about a month later for a mole check and he was alarmed by the rash and told me to watch carefully for anaphylaxis. I told my Lyme specialist (she hadn't seen the rash yet; I had only told her by email) and she immediately took me off minocycline and replaced it with rifampin. So my new protocol was rifampin, bactrim, and biaxin.

Phase 2: About six months in, I was feeling SO MUCH better. At that time, my doctor changed my antibiotic combination to bactrim, biaxin, and Mepron. As my most common symptoms were dying down, I had other symptoms suddenly becoming more pronounced, including night sweats that were leaving me drenched and other typical symptoms of babesia, another common Lyme coinfection. The Mepron was prescribed to address babesia. Babesia is pathologically much like malaria, and Mepron treats both. The night sweats went away after a few months of taking Mepron. My doctor also introduced flagyl to be taken just once every few weeks. Flagyl has been shown to be a "cyst buster" (controversial claim) that helps to break up protective biological slime coatings called "biofilms" that the bacteria surround themselves with, and which are thought to be invisible to the immune system. Flagyl helps to dissolve these, which releases the bacteria into the body, and which the other antibiotics help to eliminate. Flagyl serves the same purpose as the serrapeptase I had been taking, but I believe it's stronger.

Phase 3: I had a relapse/flare-up, and my bartonella scars were torturing me. With all my physical joint and nerve pain improving remarkably, on some days totally, and my cognition improved, my skin unfortunately has not improved much. My doctor inspected my "stretch marks" and noted how inflamed (and sensitive) they were, and she suggested that they may be colonized by candida yeast, which would explain the pain and itching. This made sense because I had developed candida overgrowth rashes on various patches of skin as a result of the antibiotics. So she prescribed diflucan, an antifungal medication, to be taken once every few weeks. It's *very* strong and I have learned that diflucan can make me "crazy." Like Lyme disease (and syphilis), when candida yeast die off in the body, their cells break apart and release toxins that make a person feel ill. In the case of candida, though, it releases up to 90 different toxins and some are neurotoxins--literally brain poison. I learned the hard way that a massive die off of candida causes very severe panic attacks with no outward trigger, and one day after I took it, my peripheral vision started to go black while I was at work, and I felt like I was either going to black out or drop dead. I ended up in the emergency room. It was terrifying. So these are the sorts of horror stories you might hear about Lyme treatment. Understanding the mechanisms that cause it is useful in being able to manage it.

I take diflucan rarely now, but aside from the whole thinking I was going to die thing, I did see immediate relief in my skin pain and sensitivity, so I believe my doctor was correct in her guess that my bartonella lesions are now colonized with candida.

It turns out a lot of infections, from bacteria to yeast, love to feast on fat, collagen and connective tissue. Lyme in particular also needs magnesium to function, and so it leaches the body's magnesium. Doing this causes metabolic dysfunction and fatigue, because magnesium is needed for proper metabolic function.

Do I feel like my past lyme treatment affected my ayahuasca experience at all?

I'm not really sure what to say about this. My past Lyme treatment is my current Lyme treatment, so I really don't know. What I can say is that my first few ayahuasca experiences took place when I was my sickest--self-medicating with alcohol and becoming out of control with that--and I had absolutely no idea what was causing the illness. None. So I was in this really dire mental place of being terribly ill with no answers from doctors after having seen a dozen specialists and having paid close to $10,000 for specialized tests. I was getting worse, and I was sure I was dying. It was, for sure, "rock bottom," except that I had managed to maintain my job. I was also on a lot of psych meds at that time because of my anxiety and panic, but I weaned myself off of all of them for about two months before I took ayahuasca. So I was on no medication other than alcohol when I first took ayahuasca. The first time I took it, I drank, even though this went against the guidance I had read.

After my second ayahuasca experience, I lost all interest in alcohol. I used to drink daily; since that experience four or five years ago, I've probably had alcohol a total of six different occasions, and never more than two beverages in any sitting. I just don't like the feeling. It's as if I am poisoning myself. So that is an undeniable benefit from ayahuasca, because alcohol does not help when a person has a severe chronic illness--obviously.

I took ayahuasca a couple of times while I was taking antibiotics. The experience was the same as prior ones until the most recent, terrifying experience. So it doesn't seem that the Lyme treatment affected my ayahuasca experiences on those occasions.

I'll also observe this: ayahuasca is famously disgusting tasting. It's bitter and pungent and earthy. I have taken a good number of herbal tinctures--cat's claw, etc.--and many of them taste very similar to ayahuasca, but milder because they're taken at much lower concentrations. I don't think this is a coincidence. I think a lot of these alkaloid plant-based remedies have similar properties, and because of the similar colors and tastes of many of these herbal tinctures to ayahuasca, I feel like there's some relationship among the way they heal. That's purely speculative, but in my experience all these things are healing.

As for my terrible ayahuasca PTSD...it's a lesson I am still integrating. Hearing from people here has been really helpful already, to be honest. at least it makes me feel like I'm not the only one who has had this reaction. Having recounted my story here has also helped me to consciously remember that ayahuasca truly was the beginning of my finding diagnosis and treatment for Lyme disease, which has affected me adversely at least since age 18 or 19--half of my life--and since I've found treatment for that, my life has improved so dramatically. I've gone from half dead to almost fully alive. And I have purpose in my life. It's remarkable.

The very first cue I ever got about ayahuasca was from the music and interviews of Tori Amos; ayahuasca is pervasive, both explicitly and subtly in her music. In interviews, she has many times mentioned "drinking tea with lucifer," which refers to her shamanic ayahuasca experiences. (Look up her songs "strong black vine," "father lucifer," and especially "sister janet" and listen to them with ayahuasca in mind.) In interviews, she has consistently said throughout her career that you have to accept and embrace darkness just as you accept and embrace the light, and as she sings in "strong black vine," "lay back/Strong Black Vine/submission/is my mission for a/Strong Black Vine/con-concentrate." She has expanded on this in saying that ayahuasca is a totally overwhelming experience that takes you to the darkest places, and if you resist (e.g., if you don't submit fully to it, which is not easy to do, and which I was not able to do during my "bad trip") then you won't be able to concentrate on learning what you need to learn and instead will suffer through the experience--you have to actually accept the darkness in order to break through it to illumination. So with her music as a guide, in addition to your experiences, I can at least rationally understand that I was too emotionally distraught about my father to "con-concentrate" and accept the lessons ayahuasca was giving me...and as a result, she beat the shit out of me. In that one, the devil--literal or proverbial--dominated the experience because I resisted. At least that's what I hope happened.
 
Wow. Oy. F this sh**, right? I'm amazed that you've made it from age 18-36 without freaking calling it quits. Super good on you (proud) for sticking it through and finding a place where you are actually hopeful about life.

I took Mepron along with Bicillin, Doxycycline and I think some other antibioitics a while ago for a year and they did absolutely nothing but make me feel gross inside. I took some herbs with it too, including cats claw, samento.

It's possible that ayahuasca is a missing link in lyme and coinfection treatments, or at least something that may speed up the process.

Sometimes I wonder if Iboga would be even better.

Have you looked into Teasel? It's supposedly indicated for lyme-induced arthritis. Currently testing that theory...

For everyone else who is peeved that there is a rambly wall of text not about psychedelics in this thread, it all makes sense if you tl;dr'd it. But this thread also might now be better suited for Healthy Living.
 
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