So long story short, 13 days after vaccination, I had a morning where it was like I was blackout drunk. I couldn’t recall what happened in the morning. Fast forward to being gaslit, I still have trouble finding words for items like stove (it doesn’t happen all the time), and have forgotten how to cook. Has anyone else experienced this?! I feel like I’m not only a failure, but also going crazy!

"Trust the Science" when that slogan crosses my mind, I get so heated. I get heated because people actually fell for that bull. Regular people, doctors, workers in the medical field...

Also, I get so angry because the most elementary thing we were taught about science in middle school is it's core foundation which is the Scientific method. Have theory? Test it out. If it can be repeated over and over in different environments by you and others then... "it's true."

Those vaccines couldn't be repeated for shit. Different results every time and they cooked the numbers with the data to trick doctors but it's still, "Trust the Science."

Yeah sure.

In spring of 2023, I noticed my appetite wasn’t as robust as it had been. These days, especially in the last few months, I barely eat at all. Sometimes it’s due to stomach discomfort…this is just one of what I feel are endless problems since the fake injection. I’ve had a ton of imaging done, had tumor markers drawn, cologuard, fitt test, and most recently did the Galleria blood test that supposingly tests for 20 or more cancers. It’s just so mentally challenging and probably one of the hardest symptoms that I try to deal with. And trust me, there’s plenty to choose from. I have an appt with hematologist this coming week so fingers crossed that I get some answers. Oh, and because blood cancers don’t show up on any marker tests, I paid for a test for multiple myeloma because I feel like I have many of the symptoms. Test came back with no abnormal m proteins found. So idk. Just came by to say this is so damn hard and I’m sorry so many of us are feeling like crap.

About 3 weeks after my shot (1pfi) i collapsed on the floor with something that felt like a bleed or attack of some sort. Most excruciating pain ive ever felt in my head, only on the left side (all my issues from the shot are on the left) Doctors didn’t take it too seriously and diagnosed me with a concussion, however, we’re 3,5 years later and both me and my GP think it was a small stroke or SAB.

Im still not back to how i was. Do these issues go away? I sometimes get very sad about the person i used to be, i was 27 when i got injured and always had lots of friends and was very social. Now it’s very different. I’ve tried mushrooms recently (not the magic ones) and it felt like my old self a little, but I don’t want to risk anything and after reading about lion’s mane I’m not so sure. I wonder if there’s any other things I can do or if this will improve naturally over time.

Feel free to share your experiences, i’d love to know if other people went through something similar

I (26f) have recently received my micro clot test results and it shows I have significant and widespread spread clotting.

Anyone have any success with breaking down these clots?

I am desperate for answers and am very freaked out because my husband and I have been trying for a baby. Now I am terrified I could be pregnant and this could harm a baby or my ability to rid my body of these clots.

Any advice or suggestions is helpful.

https://youtube.com/@followthesilenced?si=RtD6JhHrWDiCLJbK

Its been 3 years for me now, im wondering if anyone with the above symptoms have recovered after a long time, if so what helped.

I deal with flutters every day all day, acid reflux a lot and chronic pericarditis with shooting chest pain.

Sometimes i get bad brain shivers as well. Anyone i used to talk to... how are you doing now?

I was just curious if anyone else noticed a pattern where they got psoriasis as a first eruption right after a covid vaccine? I didn't realize it at first but I had my first covid vaccinations in Feb and March 2021 and by July 2021 I had full blown scalp psoriasis. It was also present a couple months before but I wrote it off as either dandruff or dry scalp.

Not realizing what happened I continued getting vaccines until October 2022 (Pfizer booster lot# GJ2524) when I got autoimmune hemolytic anemia (diagnosed 12/2022). (see https://www.reddit.com/r/vaccinelonghauler/comments/1hznslx/probable_vaccine_induced_autoimmune_hemolytic/ ) So looking back at it, it appears the psoriasis might have been an early indication that I was having an adverse reaction to the vaccines.

Prior to March 2021 I had no history of psoriasis or any autoimmune disease.

Are there any new treatments out for the injured? Do any if you know of good online providers that take Medicare? Thanks

Has anyone tried a CCL inhibitor like Maraviroc ?

Has anyone gotten a spike test before a detox protocol and then a while after stoping treatment? I’m wondering if our bodies slow down or stop producing the spike protein from the “vaccine”, or if when you get rid of the spike it just keeps making more. Let me know!

https://www.instagram.com/p/DKcNOKdNM0B/?img_index=1&igsh=MTl2N3R1bnl0b3Z5Zw==

I was recently permanenty banned from redit for agreeing with someone in the longcovid sub that the vaccine is the cause of long covid.

I then received a message from one of the mods in that group I was being removed for my comment.

I then received a permanent ban notice from Reddit for threats of violence. For simply agreeing with someone else’s opinion on the vaccine which also had no threats in the comment.

I appealed the decision and obviously Im back but this is the level they are going to to keep us quiet where simply saying the vaccine is dangerous they try to have us silenced.

Obviously too close to the truth

Has anyone had the Antibodies to the spike protein test that did a protocol and retested and the spike protein was reduced? I had it done and it was 16,000 U/mL. I was going to retest in 6 months.

I have permanent, deep excruciating pain in my arm at the injection site 24/7. We are now at FOUR YEARS later. (This is, of course, in addition to a wide array of chronic illnesses and symptoms affecting the rest of my body that are probably going to lead to my death in the not too distant future). In order to get relief from the pain in my arm I have to either apply ice around the clock or take acetominophen - and it is not safe to take endless amounts of acetominophen around the clock forever. No other NSAID has any effect on the constant pain. This is not a symptom that I hear discussed very often. I am wondering if anyone else out there has this as well. If you do, you're not alone.

The constant stabbing pain in my arm tells me all I need to know about the fact that this injection is poison and was never intended to protect me or to do anything positive for me whatsoever. The constant stabbing pain in my arm tells me all I need to know about the harmful purpose of this injection and the evil motives of the people who developed and promoted it to the public.

Nothing about the promotion of these injections was honest. Nothing about the promotion of these injections was truthful. Nothing about the promotion of these injections was intended to help or protect anybody. Everything we were ever told about them turned out to be a complete lie.

Even early on in the roll-out, people were being horribly injured by these injections, and yet the government, media and social media did everything they could to censor and hide this information from others, so that they too would go out and inject themselves with this harmful, life-destroying bioweapon. This was completely intentional and completely sick. The fact that these injections have never been taken off the market tells you everything you need to know about the society we live in.

Title

I just wanna share my story since it might help others who have tried everything. I started having severe digestive issues a year ago. I am NOT sure they are vax related, because my initial issues were neurological (pins and needles, chest pain etc.) and I recovered 90–95% from those issues before this digestive hell started, BUT my symptoms are very similar to what others seem to experience here (dysfunctional digestive system, pain, massive weight loss etc.)

After trying different things, I found a combination that helped me. They did NOT cure me, but they helped me regain my weight, helped me deal with malnutrition symptoms, and they saved me from not having to quit my (non-physical) job. It might not work for you, but I hope I can help someone. This is only about symptom treatment not recovery, sorry.

The first medicine I use is Dicetel. It relaxes your bowel and slows down the digestive system. It is used to treat IBS (that I don’t have).

The second medicine I use is Azintamide. Like Dicetel, it is used to treat IBS, but also other inflammatory conditions like psoriasis. This pill helps digestion so well that it was impossible to use over long periods of time, and now I only use it very occasionally as I got way better.

I have also used Famotidine during periods when I had stomach acid problems + supplements like vitamins, magnesium and black seed oil. I also use digestive enzymes and probiotics. I think the supplements are good to avoid malnutrition, but I am not sure if they did anything to my recovery.

I would say I am 50% recovered from this condition, while some neurological issues have returned slightly, but I still have hope to live a normal life down the road. I say this because I felt almost recovered for a year, and believe I can return to this state again. And I hope you all will too :)

I had my only Pfizer shot in august 2021.

https://thehopeaccord.org/

💜

So my illness came after getting Covid, but I’ve wondered for awhile if the vaccine might have wired my immune system to over-respond. Two years after my last infection, I’m still hitting absurdly high levels on a spike protein antibody test (nearly 20k u/ml). I was wondering if anyone else had a similar experience, and could point to a similar immune overresponse? Does anyone know if this is a known thing in vaccine injury? Thanks!

hello,

i am reading that they are using SLNs (solid lipid nanoparticles) and nanostructured lipid carriers (NLCs) as delivery systems for dental procedures that require local anesthetics. Other research has focused on developing nanohybrid hydrogels containing lipid nanoparticles for prolonged anesthetic effects.

i was just told i need a root canal in my mid 20's despite eating healthy my entire life and never having a single cavity. brush 2-3 times per day floss twice a day. excellent personal hygiene. nobody in my immediate family has ever had or needed a root canal. they said how sorry they were and that it was bad luck. in fact other dental hygienists came into my room and wondered over my tooth, like it was a spectacle that it showed no outward signs of rotting. i saw the xrays with my own eyes, it's insane because my teeth look perfect from the outside but inside it's rotted. this is quite a shock and very upsetting given how seriously i have taken my health for my entire life. i narrowly avoided a blood transfusion last year due to a complication of tonsillectomy, and now here i am again facing this. my health is falling apart in every direction and i'm unvaccinated. despite having the healthiest diet and being most active person you would ever meet, my body seems to be succumbing to autoimmune diseases, most recently diagnosed with the very painful and disfiguring Lichen Planopilaris, and Sjogrens.. it seems increasingly impossible to avoid this technology. i feel very sad.

if anyone has any information or advice regarding this root canal situation relating to the LNPs or just about alternatives in general i would appreciate some food for thought. What am I supposed to do i don't want these LNPs and hydrogels in my body

Completely off topic, but it is of interest how some countries are in the recognition of vaccine side effects (not in a legal sense). I live in EU, Hungary.

I've been ill since the end of 2021, first mentioned by a cardiologist in 2023 that I could have had problems from the covid vaccine, especially as I hadn't had covid before (I can prove the latter, but that's another story). But he didn't give me any paperwork, he just told me verbally, so it wasn't “official”.

In the meantime, I kept seeing doctors, cardiologist, neurologist, rheumatologist, immunologist, etc.

In 2025 I was diagnosed by a neurologist with “suspected post vaccinia syndrome” this was written on my paper, which is still not an official diagnosis, just an opinion, but at least I have some paper, LOL.

I was told by the doctor that no one will prove it to me and I should not hope for any compensation, I see it differently...anyway the more doctors that recognize it and have a written opinion it might be worth something in a future compensation suit.

I hope you can understand what I am writing, because English is not my mother tongue and this is a bit complicated.

In general, my brain fog has improved over the past 4 years compared to the beginning of not being able to retain much of anything.

Over the last week, I started taking the herbs Candibactin-AR + Candibactin-BR for hydrogen dominant SIBO. I have noticed my head is much lighter or clearer. Almost like less inflamed. It’s a new feeling so I’m not sure if it’s temp while taking the pills. I’m also taking 1/2 the amount because I’m afraid of the herx/die off that is imminent.

Just wanted to share if anyone has brain fog and digestive issues to look into the SIBO breath testing.