Nausea with headache

female type 1 diabetic.
I was admitted to a an er for suicidal ideation. I was being held on a 5150, upon arrival I told staff that I was sexually assaulted by an adult male. I would like to sue the hospital for negligence as well as emotional distress.
My bloodsugar reached over 350mg/dL for extended periods of time. This resulted in me having headaches, nausea, extreme thirst, blurred & frequent urination. After asking the nurse in charge of my care to confer with my endocrinologist or a specialist, they declined to do so. While I was there despite hospital policy they made me put my insulin pump on and take charge of giving myself boluses and essentially taking care of my own diabetes. I believe that any trained endocrinologist will tell you that their use of insulin was extremely dangerous, one of the times being where they switched in between giving me long acting and short acting to the point my bloodsugar was 56mg/mL.
Even though I was on a 5150 hold, I even have pictures of the CNAs who were supposed to be watching me sleep. They left equipment with long cords, which only further grew my suicidal ideation. And furthered the anxiety.
A male doctor came into my room placing his hand on my butt and shaking me to “get my attention”. He came in very aggressive which only heightened my anxiety, after seeing responding was not resulting in a resolution I stopped talking and just laid in my bed facing away from him playing 8 ball on my phone. Once I stopped responding to his threats of “them doing whatever they want to”. He grabbed my arm forcefully again and tried snatching my phone out of my hand. I turned further on to my side from the force- then looked at him while his hand was still on me and told I wasn’t going to touch him but he needed to get his hands off of me. I tossed my phone on the ground and told him he could take it and I wouldn’t fight it. I then said goodbye which I guess struck a nerve. As he was headed for the door he turned back and a bunch of grown men 6-9 grabbed me at his command. Before they grabbed me I was simply laying on my bed under the blankets on my side not moving. During this there was a person holding my wrist and bending it, to which I screamed out repeatedly that I was being hurt. I screamed repeatedly for them to get off of me, and my screams for help fell on deaf ears. After this I was left sobbing and visibly shaking from the trauma of being held down. The following night, I could not sleep despite being giving melatonin due to feeling them pinning me down everytime my eyes would shut. This has lead me to be afraid to seek further help for my mental health treatment. I was dismissed the following day.

Hi, I recently posted in a brain cancer sub. My 11 year old daughter has had headaches, fatigue, and nausea for 6+ months. She has asthma and I have had her medication adjusted thinking that they were related. She was treated in the er for something else and they found an incidental lesion during the ct scan.
She was referred to a neurosurgeon. She had an MRI with and without contrast where two tumors were discovered. They are on the smaller side, but now there is a team involved which includes an oncologist. The incidental lesion has become 2 tumors.
They want to go to surgery and remove them and then biopsy them (the larger one is in the Sylvian fissure and multi lobular, and the smaller one is on the left temporal lobe.)
My overarching concern is that the possibility of what we’re dealing with keeps escalating. First a lesion, then two tumors, now, potentially glioma grade 2. This has all taken place over the course of a month. She has lost 5 lbs, she sleeps all the time, and the nausea keeps her from playing regularly.
MRI with and without contrast:
17 x 11 x 17 mm enhancing multilobular mass at the posterior left sylvian fissure with central nonenhancing T2 hyperintensity which may represent necrosis. There is mild surrounding nonenhancing T2 and FLAIR hyperintensity which could represent edema. Peripheral rim of hemosiderin is noted. Additional 7 x 7 x 9.5 mm (AP by TR by CC) enhancing T2 hypointense mass at the left temporal pole, seemingly extra-axial versus cortically based and exophytic.

36 year old female,smoker(1/2 pack daily), do not drink & no drug use Diagnosed with: hypothyroidism, degenerative disc disease, lymphadema in both legs, tmj, adhd, depression, intercystial cystitis and had severe symphisis pubic dysfunction in one and only pregnancy
Please let me hear your thoughts on what could be causing all of this. I've seen multiple doctors & specialists & no one seems to have a clue as to what the diagnosis is as of yet.
A couple months ago I saw an endocrinologist bc I've been having lots of weird symptoms for many years, that I thought were just due to my hypothyroidism , but pcp said I shouldn't be feeling this way. Symptoms are: chronic fatigue, hot flashes, cold intolerance ( only sometimes & I can start shivering ) excessive sweating ONLY on the left side of my face/scalp & right side of face Is bone dry. This only happens when I wake up in morning or when I wake up from a nap. The sweat pours down my face into my eyes, & soaks my shirt & hair. Been happening since 2012 and has gotten worse. Chronic, severe constipation , thin nails( won't grow,split easily & have vertical lines ), knee pain ( cracking & pain ) , back pain, finger swelling, especially after waking in morning, dry & itchy eyes ( sometimes ), sugar cravings, very low libido ( like non existent ) , brain fog, forgetting words mid sentence, horrible concentration, low motivation, etc..
Endocrinologist did blood work. Came back low in iron, vit b12 & vit d. Cortisol at 8 am came back at a 4.7, so she had me do an acth stim test. Baseline 8 am cortisol was a 3.8, acth injected, and cortisol at 30 mins was a 14, at 60 mins was a 18. She doesn't know what's causing this & said cortisol is low but acth stim test showed I'm in normal range ( but on low end of normal). She does more blood work bc symptoms get worse, & I start having mild headaches. Ana panel comes back positive/abnormal. Ana antibodies come back at a 1:80 .I'm referred to a neurologist & rheumatologist, which are booked months out.
Then, a couple weeks later, the mild headaches turn into daily headaches, that are getting very painful, & lasting for hours. Start getting weird pressure in my eyes & behind my eyes. Very dry and irritated eyes. Ears popping. Dizzy episodes where the floor looks like it's moving back & forth & I start feeling like floor is vibrating beneath me. Headache won't go away for 3 days in a row, & eye pressue/pressure around my eyes & even behind bridge of nose is horrible.
I go to er. They do CT scan. Er doctor Says nothing emergency related, but I do see partial empty sella is notated on results. Er doctor refers me to an eye specialist.
Eye specialist dilated my eyes & says everything looks great. Says I might have thyroid eye disease & tells me to come back in 2 weeks for measurements without dilation.
Symptoms get worse. Nonstop headache/pressure in forehead, around / in eyes, dizziness & I'm seeing weird black things in bottom peripheral vision. Almost looks like I'm still looking through my glass frames, even when I take them off, but only the bottom sides/corner of my frames. Like dark areas.
Go to urgent care. Given steroid & toradol shot. Looks in my ears. Sees nothing. Tells me if shots don't help, go back to er.shots helped for maybe 2 hours & then symptoms are back. Also have salty liquid substance drop into my mouth from somewhere & it tasted like salty water.
I go to another er. Blood pressure not extremely high, but high compared to my normally perfect pressure. Er doctor says he's worried I have iih and does a lumbar puncture. Opening pressure is a 21. Drains csf down to a 15. Er doctor calls a neurologist & is told might not be iih bc a 21 is high but very borderline & says not to start me on meds for iih. Told I need to see a neurologist asap . Symptoms DO go away after lp, but day after lp I start having new type of dizziness where I have episodes of feeling like I'm on a spinning ride pushing me to left & nausea.
See new neurologist & she has no idea what's happening. Says doesn't sound like iih bc some symptoms don't match. Wants to do a mri of brain & orders pitutary protocol as well. Spinning feeling is horrid & I beg for a Stat mri & wishes granted. Have stat mri next day.
Havnt spoken to neurologist yet ( it's been about 1 week. ) I read my results on line. Everything looked normal except something about a concave superior margin and minimal foci t2/wave hyperintense periventricular and subcortical white matter.
Please..I need your thoughts. Thank you.

Hi,
Just wanted to share my story. In December, I had sudden onset distorted vision, intense headaches, nausea, pulsatile tinnitus, and vomiting. I went to urgent care, they ordered an MRI that I was able to get the next day, and it demonstrated elevated optic discs and suggested I had elevated intracranial pressure. I got sent to the ER, was admitted to neurology services, got an LP (opening pressure 62), had a lumbar drain for 3 days, had cerebral venous manometry testing, and followed that with stent placement. I was hospitalized for 2 weeks total.
The plavix for the stent caused super heavy periods and I almost bled to death because when I told my gyno about them, she said my hemoglobin from 10 days beforehand was normal and I didn't need to be worried. I thought my extreme weakness and shortness of breath were from the diamox and didn't go back to the ER until I started having a fluttering sensation in my chest. Ended up getting 4 units of blood transfused, which was roughly equivalent to volume I had left. After that, I started medication to stop my period but it only ever reduced it in severity.
The one thing that was drilled into my head was the importance of losing weight. I'd gained maybe 50 lbs during the past year and a half, and was at my heaviest of 300 lbs. I focused on tracking my calories and started working with a personal trainer. I couldn't do much in the beginning but gradually lost some lbs and got stronger (thank you, iron supplements and protein bars). Eventually, I got the point where I could even do barre classes, slowly started incorporation hikes, and found a friend to play pickle ball with.
I was fortunate enough to get a 6 month medical leave of absence from my job as a nurse and have used the time to work on my physical and mental health (started therapy). I just met with my neuro ophthalmologist last week and have no more papilledema, which is incredible because I was at grade 4 when I was diagnosed. We are going to have me come off diamox in a couple weeks and closely monitor with monthly follow ups to see if I'm actually in remission.
I felt compelled to share my story because I know how frustrating and hopeless it can feel to deal with this disease, but hopefully it isn't like that for us forever.

44M, 5'11", 190 pounds, caucasian, extreme fatigue and constant dizziness, no existing medical issues, slowly discontinuing SSRIs (about 10 mg duloxetine, down from 60 mg in August 2022), don't drink, don't smore, no drugs, from Canada.
So... I started to feel some serious fatigue at random times last Spring. At one point, I couldn't climb a small mountain with my kids (7 and 8 last year) when I used to be able to walk 10 miles into any mountain day or night. I wanted to do some bloodwork at the time, but I felt better soon and forgot about it. It came back in Fall, more serious, but after a couple of weeks I felt fine again.
About one month and a half ago, the extreme fatigue came back with a vengeance and never left. Also, I started to feel dizzy. And not only a bit dizzy, but enough that I sometimes feel like I've drink 3/4 of a bottle of wine. I can still function, but I need to concentrate. I feel some confusion as well (I talked to my sister today and had to ask her to slow down as she was talking too fast for me... never happened before), and has some GI problems (like constipation... which I never had in my life). I also have really bad headaches, which I never had as well. I also have a somewhat blurred vision. Not enough to impair driving, but it seems like everything is in some kind of fog. Maybe that's brain fog, maybe not, I don't know, but I don't see as well as I used to it seems. Some random nausea as well, but nothing serious yet and didn't lose more than a couple of pounds. Still, feel a bit queasy nearly all the time.
Three weeks ago I had a colonoscopy and it was fine. I had some blood test and everything is normal. Last Saturday I had a brain CT scan and I don't have the results yet but from what they told me if there was anything they would contact me first thing on Monday, so it should be OK (I hope so...).
What's left? What about multiple sclerosis? Or vagus nerve dysfunction? What else? I ate more tuna in the last months so could it be linked to mercury? What can I ask my doctor about; which test to run? My mother has some auto-immune disorder (rheumatoid arthritis) so don't now if it could mean I am more likely to get something like it.
I am pretty worried because it seems to be going fast. I feel more dizzy now than last week. More headaches too. Fatigue is constant and I feel like a hero simply because I can still work. I am slower than I used to and sometimes I space out a bit when people are talking.
What the hell is up with me? If brain scan is negative, what could it be?
Thanks!

so here are my symptoms. I say more at the bottom cause i’m concerned. please help. i’m terrified. I have a weird discomfort in my upper abdomen (left) and it’s not really painful? it’s just a vague discomfort. under my ribs just feels very very heavy when i stand up. I get really bad heartburn and nausea. I sometimes feel (this is gonna sound weird) bubbles in my stomach almost which scares me. and sometimes my right side hurts a bit but only a little. I also have only at chicken soup twice a day or once a day. so now i feel dizzy as soon as i stand up or weak. I also have back pain when the discomfort is. and now this is gonna me tmi but I had like orange specs in my stool. idk maybe it’s the carrots from the soup i’ve only been eating for literally days. and then I see these black specs in my stool as well but it looks like seeds? or like seasoning? which the sup i’ve been eating does have black seasoning it. it’s not every time I use the bathroom i see it. sometimes it’s normal but especially after i eat the soup its there? anyways here’s more at the bottom.
i’m 19 years old and I was diagnosed with gastritis a week ago. I can’t get an endoscopy because i’m like 3 weeks pregnant. so I have to wait. which scares me because I am so scared I have stomach cancer. mind you last month I thought I had a brain tumor because I had pressure in my head. had a cat scan and it was clear. so for the last month i’ve been having the WORST anxiety about having cancer or an illness. and the doctors say that the gastritis is either from me really stressing my body out (which i am finding it hard to believe that stress can actually cause this) or from the pain meds the last dr put me on for anxiety and headaches. I have really bad health anxiety and my life has been dark now. I am scared of dying. i’m not even excited about my pregnancy cause i’m too scared this is stomach cancer. Everyone is telling me it’s not but when I look up my symptoms it says it is:( I really am new to gastritis if it’s even that. I will say though I am starting to feel better after taking meds for a few days. not fully better but it’s less advanced like it was. so is that a good sign? AND the dr said she would’ve saw stomach cancer on the abdominal ultrasound she did. she also said i’m so young to even be thinking that. idk I lost my step dad 2 years ago to cancer which he always had when i was young and i think that is where my health anxiety comes from. i’m just really scared and stressed out right now. i’m starting to get in a very depressed episode from this and don’t know what to think. someone please explain gastritis to me.

I'm all up to date on my vaccines, so was hopeful I'd not get Covid again. The last time I had it I ended up in the hospital for a couple days with pneumonia.
This time I had initial symptoms that I didn't think were anything important. Started with some nausea, then I had what I assumed was an allergy flare. But, after a day of sneezing and runny nose I started getting worse. Last night I had a fever, so I decided it was worth testing. And I'm positive. Ugh.
Symptoms now are fever, body aches, watery eyes, headache, sinus congestion, cough, fatigue and loss of smell and taste. I'm hoping I don't end up with a secondary infection like last time. It's not good.
Hard to know for sure where I contracted it, but we were at a huge concert venue in Seattle on Friday, so that could've been it. I know a lot of people don't test anymore. Not sure why not, but we get the tests free, so I figure I may as well know what I'm sick with. I wish there were free at home tests for flu and RSV as well.

Has anyone experienced acute hepatitis following laparoscopic excision surgery?
I recently underwent surgery with a nook surgeon and was recovering well, until 11 days post op I started to have severe upper back pain, nausea, fever, malaise, lack of appetite, headache, and dark urine.
I went to the ER and they found my liver levels were severely elevated. They did an ultrasound on my liver and did not find any gallstones. They did a CT scan of my abdomen which was normal. They ran bloodwork for viral hepatitis (Hep A, B, C, EBV) which were all normal. My lipase was normal. I was not taking excessive amounts of Tylenol, I was not drinking alcohol, and I had a normal amount of anesthesia during the surgery. I have no known pre-existing liver disease and no family history of liver disease.
I have an appointment with a hepatology clinic soon but I’m hoping to find someone who has experienced something similar.
Thank you ❤️

I've had increasingly emotionally charged dreams, but the one last night has me feeling really weird, so I wanted to share it here. Apologies for formatting, I'm on a mobile.
It started with me having an interaction with someone that I can only describe as Mr. Doctor. He wore scrubs, but I remember feeling an innate feeling of distrust towards him. I don't really remember anything specific that was said. This is only really important later.
Afterward, a couple old friends from high school that I honestly haven't thought of in years appeared, and one of them was really, really pissed at me, telling me to "lose her number" and such. I followed and was trying to understand what I had done to make her so mad, and to try to fix it if I could. It didn't go anywhere, but I ended up in this room, standing behind a big arm chair, and I remember feeling like I was going to have an emotional breakdown, except then Mr. Doctor showed up and I felt scared and vulnerable so I crouched down behind the chair, trying to hide, and I felt that feeling like when your brain and your body are fighting over whether to cry or not - nausea, lump in the throat, headache, etc - and Mr. Doctor came over and crouched next to me and was talking to me, and I specifically remember hearing him say: "come on, you need to let it out so it doesn't just get stuck in your stomach."
I woke up very shortly after that. Idk why it's sticking with me so much, but it just feels so weird.
I'm not particularly looking for advice or insight, I just wanted to share my weird dream that has my stomach turning in uncomfortable circles.

Probably sounds dramatic, but I'm being the most serious I've ever been in my life.
Female aged 30. 5'3 and 129 lbs. No medical conditions or medications. Former smoker of both tobacco and cannabis products. Smoked about a half pack of cigarettes a day for 5 years. No substance abuse since. Never drink
About a month ago I developed a sudden general feeling of being unwell. It started with waking in the morning with headaches and nausea. The nausea is pretty much constant now and I often have a pain in my mid-back that accompanies it.
The headaches I believe are migraines. Strong throbbing often felt mainly behind my left eye. Sometimes relieved with otc meds, sometimes ending up hiding in a dark room and putting pressure on my eye which sometimes helps. Vomit almost everytime I get one.
I feel dizzy, faint and weak all the time. Pain in my neck, feet and hands.
So far I have been to my local ER for migraine relief, had a CT scan that was clear and all blood work was good.
Waiting for an appointment with a new PCP.
Today I haven't been able to get out of bed because everytime I move it is just a strong wave of nausea. The headache isn't bad, but it's always there very dull like if that makes sense.
I feel like I could sleep my life away and I have zero energy. Hardly enough energy to shower.
I'm really not depressed or anxious. This all came out of no where about exactly 5 weeks ago.
Any advice? Where do I go from here because the way I feel makes me think something is very wrong

Hi everyone, Not sure if anyone here will be able to help, but my anxiety is causing me to panic. I have gotten so many conflicting opinions about what's wrong with me right now, I don't know what to do. For context, I've been on Zoloft for 7 years now, I'm on 100mg. I've been completely fine on it until recently, when I accidentally missed 3-4 doses within a few weeks time. It has basically caused withdrawal symptoms for the last 2 weeks (constant panic attacks and high anxiety, severe nausea, internal shaking, headaches, muscle spasms, upset stomach). I have been taking it very consistently now since my missed doses, but I'm still having symptoms.
Some people here have told me to just wait it out, but others have mentioned serotonin syndrome, which is REALLY causing me to panic... any advice or reassurance would be greatly appreciated. ❤️
Also, I did CT withdrawal in 2022 (didn't know how stupid it was until it happened) from 200mg and went through 3 months of hell. Reinstated at 100 mg and have been fine on it ever since, right up until 2 weeks ago.

Hi everyone, Not sure if anyone here will be able to help, but my anxiety is causing me to panic. I have gotten so many conflicting opinions about what's wrong with me right now, I don't know what to do. For context, I've been on Zoloft for 7 years now, I'm on 100mg. I've been completely fine on it until recently, when I accidentally missed 3-4 doses within a few weeks time. It has basically caused withdrawal symptoms for the last 2 weeks (constant panic attacks and high anxiety, severe nausea, internal shaking, headaches, muscle spasms, upset stomach)
Some people here have told me to just wait it out, but others have mentioned serotonin syndrome, which is REALLY causing me to panic... any advice or reassurance would be greatly appreciated. ❤️
Also, I did CT withdrawal in 2022 (didn't know how stupid it was until it happened) from 200mg and went through 3 months of hell. Reinstated at 100 mg and have been fine on it ever since, right up until 2 weeks ago.

Hi everyone, Not sure if anyone here will be able to help, but my anxiety is causing me to panic. I have gotten so many conflicting opinions about what's wrong with me right now, I don't know what to do. For context, I've been on Zoloft for 7 years now, I'm on 100mg. I've been completely fine on it until recently, when I accidentally missed 3-4 doses within a few weeks time. It has basically caused withdrawal symptoms for the last 2 weeks (constant panic attacks and high anxiety, severe nausea, internal shaking, headaches, muscle spasms, upset stomach)
Some people here have told me to just wait it out, but others have mentioned serotonin syndrome, which is REALLY causing me to panic... any advice or reassurance would be greatly appreciated. ❤️
Also, I did CT withdrawal in 2022 (didn't know how stupid it was until it happened) from 200mg and went through 3 months of hell. Reinstated at 100 mg and have been fine on it ever since, right up until 2 weeks ago.

hey! i’m very much aware that i can’t take medical advice from strangers, but i’m desperate and need ideas on what to check for.
Basic info: 18yo female, 5”4, 85 pounds
I have been sick for ~2 years with no answers. My symptoms started as flu like symptoms and then just severe nausea all of it happened overnight. The nausea lasted 4 days and was so severe i could not eat or drink almost anything at all and ended up in the er. At the er they said everything looked fine, and sent me home with nausea medication. At this point I figured it must’ve been some kind of bug, even though it felt way different. I was still feeling very off two weeks after but I was able to go to school etc. Around a month later I got very sick again, and went back to the doctors. They, again, couldn’t find anything wrong. I kept having to skip school increasingly, and kept going back to the doctors just to get no answers. I felt malaise all the time, nausea was a daily thing, and i was fatigued. My stomach was also much more sensitive than before. I would try to eat out with friends or have sleepovers but would end up extremely nauseous, sweaty or with diarrhea. I eventually got so bad that i had to drop out of school completely, after almost passing out multiple times. I needed atleast three days to recover from one short school day. After that everything got worse.
My symptoms now include:
•nausea for 2 hours in the morning, so bad i can’t get up
•often dull pain in my upper abdomen after eating or drinking, following with terrible nausea
•nausea just all the time even without eating, so my baseline is always nauseous on some level
•early satiety and sometimes after eating i will feel extremely sick and full over 5 hours later
•excessive belching (but with a struggle to burp, so sometimes regurgitation occurs)
•exercise intolerance
•low grade fevers pretty much daily
•fatigue so bad that even talking makes me feel like i’m dying (i get dizzy and weak, run out of breath, my muscles twitch and the fatigue pretty much paralyzes me)
•orthorstatic intolerance (usually my heartrate goes from 60bpm to around 120bpm when i get up)
•low bp (85/55 and sometimes even lower like 75/45) that comes with dizziness sometimes
•headaches that feel like lighting shooting suddenly (usually on the left side of my head or left eye)
•diaphgram and ?spleen? fluttering (every once in a while)
•veins popping in eyes and burning when this happens
•super sensitive stomach (can’t tolerate fructose or any sugar, fatty foods, gluten, dairy, sweeteners)
•diarrhea and constipation
•occasional bad smelling gas
•yellowish pale-ish stools usually
•random joint pains and feeling like my entire body is inflamed and infected
•heat intolerance
•randomly cloudy pee and then normal again
Due to these symptoms i have now lost over 20 pounds.
———————————
Now when it comes to my current test results:
•bilirubin often a bit high
•wbc count consistently dropping since getting sick ~2 years ago
•almost every vitamin deficiency (i am on multivitamins and the levels are getting better, but b-vitamins and calcium don’t want to go up very well)
——————————-
in the past i had a parasite, but my parasite tests now are negative.
I have had a stomach ultrasound, gastroscopy (outruled celiac disease), blood tests and stool- and urine samples.
For some background info I’m hypermobile and we have autism running in the family.
If anyone has ideas what could be going on, please let me know, I’m desperate.

For context i had unprotected on the 11th with ovulation on the 13th and I am supposedly supposed to start on Saturday. I rarely to almost never have any pms symptoms near or on my period. So last Friday I started having nausea and didn’t think anything of it since it was very mild. I woke up on Saturday morning nauseated with with mild cramping. Since Sunday I’ve started to have more cramping, headaches , indigestion and lower back pain along with the nausea that’s started to feel more dull like motion sickness as of today. Yesterday whilst we were cooking for the holiday I became extra nauseous while smelling the meat cook and had to step outside for air. So I’m not sure if I’m just overthinking or if I could be pregnant.

1. Why am i writing this
   
2. What is it
   
3. the purpose of this technology
   
4. how it works
   
5. tips
   

Why am i writing this?
the purpose of this document is to raise awareness on the subject and provide a proper foundation of information to the public and those who may be targeted. These types of programs and technologies will become more and more common as time goes on and it may be difficult for some to get a handle on it without this information. This information is crucial in the early stages of exposure to this technology as it can help someone differentiate between schizophrenia, the voice of "god", a false conscience, an alien technology or any voice versus the actual technology being used on them. Having a trusted voice inside your head can be very dangerous and can have devastating effects on a person if they are being led the wrong way. Many dictatorship like countries have already adopted a very aggressive form of this technology, paired with their social values and strict policies it leaves millions of humans at the mercy and control of a small group of people. Behind closed doors this technology is at the forefront of government tools to use to control the population in a way that leaves them blameless.
what is this new technology?
This technology is an assortment of different directed energy weapons and a voice to skull technology that work together to project thoughts and hit the target with varying effects. The first one that most people will experience is a form of voice to skull which does exactly what it sounds like, it has the ability to project voices in your head and can be mistaken for one's "conscience" or the "voice of God" but is just a mix of human operator and conversational AI. This is usually accompanied by the same voice re-reading your internal monologue right back to you in real time. Directional voice is also commonly used, basically it sounds like someone is in the next room over or upstairs but this is just another illusion put in your head by the technology. This voice to skull is a very advanced form of conversational AI programmed with specific scripts to fit the targets life situation and the "programs" goal for said individual. The rest of the time its the actual human operator, its about 80% AI 20% Human operator. Just as they can beam outside voices in your head they can also “suggest” or “inject” thoughts that will feel like your own thoughts but will present itself as an intruding thought, yes they know how to make you think things without you even being aware. The "program" will also use an assortement of directed energy weapons (DEW) which can cause headaches, brain zaps, heart palpitations and chest pains aswell as nausea, tinnitus, very realistic hallucinations and paralysis. Another tool used is some sort of supressor which will essentially supress the electrial activity in the brain and can be turned up or down, this can cause you to feel very sleepy and if you give in then it can put you to sleep. These tools can be combined to create various effects for example, using the supressor while raising the heartrate can cause a form of sleep paralysis while you are sleeping. They can replicate almost all mental and physical health problems. Dreams are another field that this technology can manipulate with precision accuracy, dreams cannot be mistaken for anything but manipulation if you find yourself being targeted. There are hints of subconscious manipulation while you are asleep but there is not much information on this unfortunately. the program is a government level program therefore they will have access to suggest posts on the main social media’s that fits the targets situation in order to subconsciously adhere to the programs goal (instagram, Facebook, Meta apps) this fits the description for propaganda by repetition as they try to induce the illusory truth effect to double down on their goals for you. They are very well trained in psychological warfare and will use tactics like reverse psychology aswell as use/depend on cognitive biases against the target in tandem with all of these technologies.
the purpose
the purpose of this technology can vary depending on the target and the operator as well as which country it is happening in. there are a multitude of "programs" from research programs that aim to test new and existing methods and technologies on humans, this type of program is unlikely to be used on the civilian population as much as the other programs. Research programs will often leave its victims in a very disabled state often mistaken for severe mental and physical health issues. Re-education programs are used to control the population in a way to modify behavior and beliefs of the population to allign with the values and beliefs of the government that is conducting the program. Monitoring programs which are used to monitor persons of interest for potential criminal activity. People will typically fall into one or multiple programs. There is no way to tell how people are chosen for these programs.
How it works
I will begin by explaining how these different technologies work, in simple terms. The voice to skull technology essentially is a 2 way channel in which the individual and the operatoAI can communicate via thought. To achieve this, brain reading is paired with a form of microwave hearing. the way they read thoughts is the brain will give off specific electrical signals with each thought and action, they have algorithms that can decipher these specific brain signals and turn it into text which consequentially has given them a v2k word dictionary to refer to. the microwave hearing is done by sending electromagnetic energy to the skull which is then transduced by the cochlea and in turn enables the "hearing" of voices. The conversational AI is programmed with “Natural language processing” or NLP which is a field of artificial intelligence that focuses on interaction between humans and computers using language and what this means is it can interpret, understand and generate human language. This AI will talk to you 24/7 using this 2 way channel until a human takes over. This technology is also capable of thought insertion/suggestion and this will often present itself as very intruding thoughts that are abnormal to your day to day thought process but can be anything the program decides, Directed energy weapons can be classed into many subclasses, the ones i am referring to are the more subtle weapons meant for targeting, disabling and harming biological beings but i still have yet to understand how most of these work, any information missing here would be greatly appreciated.
Please note that the technology of today is more advanced then what is listed on these patents, its just to show you that alot of this was possible a very long time ago.
tips :
Here i will list a couple tips to deal with these programs and technologies altough there is no straightforward solution yet these will help.
Inform yourself on how it works, do alot of digging and verify the information with other sources.
music
Meditation
Exercise
Being outdoors
Staying off of social media.
Staying sober (very important)
Using the v2k’s natural language processing faults against it. The easiest one is sarcasm as it cannot detect sarcastic replies but there are many that i will be covering in another document.
Below i will include some useful links & patents
Here are some important patents:
US patent 4958638A (monitor vitals from a distance)
US Patent 20160375220A1 (Method to maintain peace through electromagnetic energy targeted to the brain)
US Patent 8049173B1 (this is what shows your location in real time)
US Patent 6470214B1 (voice to skull, assigned to U.S airforce in 1997)
Links
https://youtu.be/N02SK9yd60s?si=ONFisrO0ws7zuXgQ - James Giordano lecture about DEW, neuroscience
(https://www.reddit.com/emsurvival/) - survival guide
(https://www.youtube.com/watch?v=T501LHx0R_Q) - Interview
https://www.ohchr.org/sites/default/files/Documents/Issues/Torture/Call/NGOs/VIACTECAnnex.pdf) patent list (many of these are older versions of technology or just “ideas” compared to what we have today, its just to give you an idea that this did exist a long time ago and does today. Government science is always 20-30 years ahead of conventional science.
https://www.youtube.com/live/LCYH_K850Lw?si=P_kVPnJdCUSvXc35 - United states homeland security committee on AHI’S

So, I pretty much haven't had 1 single migraine or headache since starting a extremely low carb meat-heavy version of keto diet this past March. I only drink water, eat eggs, meat and sometimes eat macadamia, hazel nuts and dried seaweed. Not only did I lose weight, but my lower back and hip pain stopped immediately and I pretty much always feel good and have a good mood.
I've suffered from migraines for years probably since highschool around 15 yrs old, I'm now 40(F). I would have liked 5-7 bad migraines a month. My symptoms typically include painful throbbing on my left side, especially in the temple but all the way to the base of my neck or can be all over...it comes with a side of nausea, light sensitivity, chills and teeth chattering, slow heart rate and pounding heart. Sometimes I'd get Aura and vomiting, but usually not.
I have tried nortriptyline and amitriptyline as a preventative...couldn't take the side effects of limb numbness and severe dry eyes and mouth at night. I tried Sumitripan and Rizatriptan for migraine attacks....they don't work consistently at all and sometimes the symptoms they caused me are as bad as the migraine itself....last time I took Rizatriptan I felt I was going to die, seriously.
Things that helped me: 1) Carnivore based diet 2) Drink a lot of water, nothing else 3) Wearing pink glasses while I work on the computer and I wear dark pink sunglasses outside, always walk with a large sunhat outside. 4) I bought a forehead TENS device and wear that for an hour when I would feel a migraine coming on....it helps better than medicine. (Mine is a MYND device, from the UK, just like Cefaly but cheaper!) 5) DO NOT have artificial sweeteners, causes me a migraine every time.... especially those Zero Sugar carbonated beverages.
Hope this info helps someone!

Feel Free put me in the hospital twice during my last week of use due to vomiting, blood pressure, and heart rate.
Some quick details about me, since some of it is a little unique and could help other people with similar attributes:

• I had gastric bypass 12 years ago
• I get all of the side effects from medications and other drugs, due to bypass
• My body is more susceptible to physical addiction, due to bypass
• Liquid based drugs/meds/alcohol hit faster and stronger but the effect is shorter, due to bypass
• Used to abuse alcohol

Usage details:

• I started using FF in December around the holidays
• Quickly ramped up to using 5-6 a day since Feb
• I got caught up into the loop of "I feel like shit on it, I feel worse off of it."
• There were times when I got upwards of 10 a day and one day where I had 16, but most of the time I needed 5-6.
• Never used Kratom or Kava before FF

Quitting Details:

• Moved to Kratom Only using capsules
• The first 3 days, I took as much as I wanted to try and keep withdrawals away which was a mistake and caused side effects like nausea and temperature fluctuations.
• On day 4, I backed off to try and get on a schedule and to see how much I really needed.
• By day 7, I could take 7 g of capsules upon waking up, 7 g before lunch, and 7 g before dinner.
  • If I felt any withdrawals I would take 4 g, if I felt side effects I would back off until I felt withdrawals.
• I have started to taper the Kratom by 1 g of caps per serving, every 1 week
• I am starting week 3 of the taper and have not had any debilitating withdrawal since day 2

Side Effects during ff use:

• Lack of hunger
• Weight loss (35 pounds in 4 months)
• Occasional vomiting from overdosing
• Yellowish and dry skin
• Cracked lips, inner cheek damage, and numbed sense of taste
• Exhausted and sick feeling
• Would crash at night
• Racing heart beat
• Indigestion
• General malaise
• Rare Brain Zaps/Exploding Head Syndrome (would get this when I took SNRIs, combatted by starting to take SNRI again)

Side Effects during quitting ff using Kratom (Day 1-4):

• Body temperature fluctuations
• Cold sweats
• Mild headache
• General malaise
• Sweating after eating
• Brain Zaps/Exploding Head Syndrome in the middle of the night (every night)

Side Effects post FF with Kratom Only (Day 5 to Current):

• Rare body temperature fluctuations and sweating
• Occasional Brain Zaps/Exploding Head Syndrome middle of the night
• Occasional nausea from overdosing
• My skin is flaking off still, but looking so much better.

Other Notes:

• I feel a million times better, my quality of life is SIGNIFICANTLY BETTER
• I thought I was going to die during my last 2 days of ff use
• Kratom caps are way cheaper
• I can function perfectly well at work and as a parent and probably could have during day 1-3, if I had not taken using ff to the brink of death and if I had switched to Kratom earlier, do it ASAP.
• I was already in a ff taper trying to quit when my health took a turn and my usage bumped back up on the last 3 days trying to fix the sick with more ff.
• My taste has returned to normal
• I could eat normal again with 5 days of quitting, magnesium seemed to help
• I did 2 weeks of Prilosec starting day 5
• Join kratom and quittingkratom to learn about this beast and how to get off of it as well

Best of luck to anyone trying to quit, find a way to get off of FF as soon as you can. I plan to continue to taper off of Kratom and then taper off of the SNRI. If you have any questions or clarifications please ask here.

Hey folks! While I wait for my neurology referral, what else should I try to rule out/tick off the list of things they might want me to do?
I’m 24F, constant daily headaches for over a year with brain fog, nausea, vertigo, occasional visual aura, and some other symptoms. I drink 2-3L of water daily, have stopped drinking alcohol, cut out caffeine, quit smoking, and somewhat improved my diet. I take CoQ10, Vit B1, turmeric, cod liver oil, feverfew, magnesium, and a multivitamin. I’m not as active as I’d like to be due to other disabilities and I’m well aware I’m fat, so I look forward to that conversation. Started a headache diary, monitoring BP and pressure for it.
But what else might a neuro want me to try that I could get a head (lol) start on?

Hi all, I just need to share with someone about how I feel. (Not Diagnosed for H.pylori but my experience suspecting)
For the last 6-8 months I noticed my stomach has felt tight, a lot of pressure under my ribs it feels like I've eaten 20 massive meals in one go even if all I manage to eat is a yoghurt or a protein bar. Dealing wit constant nausea, dizziness and feeling light headed in major waves. Ive been suffering with nausea since I was 16 and im 22 now.
Started off with bloating and then the sudden and constant burping started, thought it was reflux or indigestion as my partner suffered from chronic reflux.
I got assessed, doctor assumed it was stomach ulcer and gave me tablets go treat it, said it could be H.pylori but because of my age it's "isn't likely" sent me to get blood tests and ultrasounds done.
The antibiotics didn't help, they provided a little. It of relief but it felt worse after the treatment. Ultra sound showed nothing and the blood test that were ordered they didn't even bother to test for it despite it being requested.
Getting worse now, wake up and first thing in the morning im nauseas, throwing up nearly everyday, constant fatigue, muscle weakness, i can't eat my heart constantly palpatates, I can't walk in a straight line some days I get such bad vertigo. Last few days is constant headaches, sometimes I can't keep water down, I can't focus, I get so sick I can't go to work or I have to go home and its horrendous.
I'm so scared I'm going to lose my job because I've been so chronically sick these last few weeks and months because it's been so debilitating.
Took myself to the hospital the other day because the nausea and headaches and vertigo and the tension in my stomach was so bad my ribs hurt, I felt like I couldn't breathe my heart was racing. I hate going to the hospital but I was so desperate I needed help.
The doctor who was assigned to me didn't even bother trying to help me. I felt so weak I was falling in and out of conciousness I felt like I was going to vomit or fai nt in the bed.
Didn't feel my stomach, didn't do any tests, described all my symptoms and just kept dismissing me saying it was because I have stress and that it's "just reflux" he said to me and I quote: " it could he H.pylori, but it sounds like you just have reflux, because it's been constant for to long we can't help you. I'm to busy"
Gave me reflux medication and kicked me out. I cried in the car on the way home.
Had to go home tonight from work because I felt so sick I thought I was going to pass out, Been having fevers and chills, sweating, headaches.
I've always struggled with gaining weight, mainly due to living with a severe mental health disorder and partly due to my parents relationship with food when I was growing up has formed very terrible and potentionally life threatening habits.
I'm losing so much weight I'm nervous that if I don't grt treated soon not only will it get worse but im going to end up in a ward with feeding tubed down my throat.
I've dropped so much weight that I'm now sitting at 46kg, dropping 5kg overnight, (22yrs, Male, 173cm in height)
I broke down and cried again today, the sickness is getting so much, it's destroying my life it's ruining my work, it's causing me so much anxiety and even more stress.
I can't eat, I have no desire to, the thought of eating stresses, it makes me feel sick. Nothing is appetising and I judt Don't feel hungry anymore.
I feel lost, I dont know what to do. The doctor I see flies interstate once a month (I see them cause I need certain medication) and every other doctor in my city is either not taking new patients or the waiting times to see a doctor as a new patient are around 2 months.
I can't keep living like this it's hell. It's hell being told it's just anxiety and stress, it's hell being told "it could be cancerous, but i really think it's just reflux" I'm tired of feeling guilty and stressed about being so sick I have to miss work or go home early and then spend more money and even more stress trying to organise a medical certificate for work.
I've probably spent around $350+ in medical certificates for work just because of this bacterial infection. Not including the constant repeats and refills for nausea tablets because doctors only every give me a maximum of 10 tablets at a time and some days are so bad I need 2-3 just to get some relief from the constant nausea and dizziness.

A bit of background: - In January of this year, I began to feel a shooting pain on the right side of my head. My family physician suggested it was likely radiculopathy (pinched nerve) and it would likely resolve itself within 8-12 weeks - In February, I hit my head on my truck tailgate pretty hard. Didn’t suspect anything of it as I wasn’t experienced symptoms of a concussion - I feel to Vegas a few days later and began to experience excruciating pain behind my head (base of skull & neck) - Since then, the pain has been unrelenting. It was causing me to sleep 2-3 hours a night throughout most of March & April
Treatment to date: - I’ve seen osteopaths, naturopaths, massage therapists, acupuncturists, massage therapists & psychologists. All treatments have provided little reprieve - I’ve been seeing a neurologist. Through him, I’ve managed to have MRIs of the cervical spine and brain (with contrast) done. We’ve also done CT scans. Nothing of any consequence has been found - I’m currently on 10mg of nortriptlyne daily which has somewhat managed pain but has not freed me of side effects I’ve been given Ubrelvy as a migraine abortive. He’s been treating these as chronic daily migraines - I’m not convinced as the pain has been unrelenting and while I sometimes feel as though I have a tension type headache, I don’t usually experience other symptoms I’d associate with migraines (nausea, light sensitivity, etc?
What now? - I’ve been prescribed Ajovy - and will be giving that a go despite my lack of confidence it’ll address the fundamental issue - I continue to see a psychologist - many around me have suggested that this is caused by life events/stressors which are now manifesting physically (although, I don’t know how to solve for this…)
I may be grasping (as I’m sure many due when dealing with Chronic Pain), but has anyone else ever found themselves in a similar position? Anything that helped?
I think my biggest struggle is I could mentally worm around a known, diagnosed issue that we were working to treat (even if there was no end in sight). Right now, I feel like I’m chasing and trying to treat a ghost.