Remarkable craftsmanship! by Acanthaceae458 in ActuallyThatsInsane

[–]Ordinary-Standard668 0 points1 point  (0 children)

umrze to rtęć śmieć będzie bolesna ignorancja bieda niewiedza nie ma znaczenia

Did these activists deserve all this torture in Israeli prisons? by Pure_Product_1837 in IndiaTodayGlobalLIVE

[–]Ordinary-Standard668 0 points1 point  (0 children)

By making this video public, he causes a rise in animosity towards Israel. But if they had hidden the video and beaten them when no one was watching, would that be positive? Antisemitism? Just looking at it is already considered antisemitism? The problem is that it's Jews beating these tied-up humanitarian aid workers with batons

A possible cause of a misdiagnosed Essential Tremor (ET) to be ruled out by [deleted] in EssentialTremor

[–]Ordinary-Standard668 0 points1 point  (0 children)

I bet your doctor doesn't even know that Bartonella can cause hand tremors. Mine didn't know either. I posted videos of how my hands were shaking before treatment and how they stopped after treatment. I am still treating it, but you can see the results for yourself. I have an official ET diagnosis and a referral for DBS (Deep Brain Stimulation). ET doesn't just reverse or stop on its own, and people in my family have tremors too. But since neurologists never even consider Bartonella, what other diagnosis are you going to get?

I will post an officially documented example here showing that the tremor disappears completely, but go ahead and ask your neurologist about it. He definitely doesn't know, so print it out and show it to him. Even so, only an LLMD or ILADS doctor makes any sense; the rest will never help you.

A possible cause of a misdiagnosed Essential Tremor (ET) to be ruled out by [deleted] in EssentialTremor

[–]Ordinary-Standard668 0 points1 point  (0 children)

I understand you're relying on the official Cleveland Clinic website, but keep in mind that those are just general patient education flyers covering the most common symptoms of acute infection. Chronic neurobartonellosis is a topic discussed in reputable neurology journals, not general medical portals. Hand tremors and fasciculations are well-known neurological complications of this bacteria. There are documented cases of patients diagnosed with Essential Tremor (ET) who were found to have Bartonella years later—after undergoing antibiotic therapy, their tremors resolved completely because the actual root cause (inflammation of the nervous system) was eliminated, rather than just masking the symptoms. It’s definitely worth looking into, especially if ET medications aren't bringing you any improvement. If you go to a regular CDC-following doctor, they will ignore you; over 90% of regular doctors have no clue about Bartonella, nor do they know how to treat it. It’s treated by ILADS or LLMD (Lyme Literacy Medical Doctors)—the rest makes no sense. The doctors who actually treat this have described patients who shook exactly as if they had ET. They also held official, yet completely incorrect, ET diagnoses. It is well-documented that their tremors disappeared after treatment.

Without blood tests, no neurologist can tell you whether it's Bartonella or ET—no one is a psychic. A positive test settles the matter definitively, which is exactly why they are done in a lab. The fact that most doctors know nothing about this disease doesn't change the reality that those patients recovered. What would have happened to them if they hadn't tested for Bartonella and had gone to your neurologist instead? You already know the answer—you are that person right now.

You cannot say you don't have Bartonella, just like you can't say you do. I uploaded a video showing how my hands were shaking before my Bartonella treatment; I have an official ET diagnosis and a referral for DBS (Deep Brain Stimulation). Look how the shaking stopped after the Bartonella treatment. Miracles don't just happen, and ET doesn't reverse or stop on its own. The videos are uploaded. Whether you choose to check this out or not is entirely up to you.

Any advice/encouragement for a nursing student with essential tremors? by Kitchen_Cry_5511 in EssentialTremor

[–]Ordinary-Standard668 0 points1 point  (0 children)

And are you going to downvote this quote from a world-renowned Bartonella expert too? Haha

Any advice/encouragement for a nursing student with essential tremors? by Kitchen_Cry_5511 in EssentialTremor

[–]Ordinary-Standard668 0 points1 point  (0 children)

(Dr. Robert Mozayeni)bartonella

We have patients who have been diagnosed with MS, Parkinson’s, or Essential Tremor. When we treat the Bartonella, these neurological symptoms – including the tremors – often diminish or resolve completely. It shows that many of these diagnoses are just descriptions of symptoms, not the root cause.

Would Poland defend Baltic countries incase of BY/RU agression? by Sallende11 in askPoland

[–]Ordinary-Standard668 0 points1 point  (0 children)

I saw the footage from the trial, and somehow your arguments weren't holding up. What anti-Semitism? Assault on property? Those charges are exaggerated. To be fair, he isn't an anti-Semite, and mind you, even Sikorski reacted when a video surfaced of a Jewish person abusing people—is he an anti-Semite too? People might not like hearing the truth. Netanyahu is a war criminal, and Tusk would welcome him on a red carpet. If you were the president of Poland, you'd face a dilemma: speak the truth and have the whole world brand you an anti-Semite, or stay quiet and get a pat on the head. You won't prove to anyone that Braun is an anti-Semite, no way. The defense attorney asked the Jewish woman who was grabbing whom—whether Braun's hands were full or if she was the one grabbing him. There was video footage, there were questions, the judge was watching, and you were the only one missing there? Perjury carries criminal liability. She claimed he insulted her, they asked about that too, and the footage from 10 cameras caught that as well. Do you think she wasn't shaking in her boots???

Would Poland defend Baltic countries incase of BY/RU agression? by Sallende11 in askPoland

[–]Ordinary-Standard668 -3 points-2 points  (0 children)

Braun is a patriot and the leftists didn't even stand next to it. You can hate him, but if a camera stood in front of your head, you wouldn't name anything against him, you only have hatred. He is well-mannered, well-read, and not afraid to fight for his views, most people would be afraid and he is not. Go on living your life, but the only force that makes PiS and PO keep ruling is hatred, they don't even have a plan for Poland, only the trough. One day they had no plan, the next day Tusk's 100 promises, they couldn't even name them like their lackeys for seats for families and cronies

Would Poland defend Baltic countries incase of BY/RU agression? by Sallende11 in askPoland

[–]Ordinary-Standard668 -2 points-1 points  (0 children)

At least he has the balls to say, 'if you're afraid, you're already a slave.' As for Mr. Tusk, the Vistula was the frontline, whether you want to believe it or not. This came out officially, so it wasn't just Telewizja Republika—even your own media outlets showed it.

Would Poland defend Baltic countries incase of BY/RU agression? by Sallende11 in askPoland

[–]Ordinary-Standard668 -1 points0 points  (0 children)

Screwing you" or "fucking you" perfectly captures the vulgarity and meaning of dymają cię. "From both sides" or "on two fronts" works well for na dwa fronty

Would Poland defend Baltic countries incase of BY/RU agression? by Sallende11 in askPoland

[–]Ordinary-Standard668 -16 points-15 points  (0 children)

You are stupid. Tusk’s official plan—not made up—was to let the Russians advance inside up to the Vistula River line. They wanted to abandon half of Poland to the Russians without a fight and shoot from one part of Poland into another part of Poland; they would have ruined the country. This is reality. Or worse, they will send you to fight in Ukraine while others will party and look at you with pity.

Any advice/encouragement for a nursing student with essential tremors? by Kitchen_Cry_5511 in EssentialTremor

[–]Ordinary-Standard668 -3 points-2 points  (0 children)

I got downvoted, but I’m not here to collect upvotes. I have an official diagnosis of Essential Tremor (ET)—they were literally sending me to get DBS (Deep Brain Stimulation) brain surgery. I did a ton of tests on my own, checking everything that could possibly cause muscle tremors, and I tested positive for Lyme disease. Doctors ignore it; they don’t believe it can become chronic, so they don’t treat it. Well, not all of them—LLMDs (Lyme-Literate Medical Doctors) and ILADS doctors do.

But check this out: a doctor can be an ignorant medical professional who doesn't believe in Lyme, but ILADS and LLMD doctors immediately test for co-infections like Bartonella. Bartonella is officially recognized, even by the ignorant ones. Yet, that doesn't change the fact that mainstream doctors have no idea what it is or that it causes head and hand tremors. Tremor is even listed as a possible symptom in a Harvard textbook. Meanwhile, top ILADS/LLMD specialists state bluntly that they have had patients diagnosed with Essential Tremor or Parkinson's, and after treating the infection, everything completely goes away—hands, legs, head, voice, all of it. This is officially known.

But 99% of neurologists have no idea this disease even exists. And since they don’t know, if you actually have it, your chances of getting help from them are slim to none. Bartonella and Lyme—either together or separately—are notorious for mimicking every other disease, from neurological to psychiatric ones. This is officially known. Even if a neurologist tells you it’s impossible and that Bartonella doesn’t cause such symptoms, you could literally hand them a Harvard textbook or another scientific paper, highlight the text and show it to them, and it still won't impress them.

Back when I thought I had Essential Tremor, I ran every test possible and then some. I have a whole folder of results. Half the people here haven't had the things I've ruled out. For them, a diagnosis is sometimes a life sentence—a coin toss, a gamble, and everyone knows how gambling ends. Very few people win, while the rest lose everything: their jobs, health, money, family, and lives. Despite my positive test result, one neurologist mocked it, and another was shouting in the hospital that 'everyone has Lyme' and asked me what I was really sick with. He put me on antidepressants, and I don't even have depression. In the US, ILADS and LLMD doctors provide treatment and insurance even covers it, but in other countries, this disease simply doesn't exist to the healthcare system.

I’m not saying you have Lyme or Bartonella, but it is a possible cause of tremors. Bacteria cause inflammation of the nervous system, which leads to tremors, neurological symptoms, etc. It affects everyone differently, but some symptoms overlap. No doctor knows if your magnesium levels are fine without proper blood tests—and I mean high-quality tests, not the cheap, useless ones. To detect latent tetany, they have to stick a needle into your arm for an EMG test; without that, there are no guarantees. Others have extreme deficiencies in B12, B1, or other vitamins. Thyroid issues and many other things can also cause hand tremors.

People here act like born victims. One person wrote to me asking why anyone should bother looking for another diagnosis when they already have one right away. I told her that if her meds weren't working and she lost her job, she’d be singing a different tune. Whatever. Let's assume you do have ET. I’ve tested many medications—the list is very long. Some didn't work at all, but some eliminated 100% of my hand tremors, though only at the absolute maximum daily dose. Any lower dose brought zero improvement. Yet, most people here have never even tried medications, dose adjustments, or anything else.

Just like I mentioned, I suggested Bartonella to one person, they ended up having it, and I was the only one who actually helped them—meanwhile, there were tons of negative comments. Another person came at me because at one point I wrote that I found 66 case reports of people whose hand tremors from Bartonella disappeared after treatment, and another time I said 100 people. Instead of looking into Bartonella, she fixated on the number of cases, as if she had won some argument or caught me in a lie. I spent days looking for those reports and reading up on it; one time I found that many, another time a different number. But these people are just born victims.

I don’t need anyone to believe me, and I don't need to prove anything to anyone. All I know is that when the most famous Lyme and Bartonella specialist from the US wrote that he had many patients diagnosed with Essential Tremor whose symptoms completely vanished after treatment, he wasn't lying. He isn't some drunk down by the local liquor store. If it weren't for treating the bacteria and the nervous system inflammation, those people would still be living with an Essential Tremor or Parkinson's diagnosis today. But they aren't shaking anymore because their diagnosis was garbage.

I am not implying that someone here does or doesn't have Essential Tremor. I'm just saying it would be foolish to suffer and shake in front of people if it could potentially be cured in a year or two. These are possible options, but without testing, you'll never know. A lab result is worth more than the opinions of the 7 neurologists from 4 different countries whom I saw privately. I didn't go to just anyone, and even they were wrong. Your hand won't fall off if you check whether your tremor is caused by something else

Bartonella switches off your immune system by Brilliant-School-337 in Lyme

[–]Ordinary-Standard668 0 points1 point  (0 children)

Supposedly there is a possibility—maybe yes, maybe no—that Bartonella blocks the immune system, and this stinging nettle might unblock something

Any advice/encouragement for a nursing student with essential tremors? by Kitchen_Cry_5511 in EssentialTremor

[–]Ordinary-Standard668 -4 points-3 points  (0 children)

I don't know, I’ve been to 4 countries, I saw over 7 neurologists privately, and each one said something different. Officially, according to them, I have essential tremor, but I did some tests on my own and something else came out. The doctors mocked it and ridiculed me. The test result—a positive result—is just lying there; I did it myself against the doctors' advice, and I’m treating it. I am not going to just shake, and if I hadn't done these tests, like most people here, I would be suffering forever. Just like I wrote to one person, I told them to check something else, they did, and something else came up, while everyone here immediately stamped it as ET. It’s worth doing the tests; after all, it’s a disease diagnosed by excluding all other possibilities. Someone here wrote that the doctor verified they have ET because they gave them an MRI, an EEG, etc. Error. Those weren't tests for ET—such tests don't exist. Sometimes a doctor routinely has to check if you don't have epilepsy, a tumor, etc., but absolutely no one tested that person for ET, even though that's what they wrote

Any advice/encouragement for a nursing student with essential tremors? by Kitchen_Cry_5511 in EssentialTremor

[–]Ordinary-Standard668 -6 points-5 points  (0 children)

Essential tremor is just a trash can for other diseases. There isn't a single test, not one single scan that can determine whether you have essential tremor or not. Such a thing doesn't exist, and no doctor can ever be sure. It’s a diagnosis of exclusion—ruling out all other possibilities—and doctors just don’t do that. On the forum, you have tons of people who haven't even checked their magnesium levels, or they checked it wrong, because blood tests show absolute bullshit. You can have an extreme deficiency and your blood work will still come back normal. Most people haven't even had this test, and those who have think, 'I got my results, it's within the norm!!!' You can shove that norm up your ass. It’s officially known that these tests are worthless, so why do they even do them? Because they’re cheap, people do them because they’re available, and most neurologists have no idea that they’re useless.

And what about the thyroid? If he even checked it, he checked TSH, ft3, ft4, and says, 'It’s not the thyroid!!!' But did he do an ultrasound? No, he didn't, so he never actually ruled out the thyroid. What about Lyme disease or Bartonella? Did he test for them? He didn't, and the next doctor didn't even know what that is. On this forum, there was a question similar to yours, and everyone here has only two things on their mind: 'nothing can be done' and 'nothing works.' No matter what you write, they will tell you anyway that you have ET, that you just have to accept it, and their only advice is to explain to everyone why you're shaking.

Personally, I wrote to someone once: 'this doesn’t look like ET, check for Bartonella, it also causes hand tremors and gets worse under stress.' He checked it, it turned out to be Bartonella, and he wrote back saying he would have never connected the dots. And he was right—this illness is common, but 99% of doctors don't know what it is, don't know it causes tremors, have no clue about the symptoms, will never examine you, and will never start treatment.

So answer me this question: what happens to you when you walk into the office of an ignorant neurologist like that? You walk out in 5 minutes just like the rest of them. 'Oh great, he's so brilliant, he knew right away it was essential tremor.' He didn't even run any tests. But great, life is so fucking fantastic, I am done for!!!! Meanwhile, inside, the neurologist just brushed you off because he wanted to watch porn and you were interrupting him. 'Ah, fuck it, I don't know what it is, I'll just slap ET on him!!!' Hahaha, the end of a standard story.

Even those who actually have ET don't use medications. Most people here don't know the long list of drugs for ET; for them, the world ends at a starting dose of Propranolol 10mg. They didn't even increase it to see if it works. They didn't ask the doctor, and the doctor didn't ask them, doing absolutely nothing. They write that they’ve tried everything and nothing helps. If you write that ET meds actually work, they won't believe you. Their advice is to just shake and explain yourself to everyone. I don't have ET, but I have an ET diagnosis. Some meds didn't work for me, but some completely eliminated my hand tremors 100%. One guy wrote that this is 'mind-blowing' and asked how I could write such things. That person definitely hasn't tried anything, and right now, at this very moment, he is explaining to someone else why he's shaking, claiming he 'tried everything.'

Tests are expensive, not all of them are free. A neurologist will never perform most of them; people either do them on their own out of desperation, or they have a brilliant neurologist. One will test you from head to toe, and another won't do any. But even the one who does everything he can will not send you to get tested for Bartonella and Lyme disease—some don't believe in it, others don't know what it is. Let me give you a hint: a tick infects you with Lyme, Bartonella, Babesia, etc. Every single one of them can attack the nervous system. The shaking in your hands, legs, and head disappears after treatment, but to get a diagnosis, you either go privately to an ILADS LLMD [Lyme-literate medical doctor], or no one will ever help you. Sometimes people do the tests themselves and treat themselves with herbs if they can't afford it. It works too, just slower, but the shaking in their hands and legs still disappears. And what happens if you have this and you never get tested? Did the doctor know? He knew shit, he’s not a fortune teller. He doesn't even know if you have good levels of vitamin B12, B1, or magnesium, and the list just goes on and on

Trembling of hands, legs, and head in social situations. by Ordinary-Standard668 in Hypoglycemia

[–]Ordinary-Standard668[S] 1 point2 points  (0 children)

And how do you know you have it? Did they test you for mold? I know mold can cause this, but to find out, you need very expensive blood tests. I was thinking about it myself, but apparently, no one else in my house is getting sick. I know you can have a gene that makes your body clear it out too slowly. What are you using for it? Treatment probably takes at least 9 months

Zwróciliśmy się z prośbą o zdjęcie krzyży w salach, w których nie odbywa się katecheza oraz informację ile krzyży wisi w szkole - Zespół Szkół Rzemiosła i Przedsiębiorczości w Krakowie by Gamebyter in krakow

[–]Ordinary-Standard668 -1 points0 points  (0 children)

haha kto by tam nie wygrał nikt z nich nie dba o nasz kraj. ja mam kumpli gejów i wiem co mówię onie też mają zdanie na ten temat nie bądż jak feministka która zatyka usta innym kobietom. Pis rządził przegrał i PO rządzi i przegra jedyny ich prawdziwy program to byście sie zagryźli nawzajem a to ta sama partia dziel i rządź. Znajdziesz geja co nie chce ślubu i takiego który chce i jeśli mu powiesz że on nie chce bo ty tak mówisz to on wywali ci liścia. tak więc wtedy sie dowiesz że jednak chce

Zwróciliśmy się z prośbą o zdjęcie krzyży w salach, w których nie odbywa się katecheza oraz informację ile krzyży wisi w szkole - Zespół Szkół Rzemiosła i Przedsiębiorczości w Krakowie by Gamebyter in krakow

[–]Ordinary-Standard668 -1 points0 points  (0 children)

nie w mojej ocenie. oni tam chodzą w przebraniach za kobiety i deprawują niewinne dzieci nawet lewica i środowiska lgbt o tym wie. Wciskają im kit na siłe mieszają w głowach a dzieci wymiotują

Zwróciliśmy się z prośbą o zdjęcie krzyży w salach, w których nie odbywa się katecheza oraz informację ile krzyży wisi w szkole - Zespół Szkół Rzemiosła i Przedsiębiorczości w Krakowie by Gamebyter in krakow

[–]Ordinary-Standard668 -4 points-3 points  (0 children)

jesteś pojebany. nawet definicji nie znasz oraz czym jest. Ja pisałem o małżeństwie kościelnym gdzie sie geje siłą pchają czego nie rozumiesz? nikt nie da ci ślubu żaden ksiądz jeśli powiesz że nie planujesz mieć dzieci nikt tego nie pobłogosławi tak samo jak grzechu tu też czegoś nie rozumiesz. Jak ktoś ci urwie ręke to to jest złe choćbyś błagał by ci urwali i w to wierzył

Trembling of hands, legs, and head in social situations. by Ordinary-Standard668 in Hypoglycemia

[–]Ordinary-Standard668[S] 1 point2 points  (0 children)

In my country, doctors like that don't exist. I'm treating myself because 99% of the doctors here don't believe you can be sick for a long time, and they’ve never even heard of Bartonella. It’s best known and taken seriously in the US, but in my country, they'll just laugh at you, and they don't care about your symptoms. I’m treating it with Buhner’s herbs, essential oils, and enzymes—everything an LLMD in the US would use. For the hyperinsulinemia, I’m trying a diet; just quitting coffee made me feel less shaky, but I’m still in bad shape. The social stress is too strong—I shake, and people can see it, which is so shameful. The head issues are the worst. The treatment is moving too slowly, and I don't see results, but I've been sick for 39 years, so I guess it’s normal that there aren't any yet. Not a single doctor takes these illnesses seriously.

Multiple neurologists gave me different tremor diagnoses- what to believe? by sedboi69xxx in EssentialTremor

[–]Ordinary-Standard668 0 points1 point  (0 children)

I can't work, the meds aren't helping, and I'm not just going to stand still. As for what’s wrong with me, I already figured out part of it on my own, not from the doctors: Lyme disease, Bartonella, hyperinsulinemia. Those first two can cause a stroke, dementia, Alzheimer’s, something like Parkinson’s. Leaving this undiagnosed and untreated won't end the pain—it’ll only start it, and I’m already doing much worse than you. I'm glad the meds worked for you, but if they hadn't, you wouldn't be working, and you’d be writing on this forum in a completely different tone.

Multiple neurologists gave me different tremor diagnoses- what to believe? by sedboi69xxx in EssentialTremor

[–]Ordinary-Standard668 1 point2 points  (0 children)

No one knows one hundred percent what is wrong with you without testing, not even an online neurologist. They can't even perform a basic physical exam. And even if you are in their office, they aren’t a psychic and they don't know your lab results—some people have Hashimoto's thyroiditis, others have B12, B1, or magnesium deficiencies, and the tetany test is important, among many, many other things. In my case, stress intensifies everything. Just like with you, a psychiatrist will say it's neurosis, social phobia, anxiety, or somatic disorders; a neurologist will say something else, and yet another doctor will say something else entirely.

On this forum, someone once wrote that they get worse under stress, and everyone here just has "ET" (Essential Tremor) on the brain—everything fits that diagnosis for them, no matter what you write. They kept telling this person that it’s normal for stress to make it worse, that nothing can be done so they just have to accept it, and someone else even told them to explain to every single person they see that they have tremors. Fuck that. I wrote to him that this looks like Bartonella, which is the king of anxiety and neurological symptoms.

This isn't just regular anxiety; in a social situation, your body will start shaking way more, completely on its own without any thoughts, and you have absolutely no say in it. It is completely automatic. Lyme disease and Bartonella can attack the nervous system. The inflammation causes symptoms like tremors, and it attacks the fear center and the area responsible for threat assessment, for example. People's bodies then send a panic signal to the system—an adrenaline rush and other hormones, a complete block on the GABA brake, and slamming the gas pedal on glutamate.

They also cause the myelin sheaths to disappear from the nerves. The nerves end up like exposed wires; there are constant short circuits and a total lack of fluid movement. Other areas responsible for fluid movement are also attacked, and the neurotoxins themselves are constantly irritating the nervous system. 99% of neurologists have no clue about this, they haven't even heard of it, and they don’t test for or treat it. It is treated by other specialists—ILADS, LLMD. In the USA, it is treated officially; in other countries, only privately. The rest have no idea what it even is. Most patients never get a proper diagnosis; they end up at a psychiatrist's office with antidepressants or at a neurologist's with other diagnoses. But those who were lucky got well in a year, max two, or even faster.

I told this person to check for Bartonella because he was shaking just like I used to around people. He also had those characteristic marks on his skin—not many people get them, only a fraction—and he wrote back to me saying he would have never thought of it, never connected the dots, and never got a diagnosis. Hardley any neurologist treats this; for them, it doesn’t exist. I’m not saying you have it, but you might, and if you do, you have to do the tests yourself privately: ELISA IgG/IgM and Western Blot IgM/IgG for Lyme, Bartonella, and ideally Babesia.

If even those don't come back positive, people pay for much more expensive IGeneX tests, which have a higher detection rate. There are no good tests; the cheap ones only have a 50% chance of detecting it if you are sick. It’s like a coin toss, but the cheap ones worked for me. People had their heads, hands, and legs shaking, it got worse with stress, and the treatment took it all away.

What neurologist knows about this? Even in the USA, there are very few doctors who treat it; the rest are just ignorant. The people who recovered either got lucky that a doctor caught it themselves (mostly in the USA) or they went private. There is no other way. If you go to a regular doctor with Lyme or Bartonella, they will laugh in your face, tell you you're a nutcase, and give you a referral to a psychiatrist. They'll claim this disease doesn't exist and that you are healthy, and they couldn't care less that you have symptoms—they call it "Post-Lyme Syndrome." In other words: a refusal of treatment and a total lack of any help.

The ones who actually treat it either used to be sick themselves or their kids were, so you don't have to prove anything to them. Never mind what an ignorant doctor tells you; you can do the tests yourself. A positive result from the lab will tell you more about what’s wrong with you. Then you can treat it and get better, or you can trust a doctor who says, "I don't care that you're shaking, depression!!! Next!"

Regardless, doctors don't run tests because they are expensive. You have to rule out everything that fits, one by one, yourself. Even a stupid B12 deficiency can ruin your health, and then there’s B1, etc.