A mi me hicieron estudios porque tenia sintomas de un infarto por una droga que probe recreativa como le dicen , y resulto que estaba bien, con el tiempo ya no podia ni caminar, me dolia el pecho, sentia ansiedad, mareos, distorsion, me hice un estudio de angiotac coronario, sali perfectamente , me medicaron, pero no estaba dando resultados, me daba dolor de pecho y corria a urgencias, fui como tres veces en diferentes tiempos, y no encontraban nada, que estaba sano, me dieron nuevo tratamiento, pero no funcionaba, pague otro cardiologo y le lleve mis estudios, me sentia muy debil esa vez , me reviso me dijo tu maquina suena muy bien pero lo que tu tienes y estoy muy seguro es un espasmo coronario, te recetare diltiazem, al momento de tomarlo, me senti muy bien con ganas de hacer ejercicio, ya no sentia sintomas de nada, a los meses volvi, y me dio de alta con ese medicamento, lo deje de tomar, y me dio nueva receta, pues empece a empeorar, no podia hacer ejercicio no podia hacer nada, ya estaba desesperado mi calidad de vida no era la misma, ya ni a reuniones de amigos salia, solo a trabajar porque era mi obligacion, casi no comia tampoco, volvi al medico particular haber si me daba una solucion, me hizo un examen completo de sangre, solo tenia alto el colesterol nada grabe, pues como tenia masa muscular y grasa, baje 15 kilos mido 1.80, en 3 meses aproximadamente, pero me seguia sintiento mal, aun medicado con verapamilo, metoprolol, losartan, volvi a otro cardiologo y vio mis estudios, me reviso y dijo suena muy bien tu corazon, pero quiero hacerte un Holter, aqui tienes prueba de angiotac coronario y saliste perfecto, prueba de esfuerzo saliste bien, tus electros esta bien, analisis de sangre perfectos, te falta el holter, pues me lo hize 24 horas, cuando sali de ahi pues estaba en casa, y comence hacer mi rutina de casa luego de trabajo, hacer mandados a pie no usar el carro, mucho antes de entregar el Holter me dio esedolor en el pecho, me daba miedo caminar, pero segui, me sentia muy raro, cuando entregue el Holter, al dia siguiente me dio el resultado que tengo eso taquicardia sinusal inapropiada, me dio Nevibolol, he continuado con mi vida pero no puedo ni hacer ejercicio pasar de 110 latidos porque es una carambola mi corazon, y me da miedo quedarme ahi. solo hago yoga y respiraciones, en veces me acaca el dolor de pecho solo, y lo unico que hago son respiraciones profundas, ya no pensar que es un infarto, mi estilo de vida cambio sobre todo mi alimentacion, tomaba cervezas las tube que dejar, aunque me tome dos cervezas me da angina de pecho. solo se que esto de discapacita aunque sea una taquicarsia sinusal. no eres el mismo.

I have S.T. But when I lose weight and do cardio my resting heart rate goes down to 65 and when I get up is in low 90’s. When I gain weight my heart rate can be in the high 80’s low 90’s. When I start moving sometimes in 110 without exercising. Weird how it works!

People look at me like im nuts when i tell them about this. Ive experienced it for years. My pinky is burning itchy red and swollen as we speak

El cuerpo es Divino, no enloquece nunca.

This is what I discovered. About 20 years ago people could buy a chemical online from revenge websites, legally. They would receive this stuff in a plastic box about the size of a motorcycle battery. Then they would place a little dab on anything, such as a car door handle or home doorknob. Once you touch it, it absorbs into your skin and within a week or two you begin to notice a slight burning on the tips of your toes. As months go by it progresses to your feet then a few moths later your hands. Depending on ho This is what I discovered. About 20 years ago people could buy a chemical online from revenge websites, legally. They would receive this stuff in a plastic box about the size of a motorcycle battery. Then they would place a little dab on anything, such as a car door handle or home doorknob. Once you touch it, it absorbs into your skin and within a week or two you begin to notice a slight burning on the tips of your toes. As months go by it progresses to your feet then a few moths later your hands. Depending on how much you absorbed it could affect your whole body making it extremely painful for about ten years then it kind of goes away. Doctors had no clue what the cause was/is and after a decade called it Erythromelalgia. It took an act of Congress to make the sale of this horrible toxin illegal. It was sold as a prank but it wasn’t a prank. Most people that bought this stuff contaminated themselves. It’s been covered up for unknown reasons, but I have my suspicions where it came from. There was a late-night radio interview my brother heard and told me about, but he couldn’t remember the name it was sold under. Something about 'The Shed' is all he could remember. He died shortly after telling me all this. I have been searching ever since. Was there a neighbor or ex in your past that could do something so heinous? Some of these terrible people would walk through parking lots smearing it on car door handles just out of spite or whatever, so it may not be anyone you know or knew. The world is full of evil people. If you know anything more about this, please share.

This is joe biden. 😂

I have this but my extremities are cold all the time.

I stopped eating any processed food, or anything with vegetable oils. Just rice and fresh vegetabes or pasta. Even some pasta sauces have a lot of processed ingredients so now pay more to get the better quality more simple italian brands. Symptoms improved drastically over a couple of months and I could get off my pain medicine (cymbalta), although I still have some troubles. Before that I could never seem to correlate pain my diet, although I did usually notice immediate effects after eating chips/fries full of bad oils. It doesn't take much of the wrong food to set it off and cause issues for weeks afterwards so just eating healthy for a few days wasn't enough. I never believed diet could actually make such a big difference. Vegetable oil is in so many things that you wouldn't even suspect, basically 95% of the supermarket.

A mi me detectaron taquicardia sinusal y me provoca mareos, dolor de cabeza, tonturas, tos, nauseas, manis frias, sudor frío y etc. En descanso mi corazón llegaba casi 140, entonces mi doctora me recomendó medicamento betabloqueadores.

Muito legal!

I have EDS and my life is normal but i can stretch good

About 3yrs ago my girlfriend began punching in her sleep. I feared she may do it again, so I started sleeping with my head at the feet and it worked out fine until last night. I woke up with her kicking furiously as if she was trying to kill someone. I have now upset her with me wanting to purchase another bed as I cannot sleep with someone that may kill me while in slumber. I love her but I want to live without the fear of such a fate.

As a toddler I had my ankles wrapped so I could learn to walk (in the 1940s). As I gained weight, I had stretch marks all over my lower torso. Unable to ice or roller skate because of my weak ankles. Was not able to take gym in school. Both knees dislocated when in the 10th grade. The right kneecap and tendon never returned, even after 3 surgeries. Had total right knee 24 years ago. Both shoulders are dislocated. I can't remember a time when I was not in excruciating pain, grinding of my joints, including neck and lower back. I need an exoskeleton.

I have in my whole head, neck, shoulders, arms, hand, and feet. It's caused such damage in my eyes that one is now blind. It's year 13. I won't make it to 14.

Imagine having a headache and trying to survive this video's background music. Takes away from the clinical significance of your video's message too.

Very informative and well explained video! Sarcoidosis can be daunting, but thanks to Channel for addressing it. Personally, Planet Ayurveda's supplements played a vital role in managing my sarcoidosis symptoms. Their natural formulations helped reduce inflammation and boost my immunity. Even my friend saw significant improvements with their products. Don't let sarcoidosis rule your life, give Planet Ayurveda a try! 🌱

this happens to me too, my resting hr is in the 50s at bed. My hr will sky rocket when i stand up, have anxiety but this does not feel like anxiety. I get dizzy upon standing and my heart will start to pound and of course ill get anxious right after. My chest gets heavy as well. I doubt its low blood pressure since i take 25 mg metoprolol daily. Its horrible. My hr does tend to stabilize tho after a min or 2 so i doubt its POTs

Avoid emotional draining situations ppl! 😊

1:25 that’s definitely the symptoms …: the diagnosis was today. Still trying to sort out what this means long term. I hate waiting on new appointments. I’ll be waiting almost 10 days to actually have a doctor sit me down and explain this diagnosis. I can’t help but wonder if severe osteoporosis isn’t a contributing factor but I could be way wrong. I’ve just been told I have it but has little explanation of it. I hate doctors anymore. Going to the doctor is like taking a car to automotive trade school

The truth this that most of these might not even be true and that syndrome is a bastardization of various different issues or normal varriations and inaccurate protocols definitely the most who have been diagnosed worldwide except maybe South Eastern Asian do not really have it but they will live with a fear and peacemaker forever 😢

I have cml and struggling so much with money and depression 😢

To do running simus tachycardia

You sound like Jared Owen

My mom screaming every night .. she had parkinson deases for several years .. any advise ??

Crisp and extremely informative video

Why dont they show this in every school

I have this. It can start suddenly and last for a few minutes or for hours and it returns until the trigger goes away. I have an autoimmune condition.

What sucks is you have? Doctors that don't do s*** for you. Because they look at You like a drug addict when it's because of E. D. S

Radioactive anything is a No No Wont ever be doing that

The guy talking sounds like he has a stuffy nose.

Why, why, why do posters run any kind of music in the background? It is distracting from what is being said and is insanely annoying. Teaching about leukemia deserves more respect.

Please,does someone know how to cure the GI problems?? I can't function normally without PPI,and i've been taking it for at least 5 years and the condition seems to worsen year by year

My dad had a herniated disc. The spinal doctor whose name I'm legally not allowed to say was high on heroin and botched an epidermal. My dad killed himself because of the resulting arachnoiditis

Background noise is annoying

Does the catheter ablation treat these sinus tachycardia and what are the side effects if the person presented with these sinus tachycardia and do these ablation?

Iam getting palpitations and resting rate is 118 .echo is normal wht to do to stop these extra beats iam getting

I sleep alone. When I don't use my CPAP and even sometimes when I do, I seem to be jolting myself awake with a fast slap or punch in the face. 😅 kinda scared to tape myself in case I pickup something like supernatural 😅

Yo siempre estoy por encima de 100 ! 120 a 150 todos los días pero lo mío es ansiedad! Tengo trastorno de ansiedad generalizada, fui al cardiólogo y me dijo que mi corazón está muy bien!

@tammiejones2731 we can’t claim this mess! I pray all is well with you. I was diagnosed with this stuff in 2003 I started feeling really bad with weight loss and went to the hospital and they did a CT scan of my chest and there it was smh. But to this very day I haven’t had to take no meds praise Jesus.

Mine are sweaty and hot like too wet not so red , I have to get new shoes every 3 months

You may all wish to know that back in 2014 the FDA held an advisory committee hearing on the safety and efficacy of Epidural Steroid Injection therapy to treat back pain for acute pain. (AADPAC) Although steroid injections into and around the spine were never approved by the FDA, or anywhere else in the world for that matter, pain centers found them to extremely lucrative despite reports of only short term relief in some along with reports of severe adverse medical events. After three days of presentations and public testimony, the FDA held a vote behind closed doors on whether there was enough evidence to issue an all out ban or “Contraindication" for epidural administration of particulate steroids. The vote was 15-YES, 7-NO with 1-Abstention. One year earlier, the makers of the most commonly used steroid, Pfizer’s Depo-Medrol, issued a global label-change request to have their drug not only Contraindicated for Epidural administration at ALL levels of the spine but to issue a ”MUST NOT USE via the epidural route” Black Box WARNING on the label as well. Seventeen nations including New Zealand, Australia, South Africa, etc did comply with Pfizer’s Global change request. But despite all this evidence, and votes by their own Safe Use Advisory Board along with the manufacturers’ Contraindication request, the US FDA said NO anyway and refused to comply because of industry pressures. Since then hundreds if not thousands have suffered irreversible harm such as ESI induced Arachnoiditis because of the FDA’s refusal to acknowledge the science presented at their numerous hearings. Thus we have a government agency hellbent on propping up an antiquated risky procedure that has very little proven efficacy in the name of lucrative profit$! Shame on them!

I had sinus tachycardia for 40 yrs.. must take beta blocker daily. If not lead to mi and cardiac troponin is 3000😅

I got gbs from tetanus shot 2009 .I found out there was a Lawsuit. But i didn't find about the lawsuit until 2017. Did know if the lawsuit was still active 😢😢😢

I was diagnosed thru amniocentesis i was 16 years old elected abortion in OU Medical

I am the first woman in the U.S. who was diagnosed with Dandy/Walker Syndrome in 1992 i gave my son Maxi Roger to Science for further study and research of the Dandy/ Walker Syndrome

We're really in the middle age of medecine for such conditions... And this video confirms it. Anybody with any most health conditions, even fatal ones would feel better with physiotherapy, some exercices and congnitive therapy. Even someone dying of cancer. Is this a treatment for cancer ? No. Fybromalgia is a condition where the myelin of the nerves get distroyed. These therapies are not a treatment for fybromalgia as they are not a treatment for cancer and anyone could however say it helps. I'm not saying they're bad or dangerous but it's a random therapy for a lot of things including re education after a broken knee. Now in 2023, while I'm writing this comment, most doctors have learned weird stereotypes even when freshly out of school, and take fybromalgia as a psychosomatic issue, or a catchall... When someone knows the researches on fybromalgia, the litterature about it, this video appears to not correct some stereotypes. I know it's not easy to sum up in a short clip but more correct things could be awaited in this kind of clip.

So many people have IST and POTS now after covid. It is truly unreal.

Hace 5 años me hicieron una ablación para eliminar un arritmia supraventricular por "reentrada''. El Dr. me dijo que no apareció la arritmia durante el proceso pero que "quemaron'' una parte y que con eso, quedaría bien; a parte de que, en el proceso se vio que todo mi corazón esta sano. Sin embargo, a pesar que he hecho mi vida normal (ejercicio regular como pesas o fútbol, comer de todo, beber moderadamente alcohol) me mareo al hacer burpees o ejercicios de impacto. Por ejemplo subir una cuesta muy prolongada me genera un gran esfuerzo en el ritmo y me termina en mareos, que si no me siento, puedo desmayarme. Entonces me he preguntado, que si bien la arritmia "desapareció'' pues no me aparece en reposo o en ejercicio moderado, hay posibilidades de no quedar el 100% respecto a la capacidad máxima física? Me he hecho Holter este año y todo sale normal pero no me gusta tener que pensar o limitarme para ir a un paseo que implique un gran esfuerzo físico.

I remember these images from my 1st text book

I was just diagnosed with arachnoiditis. I had never heard of the disorder. I had three lumbar spinal surgeries at age 12 and I just turned 64 years old. I'm very active working out three times a week. I didn't have any back pain until 2014 when all of a sudden, I started having severe lower back pain. The pain was also in my thighs and I had lots of muscle spasms and tingling and numbness in my feet. I went to a physical medicine/pain doctor who sent me to physical therapy. It helped, but my right hip started hurting. The doctor I was seeing was a numbskull and didn't do anything for me. I eventually saw another doctor subsequently having my left hip replaced in July 2022 and my right hip replaced in May 2023. The hips are great with no pain, but the back is as bad as every. I had an awful EMG about a month ago and an MRI yesterday getting the diagnosis today along with some other things wrong with my back. The pain specialists is recommending spinal injections. I've had plenty of them in my back and neck and wonder if they are the root of my problems. He also referred me to a neurosurgeon who I will see next Wednesday, I am generally a compliant patient but I do ask lots of questions. I always remind my medical team that I am not a novice patients having had three back surgeries, three hernia repairs, an appendectomy, gall bladder removal (all before the age of 14), removal of a blood clot from my foot and a thyroidectomy due papillary thyroid cancer. Needless to say, I am sick and tired of doctors and hospitals, but I need to continue on to get some relief. I am a college professor teaching fully online for the past three years. This was the only bright thing out of the pandemic. When my college went fully online, I was able to continue teaching and going to the numerous medical appointments without too much disruption. Thanks for letting me vent!