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The presence of clotting factors produced by bacteria are quite a serious concern.

With conditons like these, traditional therapies such as "cupping" could easily be modernised - particularly if a pressure effect could be modulated to assist bloodflow in time with the heartbrat.

Very oddly my left side was hurting. So don’t ignore any signs as I didn’t and I’m glad I didn’t! :)

thanks for the video but the normal sodium level is 135 -145 and severe hyponatremia should be less than 125 otherwise I love your way of teaching.

Thanks

3:24 - I have this rare complication. I finally had surgery when I was 33 and they removed a piece of bone a little larger than a golf ball. I still have a massive lump in my knee and my patellar tendon is filled with bone fragments that can't be removed without causing serious damage to the tendon. My knee has been in pain for over 25 years. This video mentions that the pain/symptoms go away with time. It's still incredibly tender and painful to touch. When it's really bad it keeps me from sleeping. If I try to jog or do a leg workout the pain in my knee is debilitating for a few weeks. It feels like it gets worse as I get older. My doctor told me to swim, but the pressure from just being in the water is pretty painful. I've accepted this is my lot in life, but I always wonder how far I could have gone in sports if I had a healthy knee.

Thank you so much

Dear sir I am writing to express my concern regarding a situation that, while not intentionally biased, has significant implications for the diagnosis of certain diseases in people of color. I have observed that there is a tendency among some medical professionals to overlook people of color when diagnosing conditions that are traditionally associated with white individuals. This oversight is particularly troubling in cases where an individual's heritage includes mixed ancestry, as it can lead to misdiagnosis and inadequate treatment. For example, conditions such as polymyalgia rheumatica are often presumed to predominantly affect white females. However, this assumption can be misleading and detrimental to patients of color who may have white ancestry on one or both sides of their family, as is the case in my own family. The assumption that certain diseases only affect specific racial groups can result in significant health disparities and delayed diagnosis for individuals of mixed heritage. It is crucial that medical professionals consider the full spectrum of a patient's genetic background and symptoms rather than relying on generalized assumptions based on race. This approach will help ensure that all patients receive accurate diagnoses and appropriate care. I hope that raising this concern will encourage a more inclusive and thorough diagnostic approach, ultimately improving healthcare outcomes for all individuals, regardless of their racial or ethnic background. Thank you for your attention to this important matter.

Thank you for sharing your comments Greatly helped me w/ my hbp...🙏I'm better understanding my condition & treatment. 06/23/24 Best explanations I've heard

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Your website is Awesome

Nice

I’ve had it for 3 years. This past year I’ve had several flare up 😭😭😭😭. This time it’s much worse!!! I’m so darn miserable

Hello I made a little book called Inspo for those Days on amazon. I was able to bring down fatty liver disease from 42% to 1.9%. If you ever get bored I took a good four months of making this little book to help people because so many recipes can be complicated sometimes. Hope this helps.

Thanks! I've been getting them since my 40s. 63 now.I'm pretty sure I past one last night. I was throwing up had lots of pain in my back and stomachand lots of chills. I don't understand why I ha e a headache now. I remember this happening before. Is this another symptom and why after

Amazing one ❤💥

I currently have Epidimitis and tested negetive for any bacteria and after an ultrasound my uroligist said I just aggravated it.

Add to this a new cause in the past decade: LED light high frequency flicker. LED lighting most frequently uses cheap power conversion circuitry to convert AC line power into low voltage DC to dry the LEDs. This causes the LEDs to vary in light output at frequencies twice the mains power frequency (120 hertz in the US, 100 hertz in much of the world). This high frequency flicker causes oscillation in visual signals sent to the lateral geniculate nuclei (LGNs) which extract edges from the visual field, and identify movement for the eyes to focus on. This all happens at speeds much faster than the flicker fusion limit for visual image formation, but is entirely neglected by most brain researchers and visual specialists who wrongly presume that all vision is visual scene formation, and who often are ignorant of the many wats the eyes, and many brain structures use and analyze information from the eyes. Other brain structures like the superior colliculus and pulvinar are directly involved. And beyond tinnitus, this also involves the trigeminal nerve and pain in the eyes, behind the eyes, in the face, and in the lower jaw and molars. For tinnitus, the high frequency flicker is "seen" by the LGNs as movement that they and the other aspects of the brain cannot localize. This then causes signals to be sent to the precuneus and on to the default mode network identifying unknown danger. What happens next is speculative, but goes like this. After failing to find the potential danger, the brain directs the Medial Geniculate Nuclei, and with the Inferior colliculi to instruct the ears to listen more closely for sounds to localize the sensed danger. Through several brain structures this results in the inner hair cells of the ear turning on previously disabled defective ('dead') outer hair cells. This is done despite the harm in order to best protect the body by maximizing the potential to localize the danger through sound. There isn't an actual danger though to be found. And the result instead is very loud subjective tonal tinnitus, as the dead outer hair cells circuits "ring". The brain keeps emphasizing the need to listen, and amps up the volume while adding more dead cells in the search. The result is an increasingly loud and climbing tinnitus. Simultaneously, the DMN and other circuits fail. That results in optical migraines that progress quickly to total or partial temporary blindness, often followed by migraine headaches. On removal of the flicker source (fleeing the LED light exposure), the body works to undo the harms it created. If the exposure was minot and brief, the tinnitus may fade into the background in an hour to days. More intense or longer exposure may require dats to weeks or even months, and may never fully resolve. The optical migraines will fade into about an hour, but the migraine may last hours to days until it resolves. Repeated insults of exposure to the flicker worsen the injury. Likelihood of impact and severity is dependent on nerve conduction speed. With IQs near 100, that results in sensitivity to ~60 hertz flicker. At High IQs, the risk moves to higher frequencies as the nerve conduction speed increases. Optical flicker injury from LEDs is most likely to be most severe and most apparent in high IQ individuals. However, the entire population is subject to a second impact where many of these same brain circuits lead to several types of headache from flicker up to about 5,000 hertz. This happens most commonly from dimmers using pulse width modulation, and all of the harmonics that generates. And no, you will not find this in any single scientific study or reference. Also - no, this is not yet a scientifically or medically recognized injury. And the related adverse impacts of intense blue light exposure from LEDs in sensitive individuals (~1-3% of the population) through at least three pathways involving most of these same structures, plus genetic differences associated primarily with Neanderthal or ancient hominim heritage from low light adaptation in the far north, also occur in many people. This too is not yet recognized by researchers or doctors other than in limited field reports and fMRI studies since 2017 elucidating the mechanisms involved in sensitive individuals. These have largely been masked due to the simultaneous wide spread on the SARS-CoV-2 pandemic causing brain injuries, and the severe impacts on health care and research. We are only now seeing the companion impacts from blue light suppression of melatonin production on circadian and hormone rhythms, and the consequent rapid and severe rise in hormone sensitive cancers. The first being the rapid linear rise in the rates of breast cancers from the 2015 baseline. Expect those to reach 175% of the 2015 baseline in the next ~5 years (seen 3-5 years later in national data). Prostate, Gi and rectal cancers will follow, along with skin cancers.

Can anybody explain... If secondary hyperaldosteronism is part of conn's disease or not.......

Fantastic explanation ❤

thank you for these videos they help a lot <3

Just amazing!

I have been suffering from Meniere's for last 3 years. Have constant ringing ie tinnitus 24hours a day. Unpredictable Vertigo attacks almost every week for 2 years and it lasted for hours , had to go hospital for stemetil vaccine very frequently. I ruined my everyday life. Last month I was bound to bed for whole month due to daily episodes of vertigo, had to go to hospital almost daily. Thats when my ENT suggested surgery . I had Labyrynthectomy last month and after a month my vertigo attacks have stopped. Its to soon to say but my ENT says that vertigo will stop now. Though tinnitus is present and hearing in my affected ear is lost but relief from vertigo was our main motive. I am suffering from balance problem in walking after surgery but my ENT says it will recover as soon as other ear alone will take over the role of balance the body. Hoping that it may be the end of this dreadful disease and life become normal again. I suggest to get surgery if hearing in affected ear is beyond service.

When I hit it on something I meet Jesus for a minute 😂😢

Thank you .nice lecture

Meu filho tem Dermatomiosite ha 8 anos

My thoughts are with all the people suffering from this horrible disease. Somebody I know has recently been diagnosed with scleroderma and it’s the most traumatic thing that’s ever happened in our lives. Please have an extensive read about Helminthic therapy.

My grandson is 8 yrs old and was just diagnosed with this HSP disorder. It's so heart breaking 💔 to see him struggle to walk.

I currently have this pretty bad, ever since I was around 12.5yr it started and just got worse and worse. I’m 14.5 now and it’s so bad I can’t do my main sport parkour, and weightlifting for football like squats cause pain :/

Thank you very much doc 🤍🤍🤍🤍

This is exactly the pain I have, but it also feels like my bone is popping out of place. Hurts worse when I hold my phone in my left hand in an upward position (as if laying down, but holding the phone straight up). This only started about a month ago.

Thank you for such explanation

This is the best video about immune cells

How can I download this book?

I had what appears to be vertigo for the first time in my life these last 3 days. Two days ago I woke up and the first site I saw was the bottom of my feet, the wall in front of my and the bottom end of my canopy bed all of a sudden that image stuck to my head and rotated several times the way a slot machine would after you yank the arm. It scared me and when I tried to get out the bed it felt like the room dropped at 45 degree angle. I’m pretty scientific and figured it was vertigo. The next two days the spinning would occur but not like that first rotating sight. I spoke to a pyshical therapist/doctor and she said I should go to the emergency room. I saw some causes of vertigo and see it can be something more serious. The hospital I work at is more of a trauma hospital. I’m hoping to go to a more specialized one before it gets worse. I pray for everyone’s well being. Funny thing though, my wife is on the religious side and she told me I need to stop watching them ufo shows 😂❤

My right testis is gaint

I'm 16 years old I have that pain and at night I can't sleep well.. please pray for me 😢✝️🙏🙏♥️

I Love your simple explanation , my fav medical channel so far

Just had a whipple operation this February 2024. Wished I see this video b4.

Thanks bro

❤

well done!

I was considering becoming a member because you’re beginner “Anatomy of the Skeleton” video is concise & excellent!! But I can find nothing in this Member video, or on your RUclips channel, showing a video on the “Anatomy of the Muscular” system. This is desired and would be a logical progression from the Skeleton Anatomy video.

The best i have vome across. Welldone❤

Goddamn it's very painful, and it's all because of my faulty water intake

Good work

Thank you for the video

gracias amigo

l have just got vertigo they think mine started with a real ichy ear lve only just got it but have had ear pain for years.l would advice anyone with with even the slightest ear pain to get it looked into

Can you have graves diagnosed and have no symptoms? Or opposite symptoms? Can a neck injury also stimulate or influence the thyroid gland? I have weight gain, no eyeball bulge, no myxoedema, no tremors but i was in a serious car crash that i still have pain from, including neck and back injuries. One doc said graves another said get a second opinion. Just curious