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That's excellent 👍. Thank you very much 🙏

Since pain is part of the immune system designed to change your behavior ,it is illogical to "treat pain". You treat the cause of the pain. Pain is a necessary funtion. You don't treat funtions. You don't treat immune responses. Stop.

Thanks so much...Really helpful..

Thank you very much for this. It has been very informative and has clarified some issues around my recent diagnosis of PMR.

As much as I keep learning about pain, I can still learn something new. This is a very valuable insight. Thank you!!

Good video,thank you.

Thankyou

I've osteoporosis it's so painful had that many fractures on ribcage

😂😂😂😂😂 you wont end up in a wheelchair unless you want to. What an idiot!!!!!

If you have adverse reactions to steroids are there any alternatives therapies supplements/ drug for treating PMR? Can change in diet to anti inflammatory foods help?

Thank you thank you thank you! My Dr. diagnosed me with RA but I know it is PMR. So I search for a lecture about PMR and found you. Also interesting is the Large Cell Arthritis. I was having a lot of jaw pain, I just assumed it was because I was grinding my teeth because of the pain in my shoulders was SO bad. It just recently moved to my hips. That scared the crap of me because laying on my side I literally could not lift my top leg.

terrific 😂

Very helpful and informative, that is, until the Covid part of the webinar. You missed the perfect opportunity to warn people about the inflammatory side affects of the poisonous vaccines that have more harm then benefits for the general well-being of people. Excusable in part given the date of this webinar which may not have allowed healthcare workers from saying anything contra to the Government "so-called" health advise.

Such a useful presentation. Thank you so much.

Thank you Dr., for uploading this to UA-cam. You have given me more information than my primary care doctor has ever done on this subject.

Explain this pain philosophy to your patients..... they will not come back to your clinic again..... This is a great lecture but doesn't work in day to day patient care

This talk is THE most useful I have heard on the internet (or anywhere else)! My doctor had NO idea what to offer besides drugs. Very disappointing. Also there are so many people on the internet who believe they are doing everything they can to regrow bone but sadly, only specific exercises with increasing difficulty actually help. I’m gonna go jump now. But will watch & rewatch this. 1 question I have re: strength training. I understand I need to increase the weight over time but after 2 mos of lifting, my 2 sets of 12 reps 3x/week with 5 lbs each hand, are still really hard. I shake & can barely finish my reps. Lunges too are very hard. Why don’t I seem to be getting stronger? Thank you!

😮🐍

Chronic pain patients are the forgotten and abandoned. The government want us dead. Pain is a disease in and of itself.But our pain specialist is a young female psychiatrist focussing only on the mental, knowing nothing of medications,(she has admitted this twice herself) who after our zoom appointments, writes dismissive, disparaging reports to our prescribing GPs showing her lack of knowledge.She told my incredibly supportive GP that I have a belief that chronic pain patients are treated worse than other patients. That is no belief...it is a FACT in my life, my dying daughter's life, all pain patients lives.I keep writing to health departments getting the 'pass the parcel' reaction. No answers. No action. We know what works for pain and its not meditation, visualisation, exercise, distraction although these may benefit some. What works for intractable chronic pain are opiates. They have worked for centuries. They are safe, effective and non addictive when used responsibly by genuine pain patients. I am not an addict. Of course I experimented but only 4 times with marijuana. I did not become addicted. I chose not to allow that to happen .But PAIN chose me, and like all us millions of forgotten pain patients, I suffer. Its the 21st Century. It is cruel. It is criminal. I pray for the courage to sue all the people involved with making people suffer, making people turn to other drugs, making people die by their ignorance of the lived experience of chronic pain patients.

Great presentation

Hi i have paid 24.7😢

This is outstanding information. I’ve done a lot of research on this topic but have not seen such a comprehensive explanation.

Dr emuakhe is an epitome of good treatment,the doc has every criteria to human health.......

This is junk science and a ridiculous premise that chronic intractable pain can be eased by CBT. You all have lost your damn minds

I take 2400 mg of Gabapentin for my fibromyalgia pain, as well as pain meds for back injury including torn tenden in both my biceps. I also have sclerosis of the SI joint, tailbone injuries I have collected through past accidents. My knees are always in pain, and makes it hard to sit on seats not risen a little higher to get off of. The doctor that diagnosed me with fibromyalgia said that my test showed that I supercede the point scale for the test. My body hurts to the touch, and have yet to be able to sleep through the night without muscle relaxer.

This is an excellent, very well-informed presentation. Thanks Dr. Boulos.

I would have like to ask whether the symptoms with regard to inflammatory response are reduced when the disease is not 'flaring' and whether the lowered inflammatory response leads medical practitioners to make another diagnosis (or not diagnose) in the case of early disease progression even with a long history of pain & inflammation. Also, given very long waiting times (even with top med insurance) to see a specialist rheumatologist in some Australian cities, whether the longstanding tests of heightened CRP & ESR levels & a feeling of fever & general unwellness & longstanding pain even matter? Often the flares, have long passed before seeing a specialist, only to reoccur down the track requiring more tests... and so the cycle goes on.

Glyphosate benzine atrazine fluoride chloride chlorine nitrates aluminum heavy metals and 20 more is the reason for disease, it’s in your food and hygiene products. This is why you’re all dying early with the last years of life in hell already, chemicals…….

culprit: microwaves, it can last a few years

Life changing video and great humor. Thank you.

It is my greatest joy that I discovered about Dr Aluda on UA-cam who cured my Fibromyalgia with his herbal medicine. I highly recommend him and a trial will convince you. he cures HSV I&2 and HPV too//

Very informative lecture, Dr Boulos,

I've fibromyalgia and because of it unbearable pain. I can't sleep. Every time when I fall asleep I wake up due to the pain and after 5hours or so I can't lay still at all. When I ask the doctors for help with the pain they give me the middle finger. I wish I could show them how bad the pain is. Let them feel what I feel.

This was an incredibly thorough & helpful talk. I've been doing a deep dive into hypertrophy/strength/power training as well as functional training off & on over the past few decades. Triggered not just from my own general curiosity, but my own serious chronic illness, caregiving for disabled family & teaching dance to older adults. This is fantastic information that accords with all my hard-won knowledge. Beautiful. Thank you again.

Very comprehensive and helpful presentation - thank you.

Pain is all in the brain. Load of s--t. Australia had a huge problem with repetitive motion injuries and they cut off disability payment for those who suffered these debilitating injuries, and all of a sudden case numbers went down! See, it was all in their heads!!! Or maybe they had to shut up, and go back to work and suffer the pain to feed their families. This guy is crap.

Fabulous, very informative video. I am currently having tests to see if I have this. I started getting symptoms after I had Covid. ❤️🇨🇦❤️🇨🇦

Im trying to find my ow 33:10 n doctor now where i live my doctor is clueless. I've had this for over 25 years.

Hmmm I have them all

I started to have PMR symptoms after Covid😩

I was right there with you until you said it doesn't get worse because it ABSOLUTELY DOES! I've become increasingly more disabled over the last 10 years and my pain has gone through the roof despite taking so many measures to counter this horrible disease.

Great and informative presentation! Thank you!

I think it's a lack of dopamine brought on by too much cortisol... dexamphetime works wonders😊

milnacipran caused me to have hot flashes and cymbalta gave headaches. I'm now on lyrica which takes the edge off...doesn't completely get rid of the pain. Still suffering. Amitriptyline can cause heart issues if u have heart disease

Great!

Great content.

Thank you 🤩🤩💖

Is not the same as Fibromyalgie?

Fibromyalgia is very very serious condition no doctor takes seriously I suffer very much of pain start with my ears eyes loss my hair my feet pain tremendously I can't not put shoes I can't not Walk my shoulder my back hurts I have nuts allover my body I cry every day e night I can't not sleep dizziness I can't go over e over

I suffer from Fibromyalgie for 4 years now, and I am not sure that is that the cause