Відео

I’m 51 and think I have been having this pain in my shoulders. I used to have rheumatoid arthritis with nodules and swelling in my joints but pretty much cured that through diet change so I’m assuming I can cure this by changing my diet

I kept waiting for the next slide hahahaa

Can this diagnoses...in an elderly cause frequent diarrhea?

great lecture! Thank you!

Agreed, I just realized that Mario updated his favorite way to tackle ED and it's crazy! Although what he previously talked about was pretty decent, it was difficult to follow, I just go'ogled the latest by Mario Volpstein, it's so much simpler and potent now!

Keep the gold uploading

Dr .akpamu on UA-cam cured me off hepatitis b with his herbal medication which I purchased am now totally free from the virus

bruh Brad D Tinkle lmfao

An academic approach to happiness is a little paradoxical but seems to work. Great job

This is the best medical channel on UA-cam 🤍 how the hell I didn't know it before! Really appreciate ur efforts ♥️ Thanks you sir so much 🤍

What is hydrant hot mobility???

Thank you so much for this wonderful lecture! 👏👏👏👏

I’m having on set symptoms strange symptoms that’s highly uncomfortable. I wonder if it’s my depression or something else. Someone one help me please. I don’t know what to do

My GP started with 60 mg/dly, then 40 mg for a couple days and then 20 mg for three more days for a total of 15 days starting out. I have to wonder whether the dosages are too high.

Great presentation

Thank you all

I had PMR and sadly I dx myself after an elderly person recognized my symptoms, sadly all the doctors and specialists who I went to just looked at my markers, blood work and labs and could not even help me. By coincidence I had prednisone for hammer toe about same time and that’s what stopped all the aches.. I was very disgusted with lack of care , interest and compassion of doctors

Excellent presentation. I am a case of "refractory PMR" treated with prednisone initially with the subsequent introduction of methotrexate and later on leflunomide -- both were discontinued due to side effects or infections. My lowest effective dose of prednisone was 10 mg which was only achieved after 12 years of treatment with prednisone. Many relapses occurred during my 12 years on prednisone. Actemra (tocilizumab) was initiated on January 1st, 2019 and prednisone was discontinued one year later. PMR is in remission except for a relapse when Actemra wasn't available during Covid. I have minimal side effects from Actemra in 5+ years of treatment with Actemra. Attempts at decreasing my exposure to Actemra have been unsuccessful. I would like to stop Actemra but I never want to take prednisone again.

Excellent video, thank you! I learned a lot. I feel seen.

Excellent presentation

Very useful video. I am on TMS now. The week 4. I can feel much better and my depression symptoms is disappearing 🙂

I have APS, was shocked when I found out in 2023 , I'm 68yrs old

Excellent video. I leave you to complement a list of diseases that can cause Usual Interstitial Pneumonia that I think may be useful to you. Greetings !! ua-cam.com/video/PqQI-8Ztei0/v-deo.html

Great lecture. Thankyou.

Does this video have no volume

NO WEAKNESS ????? Hahahaaa

I walked 18 holes of golf on Tuseday, felt great. Teo days later I couldn't get out of bed. Dx PMR.

Will be 59 this year… and self-diagnosing with hEDS (also have been diagnosed by physicians with MCAS, CFS, FM, Hypothyroidism, TMJD, Tinnitus, Burning Mouth Syndrome, and have a slew of symptoms, sensitivities and triggers. I had Mono at 18, and everything went downhill from there. Have had to be my own “doctor”, as I have never gotten much help or treatment; though I have been to countless doctors and specialists throughout my life. Helpful and informative video. I definitely see myself in the description. Wish doctors knew more about autoimmune and supposedly “rare” conditions, that aren’t truly rare… it’s just that many people go undiagnosed. 🙏🏼🙏🏼

Thank you so much for explaining the whole procedure in an easy precise way it has helped me to understand everything clearly

Superb presentation ❤🎉

Great talk Sir! I had to prepare a similar thing, a gentle intro to IA and was facing serious "powerpoint block" until I found your video.

Thank you very much for a fascinating presentation. I was diagnosed with pmr in November 2021 and have spent time on the 'steroid flare rollercoaster'. Luckily I have since learned how to decrease steroids slowly without flaring and am down to 3mg per day of prednisolone (I am in the UK). I would like to include a link to this presentation on a website I am currently building. Thank you again for the presentation.

Very informative!! Now I'm wondering if I need to be evaluated. I think this is the root of so many of my struggles in life 19:00

Clear and concise. Thanks

❤❤❤

Thank you for this excellent well presented informative video. I have just been diagnosed with this and I'm awaiting tests to check the artery involvement which I believe is there. I have been searching the Internet all morning and have not come across a video that can compare to yours. Thank you so much for taking the time and effort to offer this. I have made documentation of it I find it that informative and I am saving it for future reference. Forgive the people who complain the video isn't up to their quality standards. You have already given them a gift with this great information.how ungrateful they are. Shameful. I thank you.

The medication is garbage bup is puke & an awful NIGHTMARE. First how do you treat addicted doctors who work in health CARE? HOW DO YOU TREAT ADDICTED SURGEONS OR ANESTHESIOLOGISTS OR HOW DO HIDE THESE ADDICTED DOCTORS IN THE HOSPITALS? 😆 LOL THESE ARE THE MOST DANGEROUS ADDICTS. BUP IS DANGEROUS IT CAUSES SUCIDE BUT YOU REFUSE TO ADMIT IT! ITS NOT SAFE! WHY DO YOU KEEP SAYING ITS SAFE?? BC THIS DRUG MAKES PEOPLE HIGH EVEN WHEN ITS TAKEN AS PRESCRIBED ITS A POSION YOUR SADLY MISTAKEN! MUCH SAFER YOU REPEAT IT LIKE A BROKEN RECORD! Your brainwashed when it comes to this dangerous drug which has law suits IT ROTS TEETH & CAUSES SUCIDE! Try it, see how high it makes you for hours that is why the ADDICTED like taking it, but this drug gets pushed on patients in pain management at UW as all doctors in pain management treat all patients as oud nuts! You doctors push bup bc your brainwashed its sad that health care providers are now to woke & programed by big pharma. God save us 🙏 from this madness as younger generation of health care have no clue just robots repeating big pharma or what your professors are blabbing or what commie hospitas expect. What was once a wonderful health care in puget sound has fallen to nonsense in last 10 to 15 years due to woke universities. Iam glad i worked in the beautiful health care we had until you people came along brainwashed by government admin & their craziness by giving your brain over to madness of US gov CDC FDA NONSENSE. Health care is not supposed to be political doctors are supposed to think for yourself & patients. Bup is given as a punishment to the addicted or forced on patients in pain management & many doctors in western WA go to UW for advice concerning addiction or pain management the nuts AT UW WANT TO RAM IT DOWN EVERY PATIENTS THROAT TAKE BUP FOR A FEW DAYS YOU WILL CHANGE YOUR MIND ABOUT BUP POSION. Those with oud should realize what a dangerous drug this is as doctors want to force it on every one at pain clinics & ER & every where very sad. WAKE-UP!

Great ! I wish more echocardiography for beginer and breast if it is posible, thanks in advance.👏👏👏🙏🙏

Oh my, I sure wish this was more out there in the medical community earlier. I am in my mid-60s and didn't get diagnosed until then... It was a fluke that I even heard the name when I found out my dad was not my dad and a new half-sister asked me if I had it. I called my Dr and she got me a Geneticist immediately (the next day) for over an hour by phone as it was during COVID. Also probably have POTS MCAS and Dysautonomia. I was already disabled by then. All the suffering and all the meds and MRI with contrast dyes that ruined my kidneys which are now failing and on dialysis... My mom might have also had this interestingly enough! She knew something was wrong with me and took me to so many Drs. I used to sprain my ankles every weekend while running and playing. Had to buy crutches as it got so expensive to rent them! I blame the Medical Doctors for being taught that when you see Zebras, think horses because it's more probable. Guess what? There are SO MANY MORE OF US THANK THEY THOUGHT!!

Wow, he has just described my posture in every single detail. I also have hyper mobility in some joints, but not all of them. The problem I am struggling last couple of years is neck shoulder pains. Am I the only one who sleeps ON their shoulders? I mean that I just bend it towards my chest and put my cheek right on it. Waking up in morning is totally not cool! I hope I will get my diagnosis one day:( I am just 29.

Still making big errors...between AS ankylosing and others forms of spondylarthrities..spondylit ankilosing radiographic visibile radiographic and în young men...with fusing spine... and manifest different în women...

Im really interested in the link between hypermobility and ADHD, fibromyalgia and PCOS. As someone who has all of these, i see a lot of people who share these comorbidities (and usually bariatric patients too). It makes me wonder if dopamine sensors or production (secretion?) is affected by the changes in soft tissues present in EDS or hypermobility.

I have EDS and I suspect a lot of my dad's side does. I "hang on" my joints and wonder if my grandma did too, as she has had her knees hips and shoulders all replaced.

Bpc-157 can help this health condition

My GP has been seeing me for hypermobile joint injuries and instability for 4+ years and still won't write down "hypermobile" in my notes. All other healthcare professionals (physio, chiro, RMT, joint specialist) have noted me as hypermobile. I am currently on medical leave from work because I wasn't able to manage my symptoms (yet) and so I'm losing income while my doctor just keeps asking me to lift my arm (range of motion test) and earning his full income. It is so. frustrating.

Yes! The whole functionality thing is the most important thing to me! I'm 70, still very hypermobile, and movement and pain management is the key for my EDS pain control!

I think it's good to orient hypermobile people to careers sustainable for them + tneir employers. (Some joint injuries can be very long-lasting.) There's not much reason why hypermobile folks can't do pretty much any type of public service admin or other jobs with lower physical demand.

❤🎉 this video is the best

68 and just got assessed this year. Now so much makes sense, but I am going to PT all the time. Finding a PT who is hypermobile savy is so important.

my daughter has hypermobility, PCOS, soft teeth, migraines, lipedemma, only recently have I heard of EDS, it seems likely she has it