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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 !! th-cam.com/video/PqQI-8Ztei0/w-d-xo.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 ❤🎉

One study: pubmed.ncbi.nlm.nih.gov/28704600/ retrospective, "There were no differences in rates of AEs between patients with PMR and comparators for diabetes mellitus, hypertension, hyperlipidemia, or hip, vertebral, or Colles fractures (P > 0.2 for all). Cataracts were more common in patients with PMR than comparators (hazard ratio 1.72 [95% CI 1.23-2.41]).

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

this video should have million views

Can you provide bibliographical references please?

Thank u 🎉🎉🎉🎉

Great lecture, thank you

"Joint Hypermobility and It's Co-Morbidities" video. The word "IT"S" is a shortened form of "IT IS" or "IT WAS". No hyphen. Did you not learn proper grammar before getting your PHD? I stopped reading after that and questioned your credentials. Get a proof reader or go back to school and learn basic grammar.

Hi y'all! I explain TMS and nuerofeedback in laymen's terms on my channel! I will be offering free counseling and motivation too as well as following my life working at a healing center! Sub and share! Bless y'all!

Sadly because of stage 4 cirrhosis of the liver I cannot be helped. I am hoping better news on pulmonary fibrosis.

I use Aplys test. Also I screen aorta via US rather than rely on family hx

I CANNOT UNDERSTAND YOUR WAY OF SPEECH. HARD TO UNDERSTAND ACCENT.

I have joint hyper-mobility and have had dynamic movement in my shoulders, ankles and throughout my spine- causing wide spread pain,

Webinar audio quality strikes me as a scandulously under-appreciated argument, which moon landing conspiracy theorists could exploit... listen to some Apollo landing tapes. Sixty some years ago we had more intelligible speech from the surface of the moon than what we're subjected to today.

Good to know

One of the best videos on the ill returning traveler I have seen. Dr. Showler hits many of the high points. Anyone studying for a Travel/Tropical medicine certification must watch this.

I am 4 years paralisis patient I am in bed 🛏️ many treatment use but no cure my paralisis.sir cure for this rtms therapy

How do you know if Sherita is not just projecting her bigoted racist views of white people in this study? I guess if anyone knows anything about bigotry and racism, it's going to be Sherita. She is so good at labeling humans by skin color that she has even made herself a little list of what skin colors are good or bad and all the perceived privileges she thinks go along with those skin colors. It's really astounding the leaps and bounds we have made at Johns Hopkins in segregating people by skin color and labeling them for their assumed privileges. We should see her rolling out the "race brand" project soon where she will brand all the whites at the campus with a hot iron before segregating them to all white classes. When you have so much hate in your core and soul for other humans, it comes out no matter how you try to pretend it's not really there.

do you recommend PET before the biopsy or after? We are a low resource setting so infections generally are more on the higher side.

I really need help. Can't go on like this anymore. I'm suffering too much to explain and or search for help. I'm desperate.

Excellent 👌

Very informative. It seems to connect a lot of dots and explain the health problems I've had since I was little. And why I went on to develop ME/cfs and POTS.