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Are there human trials? Or are governments red-taping it out of human use any time soon? Bearing in mind the fast-tracked novel \/a##ine they literally just trialled on a GLOBAL population against the umpteen pages of detrimental side effects, going against their own standard research of 10 years “if they get it right”.
KEEP YOUR WORK HELP OTHERS. BUT IF YOU HAVE CANCER NOW, CK OUT JOE TIPPENS CANCER PROTOCOL FENBENDAZOLE RIGHT AWAY, FENBENDAZOLE REDUCES AND KILLS CANCER CELLS WITH OUT ANY SIDE EFFECTS AND JESUS LOVES YOU.
I was lucky in testing positive for SSA/Ro, and a parotid gland biopsy was also consistent with Sjögren's. I can't put together enough saliva to do a DNA test. If you touch the inside of my mouth it is completely dry. Nothing that I have tried makes a difference in that dryness.
I believe people suffering with this are hypersensitive to distractions such as music, vibrant colors, speech that is too rapid and hard to process due to the speed of speech. It was too much and I discontinued watching, unfortunate.
Isn't the most favorable way to address type 2 Diabetes and Obesity always diet? Farma needs to quite killing people with drugs. Dr. Jason Fung seems to be managing the problem without killing people.
Have you heard of the ATG 5 protein test in Sjogren's patients who have dry eyes? It's said they will have higher than normal of that protein in their tears. Do you know if this non-invasive test is part of the diagnosis now? I have heard very little about it since it came out a few years ago.
I have dry eyes and is seronegative. I do not want to do a lip biopsy either. My doctor still thinks I have Sjögren’s Syndrome even through I dun think I have dry lips. However, I have been drinking plenty of water and applying lip balm every night. I hope this new diagnostic will come to Singapore soon so that at least I get an answer.
In my last lab paperwork I saw something I had never seen before…Sjogrens I couldn’t believe it. I don’t know if it’s being used already but it was in my lab report. I’ve had Lupus for 26 years and RA so I really keep on eye on my blood work. Thank you for all the hard work !
Nice advancement in material physics, can't wait to see the studies on its various crystal structures and homogeneity 😍 >Me waiting for electro-magneto-dynamic adhesion, repulsion, and propulsion to make axial staged compressors and turbine aerofoils more efficient over a wider range of temperatures and velocities while hinting at the obsolescence of internal combustive propulsion technologies and low energy density fuel storage and atmospheric and field interactions
I would be very interested to know whether your test would show up Sjögrens in patients who have managed to get their symptoms under control through diet etc. Or would it only show positive in people whose symptoms are active?
I've had Sjogrens for 10 years despite negative bloods, I was offered the biopsy but didn't want to go through it so I refused. My symptoms have got much worse over the past 5 years but I have never had any treatment and don't even have a doctor to monitor my condition as they believe that if you don't have an official diagnosis, you don't have the disease. Thank you for your work.
Yep, we need some doctors who can start listening to patients! The longer we go untreated, the harder it gets to function. Insurance companies have to get on board too. That may be why the docs are so shy.
Telitacicept is the new kid on the block treatment for Sjogrens. Check out the sjogrens foundation. With this new test being developed and more drugs hope lies on the horizon.
This is a great design for Fission Suppressed Fusion Hybrid that produces neutrons for Uranium Fissionable material for fission reactors. This would make an unlimited amount neutrons via U238 or TH232. Reference "Ralph Moir Fission Suppressed Fusion Hybrid" .
Thank you very much !! My SSA are higher than rate but biopsie is negative but I have a sialadenite .... and I have a lot of symptom of sjogren. I have discoid lupus but not activate. I have also Hashimoto. So what should I do to be sure if I have or not Sjogren??? The medical system should assign one doctor who will be in the middle to analyse and put everything together ,work with others specialists....😤😢 Everybody works separately and the process is long to see a specialist. I'm exhausted ...the system is not helping !
The lip biopsy was nothing in the scale of human suffering . I guess it depends on the skill of the person taking the biopsy. Whatever test is used reliability should be the most important. A positive lip biopsy resulted in my parotid glands being scanned where a suspicious lesion was discovered that is now regularly scanned due to risk of conversion to malt lymphoma in Sjogrens patients. This led to
As any surgery wound, sometimes it heals wrong. You could have the best surgeon and the person's body just reacts badly. For instance keloid scarring growing and growing, and other issues. So the fewer who have to get surgery the better.
@@Call-me-Al I would prefer to have a definitive diagnosis and considered the biggest risk to be nerve damage not pain or wound healing within my mouth. The biopsy ensures a definite diagnosis and with the correct diagnosis the best treatment can be planned.
It was an absolute breeze at Guys hospital in London with minimal healing time after . At worst it felt like a small ulcer for a couple of days still fine to eat ! If it hurts it was probably done by a butcher 😮
Some people with SS are negative for Ro and La. The University of Buffalo developed the Early Sjogrens Panel to detect salivary antibodies as well as anti carbonic anhydrase and anti parotid antibodies. These results put the “seronegative” theory to rest. It’s very useful when a doc can make a clinical diagnosis but Ro and La are negative. This test helps speed up confirmation so patients can receive treatment. What exactly is your test looking for? What autoantibodies?
My Rheumatologist used the early sjogrens panel because I never would test positive for Ro and La. The positive ANA, Early Sjogrens Panel and decades long of symptoms 😢 finally gave me my diagnosis.
@@ehjohn027 Did they find any other autoimmune disorders? My rheum recently said that seronegative Sjogrens is oftentimes secondary or comorbid to other AI disorders like RA and lupus. I also have Antiphospholipid syndrome which was found incidental to the others.
I have several good ideas I'd like to be abducted into a think tank but still have some relative freedoms in case they can't let me go, I'm willing to cease any and all Interactions on all levels with everyone . I want to know what the future holds and I want to live luxuriously underground with some elements including constant monitoring if needed, but I want to help to a point but I know there isn't life on other planets for the same reason it's not ok I exist. Sometimes we take measures sometimes the measures are for political needs that are only fantasy.
As an American, living abroad in Latin America, I was diagnosed using a salivary gland scintigraphy. I'm very curious as to why this isn't standard practice as it seems pretty straightforward, non-invasive and cheap.
Rituxan has really helped me with my Sjogren's neuro symptoms. Plasmapheresis completely got rid of all my symptoms, it was insane. I'm seronegative with novality antibodies.
If you need someone to DX, I would love to help, to help myself. I won't go through my experience to find out what my extreme pain means and how no one seems to care enough to dig deeper after their first initial testing. Meanwhile, I live day to day with a pain scale from a 9/10 depending on what I have done throughout the day. I'm starting to lay down more and more because my body can't stand to be sitting or standing up at a certain point of my pain. I live in Dearborn MI, if you can help me to get there and pay for expenses to go through this, please choose me as one of your patients.
Please, please stop adding „background“ music to this kind of content. In this kind the music is even louder than the spoken content so it’s not only distracting but just dominant. And just as colored backgrounds I.e. in Facebook are not readable for blind/visually impaired people this kind of music is as non inclusive for otherwise impaired people like me as an autistic or like folks with adhd and so many more.
Only hydrogen and helium working mutually is effective all others are only experimentation projects. So we need not go for fusions .instead oceans and wave energies are environmental friendly.
