Відео

It attacks way more than hands and feet. It might start there but it ends up affecting every single part of you. Every joint.

I have been diagnosed with RA 30 years ago. Because I no longer want to take the biologics I cannot get a Rheumatologist. The one I had retired. I have been on Prednisone for the last 2.5 years. I eat a very healthy diet. I can go almost 2 weeks after being on prednisone for 11 days before an another flare up. I do everything to keep active. Today I woke up with a swollen left foot and ankle, two shoulders swollen left I could barely move while on prednisone.

I'm listening to this as a potential RA sufferer. I haven't been diagnosed, but I'm getting tested today. I feel that my doctor has overlooked my symptoms, and it's frustrating. Thank you so much!!! I needed this.

I completely cured severe seropositive Rheumatoid arthritis by going carnivore. It's been over a year with no signs of inflammation in my bloodwork, no pain or stiffness at all and have not had to take the biologic medications ever since I changed my diet. I was initially very sceptical as previous dietary changes had made no difference at all, even going completely organic whole foods plant based vegan as espoused by the Paddison program for Rheumatoid Arthritis and the McDougall Starch solution (which both gave me temporary improvements from cutting out junk food, but very quickly made me worse). The key is to cut out all sugars and carbs (which are also sugar like fuels) My rheumatologist still won't accept that the carnivore diet cured me...🤯

How does he know it's the RA is causing cardiovascular events and not the suppression of the immune system or the medications? I mean people have RA for awhile before diagnosis but the cardio numbers don't increase at that time, only years later when most patients should have had the inflammation in regression except for some flare ups? 🤔 Also, he said this was also found in Corona in the US. Where or what is Corona US? Pretty curious on these statements I see no real causality offered to back up the claims. There could be, it's just not validated at the 13:00 minute mark. I'll watch the rest to see. I'm also not sure why he looks so happy sharing this very bad news. Dude is weird! Don't trust him. My discernment of deceit is off the chart right now. JS. 😢

Just diagnosed with sevonegitive RA. Begun a carnavior diet, no plants/fruit, and and try to keep moving. Im feeling better they I have in a long time.

Chronic Fatigue...a most difficult RA symptom that gets little attention, and many people are suffering in silence. Still looking for solutions here, it's a difficult thing to cope with. I watch and listen with an open mind to any sincere soul, we must be ready to accept and make changes. I found the greatest relief so far by adopting a grain free diet first...and then finally went plant free, and doing so helped reduce 50-80% of the RA associated pain symptoms but still struggling with chronic fatigue. I have learned, if one just stops consuming seed/vegetable oil, carbs, especially from grains, they will do so much better managing RA and better health in general, no matter the issue!

I've had ra since I was 26. I'm 42 now. I can manage it with Rinvoq. Just don't like taking these medicines that causes cancer. All of them are like this

I have RA. I’m considering calling it a wrap. 41 yrs is a good run in my book.

Lmao

Oh my goodness, I hope to get a rheumatologist who is as smart as this Dr. I have been treating the symptoms of Sjogrens Syndrome for decades when I probably have RA. I recently asked for a referral to a rheumatologist to better treat my "Sjogrens" symptoms. After talking to my cousin today, who was misdiagnosed with Sjogrens, I learned that RA has many of the same symptoms as Sjogrens. Thanks for such an educational video!!

I have ulna deviation. Methotrexate did not help. I have several synovectomies and it still occurred.

Lyme disease

I have positive ANA and several other tests my rheumatologists (super young) ran. All started five months ago VERY suddenly but leaves me unable to walk, shower, get out of bed, even use toilet unaided. Shocking stuff!! I am on high level steroids to function. This doc STILL won’t diagnose RA because it’s “atypical” to have the shoulder, wrist, hands/fingers, knees, ankles/feet all swollen at the same time. She is so timid. She says ‘you don’t see thumbs effected with RA usually so let’s just wait’. WBC count also high, but she won’t even try a round of antibiotics. I am not going to drag this thing out because she is afraid. I am going to try and see if I can get an appointment with you or get a recommendation of a doctor from you. Also calling Johns Hopkins for the same. 56 years old and ain’t nobody got time for this!!!

I have RA l changed my diet gave up sweets no white flour items take tumeric supplements. No sugar drinks and l drink alot of water l feel better than I have for a long time just remember all drugs are poisonous

Chylimida pneumonia lung infection causes arthritis and Alzheimer's disease

Finding a very educated in a college natural path to help you get your immune system balanced and get the inflammation down is key, then find a myofascial release practitioner to release the restrictions in the muscles tendons and allow fluids to flow into the joints

I presented at 28 years old with shoulder, elbow, hip inflammation. Doctor outright refused to consider RA despite family history (my mom in a wheelchair with it and was his patient). He blamed it on having two toddlers and told me to take Tylenol and that I must have strained my thumb joint (also implied this was all in my head) when it swelled up and turned red. Finally changed doctors. New doctor immediately asked about family history of RA and ran an arthritis panel. RA Factor positive. Bingo. So much relief. Biologics have kept me walking but I have had lung and heart involvement….Rheumatologist insisted the lung involvement was MAC which meant going off Humira……it wasn’t - it was classic RA Lung….had to change doctors, again to get appropriate treatment.

My symptoms srarted at 10 months old. My fingers and toes were red and swollen. But it wasnt diagnosed until i was 2 and the joint damage started to become obvious. My elbows quit straightening literally overnight and theyve been stuck like that since. Im 45 now and not coping well honestly. My body and mind are worn out. I can't imagine having to deal with this for decades more as it gets even worse. Of course its progressed more and spread to many joints since then and I'm always absolutely exhausted already. It takes everything in me just to exist. Ive been hoping for a cure my entire life. I haven't worked in nearly 10 years either. I appreciate this video because you wouldn't believe how many people think its the same as osteoarthritis. I often get invalidated with "me too" when i mention my RA. 🙄

There are thousands of auto immune diseases and so called health science is totally useless. All they do is prescribe drugs with horrific side effects. There is so far no cure...unfortunately. They can suppress your immune system but that leaves you open for all kinds of other diseases.

This man saved my life 😭❤❤❤

I have RA and take methotrexate. RA also has a connection to mycoplasma bacterial infection which I tested positive for and take minocycline daily. There is also a connection to the vagus nerve and there is a surgery to implant a stimulator next to the nerve which has eliminated RA. In RA the body’s parasympathetic nerve system is inflight or fight mode causing the body to produce cytokines. There are techniques available on UA-cam to calm the vagus nerve without the surgery as well as a couple companies that sell external vagus nerve stimulators. I also take low dose naltrexone at 4.5 mg a day. My rheumatologist wouldn’t prescribe it but I got an online prescription for it. I was at a point last January where I had to be helped out of a chair by two friends because I couldn’t generate enough strength to cut through the pain. I had just gotten the LDN three days before, you’re supposed to take it at 1.5 for 10 days, then 3 for 10 then 4.5 max dose. I maxed it out that night and was able to get out of bed the next day, I had only been on methotrexate a week at that time. LDN is basically narcam at a low dose, it shuts down your opioid receptors in your body for a few hours which tricks your immune system into producing it’s own endorphins and floods your body with your own bodies painkillers. I hope this helps someone as this is from my research to try and help myself.

I’ve been dealing with this for 22 years. I’m finally good! I take methotrexate by injection once per week plus folic acid 6 days a week and a weekly injection of Brenzys (biological drug). But the kicker for me was the keto diet! 4 years now. Lost 100 pounds and kept it off. My rheumatologist is astounded by my progress!

He never gave the food to avoid I guess that wad was hook😤

It's very upsetting when the meds make you feel sick and my anxiety over methotrexate. And I have only had one clinician who truly understood my pain, nausea and tiredness...impacting on struggles with normal daily tasks. All over pain, not just the joints. Painful feet for years too. Until my pain became unbearable by 2020... eventually diagnosed with RA, by blood tests and x-rays. The specialists do not even understand or want to understand. And for the rest of everyone who are not involved in my life. It's just a bit of joint pain...and they're older than me. Why do I get tired and struggle...😥. These videos are so great, and wish hospital specialist and doctors would understand our suffering. And not brush everything away, it's somehow my fault, the nausea, the poor appetite, the anxiety and depression I suffered from anyway. And not always following my treatment for those reasons at times. We live in a world where drinking lots of water and exercise will miraculously aid in improving our health problems. Very important of course. If only a healthy life only depended on drinking lots of water and exercising. Keep moving keep moving...yeah ok. I have always been active in my job role and as a non driver, lots of walking. But have bad days and need to rest for exhaustion, needing to recharge and weak and anxiety too.

I got diagnosed with RA at the age of 29 years old, I'm 34 now, my I started treatment with Dolquine and Sulfasalazine, I was diagnosed with RA lung nodules in 2020, now I'm on Sulfasalazine/Salazopyrin whichever I find in Lebanon... I'm a smoker, work full time job, and the tiredness rarely goes away, hot summer days are very hard, and cold winter days too... I wish people would understand this disease instead of saying "stop thinking about it and you will be fine"...and my RA factor is 229

I wanted to understand this as I have a review with my consultant next week. The problem though was I couldn't read any of the script on the slides as too small.😒 Im in the UK, suffered for twenty years now, 79 y, in remission and injecting 162mg RoActemra weekly and Metotrexate 20mg and folic acid. My consultants (Bath RNDH) have never been able to define my RA, I have the physical symptoms but all the tests show negative. Im disappointed they wont discuss anything in depth. Why is the ring finger the only one completely unaffected while all other fingers (but not thumbs) have affected joints? So is the silver ring altering any electrical signals to that finger?

What????

I have a question; is it common in colder states? I just got diagnosed after a bunch of misdiagnosis. I live in Wisconsin

in fact Dr Aluda on UA-cam is a good herbalist and a trusted Dr. my wife shrunk her multiple fibroids with his herbal medicine..

In medicine , familiarity breeds contempt and kills.

U just describe what I am living. I just have my second surgery in my left ankle. The first one was In the right one. Pls help me, I got enough, I also have polychondritis. HELP ME!! B

Thank you for your share. You have shed some lite on this horrible disease

Please try ayurveda medicines they cure permanently. A friend of mine with lupus got cured completely in 1 years time.

I had juvenile arthritis which I didnt outgrow as was expected. Now close to my 40s and its been wreaking havoc to my gut health.

My oldest son is in his early 20's and he has type 1 diabetes. But thank God for this piece of article ua-cam.com/users/postUgkxVYhghKWmrUgXARZ_ydZTvmmcrw5L0I5i At first he thought he had the flu and was lying down on the bed for three days until his sister took him to the hospital. They took his blood and it was 600. What I do not understand is how he could have gotten it, since no one in the family has it. But he is winning the battle now. This is good stuff.

RA care pack by planet ayurveda consists of natural herbs such as shallaki, Guggulu, Ashwagandha etc. which is very beneficial in managing rheumatoid arthritis

I was diagnosed with rheumatoid arthritis at 40 years old but suffered with severe leg pains as a child, I had to give up my nursing job in a hospice at 45 years old as I couldn’t do my job anymore it has affected my organs I get frequent pleural effusion, pericardial effusion and a pneumothorax of my left lung which never re inflated I got a blood clot in my groin had a filter fitted in my IVC which became embedded so couldn’t be removed which caused severe ascites in my abdomen and veins swelled in abdomen and became very painful I have severe anaemia and on anticoagulants for life. The problem is all the treatments I have tried for rheumatoid arthritis has caused severe side effects so all I am taking is calcium supplements, oxynorm slow release, prednisone, iron supplements, I was on fentanyl patches but caused problems so won’t take anymore I had an emergency total hysterectomy but can’t take HRT I am in constant pain I cry myself to sleep every night because of pain my drs and specialist do seem to know what to do with me, I have other problems too but just get on with it I have nodules in my esophagus and have to have my lung drained regularly, I have synovitis in my wrists and ankles I am wheelchair bound at moment what can I do I need help desperately

I am so happy that i cured from HIV / AIDS ....... Dr forture on UA-cam shipped his herbal Treatment to me in USA that cured me from my HIV i am now living my normal life without any form of sigma i recommend his UA-cam to you he also have cure to HD4 STD , STI and many more ..... dr forture

Interesting. Thanks for the explanations.

Diagnosed at age 38. I also have lupus. Autoimmune diseases are hard to deal with

The fatigue and pain is just horrible I’m almost 42 I can’t take it no more. Have had symptoms since 5 years old got diagnosed in my 20s. I’m on Coestynx injections after methotrexate didn’t help…I’m crossing my fingers

I inject this and it doesn’t hurt at all. Very tiny needle and I hate shots. No side effects at all and I never started pills only injections.

No I have R.A. and it has been affecting my eyes. My ankles are swollen all of the time.

I am only a week into this after being blindsided with pain and paralysis.After much research i am over the shock and moving toward the depression.I am 64. Now on a positive note i have noticed changes in my bowel.I have been doing keto for high bp.I have had two teeth pulled years ago and an additional root canal.I used to use peroxide as a mouthwash.I believebibruined or killed my gut bacteria my flora no doubt in my mind.I am in a rebuilding stage,no meat or dairy,prebiotics and probiotics.Green banana and cabbage then saur kraut,kimchi,yogurt, kefir and fresh veggies and fruit...wish me well and good luck to you all.

I got my wife a herbal supplement from Dr Aluda on UA-cam which helped her shrunk her fibroids and made her conceived 2 years back, am now a Father of twin after so many years of miscarriages due to fibroids. all thanks to Dr Aluda💙

Ahhhhh he just made me realize/explained why my iron is always low and the newer constant dry eye 😑🤦‍♀️

And what about proper diet...? This is a drug guy pushing drugs and making matters worse... Lowering your needed natural immunity is harmful. Best to correct the immune system and that is the proper direction for research NOT drugs alone... All the very best in healthy and happiness

I was wondering if anybody out there with r a i Am 77 and was diagnosed a few months ago doctor wants me to start Methotrexate I'm a little bit Leery and that's why I'm listening to different doctors on UA-cam can anybody tell me if they get lightheaded or a little dizzy with this condition I'd appreciate your feedback thank you