Take a tsp of tumeric tipof tsp of black pepper and a tsp of moringa powder i buy mine from an indian spice shop an bromalian which is lobaan from an indian shop google resin ,,,,,thank you

Genius...........

Has anyone tried herbs to heal the body? Herbs heal, even the worst of the dis-eases. Please try some herbs when you get sick, God provided them for us to heal our bodies.

China? Which Chinese hospital?

My uncle was struggling with sun allergy for years, facing constant discomfort. After using IAFA Ayurveda's natural solutions, he experienced complete relief within just 3 months. The herbal remedies and personalized guidance helped soothe his skin and reduce flare-ups, offering him long-lasting comfort.

So inspiring! Are you still on medication? What helped your hair grow back? Wishing you lots of health and keep smiling! You’re absolutely beautiful!❤

Yes theres hope .. i have lupus and also had a heart attack the will to "Live" is different than being "alive" living walking smiling sunshine human contact essential 💖 I have a higher amino supplement which healed my joints my muscles my serotonin My life turned around from having lupus diagnosed at 27 years old 25 years ago I have survived the "storms" lucy in tbe sky with diamonds " song is written about Lupus Choose life find a great rheumatoid doctor as well an DO Doctor of osteopathic heal theres hope

Do patients have to have double stranded DNA to qualify for this procedure?

I wish I found you the last 6 months from this job. I was “paid to leave” severance 1 month post FMLA directly due to my Lupus - 2 versions, the standard one and Antiphospholipid syndrome (blood clotting autoimmune disease) that directly led to a major heart attack in May 2022, so mine is a more severe type of bad. I told them, and they knew about all of this when they poached me from my previous employer almost 2 years ago. Due to serious work abuse and the stress of medical discrimination (I never knew this was a thing), being mocked by my boss and ownership, I was starting to get increased flare-ups, which again I never knew was something I would go through, much less the ferocity I was having them, and still worked through all of it. My Doctor in Santa Monica (with my whole medical team there as well) told me to go on FMLA. I was afraid, but he said, "Let’s see how you do every 30 days." Needless to say, violations occurred during my medical leave, I can’t even write about the insanity they did. I returned to work after 30 days, and I was taken off of projects, my job completely changed, and all of a sudden I have this regimented schedule that I NEVER had before, like never. I requested reasonable accommodations to literally go back to the way it was before, which was hybrid and fully remote at times and for months. I was denied reasonable accommodations on the phone by ownership and threatened regarding my job. I was demoted in terms of my job responsibilities, which directly put my health in danger, plus work I’ve never done before and 4 levels down from what my job and title were. It was as if they were attempting to force my hand to quit, and I still didn’t since I thought if I did it they would stop. It just got worse. 1 month later, they marched into my office and stated my position is no longer needed and were pressuring me to sign this severance with NDA - I still haven’t. I found you because it’s hard for me to believe that someone cares for my particular illnesses, and I have never experienced this before with my previous employer. I have lawyers that want to take my case, and they all have different perspectives on it but want to take it as a case, but I feel like none of them understand the level I am autoimmune compromised. The blood clotting one leads to a heart attack, strokes, or DVT. Sorry, I had to express myself. I would love to have an advocate for this like YOU who would understand my situation. Thank You, D.

This and Just Mercy amazing performances just raw emotion

I must say that my dermatologist and the rheumatologists have been excellent. I was diagnosed with systemic lupus,and sjorgrens disease 30 years ago. It is sometimes is not easy for general physicians to diagnose these diseases. Although, many have had experience. Thank you for the comprehensive lecture.

I’ve been telling doctors for 30 years that something was wrong with me. Just now has a doctor run and ANA and it’s positive.

Thank you for this great information!

Thank you so much!😊

This is an amazing video. Loved her and how she gave her own testimonial as someone who lives with this disease. Thank you 🙏

As for exercise. I'd suggest a rowing machine. Its low impact on the joints and works 80% of the muscles. Row for 5-10 minutes several times a day. This keeps the metabolism high and its easier than one long workout. Also, take an ergothioneine supplement. Ergothioneine gets released into the blood with exercise. Our bodies don't produce Ergothioneine but we have a storage and transport system for it. Its in every cell in our bodies. Watch this video for an overview of Ergothioneine and why its important. kzbin.info/www/bejne/jImboqmCrtmmgNUsi=hbhTtUqvT2EdXSeS

Could this be a better way to turn off the B-Cells ability to create the Antibodies? kzbin.info/www/bejne/h5fXmqF5iZqMj7Msi=mEtHiD0BeJe9JNkk

I have a friend with lupus and surgical menopause and she wants to take hrt. Is this possible? She is desperate for help to stay healthy and can find no information or doctors who will work with her. Is there any Dr out there knowledgeable in this combo?

Really great information, I had never purchased these products so it was valuable to get guidance

Any information regarding levonox in pregnancy ?whether it should be given in APLA positive or even in APLA negative lupus patient during pregnancy ?

Does Methylin blue help?

I want him as my doctor. He actually gets it!!!! My rheumatologist told me today my labs look great so there's nothing wrong. Really? Then why can't I take 20 steps without being out of breath? I'm soooooooo tired of being sick. 😢

I had positive ANA, high anti-dsdna, high b12, and high alk phos, but was told I don’t have Lupus or any autoimmune condition for that matter.

Very informative. Thank you. What's a good vegan no algae option? Is flax acceptable?

can i request an inerferon test from the doctor?

Thanks for the sharing, very informative!!

it is still not clear to me why we need the engineered t-cells to attack the reactive b-cells. Shouldn't Cytoxan given first supposed to kill them all anyway? Another Q: the new incoming b-cells may still be re-active, right? Does CART therapy increase the chance of the new B-cells to be healthy?

awesome news, and great presentation. Thank you, Dr. Donald Thomas.

Thank u

Very good

Wow great

I had an ana, loads of lupus symptoms. My ana was positive but never got a teir, im uk.. is this normal?

Hi there! I’m late on finding it but the FATIGUE that comes w this DZ is overwhelming and I am now on year 20 of diagnosis. My question is the ability to qualify for CAR T CELL THERAPY without kidney dz yet bc would it not be sensible to help a patient that is suffering 20 yrs BEFORE it goes into the severest of dz? My diagnosis perfectly lines up with your ideal candidate of Lupus; Scleroderma; Polymyositis; RAYNAUD’s active syndrome. Please direct me where to go at Mayo or whom to speak to. I am not far in North Dakota, myself. Thank you! Angelina ATF

What are your thoughts on red light therapy?

Thank you so much

Hello to each everyone’s of you I have a very important message or concern regarding the lupus which I had my first rheumatologist doctor told me that I have a sign of lupus. Besides of thyroid, migraines, hot flashes, vertigo, anxiety, depression. Literarily it’s been bothering me since I can remember. I don’t know where to start but I know that I have been going through this pain for a long time. I was working hard when I kept going back and forth to see my doctor and I limit myself to say how much pain I have been having because I was afraid to take medications and I was afraid that I get fired from my job because of too many doctors appointments. Sadly the pandemic helped me to decided to take the severance package from my employer which I was still taking care of my mom health and her health was not good either so I decided to take the severance offer it was offered to people that wanted or had a difficult time or reason important than anything else. I thought I was just over work and stressed worried about my mom health. So to make the story short all my doctors and therapy’s appointments isn’t going well because of copay. I have not been able to go back to work since 2020 after 20 1/2 years and yes twenty and half years of work I can’t even get any help from the government to get my health care paid my bills. So sad and I have a lawyer that hopes to help my situation cannot wait to get back to normal body and not worry about bills filled up. As of today still hoping to get help from the government still praying hoping. To all of you who is going through any kind of pain hopefully healing and help is on the way to all of us god bless 🙏🏼🙏🏼🙏🏼🙏🏼

I'm currently waiting for tests to come back for my chronic uveitis with my optic nerve changing. Lots of stuff like diverticulitis that perforated and bells palsy in the past. I am very sensitive to the sun But I am also white and red haired. A lot of my symptoms line up with lupus and my doctor is leaning towards that right now. But yea it was weird to me because I thought that was a women's only dieses Guess Im learning new stuff. Anyways thanks for the info Its hard to find anything related to men and lupus. Also had to have my appendix taken out as a child because it was full of pinworms. probably not related but wired none the less. Also had surgery on my feet at 14 my Achilles tendon was to short they had to lengthen it. and my feet had to have bones broke and shaved down and my heels have metal bullet shaped gear in them now to keep my feet straight. I was in a wheel chair over that one for about a year and a half. I have also had the issue where When i breathe in deep it hurts. Had it happen today while I was working.

Im taking fish oil, my hair havent been falling out since

Thank you for this. My GP literally asked me what tests he should do to determine if I have lupus. I have a whole host of symptoms, but the blames all of them on my Hashimoto’s. I’m going to show this to him.

I really had a blast doing this interview and I really appreciate Lupus LA providing a great platform for us to be able to share my story and be able to let the world know about lupus and especially from a mans point of view. As I always say I'M DRUMMING TO A DIFFERENT BEAT AND THAT'S TO BEAT LUPUS. #BEATLUPUS

My joints and muscle hurt wo bad to could it be the heat,thankyou 8m tring these excercises,I to the point where anyth8ng hurts after I had a 20min seizure,thankyou for this video

I was diagnosed with SLE while in my late 40's after complaining of joint/hip pain. I am currently in my early 70's (and a white male, go figure). My PCP referred me to a rheumatologist who, after running more tests, confirmed for a fact that I had Lupus. I was handed an information pamphlet and sent home with no follow-up. I think that the only parting advice from the doctor was "Stay out of the sun." Looking back, I must have had SLE for years due to chronic anemia. I also had been diagnosed with Wolf-Parkinson-White Syndrome where the anemia exacerbated my SVT episodes. Without proper care from a qualified specialist, things went from bad to worse over the next year. Over a 6-month period, I had 2 myocardial infarctions and 3 DVT episodes. After the second DVT, I had surgery to implant a greenfield filter. After the myocardial infarctions, surgeons performed an angiogram but found no heart damage or obstructions. Every time I had a DVT event, I had to go on disability for up to 6 months and stay off my feet and be on strong pain medications and anti-coagulants. I had also lost over 30 pounds over time. I was fortunate enough to have a conversation with one of my wife's co-workers who had Lupus. She had been fighting the disease for many years. She was under the care of Dr Daniel Wallace and strongly encouraged me to get a referral and an appointment to see him. Dr Wallace did more for good for me in one month than my other doctors did in years. I honestly feel that he saved my life. I recently had my fourth clean PET scan in the last 15 months after a 5-month chemotherapy regiment for treating my stage 4 non-Hodgkins lymphoma. It would be great to meet Dion some time just to swap stories. I am also a former drummer.

Why is my alkaline phosphatase elevated. Most recentmy 990. DX 2005 connective tissue diwe are from elevated liver studies, positive ANA then +ANA panel.

Does anyone believe President Trumps had ever heard of hydroxychloroquine until Birx or Fauci mentioned it?

what about sjowgrens syndrome thank you

Please speak a little bit louder please your voice is beautiful but unsound so far away

5 or 10 minute yoga every day was very beneficial. I couldn't move much before, way too much pain.... so much better now.

Disappointed to see this multi-level marketing company on the Lupus LA channel. Lots of misleading info and unsubstantiated claims offered in this video. 😡

Which sunscreen does Dr Thomas use on himself?

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