What is lupus?

My friend just died today from lupus 😢

If lupus attacks the brain you maybe incorrectly diagnosed with bipolar or other psychiatric disorder!

I have always wanted to be a vampire and now my dream has come true yay

I haven’t been diagnosed yet but when I watched this I felt like all those people understood me and my struggle for the past 25 years

No diagnosis and doctors won’t listen to me

Lupus is hard. I want to cry from pain just sitting here

Lupus is something as a child I was diagnosed as mild my family was poor so my grandma who is native Indian and had natural cure … today dear me my face is infested with red mask on face

My eyes thyroid is always in the mix but tests show not diseased

Leave it up to woman to tell you what's wrong , so is UT a feeling or a physical condition ?

I’m in the process of being diagnosed with Lupus. All of my tests come back normal but I feel far from normal. I just seen a rheumatologist who believes I have lupus without a doubt and are being tested for it now. Reading these comments and watching this video makes me feel like I’m not alone and it’s all in my head. 🥹🫶🏾💖🌺🐝 God bless everyone whose suffering from Lupus, this disease is a silent hell show and I’m so sorry for anyone going through this 🥺😔

Lups is likely to pull over a female person of color and neal on them until . . . well, until . . . they have lupus.

If you want the 4 sec version. It’s when your autoimmune system is fighting itself. Specially targeting organs.

I've been in the battle since 2017 almost took my life twice I'm battling again waiting on blood work pray for me thanks

I just don't know what it is

My neighbor has lupus, she wanted a baby so badly and she couldnt have one. Broke my heart for her.

I was diagnosed with Lupus since 2009 right before my last semester. Unfortunately, I was not able to take my last finance major because I had a seizure the day before.

I remember I ended up on the floor surrounded by paramedics and my family. I had since suffered so much after - in and out of hospitals, doctors appointments, missed major events, had to quit my job because I was taking leave most of the time due to my lupus flare.

As I typed this comment, my kidney function is currently at Stage 4 and I've been crying almost everyday but trying my best to do whats best for my body, mind and soul. I dont want my kidneys to fail or be on dialysis or even need a transplant.

This scares me so much and it pains me to know that it can ultimately/drastically change the course of my life forever. Its scary to think Lupus can cause serious issues with your internal organs.

Best of luck to anyone suffering the same as well. I only pray that you get better ans have a good support from your family and friends because they do make it easier for you even though you are going through a tough time. ❤

As a person newly diagnosed with lupus I want to tell you how deeply horrifying and unhelpful this video was I am having palpitations and my anxiety is through the roof. Thanx

So sad your mom couldn't survive 🤣😢

Like waking up and crying cause I have to go to the bathroom and I have to walk to get there

I'm trying to learn about lupus more since i knew an amazing and wonderful person who is kind have lupus. And i wanted to know how we help. He is amazing and just wanted him to feel better. We love him.

Well, I rather have a lupus why well because I have a learning disability and it’s hard to do math. It’s hard to read but alert others. It’s hard to understand you repeat things that you don’t realize I also have a dub of vision problems with my right eye, I see double, I have a stomach issue that it’s hard for me to eat. I also have anxiety attack so honestly, I rather have lupus instead of what I have I was born with it my birth parents smoked and drink when I was in her and it causes all this terrible things that I have, my adopted family supported me so much my brother he wish I never had this problem. I’ve been wishing this stuff for 1000 years there’s no cure of when you have learning disability. It’s a gene lupus you take medicine OK so it doesn’t help it doesn’t take away but taking medicine, it’s better to take medicine than not my learning disability. There’s no medicine for it. I’m stuck with it all my life you can’t tell if someone has a learning disability or not when you’re with them for quite a lot then you find out and then you realize something interesting !

Kisi ka think huva kay

So just take your car into get a tune-up --- aweful video

Just lost a friend from college from lupus. This is really painful to deal with...

Türkçe alt yazılı lütfen

I have lupus and it’s been stressful I’m 23

Thanks for sharing this information….its always great to learn something new about the human body. Stay strong to all those who experience this condition. 😊

What about joint pain.. I'm having problems with both of my knees my left hip the lower part of my back and my left elbow.. unfortunately where I am at services are very slim.. so most of the time you get shoved under the carpet..

it's never lupus
- dr place of residence

In 1963 when I was 14, I got the sensation of one leg being huge & the other leg being teeny tiny after coming out of convulsions, now called something else, but for a long time called Grandmall seizures, while having Shingles on the left side of my back. I was already in trouble "for being sick" so I didn't tell anybody about my weird sensations. When I was 19 after having my first baby it happened again, although it wasn't my legs it was just weird sensations all over my body. I was 50 before I was diagnosed. When I was 27, exactly half of my body, my left side, was numb & tingly for months. When I was 39 I didn't have the sensation of having the need to have a BM for almost 10 months. Feeling like things are plastic on my body yet they look & move normally. I've had the butterfly rash as a preteen even. Because I eat a very clean diet without processed food I only get the butterfly rash now if I've been in the sun too long or if I'm under high stress. I'm typically guessed to be at least 10 years younger than my actual age & people tell me that I look so healthy. Fatigue is my biggest problem now. What we eat makes a huge difference & I absolutely do NOT follow what the Lupus Foundation says as far as food. I'm not underweight or overweight & I've never taken any of the drugs for it. ☮️💞🙏

When i try to change my lifestyle 2 years ago and succeed but damn lupus had to come block it almost a year now and wont let me have it. Im so done with life. Dont have motivation to do anything. 😔💔

The white blood cells are like the wolves. Its the predator starts to hunt itself. Are you afraid of dogs snd wolves? I used to be. The roots of disease is most often what you have put in your mouth. Can you remember what you had to eat? Or maybe its just germs or some metals that where in the water.

Why can't Lupus patients qualify for permanent disability? I mean this sounds worse than RA and many mailmen and army vets get disability for lame stuff. I pray for all the people with this, may God love you and keep you safe.

I'm 73 and found out last fall with lupus. I also have incontrollable diabetes, osteoporosis, CKD, bursitis from a car accident seat belt injury and because the truck was huge... I have PTSD. And i googled lupus and PTSD go together 😢😢😢😢😢😢😢😢 God bless all of you ✝️🙏❤️

If you Google PTSD 😢it can cause lupus too 😢😢😢😢😢😢

When she described driving my van, I felt that 😂

I just met a girl who I really like a lot who has lupus and I'm trying to learn all I can about it so I can help her the best I can because I want to be there for her no matter what

My mom passed away from Lupus in 1990. Seems like now at least you continue to live for much longer.

Try a long fast. Water with lemon and electrolytes only. Not intermittent fasting, but a long fast. Once you get into 20+ day range, literally miracles begin to happen. 40 days i think is optimal. Our bodies are designed to endure feast and famine. Our bodies don't function properly with the 3 meal a day approach. During a long fast, you will only struggle the first few days. Relax while you do your fast. There is no need to exercise during this time. Sleep, read, watch tv, go for walks and get sunlight. If you're not comfortable doing your fast at home there is a fasting center that will have you hooked up to an IV with a steady drip of saline and all your pills are delivered by the staff, which is i think 10k, so it's not my route but i think it's definitely the smart approach cause they will constantly monitor your levels. Insurance might cover it. Not sure. Look in to it. Best of luck

Clicked on this to see what it is and got confused all over again what a waste of time

I have been suffering from lupus since I was 9 years old and now I am 22. Every now and then I search for the disease and it seems that there is now awareness about it..

worst video

I just found out I have this

My 23 year old son was just diagnosed with lupus

I also have Lupus it is one of the Challenging deases you,never know what will you,be like next minute. Sad 😔 part we can't plan thing's
a head 😢😢😢 And people don't
Understand you.

Guys watch delafe testimonies and a video called “Jesus healed me from Lupus.” It’s uploaded just NOW ❤

Tick-Borne Pathogens are responsible for all Autoimmune Diseases including Lupus 😰😰😰