Lupus Signs & Symptoms (& Why They Occur) | Skin, Joints, Organ Systems

[@jjmedicine]

I hope you all found this lesson helpful! Please check out my lesson on the Signs & Symptoms of Fibromyalgia kzbin.info/www/bejne/bqLEkIyloLWKrac

[@brendad940]

I was diagnosed with lupus almost 30 years ago and THEN the doctors tried to say I had fibro too but don't you think one is enough? I mean they are kind of the same thing, right? So I just said no thank you.

[@nafessawaters5446]

Love this lesson this gave me more info on my type of lupus that I never know. I was walking around with this but never knew it until I was 18. I'm 42 now.

[@henrymccullough1750]

All thanks to DR.UWENBOHERBALHOME herbal protocol on KZbin

[@yvonnegilmore712]

Yes I found your lesson to be very helpful so continue the good work to educate people on different diseases

[@donnastokes2187]

I have many of the signs and symptoms the drs have tested me 3 times and say I have false positive each time now I have stage 4 kidney disease why am I getting positive but they say I dont have lupus

[@yvonnegilmore712]

I was diagnosed with Lupus when I was 34 years old back in April 99 and doctors told me it was nothing they could do for me. But God plan was for me to still be here amongst the living. I am now 55 yrs and gone back to work, doing for myself and living a normal life.

[@yvonnegilmore712]

@@shellyseaton1858 , hi Shelley yes I am I take two blood pressure pills, anti depressant cellexia , anxiety pill, take pill for acid reflux, diabetes medication metformin, rebellious, and plaquenil for my lupus and been on that for over 10 years that helps keep the inflammation down in your body. So you see I do have a lot of medicines I take but it keeps me alive and so therefore we have to sacrifice if we want to keep living so I've come to that reality and just try to live my life as possible.

[@yvonnegilmore712]

@@shellyseaton1858 , and yes before I was diagnosed with lupus I was diagnosed with rheumatoid arthritis first then the lupus came out with the butterfly rash, lost a lot of weight, lost hair, a lot of legions on my body, dry heaving, very weak and lethargic before I was diagnosed. And also I was out of work for about 2 and 1/2 years then I was able to go back and I haven't had any episodes so I'm grateful for that but before then I was in and out the hospital at least two or three times and almost died twice but I'm still here able to tell my testimony as well to help others.

[@gracekahugu3506]

Amen 🙏🏽

[@librasun1478]

If you don't mind, what were the symptoms you experienced back then? Glad you're doing fine now.

[@ayonetwork4416]

Home that was teared apart because of lupus virus has been restored back with joy, peace and harmony. Thank you dr imenHerbal on KZbin for vidicating me and my husband from lupus completely completely

[@jacquieedwards8218]

I have been diagnosed with Discoid Lupus. It began at 27 yrs, i am now 86 yrs. I AM BLESSED. I am married for 60 + years, 2 children and 3 grand children. This is why I feel blessed. I was able to cope, live a normal life inspite of the health problems. GOD has been in charge of my existence and has not left me. I probably could/should have had better medical care, but it is impossible to find anyone who would go the extra mile, therefore for me to be where I am, I know I owe it all to Our Heavenly Father. I have and feel some of the problems outlined in the narrative, but I know it could be worse. Through it all I look to Thee Heavenly Father. Jesus is Love

[@ayonetwork4416]

Home that was teared apart because of lupus virus has been restored back with joy, peace and harmony. Thank you dr imenHerbal on KZbin for vidicating me and my husband from lupus completely completely

[@lindahinojosa299]

Praise God! You are blessed

[@ayonetwork4416]

@@lindahinojosa299 amen thank God, how are you doing do you also have lupus ?

[@lindahinojosa299]

@@ayonetwork4416 I have multiple sclerosis.

[@Azet7775]

Thank you so much for sharing your wonderful story of Faith and Suffering. I admire your strength.

[@esiebold]

Excellent overview! Have had Lupus for 50 + years and still here ! Has been a challenge, but I have had a good life. Retired nurse and physician spouse, I think our educational backgrounds helped us deal with coping through the highs and lows.

[@mandronwolly]

Really do not know why people still believe in modern medicines when there are herbs as the complete cure for herpes and many other STDs. God bless HERBALIST DOCTOR KINGSLEY on KZbin for curing my herpes disease.

[@ej5376]

That’s fantastic! I’m so glad you’re powering through it! My Mother has just had a diagnoses and I’ve spent the last 48hours trying to learn everything about it. Did you ever try a Ketogenic diet with salt, or a beef only diet with salt? If so, did it help?

[@brendad940]

I was diagnosed with lupus almost 30 years ago and learned more from this video and the comments of other patients than I ever have from any of my doctors.

[@tenminutetokyo2643]

No profit in cure, only in treatment.

[@ayonetwork4416]

Home that was teared apart because of lupus virus has been restored back with joy, peace and harmony. Thank you dr imenHerbal on KZbin for vidicating me and my husband from lupus completely completely

[@maimunagarbarurum1190]

I want to thanks dr imenHerbal once again,, I'm 35 years old, and I was diagnosed with lupus 11 years ago... It's really hard to live with it bones during the winter season and very very painful extreme tiredness on summer time...but now thanks to dr imenHerbal on KZbin who cure me from lupus

[@chrisharris7649]

Ditto. Same thought as you stated. I'm in rural Iowa - even traveled to several Specialists in the bigger cities in or bordering Iowa. Every single Dr/MD I've seen is almost cluel. I have had a flair for 7 straight yrs & pray for a reprieve. Every ye I've been hospitalized due to extremely serious & life threatening computations. Been life flighted many times just to get in to a larger surgical hospital & under the knife within a crucial 30 up to 60 min. All the money I've spent yet become a widow suddenly at 47 with 2 sons to raise with not a penny left behind from my husband to finish raising them. I can't continue paying goes Cobra at $1,996 a mo just for my health insurance alone. My 14 yr old was dx'd or upgraded to Congestive Heart Failure 10 days following his father's passing. I need to endure I can keep up with his medical bills 1st but also need to regain my own health do he has at least 1 parent to be here for him at a min of 3.5 yrs until he graduated high school. I wish I could pound this point into the unintelligent Dr's I see. Ill have to beg them to either take more time to learn about my disease. Or at the very least help me by directing me to a physician who has a greater desire to either gain or already have Lupus knowledge/experience plus understands Lupus & all the ailments that goes with the disease. Hence help stop my downhill progression as I approach 50 & need to be here for my sons. . Biggest Hugs. .

[@Gypsygirl9]

Why am i not surprised..I hope you are doing well.

[@CurvyBarbieOG]

I have Lupus, RA, and diverticulitis. So many people are ignorant. It boggles my mind! Thank you for this video ❤.

[@benjaminnapoli1834]

What were your symptoms for lupus. Ive been having breathing problems/chest pain, always tired, constant headaches, bad hair loss and now "retnal tearing" I think its called (black lines in vision and white flashes)

[@melissareeves4151]

I have all those things you stated along with sjogrens syndrome

[@nana6]

I also have systemic Lupus & Sjogren’s Syndrome. I’m in my 70’s now & my youngest son has Lupus also. I think I was diagnosed 20yrs. ago & my son was diagnosed about 3yrs ago. Praying 🙏🏾 for everyone that have this illness. 🙏🏾🧎🏽‍♀️

[@micamckenzie6669]

Oh gosh!!! I hVe the same diagnosis.

[@DaiseyStone-n2w]

Treat your body for all kinds of parasites, epically amoeba, they cause all the same symptoms as mentioned in this video

[@marleneharrison8692]

I also diagnosed with lupus too for many years but God is so good am here by the mercy of God giving him all the praise glory an still following up my doctor

[@TCASpeaks]

I was diagnosed with Lupus 4 years ago & I cut out gluten, processed foods & alot of sugar. I feel better than I did 10 years ago & I'm 50.

[@Sheenasalesthriftytreasures]

I went carnivore and it put my lupus in remission ❤

[@just-a-generic-username]

I wish any of those things had helped me lol. I'm glad you found some relief.

[@TCASpeaks]

@@just-a-generic-username hopefully you find something to help because I know what Lupus can do to a person physically & emotionally!😢

[@just-a-generic-username]

@@TCASpeaks thank you

[@TCASpeaks]

@@just-a-generic-username you're welcome 🤗

[@pattih7]

Lupus, Fibromyalgia, Rheumatoid arthriti! Muscle, bone and joints, 1997 til now, I was 47, now 70. Plaquinil has been effective, for Lupus. Rheumatologist prescribed. I was able to eventually go back to work, but by 2003 began with Fibro outbreaks more frequently and back pain severely. Disabled and ill for several years. Had to stop driving, due to Neuropathy. Back surgery 2007, did well, , at this time I’m using mobility chair to get around. It’s been a wild ride, and God taught me so much! I learned to make friends with my diseases, not resent the medication and therapy, and to thank him many times a day for His help and Love. Without Christ, how would I have made it!?

[@francetogo794]

Thank you Doctor for explaining it all. I had all the clear symptoms back mid 90's, lost a spleen, only 5 platelets, and a worldwind of hospitalizations...but I survived it all. Glory Be To God!

[@scrapbookingsnoodle]

As a fellow sufferer of Lupus (20+ years) I relate to your story❗️I just wanted to tell you that I’m so sorry to hear (even just a tiny part) of your suffering❗️ I also wanted to reach out & say that I am encouraged to see that you give your thanks & praise to God❣️You are in my prayers & I pray that you will continue to TRUST in the Lord with ALL your heart & lean not on your own understanding. In ALL thy ways acknowledge Him & He WILL direct thy paths❗️God Bless You Renee & sending GENTLE Hugs❣️ ~ 🤗 Jennie 🇨🇦

[@francetogo794]

@@scrapbookingsnoodle Awe, your message touched my soul. Thank you for your encouraging words. I'm a Christian and believe in the Lord almighty. I realized in my mid 20's in 1995 when I was showing signs of all of the symptoms the doctors hadn't a clue. Fast forward 2006, I was finally diagnosed with Lupus and Arthritis. I also realized later I could've died in my 20's but I could clearly see it just wasn't my time for the Lord to call me home. He has me here for a purpose and I'm fulfilling those purposes by being a beacon of light for all humanity in their suffering. Thank you for stopping by and showing me love. Blessing to you.🥰

[@mandronwolly]

Really do not know why people still believe in modern medicines when there are herbs as the complete cure for herpes and many other STDs. God bless HERBALIST DOCTOR KINGSLEY on KZbin for curing my herpes disease.

[@francetogo794]

@@mandronwolly Western Medicine will always prevail. If only major insurance company would take on Herbal Medicine, the world could be a very healthy place to live for everyone.

[@LemireCassie]

Amen! All glory to God in Jesus name. Hallelujah!

[@nellymolotsane9428]

I was diagnosed 3 years ago but thank God it has never disrupted my life in a big way.

[@janiephillips4842]

You're lucky. I hope you continue to be ok. I have Lupus, fibromyalgia, RA, osteoarthritis, everything that causes pain and sleep disorders. Stay safe and healthy.🌹❤️

[@nellymolotsane9428]

@@janiephillips4842 thank you; hope you get better

[@ayonetwork4416]

Home that was teared apart because of lupus virus has been restored back with joy, peace and harmony. Thank you dr imenHerbal on KZbin for vidicating me and my husband from lupus completely completely

[@kimberlysmith3582]

I have this symptoms but I've gained weight???

[@mama_keikei8081]

I’ve been suffering for about 12 years and diagnosed around 4 years ago and still suffer. I also have chronic pain syndrome. The pain is just horrible and when you have a pain issue (thanks to people who misuse pain meds) you get no help. It’s nice to know I’m not alone.

[@robinaddis-vaughn7271]

Honey, I'm with you. Why didn't they crack down on the rich white doctors who were just a drive-thru for opioid medications for rich white people? They had no problem throwing black people selling weed in jail, they were just trying to provide for their families (most were, there's always the ones who push stronger drugs). The doctors should be in jail. I shouldn't be in the UK on my dream vacation and barely able to move because my US doctor wouldn't give me enough pain meds to get me through my extended vacation. Lupus sucks!

[@pameladelmonte2418]

I know the feeling. Taking imuran and paquanil. Doing some better…🙏👍

[@bryannaewing9616]

RSD/crps? I have lupus, fibromyalgia, rsd, and ankylosing spondylitis. So I understand already having lupus pain plus chronic pain

[@Alexela03]

I had lupus for 4 yrs and now in remission, I still deal with some consequences but I’m still alive and kicking , there’s hope ♥️

[@cindylou1108]

I’m so sorry. It is frustrating when we cannot get meds to help us thru our day.?

[@heirhlupuii3851]

After 8years of suffering,i was diagnosed in 2009..still facing many problems I've lost all my teen years because of lupus...but God is so good to me that He saved me till today. I hope all who suffer from lupus also got healed by our gracious Lord.. Amen

[@aft3967]

If god is so good, then why did he give you lupus in the first place?

[@heirhlupuii3851]

@@aft3967 You've got me wrong, I didn't mean that God gave me lupus because He is so good... what I meant was that here in a small state in India where medical facility is very poor many people died because of lupus including my neighbour's daughter... but God gave me a chance to live He blessed all the medicines I've taken.. Eventhough I still suffers , He saves my life and my soul i can't stop praising Him...

[@heirhlupuii3851]

@Amaya Uzumaki I'm so sorry.. May God be with you and your family..

[@gloriarouwhorst5012]

@@aft3967 k(

[@ayonetwork4416]

Home that was teared apart because of lupus virus has been restored back with joy, peace and harmony. Thank you dr imenHerbal on KZbin for vidicating me and my husband from lupus completely completely

[@cassandraberry9036]

I were diagnosed with Lupus in 1999 so good so for thank God❤

[@BridLong-y7g]

My cousin had lupus. She received dialysis, had to remove her leg from the knee about three years ago but contracted covid while recovering in hospital. She didn't make it and sadly passed away alone in hospital due to covid restrictions. She would have been 50 years old this summer. She couldn't have children because of her condition but was married. RIP Tracy ❤❤❤

[@treehouse8175]

SOO SORRY MAY HER SOUL RIP 💔🫂

[@Zephan-y2w]

She's with you her soul

[@Jen-wo6on]

That is awful 😢, i’m very greatful the hospital my mom was at , let her sister, and my 2 sisters and myself be and visit with my mom ,for bout a wk, then i had to make that horrible decision ,to take her off life support, but it wasn’t from covid tho, her heart was too weak, i’m so sorry so many had to pass alone during that time, that whole mess was very unnecessary

[@jaydavis8394]

A few months ago I found myself unable to walk, use my hands and lift my arms. This came on overnight. Had someone not stopped by to see me I have no idea what would have happened. Luckily, my nephew actually lifted me and helped me get into the car. A friend took me to my doctor's office and then the doctor sent me to a hospital not knowing what was wrong with me. I have fibromyalgia also. The doctors diagnosed me with lupus and within two days of a new medicine I was once again able to walk and use my arms and hands. I've had surgeries and automobile accidents but nothing was as frightening as thinking I was ready for the nursing home. It was a terrible thought. I'm still doing well but I am waiting to see a specialist who treats lupus. So if any of you suddenly find yourself in my situation please relay to the doc that you could have lupus. God bless.

[@samanthaabel1079]

I limp sometimes in morning and sometimes i cannot walk without a severe limp my left side extremely weaker than my right. my orthopedic dr who got me physical therapy argued it wasnt fake with my neurologist who said it was anxiety ... it just takes alot of work they didnt want to do cuz im on medical assistance so thye dont make alot off me . greed is terrible

[@donnastevenson6700]

I have had lupus/ fibromyalgia for 27 years. The sun is my worst enemy. If I go into the Sun for a period of time, sometimes can’t walk for 3 days. My input on this is everyday you have to force yourself to get up, get dressed, and try to do whatever can that relaxes you and bring you some peace. This disease and the pain will wear you down quick. Break your day into sections. After 3 pm my body starts shutting down hard. Do little chores at a time and rest. Learn and recognize different levels of pain, and types of pain. I know the difference between muscle and joint pain and nerve pain. If you take narcotics , don’t abuse them. Try Motrin first or hot shower, or hot water bottle, or Tylenol. Save narcotics for really intense pain. Your body will tell you when you need to rest. Get use to symptoms and what your body is telling you. Every day you must plan ahead for your day so it doesn’t become overwhelming. Definitely find things that relaxes just you. Stress will make this so much worse. This disease has taken a lot from me. Had to give up my nursing because of it after 35 years of being a RN. I refuse for it to take anything else from me. I will continue to fight and give this disease a back seat

[@nancycarlos5695]

I have been suffering from Lupus disease for some year without having a solution to it until i done a research on KZbin i come and cross Dr.Auchi on KZbin channel. That was were i find effective herbal medicine to cure my Lupus disease permanently without having side effect from the herbal product.. i recommend Dr.Auchi herbal medicine for Lupus disease cure....

[@juliecramer7768]

Thank you for sharing your story

[@lauriewilson4741]

Thank you. I’m scared out of my mind. Not getting medical interest. Have to work full time.

[@lauriewilson4741]

@No. I’m new to this shite but seems everyday can be different. Don’t make plans bc you might just have to sleep through them. And no Rhuemotologist ? No help for anything. Discouraging

[@Sketchbook999]

Black seeds kalonji (nigella) great for covid/ and Lupus- it's got hydrochrloroquine- VIT D3- VIT C- important aswell. I got all of my fallen hair back after covid- and my energy levels- must spend time in NATURE. - I have recently grinded kalongi ( nigella seeds) - add half a teaspoon in water to LOWER blood sugar- that's how my friend in her 60s cured her DIEBETES- and another lady age 70 reversed her bad eyesight ( info below)- read everything PLEASE- you can prevent having operation for many things- HERBS are the answer- Turmeric great for inflammation- Moringa great for pains in body. - not eating after 6:pm - avoiding buffets- fried foods for breakfast- instead boil/ steam VEG. things- I have replaced 2 fruit with celery and boiled kale - grill instead of fried food for lunch- - stop watching television ( tell a LIE to your vision)- I threw tv out years ago. - eyesight can be REVERSED- optition told me the SECRET was to go out each day - look outside- - do eye yoga- eye exercises each day- videos on KZbin. - replace 1 unhealthy food with carrots/ spinach/ beetroot. ( the also reverse aging process for skin- hair- nails - memory- and energy.

[@MITCH31785]

I was diagnosed with lupus around 10 years ago. I also have Sjogren's and fibromyalgia. The uncertainty that comes with these diseases is the worst thing but you take each day as it comes. I also get serious issues with sunshine. Rashes and feeling ill with too much sun. There is a long list of issues but you learn to live with it!

[@genericamerican7574]

When I was a kid I took my moms umbrella because I didn't feel good in the sun. I had all the symptoms by that time. I was 33 when I was diagnosed. I have also been diagnosed with CRPS/RSD (similar to fibromyalgia).

[@blumerlredpilledgirl8958]

Yes agree and suffer all of the symptoms including hashimotos thyroid.

[@bolinhong2598]

I have suffered Lupus for many years and I finally got rid of it with help of herbal remedy from Dr Oyalo on KZbin channel. I used his herbs and I was cured completely with his herbs and up till now I’m negative

[@blumerlredpilledgirl8958]

I’m not finding that channel for the Dr.

[@genericamerican7574]

@@bolinhong2598 you can not cure it bot. Hopefully we can cure bots... maybe not in my lifetime though. ugh

[@j.a.whittler6983]

Thank you for sharing so much information. My older sister has Lupus. We talk via phone quite often. I live out of state. I miss her deeply. My sister talks alot about her symptoms. She suffers from the alopecia, canker sores inside and outside of her mouth, the fatigue according to her is unfathomable. She has the hot/cold flashes at night , severe arthritis in her extremities. As far as weight loss...not so much. One of her specialist doctors has her on steroids in which has caused her to gain extreme amounts of weight. When I see her in pictures, I can't believe how this medicine has caused such a weight gain on her. As a younger woman my sister was a very small woman. This really bums her out. I pray that a miracle medicine 💊 can erase this horrible disease out of her life. She's a fighter. I love this about her.

[@elizafaulhammer2203]

Get her off steroids, what an insane "medication"!

[@johnsonlee4130]

I have suffered Lupus for many years and I finally got rid of it with help of herbal remedy from Dr ehime on KZbin channel . I used his herbs and I was cured completely with his herbs and up till now I'm negative

[@cathybedwell1877]

Celery juice for healing - 2 cups every morning, pulp removed, 30 minutes before breakfast. God bless. ❤️

[@patritablackston2064]

J. A. I'll be praying for your sister although; I know God is in control and he has his arms all around her. God Bless you.

[@j.a.whittler6983]

@@patritablackston2064 thank you so much.

[@tarinachickadaunce8011]

I was diagnosed at 38 2 years after i was originally diagnosed with RA. Between my hair thinning so bad, always being so tired it was hard to function, my feet, toes, fingers, etc swelling up & constantly aching, and the sun bothering my skin & eyes, and the constant fluctuation of my weight along with a number of other irritating and painful symptoms I seriously had days I thought it would never get better and that i had to be crazy because no normal person should or could really be experiencing all that stuff and not have a solid reason and understanding of the cause of it all and how real this disease really is. Learning what Lupus is, how it effects the body, & what to do to help control & minimize the symptoms of it has helped me learn to live with the disease and live a much more normal life. I was lucky getting an experienced doctor that really cares and took the time to listen and educate me from the get go.

[@brendad940]

I wish my doctor were that good.

[@kimjohnson5385]

I was diagnosed with discoid lupus 10 years ago, I'm now 57 and don't take any medication only because I'm afraid of the side effects, they want to put my on medication that can cause blindness, do you take anything?

[@brendad940]

@@kimjohnson5385 I don't and haven't ever taken anything for it except steroids for a very short time years and years ago, I couldn't tolerate the side effects. It's getting so bad now, the joint pain, that I'm going to have to look into something to help alleviate it if possible.

[@tarinachickadaunce8011]

I didnt have insurance for awhile and didnt have the money to go to my doctor. The doctor that i went to at the free clinic in my area told me " Me prescribing Plaquenil is like me giving chemo to a cancer patient". Lupus medicine has to be prescribed by a Rheumatologist. Unfortunately, by the time i obtained the insurance to be able to go my Rheumatologist again I was diagnosed with Throat Cancer and have been dealing with that.

[@brendad940]

@@tarinachickadaunce8011 I'm so sorry. Saying a prayer for you.

[@BAGO440]

Tengo 36 años y me diagnosticaron lupus en el 2006 y si es un cambio drástico pero a pesar de todo lo que tenemos que aguantar e tratado de ser paciente y no renegar de esta enfermedad🙂 gracias por la información.

[@natasha_t]

This video is about 20yrs too late for me but still very interesting. I've was diagnosed with lupus nephritis about 20yrs ago been on dialysis for 4yrs...let me say its a BIG LIFE ADJUSTMENT and I had no systoms and 2 flares about 10yrs part. Lupus should be talked about more in the media!! Thank you for this 😊

[@irishchick5528]

Your never too late, I’m watching this video and saw your comment, I don’t know why but I think after almost 4 years I should be use to this by now. We sound like the person but in 2 different worlds, this disease is horrible and painful at the same time. Right now at this time I’m in so much pain my husband woke up and ask what’s wrong I told him I was having very bad pains in my legs a I needed to stand but I was so numb. Lupus is nothing to play around with, everyone looks at us like they look fine to me! We are suffering inside and want you all to this disease “LUPUS” is known to be silent until you get us into the SUN ☀️. Lupus causes so much pain from different body parts, we never know how we are going to feel the next day we can’t plan events due to lupus. My Story: I was diagnosed February 2017 after seeing a red rash on my face, it wasn’t the 1st one about 5th or 6th. Still continued going to beach, but each time was the same thing another strange looking red rash on face. The only thing I can say it happened when I in the sun, Finally I go to the Rheumatologist he ran test and diagnosed me with LUPUS SLE. I had one thing different then others during this time I didn’t test POSITIVE FOR LUPUS yet, it took 21/2 years to get a positive result. Then I had chronic lupus due to the sun, if I’m in the sun for more then 10-15 seconds my face starts to burn up and causes me to be in pain for hours to days. My Story.

[@tstarr7620]

@@irishchick5528 Yes, I just say I’m allergic to the sun and the heat but on the other hand the cold makes me hurt and swell to……both in two different ways……so unbelievable, this LUPUS…….Ty

[@bolinhong2598]

I have suffered Lupus for many years and I finally got rid of it with help of herbal remedy from Dr Oyalo on KZbin channel. I used his herbs and I was cured completely with his herbs and up till now I’m negative

[@AmariDJMonaLisa1]

Natasha I wish you all the best. Youre strong and courageous. I applaud you for learning to adjust despite the sacrifice. Youre in my prayers.

[@natasha_t]

@@bolinhong2598 i was told there is no cure for lupus...but if u are really cured congratulations. Could u pass on what cured you and how long have u had negative diagnosis...and again congrats 👏

[@skybluemoon4077]

I was diagnosed when I was 19 years old I do my best to ignore it 💯 thank you for sharing ! No matter what I keep pushing!

[@nancycarlos5695]

I have been suffering from Lupus disease for some year without having a solution to it until i done a research on KZbin i come and cross Dr.Auchi on KZbin channel. That was were i find effective herbal medicine to cure my Lupus disease permanently without having side effect from the herbal product.. i recommend Dr.Auchi herbal medicine for Lupus disease cure....

[@nigerianavyreciutement9571]

Am so excited to be permanently cured from Syphilis virus/hsv with the help of Doctor Ani herbal medicine on KZbin channel it’s works perfectly without any side effects Thank you so much Doctor..

[@louisethompson2044]

I've had lupus for some years and this is the VERY best and inclusive information on lupus I have ever heard.Thankyou so much

[@johnsonlee4130]

I want you to know that there is a cure for lupus and I cured mine with herbal remedy form Dr Ehime who I met on KZbin channel. His name is Dr Ehime.

[@louisethompson2044]

@@johnsonlee4130 thankyou so much i will check that out

[@johnsonlee4130]

@@louisethompson2044 yeah, he can cure you

[@johnsonlee4130]

Yeah, he can help you

[@louisethompson2044]

@@johnsonlee4130 thankyou so much i never knew there was a way put 💓

[@Stargirl622]

I was diagnosed with Lupus 6 years ago, I have only managed to start living my life this year and I am so determined, I won't wallow in self pity. I have gone back to school although it's hard to remember things I would have studied I don't give up. I believe there is a reason why I am still alive and I will do anything possible to reclaim my life. Thank you for this video

[@leandragilmour2806]

The only symptom my daughter showed was the joints, doctors wouldn’t test her for years because of it. They finally tested her when other symptoms started to appear for other autoimmune disorders. She ended up with Lupus SLE, Scleroderma, Raynaud's, RA, Connective Tissue disease, Sjogrins etc. By the time they started to take her seriously it was too late, they told her she still had 5-10 years of quality life, called her in 3 months later to tell her that it was more like 3-5 years, she passed away in under 18 months from that day. NOT everyone exhibits the classic signs, it was the physical signs of Scleroderma that appeared and got the testing done. The hardest thing as a mother to watch is the pain she was in and can’t do a damned thing about it. Be diligent, it’s your body, don’t take no for an answer, keep going back until they just do the tests to get rid of you. Sometimes that is what it will take.

[@leandragilmour2806]

I’m not sure why you are suggesting this?

[@leandragilmour2806]

Marian, like my comment says...my daughter died. I don’t need remedies.

[@alicew3563]

@leandra Gilmour I so feel for you! And the horrific thoughts of what your daughter had to go through before taken serious or even getting a diagnosis Horrible.. And you are right, these days you really have to stand up for yourself (which is not easy to begin with, when ill) if wanting to get the right diagnosis and treatments. The Hippocratic oath doctors take when exam, says sort of "if I cannot cure you then I should give you ease and relief" (I am Swedish so do not know the correct translation) but it seems to have lost it's meaning nowadays.💕

[@ttlola5515]

I am sorry for your loss. But you are so right. These doctors will put you off and tell you something else you have anxiety, They need to do better in the health industry. Too many people are dying do to neglect

[@natashajohnson5119]

Thank you for the detailed information. The Healthcare system really sucks sometimes so you definitely have to advocate for yourself and not take no for an answer. Sorry to hear of your daughter's passing. Blessings to you.

[@michelleb6363]

Thank you so much! This information was very well covered. Every question I had along the way was covered in full and very well explained. Tip - A lot of people do this, but you need to also show what some of these rashes and other skin conditions look like on different skin tones. It absolutely looks different on skin of color and can be missed, mistaken, or even dismissed from lack of understanding what it should look like. Appreciate this thorough information🙏

[@crazycajunsunshine]

I have Lupus and Fibromyalgia. My teeth and gums are affected more than I ever dreamed possible. I have started taking different natural remedies and vitamins. I had hair loss, but prayed against it and added different vitamins. If your patients tell you they want to die or feel like they are dying please understand that some days you have minimal symptons, but on important days out of no where our face breaks into the rash and we have insane amounts of pain. I get my bloodwork done every 6 months. I am well aware that I have a considerablly higher risk ok kidney or heart failure. It has helped me to only be on 2 medicatins not 7 as originally. The less medication and more prayers and positive thinking. Anyone, however that has Lupus who says they don't think about dying too young in horrible pain is not being truthful. Please advocate for your patients to your collegues. I can not tell you the level of disrepect and outright ignorance there still is within the medical field. Even my Board Certified Rheamatologist said she knew very little about it. Thank You

[@ASheepNoMore]

Look up Medical Medium aka Anthony William. His info will help you since you are not going the big pharma route.

[@marilynwelch7083]

I’m so sorry for any person who suffers from Lupus 🥺 this is heart breaking 💔💔💔

[@marilynwelch7083]

@@Gautam-r1v sorry your dealing with this try to keep a stiff upper lip and find something that makes you happy life is short and I pray for your health and healing 🤗❤️

[@beatrizperez3256]

THANK YOU FOR YOUR COMPASSION HEART! ITS VERY DIFFICULT TO LIVE A NORMAL LIFE WITH LUPUS! I

[@maimunagarbarurum1190]

I want to thanks dr imenHerbal once again,, I'm 35 years old, and I was diagnosed with lupus 11 years ago... It's really hard to live with it bones during the winter season and very very painful extreme tiredness on summer time...but now thanks to dr imenHerbal on KZbin who cure me from lupus

[@nidzainfante6022]

Thank you had made me so sad 25 yrs marriage gone but God has me I'm caring for my 84 yrs young mother fragile she helps me every day. I'm blessed

[@maimunagarbarurum1190]

@@nidzainfante6022 oh really, just connect Dr imenherbal on KZbin channel to give you the herbal medicine to cure your lupus and be free just like me..

[@melanytodd2929]

Thank you ❣ I was diagnosed a year ago, during the first wave of the pandemic. I'm so grateful that the specialists took the time to do all the tests necessary. They could simply have called it 'the virus '.

[@ayonetwork4416]

Home that was teared apart because of lupus virus has been restored back with joy, peace and harmony. Thank you dr imenHerbal on KZbin for vidicating me and my husband from lupus completely completely

[@maimunagarbarurum1190]

I want to thanks dr imenHerbal once again,, I'm 35 years old, and I was diagnosed with lupus 11 years ago... It's really hard to live with it bones during the winter season and very very painful extreme tiredness on summer time...but now thanks to dr imenHerbal on KZbin who cure me from lupus

[@JaniLo05]

Where did you go???

[@deecee901]

They called mine fibromyalgia for years. It was awful .

[@melanytodd2929]

@@deecee901 . What was it???

[@Azet7775]

Thank you for posting one of the best and most informative videos online covering the causes and symptoms of Systemic Lupus Erythematosus. Having this condition for over 10 years, I am familiar with a lot of the symptoms and terminology, but commend the production so that people who are not as well informed can glean invaluable knowledge and insights. It helps that the speaker has a pleasant and clear speaking voice. 100% Brilliant.

[@henrymccullough1750]

I suggest you to ( Dr.uwenboherbalhome ) we’re my wife was able to reverse my Sle Symptoms with Effective natural remedies and a natural diet..❤️👆..

[@mandronwolly]

Really do not know why people still believe in modern medicines when there are herbs as the complete cure for herpes and many other STDs. God bless HERBALIST DOCTOR KINGSLEY on KZbin for curing my herpes disease.

[@Azet7775]

@@mandronwolly Thank You for sharing your comments which I received in my Inbox. Can I proffer an answer to your question. Answer, is One Word "Choice!!" I get very irritated when people who are clueless about the amount of pain and suffering people with S.L.E. suffer, including damage to our vital organs, and then have the bare faced cheek to question why we use Prescription Medications? No one can know how another person tolerates or cannot tolerate pain. Who is able to judge us? Only God has the right, we are all flesh and blood, no man or woman is better than another, just some suffer with physical ailments.

[@jacobcutrer]

I don’t think I have lupus but I have noticed eating less starchy and processed food reduces my inflammation. Sometimes I get a joint or area that is inflamed and it reduces the symptoms. Also my headaches tend to form because of caffeine, so I’ve been reducing my intake and that helped greatly. Seems like that’s the way to go. Less processed sugary starchy foods and toxins.

[@tstarr7620]

Thank you for explaining what goes along with lupus…… My first time seeing anyone explaining it like this, thank you

[@bolinhong2598]

I have suffered Lupus for many years and I finally got rid of it with help of herbal remedy from Dr Oyalo on KZbin channel. I used his herbs and I was cured completely with his herbs and up till now I’m negative

[@blessbless3527]

Thank you. Have lupus diagnosed in 2011. The doctor never explained fully detailed like you have. Been denied help from someone. Can't even get Insurance. Went to herbs. And keep strong faith. Tks

[@reneeyates2149]

I've had symptoms of lupus for years but every time they did a blood test it was negative. I was told without a positive blood test I couldn't be treated. I have a lot of the symptoms in your video. Very informative 👍

[@karendalsadik7119]

I’ve had a biopsy and blood test they say inconclusive.

[@NonaWondersWhy]

Fibromyalgia and Multiple Sclerosis have many of these same symptoms, as well as others. If this comes back negative, keep looking! I finally got a Chronic Fatigue & Epstein Barr Diagnosis, along with fibromyalgia and probable MS. As far as I know there's still no Fibro test, but an MRI can look for MS lesions on the brain.

[@carolweaver3269]

@@NonaWondersWhy You are correct. Many of these symptoms seem to shadow or look much alike, with symptoms of Lupus. It would be hard to see a difference and if not showing up in the blood as Lupus, it can be any of the other problems. Fibro, Osteo Arthritis, and just about all will do the same thing, Often people have several of these DX. all at once. They just keep coming. This video helps alot, but we certainly see how closely they all work together. Did nursing many years ago, and never saw so much of this. Just wondering when it all came and why and how? Many autoimmune problems. Many cannot function and it can change your lifestyle so much. Active people become inactive and yet they need 'some activity' but it keeps them down as they do not like pain ( Who does?) If stressed the pain is worse and you can be stressed trying hard to work or keep up with what people want as you "Look good"

[@mandronwolly]

Really do not know why people still believe in modern medicines when there are herbs as the complete cure for herpes and many other STDs. God bless HERBALIST DOCTOR KINGSLEY on KZbin for curing my herpes disease.

[@belleve5709]

Rene Yates get another test, do not let them know what you think you have,let them figure it out! And don't give up

[@MsNailgun]

I was diagnosed in 2000 at the age of 34 along with Rheumatoid Arthritis. I do think I had it much longer prior to diagnosis. In my mid 20's I went through bouts of pleurisy and had one bout of pericarditis. I started having joint pain as a pre-teen. I remember constantly going to the nurse cause my knees would ache so bad I would cry. The general consensus during that era was kids don't get arthritis. The years of battling awful pain, going undiagnosed made me one helluva strong person.

[@ngoziobidiegwu2687]

Lupus {SLE} is very horrible. I have been battling with lupus since in my twenties. Thanks for sharing.

[@dorisjohns8124]

Me too

[@hollaturgirl33]

I was diagnosed with lupus in 2019 and sometimes the pain can be very unbearable. What works for me is heating pad, some medication and rest

[@em945]

Thank you JJ Medicine. I really enjoy your teaching / communication skills.

[@melissakoko8154]

I'm 35 years old, and I was diagnosed with lupus 11 years ago... It's really hard to live with it 😢 very painful bones during the winter season and very extreme tiredness on summer time...

[@ayonetwork4416]

Home that was teared apart because of lupus virus has been restored back with joy, peace and harmony. Thank you dr imenHerbal on KZbin for vidicating me and my husband from lupus completely completely

[@maimunagarbarurum1190]

I want to thanks dr imenHerbal once again,, I'm 35 years old, and I was diagnosed with lupus 11 years ago... It's really hard to live with it bones during the winter season and very very painful extreme tiredness on summer time...but now thanks to dr imenHerbal on KZbin who cure me from lupus

[@abbyortiz9669]

I get rashes when being in the sun and its painful looks like a butterfly shape my bones ache i feel week certain days so fatigue and i get headache and feel feverish when i get the rash but i was checked and they find nothing.

[@abbyortiz9669]

Oh summer is the worst i get swollen in my face flushed and feel do weak

[@ayonetwork4416]

@@abbyortiz9669 I was diagnosed 3 years ago but I got cured with the help of dr imenherbal on KZbin but thank God it has never disrupted my life in a big way.

[@dailydoseofcoy9846]

It's not easy living with lupus my sister who's 42 yrs old was diagnosed in 2004 and trust me it's not an easy road for her she suffers from hair loss, fainting spells, seizures, butterfly rashes, she gets pneumonia often, she had 2 strokes due to another condition that she developed because of the lupus I could go on and on but that would take too long. I'm praying for everyone who is suffering from lupus and other autoimmune disorders I myself have 2 types rheumatic heart disease and sympathetic nervous system disorder it's not easy at times but by God grace and mercies I'm pushing through I pray for all the person here battling this disease and other autoimmune disorder God bless you 🙌🙏

[@donnahilton471]

He mentions the heart problem.

[@donnamst.perrier5526]

I understand how you feel,my mom has Lupus.Had it since she was in her late twenties.I am thankful for every day . She's had some really bad days,and good daysThe best thing to do is talk about it,talk about what you're feeling, don't hold it inside.We care and do "want to hear about it"

[@donnamst.perrier5526]

Having this site available is appreciated, getting more doctors on board is greatly needed.Doctors who will listen,my mom would say"sometimes when I tell them about my new symptoms,it was like talking to a brick wall"For those who are Listening,Thank you for doing so.

[@JustMe-vo9bq]

I was diagnosed in my 40’s however, the doctor felt I might have had it for many years due to all the symptoms I had, but went undiagnosed. In fact, when I was finally diagnosed, I asked my doctor, who was young, to be tested for it because a friend’s daughter had been recently diagnosed with similar symptoms. The doctor was certain I had Hodgkins and was going to do a bone marrow test…however, I asked to be tested for Lupus before he did the bone marrow. He got snippy with me and insisted I didn’t have it, then reluctantly agreed to do the test.. Several days later, early in the morning, my husband answered the the phone it was MY Doctor! He was apologizing profusely because I tested positive! He said he was ‘tunnel visioning’ because he was certain I had Hodgkins.. and said it was a learned lesson - Not to do that ever again! Thank God, I finally found out what was wrong with me..but I was most thankful too, that he Didn’t do the bone marrow.

[@Karlen53]

Lupus is often associated with Hodgkins and studies have shown linking the two! I wish you all the best but be sure to get a second opinion if possible!

[@JustMe-vo9bq]

@@Karlen53 Thank you..

[@ayonetwork4416]

Home that was teared apart because of lupus virus has been restored back with joy, peace and harmony. Thank you dr imenHerbal on KZbin for vidicating me and my husband from lupus completely completely

[@maimunagarbarurum1190]

I was diagnosed 3 years ago but I got cured with the help of dr imenHerbal on KZbin but thank God it has never disrupted my life in a big way.

[@judywilson5775]

Yeah, those things hurt. As a matter of fact, I was in the hospital for 5 days bc of having an epidural. I had a hysterectomy and the hole in my back didn't close up. Could not lift my head off the bed due to headache and najsea. I lost 11 pounds and didn't really care anymor if I lived. It was bad. If you don't need one, dont get it.

[@ellasmommy9278]

My daughter was diagnosed with lupus about 10 years ago and she swears that I have it. After some testing I was told I did not have it, but after going through this lesson, I'm not sure that I wasn't misdiagnosed all those years ago. Blood clots, renal failure, mysterious migraines I can't get rid of, constant sharp chest pain. I was told about 5 years ago I had a pericardial effusion and costochondritis. Actually I'm once again dealing with costochondritis. Joint pain that gets worse when I lay down and stand back up. God knows I'm constantly tired. I'm a walking medical disaster

[@petrprecious4345]

his herbal medication is 100% Cure for Shingles virus and any disease virus and STDs I was cured after 12days of using the herbal medicine I ordered from Dr.Ani John contact him now and get your permanent cure

[@onahginika3203]

Am so glad I came across Doctor Ani John on KZbin, cause he has turned my sorrow into joy. I have been having this lupus disease since I was a teenager, but now am permanently healed

[@smc130]

These people who are promoting this herbal medicine doctor are trolling for sick people with lupus. If herbs worked my rheumatologist who also has autoimmune disease would know about them. It’s a scam so please don’t get hooked by these crooks!

[@aashiraali6864]

@Fatai Isamot which herbs, pls share

[@jennahursh8086]

I have lupus and costochondritis it Def sucks

[@Aliali817]

May God protect us from such diseases 🙏🥰

[@saleemahfareed4790]

🙏🏿🙏🏿

[@itsmesexyme8137]

Yes, Amen🙏🙏🙏🙏

[@smc130]

Too late for me. Sorry 😢

[@Aliali817]

@@smc130 God can heal. X

[@hopendembo7403]

Amen🙏

[@dragonfly2117]

Thank you 🙏🏽 for your work the psychology factor is a huge part that misses or doctors sometimes don’t want to engage

[@gingerweber51]

My daughter has had SLE for 20 years. She was on peritoneal dialysis for a long time and has had two kidney transplants. She has spent a lot of time in hospitals. She had an episode of endocarditis. Bowel obstruction with perforation. Seizures, anemia, leukopenia, thrombocytopenia, malaise. It's a mean disease.

[@pameladelmonte2418]

Yes it is!☠️

[@LemireCassie]

Oh my... I am so sorry to read this. How is she today? God have mercy please in Jesus' name. Amen.

[@eloquentlyspoken1525]

I just want to say Thank you. For so long I have suffered in silence because no one really understands Lupus. Thank you for this video.

[@shailugeorge1991]

I I'm very thankful to the almighty God for blessing me by good health I'm suffering with lupus since 11 years and still I'm good and healthy by using my medication regular love you God for everything

[@wandal.rodriguez7253]

Thank you I wasn't diagnose until I was 65. Had many of these symptoms but no one ever caught it until I moved to California from NYC. Again thank you for filling me in more about Lupus Hydroxychoroquine 300mg 1xday doesn't do much to me. I have alot of those systems you spoke on. My primary doctor want me to talk with my Rheumatoidis to see if I could get other medications to help with symptoms. Was afraid to learn more so this is my first time really hearing about Lupus and the effects on body.

[@onahginika3203]

Am so glad I came across Doctor Ani John on KZbin, cause he has turned my sorrow into joy. I have been having this lupus disease since I was a teenager, but now am permanently healed

[@ElsaGuevara8469]

Im currently going thru many of these symptoms everyday my legs are killing me and from time to time i my ankles will swell up. Cheat palpitations shortness of breath loss of concentration have a difficulty with my speech. I constantly have to repeat my self trying to explain something that is so simple. Bleeding of my gums. Falling asleep, anxiety , stress … im scared of going to the doctor … i have many excuses…but definetly this video has made me take action.

[@nancycarlos5695]

I have been suffering from Lupus disease for some year without having a solution to it until i done a research on KZbin i come and cross Dr.Auchi on KZbin channel. That was were i find effective herbal medicine to cure my Lupus disease permanently without having side effect from the herbal product.. i recommend Dr.Auchi herbal medicine for Lupus disease cure....

[@kelligray1848]

Have Systematic and Discoid Lupus plus Reynauds. Been diagnosed for 20 years or so but showed signs since I was about 7. I had to retire. I miss the old me. Thank God I have wonderful doctors.

[@Dulcimerist]

Thanks so much for posting this! Doctors had suspected that I had Lupus back in 1996, but then ruled it out. It turned out that I have hypermobile type Ehlers Danlos syndrome, which has many of the same symptoms of Lupus. There are several differences between the two, though.

[@ayonetwork4416]

Home that was teared apart because of lupus virus has been restored back with joy, peace and harmony. Thank you dr imenHerbal on KZbin for vidicating me and my husband from lupus completely completely

[@maimunagarbarurum1190]

I was diagnosed 3 years ago but I got cured with the help of dr imenHerbal on KZbin but thank God it has never disrupted my life in a big way.

[@Dulcimerist]

@@maimunagarbarurum1190 My post is about Ehlers Danlos syndrome, which is a genetic mutation that has no cure. It's a defect in the body's collagen, and collagen in the body (organs, blood vessels, etc.) can't be replaced. Please don't mislead people by suggesting there's a cure for Ehlers Danlos syndrome.

[@thereseshaffer9925]

You can have both also at the same time, as I do.

[@kathleenarapoglou7724]

Hello...and I am not selling anything. I was diagnosed with Ehlers Danlos 50 years ago...and also have some Lupus symptoms (canker sores, alopecia) When I went to my first cardiologist appointment, 40 years ago, he had no idea what Ehlers was, looked it up in a diagnostic book as I was waiting for hope. Heal thyself. I have dislocated my right knee at least 50 times to the point there is not much of a patella left. I was a candidate for knee replacement surgery at 30. Fast forward twenty years...I did strict Keto for a year, I took myself off knee replacement surgery list, the rest of my joint pain is reduced. Two hours after a bite of something sweet, the pain returns. Blessings on your journey.

[@karinasulger9431]

i have discoid lupus , and have had it 18 yrs , i do have the red patches on my head , in my mouth , and in my eyes , i am forever tired , headaches , and tingling in my fingers , but i have been on meds n for the most part it helps alot but def not a fun disease , ty for sharing this info , im always learning

[@blueswallowtail4628]

I wish my Dr. new this much about Lupus

[@johnsonlee4130]

I have suffered Lupus for many years and I finally got rid of it with help of herbal remedy from Dr ehime on KZbin channel . I used his herbs and I was cured completely with his herbs and up till now I'm negative

[@nicholemariejohnsonforbis3482]

I have lupus. I wish I had never gotten it, I have had many issues. Over the years I have begun to have more and more issues due to my lupus. It definitely does make me very tired and sick. I had anemia when I was really young so I don't think that me having lupus caused me to be anemic but, I have had seizures, I have kidney problems also and my liver has issues, I lose feeling in my hands and feet a lot mainly in the winter or just cold period. It's not fun. I also get headaches or migraines so bad I have to go to the hospital to help get rid of them. I was told that lupus can be hereditary, the reason I had asked was bc my cousin and my little sister also have it. My 15 year old son has low platelet count and I have to take him to a hematologist to get seen. I'm praying he doesn't have it. It's hard but I still work and I am able to take care of my family but it's definitely not easy. I definitely pray for anyone who has Lupus!!!God bless you all!!!

[@ab5680]

Prayers for you and your family. How is your son now?

[@tshep173]

I have Hashimotos thyroiditis. Many similar symptoms. Also an autoimmune disease. Once you have one, you can easily get others.

[@tramey01]

One major one he didn’t have in here is Raynauds . When you lose blood flow to your hands and feet and they get extremely cold and can turn white. This is one of the symptoms I have and is very miserable. But better than failing kidneys or heart problems.

[@NormanF62]

I’m the rare male victim of systemic lupus. Its an experience living with an autoimmune condition. I wouldn’t wish it on my worst enemy!

[@bonniemoerdyk9809]

My best friend and her father both had Lupus, then 30 yrs ago they told me I had the LE Cell, but mine might be one of the other 4 or 5 diseases that also has the LE Cell in it, like Dermatomyositis. I'm 66 yrs old, I've been ill off and on the whole time, I Still don't fully know what I have. I hope and pray you get all the help you need and feel better soon.

[@reenaicha]

@Fatai Isamot hello! Can you please put me in contact with the doctor??? Please🙏🙏🙏 my mom is going through it😢😭

[@davetinoco]

I often wonder if I have Lupus. In 2012 I developed a severe butterfly rash on my face. To the point that I would bleed, it was so raw. Then I developed sever nerve pain and numbness/tingling in my arms. After 6 years the rash finally went away and my skin healed. But i deal with constant headaches and chest pain.

[@Chippy88]

I was diagnosed with Lupus when I was 16. I am now 50. I have had only 3 major flare ups. What helped me a lot is that I was diagnosed right away. Unfortunately as it mimics other diseases sometimes lupus has already affected the organs before they find out what it is. All of my joints hurt and I mean literally every single joint hurt it started with my wrists. Before you know what I could barely walk so my mother took me to a doctor and then I was referred to a rheumatologist and he said it could be limes disease, juvenile arthritis or lupus. So I went back in two weeks and it was lupus I was put on plaquenil and within 2 to 3 weeks it went into complete remission. Then after like four years I had a flareup and I had to take prednisone and Only one hospital stay and they gave me chemotherapy. And that was only because the doctor did not think it was my lupus if you had increased my prednisone I would not have even been in the hospital. But I was blessed to be diagnosed right away in early. I also know a lot of people that either stop the medicine or they don’t want to take it etc. I can tell everyone right now I was 16 years old and from that day he n I took whatever medicine I was told to take and how I was told to take it. People get afraid of the side effects etc. but you have to realize this is your life you need this. Sometimes you can get weaned off of the medicine. I also have had two kids and I did great with it! I know unfortunately some people have it worse but please take your medicine! God bless

[@mrsg.9224]

My Daughter is 13.5 we are now seeing a lot of symptoms! I’m scared to death. Thank you for sharing your story.

[@jayugly8284]

Thank u for sharing

[@marymolina6159]

I was always getting sick they send me to a dermatologist and they did a biopsy on my ear the test came back saying I had lupus my doctor sat down with me and told me I had exactly 10 years to live to sit down and tell my kids this that was in 2009 here we are in 2022 and I am still here with the grace of God feel blessed and thank God everyday because GOD is the in control he's the driver I'm just the passenger I trust in all he do Amen🙏❤️

[@starshowers8312]

You need a different doctor

[@dr.reviewsfrompersonalexpe7603]

@@starshowers8312 She has the master physician in Christ, Jesus ! All Praise and Glory to Jesus Christ, King of King’s and Lord of Lord’s!

[@kellylestig4941]

This video is very well-made and very informative you get right to the point, thanks for sharing job well done

[@elizabethconroy7665]

Thank you for all the interesting information

[@johnsonlee4130]

I have suffered Lupus for many years and I finally got rid of it with help of herbal remedy from Dr ehime on KZbin channel . I used his herbs and I was cured completely with his herbs and up till now I'm negative

[@shandaa2007]

Symptoms since 21 and diagnosis in 2017 and I was relieved for the diagnosis because I saw multiple doctors with multiple diagnosis.

[@kayladurham8119]

I just got diagnosed and only found out because I’m pregnant and my ob wanted to figure out why I had 9 previous miscarriages. On the bright side. This baby is healthy and I’m about to hit my 3rd trimester. My whole life makes sense now that I know why I’ve always been sick and in pain.

[@annelyceyawingu6678]

This gives me hope! I want a second child bad. I was also diagnosed last year with Lupus and currently taking contraceptive pills..

[@karenmeer2320]

Praise God! I hope all went well with the baby!!

[@joannejohnson7006]

Really good information and presentation. Thank you

[@tarshaneilly518]

I suffer from RA and I have lupus "symptoms". Can you do a video on RA please? Supplements etc....the stiffness, inflammation, lymphatic pain etc is just rough.

[@vicBellamonkey]

So sorry me as well 27 years now it's hell..

[@tarshaneilly518]

@@vicBellamonkey 27yrs I would say you are strong? I pray you find relief. It's good when you can relate. The pain, fatigue, fear etc is alot. Take care!

[@kathleenarapoglou7724]

Ladies.... Do an ANTI INFLAMMATORY DIET, super low carbohydrate diet with no dairy, eggs, nightshade vegetables. Try it for a month. Sugar is extremely inflammatory and is in nearly every processed food. Blessings to you. I took myself off knee replacement surgery list. Xx

[@leanc8906]

Excellent breakdown of SLE.

[@KukLuv]

I have lupus and I have a dark purple rash it goes around my arms at the top. I've had stroke symptoms but had no stroke. My bones ache constantly I can't get any operations that I need because of Lupus. I live my life being as happy as I can. Positive thoughts do help though.

[@Sorchia56]

Very well presented, cheers. Raynaud’s is a big one as well. I was dx’d when I was 29. At the age of 14, I had what they thought was mono but it lasted a year. Followed by shingles and extreme malnutrition. I’ve had the Chickenpox 3x and those pesky seizures presented in 2015. Oddly, I only get sinus infections and pneumonia. I haven’t had a regular cold since I was a wee lass. I had Covid in January 2019, yes the medical profession knew all about it. I was fine. It was basically a flare up with a bit of a punch. No hospital needed. My hands have become so swollen that the skin cracks and they bleed. I started Millipress and no more swelling to the point of bleeding but they still swell and hurt like Hades. It’s a bugger to have but I forget sometimes. NEVER if I’m going to be in high heat or the sun though.

[@Sorchia56]

@Victor Louisville Wow! That’s two recommendations. I’m checking into him more. Cheers!

[@Sorchia56]

@Fatai Isamot I’ll definitely be checking into his channel. Thank you. I refuse to take all the medications and steroids the doctors keep pushing.

[@sherrizanoli1398]

You need to do a video on Sarcoidosis and all of its mimicks.

[@boldandcourageous4176]

Yes my Dad died from that

[@sherrizanoli1398]

@@boldandcourageous4176 I have it and am having problems with it.

[@boldandcourageous4176]

@@sherrizanoli1398 consider reducing gluten and certain grains Sherri after my dad passed and immunologist called me and told me that avoiding certain grains really helps. Eat a lot of antioxidant Foods like blueberries to protect your kidneys . Take co Q 10 to keep electricity going to your heart. Have you had to have a pacemaker put in yet? I'm so sorry you've had to battle this terrible disease.

[@sherrizanoli1398]

@@boldandcourageous4176 No, but my skin keeps breaking out and it is horrible, not to mention it looks like I have glass beads in my lungs.

[@Mr93sharpei]

I suffer systemic lupus, discoud lupus, sjogrens, and scleroderma... Thank you....

[@jennifermartinello5172]

I have Bechet's disease, two doctors thought I may have lupus as well as they are almost a layover of the symptoms minus the the malar rash those discoid rash reminds me of bechet's but painful and DEEP.

[@amberrose647]

Watched again. Thank you so much. Calm and informative.

[@vixroberts759]

Thank you for this video! I've been in an 8 year battle since I was 14, all booked normal and told it was so in my head till month I demanded my ANA to be redone and it's very high at 1:1280. So definitely something Autoimmune, now waiting for my Rheumatology app in 7 seems for a much needed answet

[@ldjt6184]

Look into how Dr. Brooke Goldner healed her Lupus.

[@shaneluke346]

What does Ĺupus look like / what are the the symtoms ?

[@MariaMaria-wv1sy]

Have you been diagnosed with Herpes, has that been Ruled out?

[@vixroberts759]

@@MariaMaria-wv1sy yep definitely don't have herpes 😂 it's autoimmune

[@vixroberts759]

@@shaneluke346 everyone is different lupus is called the disease of a 1000 faces as it looks like and can mimic other things but most common are joint pain/swelling/redness, hair thinning or loss, sun sensitivity then you get the more serious type like Lupus Nephritis which is to do with your kidneys it's a very hard and long road to be diagnosed

[@tammydunn4664]

Loved this..very helpful..

[@fabiwilliams4644]

I didn't develop symptoms until my twenties & that was hair loss. I was diagnosed in 1987 but no one could tell me how I got it. It was only when I was in my 40's that I found out my biological father had lupus so it was inherited. I'm the only one of his 4 children to have it. I have now developed most of the symptoms & will have my daughter tested to see if she has it.

[@samanthakwnsnziao9085]

How was your hair loss tho? I’m currently having hair loss and I’m scared I’m only 16 :(

[@fabiwilliams4644]

@@samanthakwnsnziao9085 Sorry Samantha. I'm much older than you & my hair is quite thin now. I have my hair cut in styles that make it look thicker. You tend to adapt to the situation over time

[@samanthakwnsnziao9085]

@@fabiwilliams4644 mine is getting thin as well I used to have super thick hair & my doc dismisses me all the time cuz she says I’m too “young” and it’s just stress like bye it’s not stress there’s literally nothing I stress about.

[@fabiwilliams4644]

@@samanthakwnsnziao9085 My hair also started out thick & it was through blood tests to discover why I was losing my hair that they discovered I had Lupus

[@Victoria-fw9xn]

Very informative... Excellent video

[@lindatorres7003]

This was such a well explained video. Very clear and easy to understand.

[@rabiaafzal1815]

what a lecture .. very nice thans

[@klaritydawn]

You are INCREDIBLE.. Thank you so much. I've had SLE for YEARS and I've never understood it like this. You are so clear and it sure makes a lot of sense as to the Multiple I call (break off) diseases or health issues that come with SLE. I used to have an Amazing doctor and he quit and went into research (I miss him terribly). The doc I have had for years now is....idk I feel lost bc he doesn't pay attention to a lot of issues. For instance my first SLE doc did scans and found out I had osteoporosis really bad at age 26 and started me on medication and told me to start using a cane way back then. I begged my now doc to please scan and look at my records but we went 12 years without looking...guess what..I have osteoporosis way worse now. I do prolia shots but not the point right? He won't listen and it's scary to change docs when you are fighting so many issues.

[@johnsonlee4130]

I have suffered Lupus for many years and I finally got rid of it with help of herbal remedy from Dr ehime on KZbin channel . I used his herbs and I was cured completely with his herbs and up till now I'm negative

[@LindaKennedy-kf3ws]

Alot of information. Thank you ❤

[@catfrigames]

I had a sister that developed lupus in the '70s she was 16 and was died before her 17th birthday. It was a slow painful death. I was only 11 at the time and I remember the pain and suffering she went through. No one else in our family has lupus that I know of.

[@nancycarlos5695]

I have been suffering from Lupus disease for some year without having a solution to it until i done a research on KZbin i come and cross Dr.Auchi on KZbin channel. That was were i find effective herbal medicine to cure my Lupus disease permanently without having side effect from the herbal product.. i recommend Dr.Auchi herbal medicine for Lupus disease cure....

[@nigerianavyreciutement9571]

Am so excited to be permanently cured from Syphilis virus/hsv with the help of Doctor Ani herbal medicine on KZbin channel it’s works perfectly without any side effects Thank you so much Doctor..

[@haywatteesingh1144]

I know how that is because my niece died on Saturday the 25 February 2023..it very painful and she have plenty fluid an she gets plenty short breath an coughing she was only 32 years it really sad 😭😭😭

[@TracyCordero-vv5ky]

I have had a lot of these symptoms for a while now. What got me going to the doctor to find out what is wrong with me. The night sweats the highs and lowes in temperature it was driving me nuts. So a does doctor visits and about 10 vilies of blood later is Lupus. I was glad to have an answer but said because I already have GBS

[@mohamedabdullahi1931]

Thank you for your explanation and I hope you will prepare soon Mx of Lupus and other connective tissue disorders like Scleroderma and Dermatomyositis

[@johnsonlee4130]

I have suffered Lupus for many years and I finally got rid of it with help of herbal remedy from Dr ehime on KZbin channel . I used his herbs and I was cured completely with his herbs and up till now I'm negative

[@NihouNi]

What clarity! Thankyou

[@nigerianavyreciutement9571]

Am so excited to be permanently cured from Syphilis virus/hsv with the help of Doctor Ani herbal medicine on KZbin channel it’s works perfectly without any side effects Thank you so much Doctor..

[@MrsJAZack]

How incredibly informative! Thank you!

[@dannyallbritton977]

I enjoyed watching this. It runs on my dad's side of the family. I've had one cousin past away from complications of Lupus and besides myself, I have two cousins, females. I'm the only male with it. Would like to talk with you.

[@christinanewcomb1718]

I was glad to see the part about the brain. I try to explain that the lining in my skull around my brain is inflamed and people think I'm making this up.

[@fabiwilliams4644]

Yeah I feel like my head is in a vice & tightening

[@nope516]

Add iodine and black cumin seed to your daily after research and reading up to see if they'd be helpful.

[@subasinicole6067]

THANK YOU SO MUCH. I Just found out that I tested positive for Lupus this year and I have been having the symptoms of it since I was a teen, but the doctors kept telling me it was growing pains. I'm now 36 and still have the same symptoms and just had my gallbladder removed because it was full of stones. And then when they did blood tests they found out that I have Lupus. If the other 10 doctors just did some testing instilled or kept telling me it was growing pains i would not have had my gallbladder removed or still be having this much pain.

[@trussiamontgomery3125]

Thank you! I agree with Dimps The Patriot, please do one on MCTD/UCTD

[@koryryon4177]

Excellent lecture . Thank you very much.

[@rochelle5266]

I was dx at 29. My life has completely been charged. You have to let go of who you were and accept who you now are. I was sick for 6 mo before my friend said you have to go to the Dr. I thought he'd say I had too many kids and needed a nap. I had no idea what I was in for. I am now in stage 3 renal failure, among too many other symptoms to list.

[@shaylouise4436]

Take care of yourself, my daughter passed away she had lupus, she was only 31.

[@rochelle5266]

@@shaylouise4436 im so sorry for your loss. Unfortunately I know how she felt. They refer to us as the missing because we are missing out on living. Sometimes I feel as if im just existing.

[@saurabhbhalla90]

How old are you now

[@rochelle5266]

@@saurabhbhalla90 early 50s

[@tessygreg5003]

Your endless compassion towards humanity Dr.Obaedo has broader my heart, and prove all the doctors here that they were wrong and I really didn't know what else to do than believe in your medicine,thanks so much for curing my lupus

[@Merikahnii]

Tell me I am also suffering lupus

[@sitarasarfaraziqbal4789]

Hello Doc, amazing lecture. You are blessing for medical students. Kindly share the link for Diagnosis & Treatment part. As I couldn't find in the playlist. Thanks

[@blancabulgrin5560]

My god this sad thank you i never knew what the effects were best wishes to any who has this .

[@simonjones3863]

I have RA 30y but also straddle some lines with Lupus. Sun exposure causes pleurisy within 12h, I have a face rash, but in the wrong place, I've had pericarditis several times (Terribly painful, even worse laying flat), and my hands and feet are wrecked. Humans are so darn complicated!

[@michellelangdon5134]

Lots of people with SLE never get a rash. I get a rash all over my face, neck, scalp, and arms. Don't let the fact that you don't have the butterfly rash stop you from getting checked for Lupus.

[@drsabirkakar]

It is too much helful for me thank you 👍🏻

[@brucemcfarland5994]

I’m 23 year old male who’s doctor just diagnosed me with lupus. She came to this conclusion through blood work and butterfly rash on the face. I have yet to get a appointment with the specialist.

[@nancycarlos5695]

I have been suffering from Lupus disease for some year without having a solution to it until i done a research on KZbin i come and cross Dr.Auchi on KZbin channel. That was were i find effective herbal medicine to cure my Lupus disease permanently without having side effect from the herbal product.. i recommend Dr.Auchi herbal medicine for Lupus disease cure....

[@fayekalan]

Wishing you a well planned approach to dealing with symptoms forever.

[@macadocious1103]

I was diagnosed with lupus at age 6 I’m 26 now and Watching this is pretty crazy I have the malar rash right now but it’s only on my right side I have never met someone else with lupus