Understanding Lupus: Activist Spreads Awareness, Breaks Stigmas

[@idonhadenuff5979]

I’m laying in my bed right now with Lupus watching this story. Thank for bringing awareness to the struggles of Lupus.

[@hermithollow2024]

Me, too. I wasn’t diagnosed until my late 40’s and it effects me in more extreme ways. But each one of us who “soldier on” can be an inspiration to each other just like this young lady. 😊

[@pierrettelaf9728]

I have a naturopath that can help you. It's not a commercial. Not for me. Just want to help .

[@shedejadlockett8274]

Me too!

[@nicolettesnyder5866]

Same :( laying in agonizing pain

[@RebaMiran]

Me too

[@janecoffey3330]

Lupus is cruel,my brother passed away February 24 2022 from lupus, his last months were horrible. He is no longer in pain and is happy in heaven.

[@m.layfette6249]

Rest in Peace 🕊️ Sweet Prince may flights of Angels carry thee to thy Rest 💜💪🏾🦋

[@mariawhite2760]

God bless you and your brother,he is definitely happy and pain free physically and mentally,love to you and your family 💕🙏🏼

[@donnam4305]

Maria did a wonderful job describing this disease. Lupus has many faces, effecting millions of people in many ways. I have had Lupus and Lupus Nephritis for 32 years with many ups and downs. Thankfully, I am in a good place right now. I wish Maria and everyone with this disease the best of health and hope for a cure!

[@moneemitchell1227]

I have systemic lupus for 19 years and still learning about symptoms

[@m.layfette6249]

@@moneemitchell1227 I too have SLE and with every doctor's appointment, every minute, moment, day I learn something new. Stay Strong! 💪🏾💜🦋

[@melissamartin1485]

Amen!

[@patticakes74]

32 year's you've suffered? Definitely change your doctor's they are not helping....

[@Holly.Brewer]

God bless the day I came across Dr ubarlo on KZbin, ever since I was recommended to him, my health has been on the best condition. Thank you for coming through for me during my hard time with lupus disease

[@courtneymcleod7283]

Lupus unfortunately took my mom. Her organs were failing. She was on hemodialysis and was in need of s kidney and a liver transplant. Her heart was so weak and she went into cardiac arrest in the hospital and couldn't be resuscitated. My mom lasted 15 years after her diagnosis and she lived life well. She was a manager at Disney and she had many friends. I miss her so much.

[@garlandowls1134]

I'm so sorry for your loss. My condolences goes out to you and your family. 🙏🏾❤️🕊

[@MindyMontes75]

I’m so sorry for your loss! I suffer with lupus so I know the struggles. Your mom sounds amazing! ❤

[@lesleyd2448]

It’s absolutely horrible. This Disease needs to be talked about more and doctors need more awareness. I was told I had chronic pain and menopause for years before diagnosed.

[@joycehernma3541]

Herbal medicine is the best to treat our body system naturally Hi I’ve been living with lupus😭 for more than 5years now but I got rid of it naturally after using dr Omo herbal medicine

[@Happypucks]

But they never will. Its all business

[@Holly.Brewer]

What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last

[@oddlilbird]

It’s easy to see why her husband wouldn’t leave her; what an incredible woman!

[@BrooklynBaby100]

Women like her get left all the time, bird… and he may do so later

[@oddlilbird]

@@BrooklynBaby100 I know that’s true, but I hope the best for her.

[@rahulmiya5496]

Dr Ewi1 on have the cure for it

[@mahmudrza191]

With the help of Dr Ewi1 herbes my Lupus was cure thank you sir you are a great man

[@Donna-cc1kt]

It’s not that easy. I say that with love for all the family members that could not deal with it. It’s pain for them too.

[@TheBritot]

Girl, I am right here with you. I was diagnosed over 10 years ago and there were times when I would just sob out of pain and frustration. The minute I started eating better and exercising I felt better and I believe I am in remission. Keep going, you are on the right track..and don't give up on having your family...it is possible, speaking from experience. God Bless you and thank you for sharing your story.💜💜💜💜💜💜💜💜

[@Zisjejk]

what test is used to diagnose lupus pls

[@TheBritot]

@@Zisjejk it's very hard to detect...its done through blood. I was tested in my 20s and it showed negative all the way up until my 30's. They caught it when I was going in for a colonoscopy. The dr told me that I had double stranded DNA (really unsure how to explain that myself) and it was Lupus. My mother has it as well, so I honestly think it's passed on, but I can't say for certain. It's a young woman's disease and if you are weak in the muscles and joints, constantly tired with no energy, hair loss, rashes on your face you should seek out a rheumatologist and get tested. As you can see from my story it lied dormant in my body for a long time. I hope this helps and not scares you. GOD BLESS ❤️

[@vlogsofsamiyusuf6651]

I have lupus I eat healthy most of the time and exercise makes it worse every single time and I like walking come to exercise I'm glad it's work for you

[@brittneybabeee4031]

@@vlogsofsamiyusuf6651Thank you for commenting this because while eating right & exercising can definitely help many people, many other people struggle with it because it doesn’t make a difference for them. I spent 5 years eating right & working out & not only was I miserable from constantly forcing myself to work out through the pain, fatigue, etc., but it wasn’t helping at all & no matter what workouts I did, the pain would stay and sometimes even worsen. I ended up giving up entirely & over the years following, I gained so much weight & progressively got worse. Now, I’m back to portion control, eating better, and trying to be as active as I can between the pain, insane fatigue, and constantly getting sick, and I’m down 40 pounds, which makes me so happy to say. Still, my symptoms aren’t any better. So, eating right (but allowing yourself some treats still) and working out are great things to do & those who are capable of doing so should, but the idea that it will cure everyone who struggles with lupus or other chronic illnesses is not only false, but it’s harmful. Doing these things are beneficial in their own right & they can help us in many ways, but curing or bettering illnesses, chronic or otherwise, is not something they do for everyone. It’s great that there are those who got better after eating right & exercising, but it’s just not the case for everyone. I promise that you’re not alone & it’s not anything you’re doing or not doing that’s causing your lupus or preventing you from getting better. All that said, OP is not wrong in their comment & sharing what’s worked for them was a good choice as it may work for others. I just think we should be careful & add disclaimers when sharing what’s worked for us so that others know that it may not work for them & that that’s okay & it doesn’t mean they’re doing anything wrong or that it’s their fault they’re sick.

[@IvySnowFillyVideos]

Its not just a young women's disease...it can happen @any age.

[@kristibbradshaw]

I have SLE and it’s so hard. Mine began when I was 9. My hair began falling out by the handful and I started getting tired. Children aren’t supposed to feel that way. Now I’m 58 and still having daily symptoms, but I’ll never stop. Sending hugs to the other lupus carriers out there.

[@kerrividler6571]

OMG that was me. Diagnosed at 25, all the symptoms Maria has. The way lupus travels is frightening. I used to sit down, able to walk but try to get up half an hour later and can’t walk. The dr came in one day and said ‘you have rheumatoid arthritis’ the next day he came in and said ‘you have lupus too’ and then he came back and said ‘oh you have hashimoto’s thyroiditis’ - a trifecta! Mind you, I wasn’t celebrating thats for sure. It’s a very cruel disease.

[@Holly.Brewer]

You have my utmost respect Dr ubarlo and I want to appreciate you for all the glorious things you are accomplishing you are my hero I never thought there will be a way to cure lupus, I'm totally in awe of what you are doing to help others who are suffering from this so - called ailment lupus" I appreciate your hard work.

[@ShyFly1000]

I’m so grateful people are talking about this. So grateful! I have been diagnosed for 20 years and it took 4 years to finally be diagnosed. Awareness is so important. Maria is a warrior. I am a warrior. We can own our tragedies and turn them in to growth and support for one another.

[@Holly.Brewer]

What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last❤

[@L.Spencer]

A few years ago we lost a dear, young friend in Mexico who had lupus and died of a heart attack at 16. She's resting, awaiting the resurrection.

[@mahmudrza191]

With the help of Dr Ewi1 herbes my Lupus was cure thank you sir you are a great man

[@Real_Life_Is_More_Important]

I'm in the tub crying because of my lupus flare and I have so much hope for you. It's a hard life, but blessing are rich when they come.

[@Holly.Brewer]

What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last

[@lunamoran2463]

This made me cry. I had my daughter at 21 before I was diagnosed and I’m 34 now and can’t have more children because I could die if I got pregnant due to antiphospholipid syndrome and lupus. I’m happy and grateful I had a successful pregnancy at 21 though. I cried when she said “there’s no cure?” … some days I just want to cry and say why me? But then I say why not me? I’m not special. I just have to get through it. Life on life’s terms. To all the other lupus warriors out there, stay strong, life is tough but so are you ❤

[@Holly.Brewer]

What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last

[@kotybear0828]

I didn’t get diagnosed until I was 31, but had symptoms at least from 24-26yrs old. I had my first at 20,22,24. I had to have a full hysterectomy at 29. I have been diagnosed with the lupus anticoagulant disorder or antiphospholipid syndrome as well. I had been hospitalized three times for PE’s before they finally figured out it wasn’t bc of the estrogen I was taking due to the hysterectomy. 🤦‍♀️🙄

[@cyborg-2.1]

I was diagnosed 1 year ago. I had symptoms a few months before the diagnosis. Loss of hair, severe pain in joints, lost 30 lbs in 1 1/2 month, bleeding, throwing up everyday. I thank God that I recovered so fast. 🙏

[@Holly.Brewer]

.What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last

[@laurakelly631]

What a lovely woman! And good to know there are men like her husband. I wish them the best. I lost a best friend to lupus and my sister has it. People often get very ill in their late 30's, and if they make it through, have perhaps remissions (but with ups and downs) till the 60's... when many succumb. Lupus can attack any organ, so the symptoms are variable. My friend had crisis in the lungs in her late 30's and made it through. Then in her 50's her kidneys were the problem till she needed dialysis. She was a warrior also and lived well with all of the difficulties till she died at 63. My sister has had several crisis involving kidneys and lungs also, almost died a couple of times...still hanging in there at 65. People with Lupus like other immune dysfunction diseases, can look perfectly normal but be very sick. It is not necessarily something you can see. They often suffer from debilitating fatigue and pain that is not visible. Exertion is dangerous. They have disabled parking stickers and get yelled at for it. (Think twice people)

[@patticakes74]

What did they prescribed for infection 😕? This will create alot of havoc for the body....

[@buttaflyantics8618]

Many people succumb to what ever they develop in life in their 60’s. Don’t put a timeline on anyone but yourself. Everyone is different and God has the last say not an imaginary timeline. Sorry for your loss and prays for you loved ones that are still thriving with Lupus.

[@evaang3616]

omgoodness love you comment! Amen! my daughter got diagnosed with lupus nephritis at only 15 and a half we gone thru so much in that short time, her poor figure changed amongst soooo much more…We need support and others for the battle. She’s a warrior for sure🙏🏼

[@Holly.Brewer]

What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last😊

[@sydneyrogers9697]

I've had Lupus for 50 years! At the time the prognosis was 10 years max. I've had some hard times to be sure but I'm still alive and living independently (with my 2 cats). Saw my rheumatologist yesterday and I'm stable. New treatments on the way I'm sure for younger patients.

[@IvySnowFillyVideos]

Your story is so inspiring. Thank you for sharing

[@Holly.Brewer]

What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last❤

[@Sheloyigamer]

I’m trying to get a diagnosis; not that I want to have Lupus. But I have so many symptoms that come and go and change. Even with health insurance, I simply cannot afford constant visits and labs and no answers. Also feel like I am brushed off by doctors and even my own family. It’s so overwhelming to feel sick most of the time and have to fight to justify how I feel. Again, I don’t want to have Lupus or any other chronic condition but feeling horrible for the past 4-5 years with no help, no answers is debilitating

[@funnyadorabledonna]

Same here. Don't stop until you find answers

[@gabyrubio6647]

Hi Chaya, i’m no doctor here, but myself I suffer from hypothyroidism along with Hashimoto’s disease which is an autoimmune disease. That if not treated makes you feel A lot of fatigue, lethargic, depressed, constipated , low libido, weight gain , intolerance to cold, brain fog. As much as you sleep you’re still sleepy. Some days are good and other days are not. Also Mood swings. In case you want to start from there. I hope you find answers. 🙏🏻

[@Sheloyigamer]

@@gabyrubio6647 Thanks Gaby

[@manishajaswal1577]

Same with me I am suffering since last 3 to 4 years all test negative.... But I know there is something wrong

[@Holly.Brewer]

What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last.

[@AlejandraXio]

April 2021, due to a severe lupus flare, I went to the ER due to dysphagia and ended up getting a feeding tube. A few days later I had a PRES seizure and got acute respiratory failure. I was on a ventilator 10 days and miraculously survived. My doctors told my family to start planning my funeral but here I am. I woke up with a tracheostomy and paralyzed. I had to relearn how to breathe, swallow, talk with a speaking valve, and can move in bed some. I still can’t walk but my next goal is to be able to transfer to a wheelchair. Lupus is a real battle. For those of you who haven’t faced the scary life threatening side of the disease please please do what you can to prevent it. It can leave so much damage if you survive it.

[@aquamarine2416]

but some doctors can't do the test, sometimes it doesn't show and other times yes , I need medication but they can't give me, my results come out good but I am not Good. this is very Hard.

[@sierralima1433]

@@aquamarine2416 Hi! How are you doing now? I totally understand how you must have felt

[@sydneyrogers9697]

I'm sorry, you can't prevent it. I've had Lupus for 59 years. It's been tough but I'm alive.

[@AlejandraXio]

@@aquamarine2416 I would get a second opinion at least. It took me 4 rheumatologists to finally get results. It was my moms idea and if she hadn’t done that the doctors probably wouldn’t have treated me for that in the hospital and I probably wouldn’t be here.

[@AlejandraXio]

@@sierralima1433 oh my this comment was 10 months ago! After going through another 3 month health crisis where I needed an emergency nephrostomy tube, kidney stone removal surgery and the flu I’m finally able to sit in my wheelchair 2 hours. My next goal is four hours

[@laurad3497]

Wishing her the absolute best

[@rahulmiya5496]

Dr Ewi1 on have the cure for it

[@cinephile1712]

Spreading awareness isn’t enough. It’s all about teaching people how to advocate within medical and social service systems, deciphering dense jargon, and providing the resources and other tools so people with lupus (or other autoimmune conditions) can get what they need :)

[@m.layfette6249]

Raising Awareness 💜, Being an Advocate 💜, Telling Your/Our/Their Story 💜 that and so much more makes YOU an Lupus 💜 Warrior!!

[@Holly.Brewer]

What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last

[@denisedean8503]

I have lupus we will be alright do not lose hope keep God first place keep praying God Bless you Maria. 🙏🏾❤

[@m.layfette6249]

💜💜💜💜💜💜💜💜💜

[@rahulmiya5496]

Dr Ewi1 on have the cure for it

[@Holly.Brewer]

.What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last

[@strawberrycupcakes0084]

Last year on August,i was diagnosed with lupus and when the doctor said it there's no cure,i was crushed from the inside,i tried to look okay but it's never okay,i started having the symptom whe i was 13 by having a excruciating pain on my back and on my shoulder blade but i always dismissed it as a stress,years passed by and it getting more painful to the point that i can't even stand up from bad or sleep at night,then i start sleeping for a several hours and still feel sleepy after a long sleep,i told my family about it just so they will understand a lil' bit about my condition but all of them dismiss it and said that i only used that as an excuses,now watching this kind of video give me hope and i don't feel alone anymore,thank you

[@barbaralkennedy1870]

I’m a Lupus Warrior too. I have 5 beautiful, and healthy adult children, and we just had grand baby 13 on Friday. Hang in there. Anyone who gets a Lupus diagnosis may feel depressed, but with adjustments in diet (a lot of adjustments), exercise (when you can) and listening to your body and not overdoing, things will get better. I refused to be on meds due to side effects. But I saw a great holistic healer and am on supplements and juices (and kombucha). I’ve learned what I can’t eat, not even once, and things I needed to include in my diet on a regular basis. I’m doing so much better. With each trial comes learning, and I’ve learned it’s ok to slow down (I’m very task oriented), and it’s ok to say ‘no’ when you need to (I was also very, very volunteer oriented). But I’ve also learned a great appreciation for my life, for my family, and I thank God everyday (literally) for all He has given me. I have much more than I deserve. Years ago when I started this journey I honestly thought my life was over. It’s not. It changed, I’m writing a new chapter, but I have much more living and loving to do! You are blessed to have a great husband by your side. I’m very blessed in that way too! I wish you and all Lupus warriors (all chronic illness warriors) the very best. Do your research! You can win this. 💪

[@aashiraali6864]

Pls let me know what diet you followed

[@jamilathomas6199]

​@@aashiraali6864 Look up Dr. Brooke Goldner

[@Holly.Brewer]

What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last❤❤

[@yajairapartida]

Maria's story touched me. Omg she's so beautiful. I wish her the best in this difficult journey ❤️

[@lea9977]

I understand , don’t have Lupus, but have multiple sclerosis. Once diagnosed, you think medication is enough, but the reality hits. Stay strong anyone who’s suffering.

[@Holly.Brewer]

What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last

[@9doyouknow09]

Seriously??? Lupus can be cured????​@@Holly.Brewer

[@Holly.Brewer]

@@9doyouknow09 of course

[@Bee-xz4sh]

​@@Holly.BrewerHow

[@charonbecker4630]

Lupus cannot be cured but you can go into a type of remission

[@dawnbarber7980]

Awesome woman is an excellent lupus warrior that certainly inspires with words and her incredible spirit. Thank you!

[@dawnbarber7980]

@Kim Sonn Excellent news to read, thank you for sharing your wonderful news!!

[@rahulmiya5496]

Dr Ewi1 on have the cure for it

[@MariaLopez-nq4tf]

I found out when my kidney failed. But I knew something was wrong years before that. I kept hearing from doctors " your young and your fine. I had to fight for myself to get treatment. Push! You have to advocate for yourself.

[@paulw9068]

This made me emotional. I have sle lupus in 2009 my world fell apart when I was diagnosed I was told I could never have children. 15 years later I have two amazing wonderful boys 3 and 5. If you was meant to be a parent him up there will find a way.

[@jenceepooh4520]

That's exactly how I started with a lot of pain and could not even put on my own clothes...then the rashes and swelling in my ankles....I was diagnosed with lupus

[@Holly.Brewer]

What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last

[@LupusOrg]

Thank you so much for raising awareness about lupus!

[@rahulmiya5496]

Dr Ewi1 on have the cure for it

[@mahmudrza191]

With the help of Dr Ewi1 herbes my Lupus was cure thank you sir you are a great man

[@Holly.Brewer]

.What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last.

[@theamp1986]

I was diagnosed at 16 and now 35. I’m fortunate to have been able to manage it majority of my life. It’s gradually developed into more problem list/diagnosis. when treatment was not affordable, I dipped. It’s Unpredictable flare ups disrupt productivity/career. Outside nothing is noticeable, so sometimes I feel able body people aren’t as patient with me. I know others deal with more intense pain/dialysis or it becomes fatal upon being first diagnosed. I am one that doesn’t want to conceive because I don’t want my biological child to suffer; but I’ll adopt once I can be financially stable:)

[@Holly.Brewer]

What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last❤

[@fallen605]

I have had this for over 14years your amazing and strong this is a ride please be blessed with everything life has thank you

[@Holly.Brewer]

What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last❤❤😊

[@fallen605]

@@Holly.Brewer oo congratulations 🎊🎊🎉🎉 you are awesome stuff I'm so happy for you your blessings are going to be amazing 🌹

[@Holly.Brewer]

God bless you dear. You can also contact Dr ubarlo for help

[@shellyrae777]

I have Ankylosing Spondylitis ( inflammatory spinal arthritis) I took a medication to help it and it caused temporary lupus for a year. I had hair loss, mouth sores, face rash and horrible fatigue. Lupus is no joke.

[@shellyrae777]

@@lufufydlitslirairarztxthank you for the hugs 💕, Yeah it’s very painful, I take Advil and morphine daily just to get out of bed. I guess all chronic illness is horrible in it’s own way.

[@debrabenavidez3382]

Temporarily lupus? I thought lupus wasn’t curable?

[@shellyrae777]

@@debrabenavidez3382 it was drug induced. It wasn’t actual incurable Lupus, it caused all of the horrible symptoms though including a positive ANA blood test, but went away after the medication was stopped about a year after stopping. I was taking a TNF blocker, but there are other meds that rarely cause this as well for epilepsy etc.

[@Holly.Brewer]

What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last

[@TheSmartBarbie]

I was just diagnosed a few weeks ago…I’ve been surfing Google for days…surfing KZbin for days…thank you so much for your story…I’ve been so tired of crying but it feels so good to actually cry from *joy* rather than from the pain and shock of learning this….so I greatly appreciate it the positive videos about this disease…🫶🏽Thank you.❤️

[@Holly.Brewer]

❤What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last

[@ayyb6789]

I wish her the best in life.

[@rahulmiya5496]

Dr Ewi1 on have the cure for it

[@LuLu-kk5gs]

Aww what a great Husband she has… I pray for her wellness!!

[@tashab1628]

Your story is beautiful. Your husband is amazing giving you the support he does. Stay faithful in God, stay positive and hopeful.🎉🙏🏾

[@brittenyevans1101]

I too, have lupus. And in the beginning : the not knowing phase. Was the worst, I thought I was going to die. But, thanks to medication I’m here. I even know some women, who have it worse than my symptoms that have given birth. So yes , don’t give up.

[@Holly.Brewer]

What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last❤❤❤

[@Bee-xz4sh]

​@@Holly.Brewerof coarse your a bot or a troll

[@Bee-xz4sh]

What medicine are you on

[@marandamarvin]

I am so thankful for positive people! Yes! "Let's be light together!". 🥰

[@rahulmiya5496]

Dr Ewi1 on have the cure for it

[@Holly.Brewer]

What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last.

[@shanabenjamin8945]

Seeing the specialist on 28/07 to hopefully get a diagnosis on which auto immune desease I have. Many years in the making. Prayers are always 🙏 ❤ welcome 🙏

[@Holly.Brewer]

What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last..❤

[@Lani-jy2hv]

I was diagnosed at 8 and I am now 18… and I can tell you its such a tough journey…. Especially as long as it took for doctors to figure out what was wrong and to give me a diagnosis. One moment you can be fine , the next you can be going through flares. I am currently 9 months into my flare( my last was 3 years ago when I went on chemo) I am trying to reduce inflammation without chemotherapy as it is very toxic. Currently have been on prednisone since March, the lupus inflamed my lungs making it harder to breathe and shortness of breath, prednisone has been definitely helping. But the side effects of prednisone do play a negative role on self esteem. Hoping I get through and pass this flare to at least put my lupus to sleep.

[@evaang3616]

God bless you dear one, My daughter got diagnosed at 15. She is only 19 now it’s been a tough journey for sure and we are trying to keep meds at bay, she is going through a flare as well. Sending you so much love❤

[@Holly.Brewer]

What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last❤

[@leonmorris5602]

Just found out my mum was diagnosed with lupus 3 years ago and it’s a big sock to me, I noticed that she complained about her eyes driving, her shoulders hurt and she was feeling like she had no energy mum is still going strong and regularly exercising, working doing everything she did before the diagnosis but she has become a health freak and she only eats healthy organic foods this has made her much more comfortable and she is doing very well, she has aches and pains but she pushes through that I just hope she will live for a long time I am 27 years old and my mum is only 51 years old plz let me know if you guys have any remedies or medicines to help her, she’s the only family I have left and love her so much

[@imenrhouma8808]

I really need some stories like this🥺 Thank you so much🙏

[@Holly.Brewer]

What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last❤

[@rosam578]

Amen Maria thank you with all the great powerful words don’t loose hope❤

[@peacepocket]

That’s true love! God bless her and her husband

[@antreaserobinson7995]

Keep fighting Maria 🥰

[@rahulmiya5496]

Dr Ewi1 on have the cure for it

[@mahmudrza191]

With the help of Dr Ewi1 herbes my Lupus was cure thank you sir you are a great man

[@happydays5989]

I have the opposite- I cant seem to gain a pound without losing it if I miss a meal. 110 is what I've been at for years- drives me nuts when people say "I wish I had thatc I have lupus and auto immune immunothrombocytapenia This makes me happy to know I'm not alone God bless all the lupus and ITP warriors

[@Holly.Brewer]

.What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last❤

[@dullfairie5886]

Dealing with the worst lupus pain of my life, hearing her motivates me sm!

[@Holly.Brewer]

..What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last

[@rukhsanagulshairrukhsana7538]

My sister passed away 7march 2022 with lupus age 35 center nevrous system damage and sepsis diagnosed and 13 years before diagnosed lupus both hip are damage very pain ful death

[@Holly.Brewer]

What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last🎉

[@servicioslinguisticos5502]

What an inspiration! Thank you so much for covering this story, I sure needed this.

[@Holly.Brewer]

What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last

[@jacquelynmunilla538]

What a trouper! I have Lupus as well and it can be very disabling. The fatigue and aches when one flares really bring one down. People don’t always understand either. But, you keep moving forward, make the best of your good days, eat healthy, take your meds; and, rest on your bad days. 🙏🏻😊

[@Holly.Brewer]

What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last.,

[@pamelamays4186]

My Mom passed from lupus in 2018😢

[@buttaflyantics8618]

So sorry for your loss

[@m.layfette6249]

Rest in Peace 🕊️ Sweet Princess may flights of Angels carry thee to thy Rest 💜 🦋🙏🏾

[@everythingtaken19]

I’m sorry for your loss. My mom passed away from rheumatoid arthritis wearing her body down over the years. It was the hardest thing I’ve ever witnessed, and also have been struggling since her death. You’re not alone. ʚ♡⃛ɞ

[@alisonbear7114]

I have lived with lupus for 10 years now. The pain I can deal with. The disfiguring rash on my face, arms, chest and hands tho, not so much. Hard to leave the house feeling like a freak.

[@Holly.Brewer]

.What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last❤

[@jlf1309]

God bless you! I have lupus and have been miserable. You are such an inspiration! ❤

[@Holly.Brewer]

....What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last

[@TheresaDeVries]

I was diagnosed in 2006 if i hadn't listened to the voice in my head telling me something was wrong i wouldn't be here now. My lupus is under control but now I'm dealing with Fibromyalgia, Sjogren's Syndrome etc. Even with all the medications etc I am soaking up every sunrise and sunset taking it day by day.

[@GeneleaMarion]

When I was about 35 I was diagnosed with fibromyalgia and in April 2024 I had to have shoulder replacement surgery and they said it was arthritis that ate my joint up well in July or August I took a arthritis blood panel come back arthritis was negative. My auto immune disease was positive, I talked to the nurse and the doctor. They said it was lupus and I’m learning more about lupus. I’m finding out that doctors sometimes misdiagnosed lupus for Fabro so all these years I thought I had fibromyalgia and it turned out. I have lupus so now I’m trying to get help going to a rheumatologist. It’s going to be tough cause I have no insurance not gonna have to pay out-of-pocket, but I will make it. That’s why I’m trying to learn all I can about this disease, so thank you for this video.

[@ayyb6789]

Her words are encouraging.

[@rahulmiya5496]

Dr Ewi1 on have the cure for it

[@Holly.Brewer]

..What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last❤

[@g.c.m.productionsny]

Thank you for this interview 🙏🏻💜 means a lot to us 🙏🏻

[@RebaMiran]

I have lupus and it it’s so hard…. I had it for 8 years now. It’s a bumpy road with lupus, some days you’ll have good days and some days are just awful, but you make the best of your situation. I’m a lupus warrior too and we are so strong but can be fragile in many ways… but we keep pushing because life is beautiful, yes we suffer but life itself is beautiful. So though we suffer we keep going.

[@Holly.Brewer]

What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last.

[@sari5280]

😮😮😮😮😮😮😮😮😮😮had sle lupus for 30 painful years and I am still here never heard of it before but now I have COPD and RA and seizures and migraines and kidneys hurt but I just talk to God and pray been hospitalized 45 times So. Blessings to you all you lupus patients because people don't believe we are tried and in pain. But my sis

[@Holly.Brewer]

.What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last.

[@m.layfette6249]

I was diagnosed with Lupus 💜 back in December 2015. It was a case of had I known then what I know now. Rewind back to 2012-2014 I had multiple Alopecia spots/bald spots in my hair. Rewind back to 2011-2013 I contracted rashes on my face and mouth. TBH I just summed up my rashes to something my daughter caught at daycare. Instead mine would never go away, they grew and created dark and scale-like circles on my cheeks and under my eyes. Fast forwarding to 2018, when at 40-years old I had total hip replacement surgery. Before my surgery I was in excruciating pain and was walking with a cane. Since that time I've had over 10-Ten surgeries and medical procedures. My life has turned upside down. I was active, working, moving, grooving, always on the go. Now I am a Stay at Home Mom, my daughter is now my Little Trooper. She can recognize when I'm having a flare up, before I'm ready to admit it to myself. It hurts even more when I'm crashing, drained of All energy, struggling just to get in and out of bed. Despite all of the trials and tribulations, I Am a Lupus 💜 Warrior! I wear my Butterfly 🦋 wings with Pride and Strength and Courage and Wisdom, to tell the world and myself that, "I may have Lupus but Lupus does not have me." 💜🦋💜🦋💜

[@auntbeth6794]

Preservere good Buterfly ❤

[@Holly.Brewer]

What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last❤

[@ayofefe3976]

I have Lupus and it’s crazy! Bless you💜

[@Holly.Brewer]

What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last

[@bexxs2245]

It's nice to hear that someone else gained weight with lupus. I though I was the only one.

[@rahulmiya5496]

Dr Ewi1 on have the cure for it

[@Holly.Brewer]

What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last❤❤

[@pixpusha]

I came here to say Lupus is not understandable. No rhyme or reason to Lupus symptoms. Pretty much anything can happen. Anything.

[@Holly.Brewer]

.What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last.

[@rabinaneupane75]

I'm suffering from SLE with lupus nephritis from 3year ago .. my situation is going worst day by day 🥺💔

[@Holly.Brewer]

.What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last😊😊

[@JustRaine97]

My niece is a Lupus warrior. She was diagnosed at 14. The journey has been hard but she perseveres. She had to go on homebound school for a few years, but was able to return to school for junior and senior year. She got her associates degree a year later and 3 years after that she got her Bachelors degree. She achieved all of the this while gong in and out of the hospital and dealing with lots of pain. Unfortunately she is unable to hold a job because everyday is different and there are many days where she can't get out of bed. So she does light work part time. She's been on many many meds because she has 6 other autoimmune illnesses as well. So trying to stay insured and battle the insurance companies to pay for meds and treatments has been a full-time job. And finding a good Rheumatologist has been difficult. Before this we had never really heard of Lupus. So to all of the Lupus warriors, keep fighting. There needs to be more research and more advanced meds to help manage this disease. At 18 my niece had to have a hip replacement and at the age of 24 she needs another one. There needs to be more awareness of this disease.

[@Holly.Brewer]

.What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last.

[@davidserrano4716]

I am amazed to know you and Chris both as Family. Que Dios te bendiga ❤❤.

[@emusedone]

Thank you for covering this. 💜

[@rahulmiya5496]

Dr Ewi1 on have the cure for it

[@rocksofoffence.righteousam2422]

She's beautiful.

[@freshfaced625]

A brave woman and a wonderful story

[@rahulmiya5496]

Dr Ewi1 on have the cure for it

[@lefromthecity]

Unfortunately I’ve known many people with Lupus, and for this who have passed…they haven’t lived past 50 years old. It just seems like their is no reason, it’s random and no cure. Just living with it until maybe one day one bad week it will take you smh

[@ronnieking3848]

My cousin who died from Lupus was 70.

[@tlkayaks8225]

My sister in law is 63 with lupus for over 30 + years. There's no expiration date on anyone's foot. Keep living and seeking joy.

[@moneemitchell1227]

I am 52 and still enduring this wretched disease. Prayers and positivity keep me going

[@sydneyrogers9697]

I'm 70 and have had Lupus since 22. It's been a long road but I'm stable. It affects us all in different ways.

[@Holly.Brewer]

What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last.

[@lisakitzberger3931]

I was diagnosed with lupus in 96, I'm 60 years old now. I have my good days and bad days.

[@Godblessyou10100]

God bless you ❤❤❤❤🙏🏼🙏🏼🙏🏼🙏🏼🙏🏼🙏🏼

[@Starrr-ro8hg]

God heal her 🙏🏼

[@LeonaLilly-gx8fj]

Keep fighting Maria, your not alone. I also have lupus! We'll just keep on fighting all of us together. And prayers ❤

[@Holly.Brewer]

.What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last❤❤

[@monserratebarbosa5850]

I am fighting my lupus and I understand the pain that every day I have to go through and I am taking care of my son that is in a wheelchair

[@Holly.Brewer]

What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last❤❤❤

[@jackiealv6547]

Not only she’s physically beautiful but she also seems to be a very good person and I hope she continues getting better . I was diagnosed with Still’s disease (very similar to lupus ) at the age of 26 (I’m currently 42) and I still have painful flare ups . I got tired of immunosuppressants (including chemotherapy) and I haven’t taken medications in 2 years but I live in constant pain and extreme fatigue . Like her , I thought I would never have kids but after a long treatment I got into remission, feeling so well that I thought it would never come back but it always did . My kids are 6 & 9 and I’m always concerned that they could develop something like this . My daughter has asthma and eczema (also autoimmune ) and I feel so guilty . The pain in my knees is unbearable and I also have alopecia and skin issues . It really affects everything and good times come but they also go and the pain gets chronic. Prayers for this young and beautiful woman .

[@kimb2379]

Living with the pain of lupus. Was doing well with my symptoms since acquired after birth until getting Covid-19. It is my theory that the vaccinations given to us as children are responsible for all of our diseases. GOD designed our immune system and it does not need help from man-made vaccinations.

[@Holly.Brewer]

What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last❤❤❤

[@elizabethsamuel2894]

It’s nice that you have a supportive family but without that it would have been very hard

[@shihtzuwhisperer9069]

Anyone heard of Dr Brooke Goldner. A physician with Lupus. Her protocol has helped my friend with Lupus. Good luck to all of you!

[@kasmaineheyoka540]

Dealing with flare up right now. It’s been a tough weekend and trying to hold a straight face in front of my children. I’m worried I may lose my job because of this crap. I feel like have the flu.

[@yvonneboaten8289]

I know two people with it. Keep educating and inspiring.

[@Holly.Brewer]

..What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last😊

[@gdsfamily_]

😭😭😭 its so pain and hopeless to survive

[@Holly.Brewer]

What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last😊

[@axel.cruz47]

My mom got diagnosed with lupus at age 45, she was bed ridden for 6 months and no medicine could help her, she fasted for a while and over time it got better and she started an extremely healthy diet, now she is 50 and is perfectly normal and more flexible than a 30 year old, you are what you eat.

[@Holly.Brewer]

.What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last..

[@jeancoultas4312]

I am an anomaly, I have a very high blood test result saying I should have lupus but I have no symptoms. My rheumatologist has now started looking at connective tissue disease. He believes that having my thymus gland (t-cell producer when younger) removed due to a tumour growing on it (thymoma) has awakened auto immune responses. I have dry eyes and mouth but not enough to be Sjogrens syndrome and white cold toes but not fingers to indicate Raynauds. I am now faced with an ever evolving issue of spot the cause

[@Samchi8712]

I have lupus and it take so many years to diagnosed.

[@anthonylaszlo7487]

I was diagnosed with Lupus, Erythromelalgia and Raynaud's. I feel horrible everyday. I don't have any support from my family besides my brother and his girlfriend. I'm trying to get on disability and work part time but working has been really hard for me. Nobody in my family seems to care or understand that I'm sick and have turned their back on me. It sucks because before I got sick, I worked two jobs, went to college, and exercised daily. Now I feel like I can barely get out of bed every morning. I'm on methotrexate, Hydroxychloroquine, Prednisone, and a vitamin, but my kidneys hurt, and I still feel so tired all the time. I really hope I get approved for disability. I can work part time, but I need the disability money bad.

[@benitaj100]

What medication are you taking?

[@roquebrown2352]

Ive been sick for 24 yrs an i just found out i have SLE lupus an high blood pressure all my joints from head to toe have been killing me everyday for 24 years ive been bed ridden 3 times for over 6 months with no help or support from my kids im a single mom so its hard but im strong an im fighting it until i die

[@memyselfi1828]

I have had Lupus since 2009.

[@Holly.Brewer]

.What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last...

[@eyesrblue73j46]

My sister died at 56 from lupus. Well a heart attack from it. I didn't know about lupus. The last few months I can barely walk. I have all the classic symptoms. My Dr keeps telling me I need antidepressants. I even went to a neurologist. He did nerve conduction tests and tested reflexes. He said he did even know how I was walking. But yet my Dr says I'm depressed. I'm not. I know the difference. I have msk. A kidney disease, congestive heart failure and have had 27 surgeries. I know depressed. But all my symptoms came after a fall in fall last year and gradually have gotten worse. The rashes came 2 months ago. I can't even roll over in bed. This came across my feed. Seeing this made me cry. Because I was thinking there's no point in living if the Dr's don't care and I have to live this way. I'm going to ask for another opinion now.

[@Delious07]

going on the 7th to get tested currently something is attacking my eyes and brain

[@amzderdamn]

Finally diagnosed with lupus. I'm 30. 20 years of symptoms. They misdiagnosed me for 20 years

[@rahulmiya5496]

Dr Ewi1 on have the cure for it

[@Holly.Brewer]

What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last

[@mariehoadley2075]

I have Lupus, Fibermyalgia, & Rheumatoid arthritis, they are all very painful, but I,m trying to coup.

[@Aliciae2009]

I am.have trouble getting it diagnosed 😢

[@charonbecker4630]

Same. I also didn’t know what Lupus was until my rheumatologist told me it’s what he suspected I have.

[@Holly.Brewer]

What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last

[@rainydays9504]

OmG my sister symptoms started like that, her finger was hurting than her arms. Now she is getting studies to see if she has lupus 😢

[@Holly.Brewer]

What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last..

[@megramos2888]

I'm trying so hard to get out of bed today Ihave four children and I can't get up. It's all I want to do.

[@ashleygary1724]

I’m glad I found you here on KZbin Doc Kham. Curing me from herpes is something I never imagined. I’m so excited to be cured!.

[@sydneyrogers9697]

Getting out of bed is the hardest part and staying out is harder. You just want to crawl back in again.

[@Holly.Brewer]

.What a wonderful blessing and encouragement you are Dr ubarlo. I don't have words to thank you enough, I blessed the day I came across your KZbin channel, I'm free from my Lupus, victory at last.

[@sherylousison981]

Sending love ❤

[@pbg1949]

Thank you for spreading the message…but, unfortunately, if you look at the number of views and comments, the message still be sent

[@m.layfette6249]

All it takes is One-1 ripple in the water to create a mighty wave 🌊 of support, hope, advocacy, awareness and Love 💜.