Lupus is very serious and difficult to deal with physically and emotionally. I was diagnosed in Highschool at 17. I am now 38! Grace of God I am.here and will continue to be. As my prayer for all of you battling through the disease. I have lost a lot physically but have gained strength I didn't know that I had😇✨💜💎.
czcams.com/users/StephenSolowayMD love your story!!! My daughter has autoimmune!!! It’s the worst! God bless you!!!!! if u need second opinion see czcams.com/users/StephenSolowayMD he’s the best dr
I have suffered Lupus for many years and I finally got rid of it with help of herbal remedy from Dr Oyalo on CZcams channel. I used his herbs and I was cured completely with his herbs and up till now I’m negative
Lupus is a BULLY ... Together we stand & FIGHT this chronic & life threatening condition. I’ve been diagnosed in 2007, I’ve SLE & Lupus Nephritis.. GOD IS IN CONTROL 🙏🏾🙏🏾💜💜
I have Lupus Nephritis and I ended up on dialysis and I am soon getting a kidney I hope he gets and stays feeling well! At least as long to enjoy his children !!!
I have suffered Lupus for many years and I finally got rid of it with help of herbal remedy from Dr Oyalo on CZcams channel. I used his herbs and I was cured completely with his herbs and up till now I’m negative
I have lupus and i have all of the systems from all of the lupus definitions. I was diagnosed at the age of 19 I'm now 54yrs of age. I've dealt with a lot of things due to lupus. Its a lot i would like to say but hey carry on.
I think he’s lying about having lupus. He’s had lupus for 10 years he claims but that’s as long as Jena Tew has had Aids. I think Nick gave ig model Jena Tew HIV. And saying he has lupus so his reputation doesn’t get destroyed.
Remember his son just passed from a rare brain cancer. Mind you people who are hiv/AIDS often die from this same secondary disease 🦠 There’s been rumors of this for years.🤷🏻♀️
The timing to a T. The fact he too ended up on his death bed!!! If you remember he didn’t speak on his so called lupus at first. Then I look at Chris Brown and he has that skeleton face Gena has. Give it 20 years and all the pieces will fit together perfectly well
It’s so crazy to me how common it is now to have an autoimmune disease or some kind of health / mental health issue. I thought only truly unhealthy people go through that but it’s now going to people who we’d think have the money to afford to stay healthy with the right nutritionist & doctors
Sad that this condition arose. Glad he got the treatment he needed and a way forward. Mariah loves him and his kids need him. Best of luck to Nick and his lovely wife and family.
He is so likeable. I can see why Mariah fell for him. On another note, I want to put in a plug for sleep. I read recently that sleep is to the immune system what stress is to the immune system. Stress can cause stroke and so can a lack of sleep. I didn't know that. So it's important to not abuse the body thru sleep deprivation. Sleep, people!
You make it sound like people don't want to sleep. Of course we all want to sleep with no problems but it's not that easy to make your body stay asleep for 8 hours. Stress causes people to lose alot of sleep.
At my worse I slept 20+ hours a day, just getting up to drink, pee and take meds, couldn't stop sleeping. Now diagnosed took 12 years to be diagnosed, on strong meds and sleep 12 hours a day, although 11 years after diagnosis I'm gradually creeping down to 10 hours. That feels great
I have SLE , && it's affecting my kidneys but low sodium is most important ! good luck Nick Cannon , you're doing the right thing for making lupus awareness
I've got "Systemic Lupus, Erythematosus" I was diagnosed last year on ( Sept 28th 2016 ) its completely awful the exposure to fluorescent lights and even Sunlight can make me sick and nauseated. I get extremely tired at times from fatigue. And I have to sleep for like 3 - 4 hours at a time. My body temperature tends to go up and I get fevers in the back of my head. It goes down my spine then disappears
I just got diagnosed with SLE this month which inflamed my kidneys. I'm female mid 50's. I was lucky the rheumatologist who diagnosed me called a kidney specialist the next day and the inflammation was caught early enough so I am being treated aggressively. I had to change my diet as well. I too am eating egg whites- not bad with some Mrs. Dash:) A lot of meds for now though. It's a little scary but I am determined to keep a positive mindset. Support of family and friends has helped greatly.
ME as a LUPUS PATIENT that has been living with LUPUS for 44 years now there are plenty of actors and actresses that has LUPUS or know someone that has LUPUS, will not help spread the word of us people that is living with LUPUS. I have SLE the worst of the worst of the LUPUSES and wish and pray that it get spreaded more than it is or has been.
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
God is able I've had lupus since 98 and now I'm on dialysis due to the lupus attacking my KIDNEYS it's not the end of the world but you must take care of your self.GOOD LUCK TO ALL THE BUTTERFLIES....
I was just diagnosed with lupus yesterday. Both biopsies on some bumps of my leg tested positive. They are doing an even deeper biopsy tomorrow and I will hopefully have some more information on what strand I have been diagnosed with. I have about 60 or so red “bumps” on my body. Most of them are on my legs. A few on my hips and a few on my arm. Not itchy at all. Just very painful and red. I am a 28 year old father of two boys. I’d be lying if I said I wasn’t pretty scared as to what the future is going to look like. I am currently a CDL A truck driver and my life has always consisted of very labor heavy jobs. I found it hard to even walk last night because the bumps felt like they were popping out of my legs. My dermatologist prescribed me prednisone to help with the swelling. Should I seek a lupus specialist or something like that? I just want to make sure everything gets done correctly for the remainder of my life
OzZy401 yep. You need an auto immune doctor and regular therapy. If not treated it gets worse all at once. Praying for you but yes get scheduled for an ongoing doctor for your lupus.
Nick, Lupus Nephritis is Lupus. Its an autoimmune disease..Lupus that attacks the kidneys. I have Lupus myself and it has enlarged my liver and spleen many times in the past. I hope you are on some strong meds like Imuran or Methtrexate. Keep strong and continue doin you. Make sure to rest though as getting fatigued with Lupus isnt the best thing. Congrats on the babies!
I have lupus and its starting to effect my organs its already taken some babies from me just days before delivery its very tiring and exhausting and genetic.. I know what Nick is going through I've had and get still all that shit. wish there was a cure....
Insomnia is a symptom of Lupus so being on the go feels like the right thing to do, until of course the disease won't allow it anymore because you are too exhausted and in too much pain.
LUPUS {SLE} and suffering in silence since 2011. Why isn't there a PSA for LUPUS? There's a PSA for everything else except this disease here in Ohio at least? #Frustrated777
And look at the creator of the Universe! He is Still here even made it through the pandemic! Our body never does well on fast food we suffer sooner or later for it. All praises to the most high God for sustaining!🙌🏾
no matter what he does the only cure for lupus nephritus is having a kidney transplant. People who have this form there lupus symptoms subsides as long as the transplant doesnt fail. I have it and ive finally reached kidney failure after 7 years of medications. Waiting for a donor is another issue....
No, quite the opposite actually. HIV is contagious and weakens the immune system, while Lupus causes an over-active immune system and is not contagious.
Have a doctor check you for neurological celiac disease or non celiac gluten sensitivit and autoimmunity. I had lupus antibodies but gluten ataxia symptoms. Nobody thought to check me for gluten ataxia!
Lupus is very serious and difficult to deal with physically and emotionally. I was diagnosed in Highschool at 17. I am now 38! Grace of God I am.here and will continue to be. As my prayer for all of you battling through the disease. I have lost a lot physically but have gained strength I didn't know that I had😇✨💜💎.
what medications have you been taking to battle Lupus..what meds worked for you and didnt work for you?
czcams.com/users/StephenSolowayMD love your story!!! My daughter has autoimmune!!! It’s the worst! God bless you!!!!! if u need second opinion see czcams.com/users/StephenSolowayMD he’s the best dr
I have suffered Lupus for many years and I finally got rid of it with help of herbal remedy from Dr Oyalo on CZcams channel. I used his herbs and I was cured completely with his herbs and up till now I’m negative
@Ignace Alli how long did it take for you to be cured ?
thank you 💜💜 i was diagnosed 3 years ago
My mum is a Lupus survivor I am undiagnosed but look at you guys , for inspiration and motivation especially in those moments when I get exhausted.
As a 58 yr old male with lupus I appreciate this interview
My bf has Lupus as a male, and if you don't mind me asking when did you got diagnosed? Also you're so strong!! ❤
Hey bud, 52 just diagnosed. Got any tips? Stay strong.
Lupus is a BULLY ... Together we stand & FIGHT this chronic & life threatening condition. I’ve been diagnosed in 2007, I’ve SLE & Lupus Nephritis.. GOD IS IN CONTROL 🙏🏾🙏🏾💜💜
I have Lupus Nephritis and I ended up on dialysis and I am soon getting a kidney I hope he gets and stays feeling well! At least as long to enjoy his children !!!
How are you?
bless you 🙌🏽
All 7 of them lol
I have suffered Lupus for many years and I finally got rid of it with help of herbal remedy from Dr Oyalo on CZcams channel. I used his herbs and I was cured completely with his herbs and up till now I’m negative
@Ignace Alli can you tell how can we contact him?
Ty for speaking on this. My mother passed from Lupus and I had no idea what it actually was. Thanks for speaking on it
I have Lupus and i did not even know Nick Cannon had i. The word needs to be spread more and more research is needed.
Thanks so much for all your information Nick I was diagnosed with lupus in 2019 and I’m still learning a lot about it keep up the good work #💜
I have lupus and i have all of the systems from all of the lupus definitions. I was diagnosed at the age of 19 I'm now 54yrs of age. I've dealt with a lot of things due to lupus. Its a lot i would like to say but hey carry on.
nice keep up good diet
I think he’s lying about having lupus. He’s had lupus for 10 years he claims but that’s as long as Jena Tew has had Aids. I think Nick gave ig model Jena Tew HIV. And saying he has lupus so his reputation doesn’t get destroyed.
All those babies he having 😳
Remember his son just passed from a rare brain cancer. Mind you people who are hiv/AIDS often die from this same secondary disease 🦠 There’s been rumors of this for years.🤷🏻♀️
@@sandalust1481 medicine is advance the odds of them kids contracting it are slim to none, and
I don’t think nick gave it to her, I think she did give it to him tho and it is a cover
The timing to a T. The fact he too ended up on his death bed!!! If you remember he didn’t speak on his so called lupus at first. Then I look at Chris Brown and he has that skeleton face Gena has. Give it 20 years and all the pieces will fit together perfectly well
This make me think of Gena Tew situation now. Its been almost 10 years since he was in his death bed. Now she come out she been sick almost 10 years
My thoughts exactly ..
I'm sure he was tested for HIV😏
The fact this came up on my recommendations after that Gena /insta model came out
It’s so crazy to me how common it is now to have an autoimmune disease or some kind of health / mental health issue. I thought only truly unhealthy people go through that but it’s now going to people who we’d think have the money to afford to stay healthy with the right nutritionist & doctors
Hopefully there will be a cure for autoimmune disease such as Lupus it’s rough on the body
Sad that this condition arose. Glad he got the treatment he needed and a way forward. Mariah loves him and his kids need him. Best of luck to Nick and his lovely wife and family.
God bless Nick Cannon. 🙏🏾❤️🙏🏾
He is so likeable. I can see why Mariah fell for him. On another note, I want to put in a plug for sleep. I read recently that sleep is to the immune system what stress is to the immune system. Stress can cause stroke and so can a lack of sleep. I didn't know that. So it's important to not abuse the body thru sleep deprivation. Sleep, people!
You make it sound like people don't want to sleep. Of course we all want to sleep with no problems but it's not that easy to make your body stay asleep for 8 hours. Stress causes people to lose alot of sleep.
At my worse I slept 20+ hours a day, just getting up to drink, pee and take meds, couldn't stop sleeping. Now diagnosed took 12 years to be diagnosed, on strong meds and sleep 12 hours a day, although 11 years after diagnosis I'm gradually creeping down to 10 hours. That feels great
Mr. Cannon is a wonderful man
I love Nick and his family. He seems like such a nice guy! Please Nick take care of yourself! :)
I have SLE , && it's affecting my kidneys but low sodium is most important ! good luck Nick Cannon , you're doing the right thing for making lupus awareness
Alexis Baez How long have you had it?
Deschamsify not even 3 years
I've got "Systemic Lupus, Erythematosus" I was diagnosed last year on ( Sept 28th 2016 ) its completely awful the exposure to fluorescent lights and even Sunlight can make me sick and nauseated. I get extremely tired at times from fatigue. And I have to sleep for like 3 - 4 hours at a time. My body temperature tends to go up and I get fevers in the back of my head. It goes down my spine then disappears
How are you now? Same problem here.
I just got diagnosed with SLE this month which inflamed my kidneys. I'm female mid 50's. I was lucky the rheumatologist who diagnosed me called a kidney specialist the next day and the inflammation was caught early enough so I am being treated aggressively. I had to change my diet as well. I too am eating egg whites- not bad with some Mrs. Dash:) A lot of meds for now though. It's a little scary but I am determined to keep a positive mindset. Support of family and friends has helped greatly.
MegensBay Family and friends make a big difference, stay positive... You will be okay.
I feel your Pain Nick I just tested positive so its all still new to me prayers going your way
Ur blessed no matter what they have to say about you and ur health
im glad that hes doing well
ME as a LUPUS PATIENT that has been living with LUPUS for 44 years now there are plenty of actors and actresses that has LUPUS or know someone that has LUPUS, will not help spread the word of us people that is living with LUPUS. I have SLE the worst of the worst of the LUPUSES and wish and pray that it get spreaded more than it is or has been.
Carla Williams how are you doing today?
I’m 15 with lupus I’ve been diagnosed since 2013 but I’ve have symptoms since I was a baby
Sheila Acosta what kind? Please describe the symtoms..
Nick you will defeat this. I love you stay strong.
More awareness. Thanks Nick!
God bless you Nick...y your beautiful little cuties...💕🎶💜😇
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
I have the same illness! and yes, it requires a lifestyle change.
God is able I've had lupus since 98 and now I'm on dialysis due to the lupus attacking my
KIDNEYS it's not the end of the world but you must take care of your self.GOOD LUCK TO ALL THE BUTTERFLIES....
God BLESS you Monique and HEAL you of Lupus completely IN JESUS'S NAME!
I love this man💖He inspires me
Am glad he was okay, they make a cute couple.. and he is to funny.
i am a 12 yearold female with the same problems all u gottah do iz stay strong
Here after gena tew
Prayers Nick
My daughter suffers from Lupus also.
I have lupus and I go too dialisys now😢😢😢😢
Not confirmed yet, but tests results highly suggests it. People seem pretty chill towards eachother about it! 🙏♥️
I was just diagnosed with lupus yesterday. Both biopsies on some bumps of my leg tested positive. They are doing an even deeper biopsy tomorrow and I will hopefully have some more information on what strand I have been diagnosed with. I have about 60 or so red “bumps” on my body. Most of them are on my legs. A few on my hips and a few on my arm. Not itchy at all. Just very painful and red. I am a 28 year old father of two boys. I’d be lying if I said I wasn’t pretty scared as to what the future is going to look like. I am currently a CDL A truck driver and my life has always consisted of very labor heavy jobs. I found it hard to even walk last night because the bumps felt like they were popping out of my legs. My dermatologist prescribed me prednisone to help with the swelling. Should I seek a lupus specialist or something like that? I just want to make sure everything gets done correctly for the remainder of my life
OzZy401 yep. You need an auto immune doctor and regular therapy. If not treated it gets worse all at once. Praying for you but yes get scheduled for an ongoing doctor for your lupus.
How are you these days brotha? Did you ever get the evaluations and treatments you needed? Hope all is good
Nick, Lupus Nephritis is Lupus. Its an autoimmune disease..Lupus that attacks the kidneys. I have Lupus myself and it has enlarged my liver and spleen many times in the past. I hope you are on some strong meds like Imuran or Methtrexate. Keep strong and continue doin you. Make sure to rest though as getting fatigued with Lupus isnt the best thing. Congrats on the babies!
Yeah that is not lupus like, it is lupus.
I have 2 kinds of Lupus I don't know where to begin my life sux,so much pain
O really really love him Oh my gosh
God Bless him, pray hes well!! Thank you Jesus!
good man, Nick
stay strong and keep fighting. we support you all.
Fast forward, “Lupus LIKE?!”👀🙄.
I came her because of gena tew
Me too
Gena Tew, Got you😮
I have lupus and its starting to effect my organs its already taken some babies from me just days before delivery its very tiring and exhausting and genetic.. I know what Nick is going through I've had and get still all that shit. wish there was a cure....
Sorry try stay healthy.
Yeah taking care of your body with supplements and exercise but sleeping with tons of women with no protection is not the way.
I thought he said in the video it is a "lupus like disease"??? Or am I hearing things.
I have lupus for three years now
His lupus causes so much fatigue he can't pull out.
I wonder what are the holistic things he takes to help him?
Sickness and in health not only good times linda j ☮️
Rare? Actually it is not rare.
Lupus Nephritis is one of the most rare forms of Lupus. So he's right.
As many as %40 of people with Lupus have kidney involvement. %50 of those with SLE diagnosis are also at some point diagnosed with lupus nephritis.
Brandi Watts Are you serious? Thats not at all true. Less than 10% of Lupus cases are Lupus Nephritis.
www.lupusresearch.org/research/acr/lupus_nephritis.html#.U2kJP_ldXng
www.kidneyabc.com/lupus-nephritis/
www.kidney-support.org/lupus-nephritis/
www.webmd.com/lupus/lupus-nephritis
www.kidney.niddk.nih.gov/kudiseases/pubs/lupusnephritis/
Brandi Watts its rare for men
Insomnia is a symptom of Lupus so being on the go feels like the right thing to do, until of course the disease won't allow it anymore because you are too exhausted and in too much pain.
#LUPUSSTRONG 💜
🙏💖
"Lupus-Like"...ok
I'm surprised they didn't diagnose him with sarcoidosis like they're doing everyone else.
I'm ten and I have the same lupus he has and I do chemo and I hate the renal diet too my kidneys r in damaged
He said it's lupus nephyritis...stop being ignorant...
sexyjb1975 nephritis...
Now I see how he discovered Sebi lol.
LUPUS {SLE} and suffering in silence since 2011. Why isn't there a PSA for LUPUS? There's a PSA for everything else except this disease here in Ohio at least? #Frustrated777
it is a different form of lupus.
Gena tew
Gm edagdwg love this video young man God it work he is a real man she loves him this what makes married ppl understand for better or worst linda j ☮️
I have lupus and take no medicine!!#!!!!!!!!!
Why not?
Lupus like??
Nick cannon gets what he sows. So glad he won't be here long.
I have kidney damage. But not the right diagnoses.
They say it is a different form of Lupus.
And look at the creator of the Universe! He is Still here even made it through the pandemic! Our body never does well on fast food we suffer sooner or later for it. All praises to the most high God for sustaining!🙌🏾
All of a sudden many HOLLYWEIRD PEOPLE have Lupus??? Hmmmmmm that's very odd!🤔
Well it might be lupus like bur it isn't lupus.
life style choice after the incident. ok. what is the incident? Lupus? are you sure?
we idolizing this people we not even praying God
no matter what he does the only cure for lupus nephritus is having a kidney transplant. People who have this form there lupus symptoms subsides as long as the transplant doesnt fail. I have it and ive finally reached kidney failure after 7 years of medications. Waiting for a donor is another issue....
How old are tho? Not everyone goes through the same thing with lupus nephritis
Ill give him a kidney
get your kids checked its hereditary!!!!!
Was thinking the same
No it is not
It's not
Aw Mann that's bad
O.o
So…lupus doesn’t allow you to pay child support for your 12 kids?!
I’m a lupus warrior, a RN, and a mother.
Nick is trash.
1st
is lupus HIV or na
No, quite the opposite actually. HIV is contagious and weakens the immune system, while Lupus causes an over-active immune system and is not contagious.
You really need to educate yourself...Its far from it
Dum ass
And now your question is a great question!!5 years later
Have a doctor check you for neurological celiac disease or non celiac gluten sensitivit and autoimmunity. I had lupus antibodies but gluten ataxia symptoms.
Nobody thought to check me for gluten ataxia!