To God be the glory in all things. Nicks on my prayer list ✔

I have lupus also..since i was 18 years old I'm 40 years old now.. been though alot but i'm o bleesed to still be here.. Just thought i would tell my testimony..

I have Lupus (SLE) too; I was diagnosed over 30 years ago. I have gone through a lot, but I can't quit because quitting is not in my vocabulary. Yes, it gets very difficult at times, but I know God hasn't brought me this far to leave me and the same for my Lupus Warrior Brothers and Sisters.

Who else is here after the Gena Tew story am proud of her for coming out.

I Have Lupus Too & Its Exactly What He's Saying. It's So Tuff & Ruff Ty So Much Nick Cannon For Telling Your Story Because This Is Exactly What I feel All The Time. I Feel So Alone At Times Dealing With This & Facing Death In The Same Ways. Than After All The Medications Side Effects Can Cause Added Illness.Yes This Opens The Door 4 You To Obtain More Illness, Your Body Is More Sensitive. But Now I Want 2 Say TY & I Don't Feel So Alone Anymore. Finally Someone Understands ME💜Thanks😘❤🙏 @NickCannon U WILL LIVE A LONG PROSPEROUS LIFE BLESSING SENT 2 U & YOUR WAY. REMEMBER TO PRAY WITH FAITH, NAMESTE 💜 💞💜

Toni Braxton battles the same thing too. I can't imagine what her and Nick be going through, by the way he describes this, it's something very unpleasant to have. I will say that he is thinking very positive on this issue and is trying to live his life.

I knew that Nick had lupus but I never knew the things he has to go through dealing with it. I’m glad that he told his story because now I know more about this illness.

Lupus hurts.. it took years for me to understand what was wrong! I have to fight my body to work .. I will tell myself get up! Don’t be weak..

So inspiring! I wish I could hear him speak more. It would be amazing if he decided to have his own podcast. Great guy!

I basically grew up with this man.. I was a kid watching him on All That... faithfully watch Wild ‘n’ out. I take my hat off to him because no matter what, he still doing his thing despite it all!! 👏🏾

I love your spirit, God's hand is on you...

No one deserves to be sick stay strong also brother

That vibe was so strong, I felt it! Living stress free is the key.

Nick never complains about his sickness. He always looks healthy. I pray he lives a long life.

I recently found out I have Lupus when I went into to my doctors office to take a pregnancy test. They told me Congratulations you have a baby, bad side to it your at a high risk pregnancy because you also have lupus. I'll never forget how I felt sitting in that chair trying to take in everything I was being told. I'm scared for my health, for my baby's health but most importantly how I'll be able to mentally take it all it in. He makes it look so easy & I guess as time goes on it will be, but he gives me hope that if can deal with it & be okay & learn to cope in a very positive way, hopefully I'll be able to do the same soon.

I have lupus and was diagnosed in 2013, my last semester in college. I still walked across that stage with a BA in Mass Communication. I'm still fighting everyday and currently teaching Journalism at a local high school. I take prednisone, plaqunil, methotrexate, and imuran. Stay strong brother, you are not alone!!

I Have Had The Lupus Systems As Well, OH BUT FOR GOD AND HIS GLORY IM STILL HERE IN JESUS NAME!!! Our God Is A Healer!!!!

3 years ago yesterday i lost my love my heart my big brother he was only 27 and he lost his battle to lupus and that was the worst day of my life. I watched the life leave his eyes and still to this day i see his face i feel i could have done more for him. My father also suffers from this disease.. Lupus is very real it is still a fight that has no winner in the end. Thanks for the love guys it's not going unnoticed!!! I appreciate all the words of encouragement. I've never spoke on this before so it was a great somewhat release on some of the bottled emotions and i appreciate all of you..

Fellow lupus warrior...thanks for your inspiration! Sending you love and hugs!

I was diagnosed with lupus in 2014. I was devastated at hearing the diagnoses and was in denial for months. With my first appointment with my rheumatologist, I was so sick and I felt so old, it was difficult to move. It's exactly as Nick says, some days you can hardly move and get out of bed so I decided that I will not allow lupus to define me and I will beat it every morning. Now I wake up with a prayer of gratitude and before getting out of bed, I decide what my day would be like. Oh my, I so relate with everything he says. It's exactly the attitude and outlook I have about life. I was always wondering about my purpose on earth. Now, with lupus, if I can make a difference in one person's life, that question is no longer needed. I know I am Blessed when I open my eyes in the morning.

30 year survivor.. it's an every day struggle.. thank you for making those aware of this disease you cannot see and the painful effects on you every day.. take care Nick! God bless

Beautiful spirit this man has. I struggle with fibromyalgia and I don't know if I can stay that positive through the pain all the time. Thank you, Nick, for your perseverance and your beautiful spirit!

By The Grace Of God 🙏🏽

God has him here for a REASON...he's a very strong mind and has very positive attitude may God BLESS you Nick🙏

He’s so positive and busy I forget he’s fighting. I love me some Nick Cannon!!

Your not alone Nick cannon I have lupus too

U can look good to others while in a flare up but when you look in the eyes they don't lie 👀👀💜💜💜💜💜💜💜💜💜💜💜💜💜💜💜

I truly understand. thats how i feel sometime. I have Multiple Sclerosis which is another auto immune disease like Lupus. Nick is a good guy and a fighter u would never know what he was going through from watching Wild n Out. I have always loved Nick. I actually like some of his movies. Lol im being brave and admitting it. Keep pushing Nick!!!

I will be praying for Nick for healing and wholeness. He’s such a BLESSING to us!!!

I look up to you your sooo blessed! I know how you feel.... I was diagnosed with cancer and had my first surgery on my 38th birthday March 9,2018. I'm a single mom of 3. It was the worst pain I've ever experienced... I think the hardest part was telling my kids that I had cancer... I was diagnosed with rare rare cancer of my muscles and flesh in my back I'm that 1% It looked like I was attacked by a shark and I have pain every day. I thank God I'm alive... Its been tough fighting for my life, working, stressing over bills and trying to hide my pain from my kids. I had a total of 3 surgeries a few months ago. My surgeon said it was pretty bad... I go for another PET scan hopefully November 1,2018. I thank God for holding me up.... and I pray for everyone that's battling for their lives. It's funny I work at a hospital in San Antonio and most don't know because I smile and hide my pain.... my passion is helping others... I LOVE encouraging others to never give up.we have to give the baton to God. I thank God for everything, my kids making airplane sounds as they hand fed me after surgery 😊 I had to learn how to eat and brush my teeth all over again. I thank God for all the love from my family,friends, and coworkers.. it has been quite a journey 🙏. God bless you always Nick and anybody going through some tough times

Battled lupus since sle Dec 2005. He broke it down so very well. I rejoice on my good days. Praise God for every day. Lupus is frustrating exhausting and something most people don't understand. Praying for Nick a good man.

Thank you so much for sharing your story Nick. God Bless you!!! Prayers

Grateful for this testimony. I was diagnosed 10 years ago and spent a good 3 years in and out of hospitals. By the grace of God my life has taken a turn that even my doctors have referred to as a miracle. The last few weeks have been a little rough but I have slot to be grateful for. I've managed to build a 6 figure business and that business is designed to keep running even on days when I can't. I think in life you take what you have and do with it what you can. It's been my experience that as long as I keep doing this God fills in the gaps and then some. Many blessings for all those in the fight. Keep your head up. Keep coming back to stories like this one above and rest whenever rest is needed.

In am just starting my lupus journey now. I live in daily agony, but keep getting up everyday for my family. I love the mindset of "live for right now". I know it is easier said than done, but when you don't know whether you're going to live to see tomorrow, you have to treat every day as a blessing. Cheers to all of us just surviving, and trying to live in the moment.

Wow gave me chills!!!! You got this !!!! You are highly favored ❤️🙏

My mother was diagnosed with lupus at the age of 16 suffered a mild heart attack and both kidneys failed. She got a transplant in the largest kidney swap back in 2010 and has been healthy and happy since. She will be 50 next year. My second oldest sister was diagnosed with lupus January 2010 at the age of 17 after she suffered a stroke she’s had 1 flare back in 2013 but has been healthy and happy and even put on a few pounds since then. My oldest sister was diagnosed with lupus February 2018 and has since become vegan and works out and lives a healthy lifestyle she’s 27. Lupus can be a scary thing but having these 3 amazing women in my life fighting a great fight and pushing through no matter how rough the rough days get just reminds me that having God #1 in your life anything is possible! He’s brought us through our storms and continues to show us there are brighter days ahead!

This was so inspiring, you never know what anyone is going through behind closed doors.

Lupus is very hard to diagnose because it mimics other diseases.. I like that he lives for today & doesn't worry about the future.. God has you Nick & you are definitely in my prayers!

Love this! His words really touched me. I Was diagnosed with lupus at the age of 14 and I just celebrated my 29th bday this past month. It's a rough ride so being positive becomes so difficult. But I'm learning. God would never put more on us than we can bear. Stay strong yall 💜💜

I had lupus for 5 years now and it’s been a bumpy road but I made it and I’m still in battle we are all still in battle...but I learned that it’s best to stay positive and be thankful for being able to move and just being able to go into the kitchen and make breakfast... 🙂 cause it was days where I couldn’t make my own food or bathe myself... but I thank God and the support from family and friends that I can do that now...some days are still bumpy but I’m pushing.. last year I wrote a song about my lupus experience and I just recently uploaded it on my channel if you listen to it I hope you get some motivation from it and continue to live each day at your best ❤️🌸

I knew something was going on. I have Sickle Cell Disease it does the same thing. Thank you for sharing because I educate everywhere I go.

Sounds like me with my three successive mini strokes. I'm still here...for some reason. I try to spread love and kindness with whatever time I have left.

I have lupus & it's no joke but glory be to God & my amazing doctor. Everything he says I've gone through minus the chemo. I was diagnosed in 2016 & now i am in remission. God is good!

Lupus has changed my entire life. ...I use to could say those things, when first diagnosed. Now it turned my world upside down. .Pray one day I can get to a space where having life is good again. ..

Very inspiring Nick. I have Sickle Cell but Sickle cell doesn't have me. I never knew how similar Lupus & Sickle Cell are. We gotta not take Today for granted.

I can understand because I have RA and I have my bad days but I learned to push through. This was so inspiring to listen to.

Live your best life

God continue to bless you. My sister died at age 63. She was very strong. She was my hero. She never complaint about her illness. Thanks for your testimony

Continue to stay prayed up and en joy each and every moment of your life. I had a cousin that had it. She was only 17 but she kept pushing with smiles every day. Remember our God know your pain and that every day is another blessing.

I hope he is here forever! I have Lupus also and this video and him talking about his personal battle is a HUGE help to me! Thank you for sharing! God be with you and everybody who sees this video.

Ive had lupus since 1997. I know everything he has n is going thru. But were fighter's and I'm now 38 n still here fighting

Wonderful show of strength and faith!!! I truly admire your heart and resilience💝

Thanks for sharing. I've had it for 33 years now and i feel so happy because I've willed myself to stay strong, well and positive. Thank God, i have been able to go to work every day. Working to pursue my Masters in Accounting. God bless.

Lupus patient can have a normal life if they take care of themselves and follow doctor's advices, my wife has been a lupus patient since 2014;indeed, sometimes she had some headache , pain joint, stiffness, but overall she has a normal life: she works, she takes care of the baby and me.... A point I can say she is stranger then me ... I am proud of her, she never give up and I will be on her side until death I love her too much. I want to say to all lupus patients: you can have a normal life just follow up with your doctors and be a vegetarians, workout, no processed food , no meat just fish, fresh air and meditation practices like prayers, yoga, meditation ( avoid stress maximum) I love you all and take care god bless you.

This is inspiring for all those with lupus and related diseases . What u and Toni are doing is beyond admirable! God bless you with many healthy days

Thanks Nick Cannon for sharing your I too am a Lupus Survivor 💜 God Bless you and Heal you from the inside out!!!

My Mom is living with Lupus n Fibromyalgia n she has described it just like Nick has... It is so wonderful to hear someone share their private battles with this tyrant of a disease. Kudos to Nick Cannon for being so open yet remaining enthusiastically positive 💯👍🏾 There isn't a soul on the face of this earth that isn't battling something.... My thghts n prayers go out to those strong warriors - God bless! 🤗

Man I really applaud him for having such a positive attitude 24/7. I had no idea his disease was this bad. But yet he continues the always uplift those around him and walk around with a smile on his face! I learned a lesson today well watching this. I don't have Lupus I don't have any life-threatening disease so I have no reason to complain or grumble about anything! I need to embrace life and love those around me with all I have and treat my body better than I have been doing. Thank you Nick for sharing you're amazing story. You are an amazing person and you will be continually in my prayers.

What a great explanation. Been living with it for 29 years and I’m 40 now. Lupies... make sure that you have a plan A, B and C. Appreciate life and live as best as you can 😘🇬🇧

Doctors treat but God heals! I pray you live long Nick! You’re a big inspiration to many young people!!

Much blessings on your life. I grew up watching you and your talent evolve. Much respect to you for sharing your struggle it sheds light on a very misunderstood disease.

I also have an autoimmune, called ME/CFS. It does not have as much research as Lupus, so we have very little information about how to treat it. I'm glad that there are treatments available for Nick. He has such a great temperament: there's no anger visible here, only acceptance and love 💜

Such a great spirit...I'm inspired, truly.

Wow! I love his motivation and faith in God in spite of.💕🙏🏽

So sorry for anyone who suffers from this or any illnesses. Wishing Nick the best. This was very humbling.

Inspiration 💜💜💜 i also have lupus, scleroderma(recently diagnosed), sjogrens, Raynauds and other autoimmune diseases.. and I really needed to hear this .. thank you.

Ncredible, such positivity!! So much respect for him and prayers going up for a miracle healing for him. God bless!!!

Awwww especially touched my heart. May he live a long, powerful life.

I hope he lives a long happy life. thanks for the little insight on what my friend is going through.

Wise words and very inteligent man honestly its true his outlook on life is one we shouldnt take for granted. Each day is a blessing and surround yourself with people who lift you up and see the beauty in you.

I have MS (also an autoimmune diease )and this hurt my heart. He explained it perfectly

Sending you Nick Cannon and all of you with Lupus so much Love and healing light.

Thanks for sharing your an inspiration to persevere through it, May God give you comfort and strength.

You are truly blessed and highly favored! God continue to bless and strengthen you!

Love you, Nick. Than you for speaking your truth. I lost my Mom 11 days before my 19th birthday, she was 38 and wasn't able to live in a time of medical advances of today. I'm sure she's proud to hear you.

I can relate to the chest pain and everything you are describing. Definitely not easy to live with having but keep fighting 🙏🏾👑 we've got this! #LupusWarrior

Man Nick is a strong dude.Grew up watching him he always smiles and he loves to make people laugh with or at him. Nick doesn't have nothing to lose he always have a good attitude.

Exactly as he said "he has Lupus it doesn't have him"...many other people need to think about that also with whatever they may be facing, dealing with etc. Nicely done Nick.

God Bless Nick - did not even know he was experiencing this illness. I totally get his perspective about living in the now; tomorrow is not promised to anyone.

I have lupus nephritis syndrome. I definitely can relate to what Nick is saying. It’s a day by day living arrangement. Thanks for sharing 🙏

Wow I needed to hear this , so uplifting and inspiring . Me myself battling with lupus it’s a very hard struggle but also manageable. Being diagnosed at 23 was devastating . It was definitely a stressful time for me to take all of that in and changing my whole lifestyle up. I still am today a little in denial so I run to things like this . ❤ thank you for that .

All the best Nick Cannon. I have loved and respected you for so long- Good luck with your health- I love your enthusiasm and wisdom- it is so wonderful

I was diagnosed last month and I also got a serious blood clot like him too. It was the time when I’m planning to step forward in my career/business/ambitions and applying for a scholarship abroad. After I got the test result, my dreams shattered. I cried endlessly for nearly 2 weeks. I used to think it’s that I was just like other lazy person. My stress/body ache was probably caused by school and works I’d been doing. I’ve been working real hard and always think ahead in life. Now I had to quit all energy consuming activities. I can’t do the same as a normal woman in her mid-20s?? However just want to say I do appreciate this video I found after I just came out of my depressive cave. He really inspired me at some points. Maybe god would like me to slow down a bit and enjoy the moment which I often neglected this whole time. I stopped for a second and embracing some self love and know my own limits. It’s blessing and curse sometimes when I know I couldn’t go further with this shitty energy level I have. Truly it’s really hurt sometimes to watch my friends getting successful and having a normal family/healthy kids, which I don’t think I ever could...

My prayers are with you.i also have an autoimmune disease.i have Sarcoidosis, with mulit organ involvement.no one can quite understand what we go through unless they are going through it as well.

2012 was a big year for the beginning of spiritual awakenings. I can tell by his words of vibrations, frequency and love that he's in that space where energy is EVERYTHING. What you project and allow yourself to take in will make or break you. Namaste Nick!

So positive.. keep ur head up Nick!!

Wow... every time I see this brother he is always smiling, positilve and joking. Who knew that he regularly faces serious health conditions. He is someone to celebrate and look up too. He is a warrior!!

Praying for the manifestation of complete healing!!! 💙

My Mom died from Lupus at 38. When He was talking about His experiences I literally seen Her. Nick You're fighting a fucking tough battle and I can tell Your a Soldier. Man I have a totally different perspective and level of respect for You. ✊🏽✊🏽✊🏽✊🏽✊🏽✊🏽

I know this is going to sound messed up but it feels good to hear someone say what I've been saying for years. I swear people think I'm being overdramatic. It gets frustrating having to explain this.

Live On, Nick! We love you! My best friend in the whole world passed away from it 5 years ago...she lived 1 year after finding out then she was gone! I.ve never ever gotten over it* Stay happy and healthy...we.re praying for you!💝

God bless you Nick Canon....my prayers are with you....thank you for sharing your story....trust me it's helping someone out there going through the same thing.....

Thank you for your openness and honesty. I was just diagnosed 10 months ago.

My heart completely goes out to him. For someone who lost a mother to lupus. To see him still so full of life and still fighting brings tears to my eyes. I commend him for all he has done. For everyone who has lupus keep fighting stay strong 💪🏾 this is but a battle that’ll make you a solider of GOD.

Speaking things into right now. Thanks for your wisdom. I pray for you Nick.

Very very inspiring Nick. U have an unbreakable spirit and i admire u for being able to handle ur illness the way u do. Sometimes i forget that u even have it bc of energy and how u laugh and smile and still carry on like u do. #Blessings ❤

Thank you for sharing your testimony1

My best friend has lupus God bless you Nick Cannon🙏🙏🙏🙏🙏🙏🙏🙏💜💜💜💜💜💜💜💜💜💜

That's some serious words. Thank you Nick. May God continue to bless you and your family.

Wow! What an incredible testimony!! God Bless you Nick Cannon!🙏❤️🙏