Lupus Awareness Infomercial

[modelnsinginme19]

Thanks for the video =)

[evilmonkeyzoey]

my mom might have this and knowing that its heratitary scares me but i cant help but think the docter says that its possbile if she ends up having it the next stage is it attacking her organs and i cant help but break down in tears... :'(

[AsialovesBieber19]

I might have lupus, and im not over 13, my cousin has it, he's 19, he will probably die or won't be able to move by late 20's, He was my bestfriend but we grew apart when he got older, He has had it sence he was 2, he can barley open the door or hardly do anything, I feel so sorry for him! I'm scared i might have it, i went to childerns hospital to see if i had it and they don't no, Im very scared! My cousin that has it means the world to me & i love him.. I don't want anything to happen to him

[karinachabela]

I've got Celiacs and Autoimmune Liver disease. It's not Lupus, but our diseases started the EXACT same way, molecular mimicry. Ask YOUR doctor if they even know how autoimmune diseases start, and then come talk to me because I can assure you they don't.

Keep taking your pills then. BTW, I don't make a dime off of people, again this is you being ignorant.

[miragemammaries]

@karinachabela Apparently you misread my reply. YOU ARE DONE HERE. You are a fraud who endangers peoples lives, The appropriate information concerning your activites has been forwarded to, and brought to the attention of the appropriate agency/authorities.

[karinachabela]

@miragemammaries

Oh wow. Youtube authorities. Very scary.

If you have Lupus, you are doing yourself a major disservice by not investigating that information. I did you a favor.

[miragemammaries]

@karinachabela Your info has been given to the BBB and to the A.G.'s office. Fraud is a crime. Good luck.

[karinachabela]

@miragemammaries

You're wasting their time, my time, and your time.

[miragemammaries]

Here's a word of advice to all of you who don't have Lupus, and would like to tell those of us with Lupus that we are stupid for taking the proven meds that keep our disease in check and allow us to live long productive lives-

MIND YOUR OWN GODDAMN BUSINESS!

[RawClorophile]

If U don't try anything that is a real cure, to change all your system, blood cells, by getting rid of toxins from your foods and bringing real Live Food in your diet, If you keep taking pills and especially if you believe that stupid f** that tells you "there is no cure for it " ,it means your doctor scared you and you do not trust enough to change anything. Ask the Dr how many ppl he CURED ! then go to someone that KNOWS HOW to CURE IT. If you intend to live on drugs,then U got a death wish :(

[miragemammaries]

@RawClorophile Do you have Lupus?

[karinachabela]

You have to pause that at 0:56 where it says there is no cure for Lupus.

There is a cure, it just doesn't come in a pill form.

According to the study done by Dr. Seignalet, The Paleo Diet cures 100% of patients with Lupus.

Want proof? There it is ----> youtube.com/watch?v=BVn-jmCi4z­I

[miragemammaries]

@karinachabela There is no cure for Lupus you fucking fraud asshole. I'm sick of people like you insulting those of us who have this disease with your uneducated and ignorant remarks.

[karinachabela]

@miragemammaries

I'm neither uneducated nor ignorant on this topic. Do yourself a favor, and look into the video that I provided. It's people like you that stifle progression. Instead of looking into the facts, you bury your head in the sand. It's people like you that wear your disease as a badge, as if you were in some elusive club.

People die every day from Lupus, and it sucks. If you could get better, for free, why wouldn't you want to?

[miragemammaries]

@karinachabela Bury my face in the sand-wear my disease like a badge? Like an elusive club? Do you have and fucking idea what the hell you are talking about? You know ABSOLUTELY NOTHING about me. But I know quite a few things about you, and I will make it my mission to have you REMOVED PERMANENTLY from Youtube. Your fraud costs lives. How does it feel to turn people away from REAL MEDS, and then have them die so charlatans like you can make a few bucks? You just fucked up asshole...

[crimberland]

@Firagax2 I will agree with this guy/girl here. There is nothing worse in this life than government bodies and even so called charities telling people there is no cure for this and that when they have been staring you in the face for years. The diabetic association still says you cannot cure the diabetes though i personally know five off drugs altogether and all they did was change their diet to raw food. Bob beck and dr clements from food that kill are two great men who tried to help years ago.

[crimberland]

@crimberland In his old lecture video he pointed out a huge flaw in our society. He says that out of 100% of the people he told and showed how to cure all these so called incurable diseases 15% would research and practice it for themselves while the other 85% had a death wish, they couldn't be bothered to change anything or would do a half asses job while still smoking,drinking and poisoning themselves in other ways. Im lucky to be in the 15%.

[crimberland]

@crimberland Do as firagax2 said and look up bob beck protocol, or search bob beck pdf. With any illness or cause and effect ( I dont say disease because most of what we hear is bullshit) its best to eat the best you can as much raw food as possible. Not meat or dairy or any animal fats, preservatives, additives,alcohol, give up the smoking.. cyanide has worse effects in the body than death. While at this stage is best to use bob beck protocol..after you have given up the things that harm u.

[grettagrids]

I keep getting strictures in like my esophagus,colon and cervix and was diagnosed with lupus. Plus the constant "bite" mark rashes I seem to always be getting. Can LUPUS cause strictures of organs?

[h00ddiva]

This video is GREAT! it really lifts me up on those days I am down and out due to my SLE...it is also a great way to inform the world about Lupus. Thanks for help spreading the word for me and others with Lupus

[SxEshawn]

Im in tons of pain still...I know it well, I am also getting bounced to numerous doctors

[poosaypirate]

@SxEshawn ugh good luck! try not to give up.

im in the same boat and i even have symptoms of Kidney damage and we have at least establisthed ( AT THIS POINT ONLY) That I have " polyartrittis" as a side note in the vid it says theres no test but there is the ANA i dont understand why they make this claim

[hirich1]

I have Lupus. Today i couldn't get out of bed. I feel like im burning even when i dont move. Its like living in Hell. The pain is so bad i can't if make a fist. It took 5 years and 8 doctors for my diagnosis. PLEASE HELP GET THE MESSAGE ACROSS.

[poosaypirate]

@hirich1 same here good luck

[SxEshawn]

I have just been diagnosed with lupus at one of the worst points in my life already, I already have so many problems its just too much.

[seseanjones]

well today is your lucky day: if i were you i would clean the inside of my body out, meaning a colon clensing. then i would stay away from all sweets and sugars! then i would only eat vegies and fruit! organic apples are great after 72hours in your body it turns into vinigar! vinigar cleans all the majour organs or have a shot of apple cyder vinigar every day. last order some PRO ALGA ZYME THIS IS A HIGH PH ALGA WATER THAT WILL DO THE JOB. 1-800 881-2312 WORK 4 ME..

[MalfoyFemDom]

I too am looking at being diagnosed with lupus, and I too am going through a lot of other stressful things, a new life transition, struggling financially, and all this other stuff. I even have a mental disability. Anyway, if you wanna talk, I'll talk with you. Basically, don't give up; there are other people in situations similar to yours. Together, we can make it.

Here's to life without lupus.

[91tiga]

don't let your mind psych you out. stay strong

[Curttehmurt]

It's Not Lupus

[lOveMW]

Hi, beautiful vid, can you tell me what the title of the song is, please ? x

[am6662006]

Stand Up For Love -Destiny's Child

[lOveMW]

ThQ ! x

[am6662006]

Tell your friends about this video and the "Lupus Awareness Video" thanks

[patientspride]

Lupus awareness is so important, especially with doctors! Sheila Shaw survived Lupus, which knocked out her kidney function. She teaches all about taking control of your life despite living with chronic illness.I have talked with so many Lupus patients who all said that their Lupus flared out at the most stressful point in their lives. This was Sheila's case as well. Stress control seems to be important with Lupus. If you have Lupus, seek success stories- they are out there!

[janster20]

I believe there is a cure for Lupus. Don't giveup!

[djpmode]

I have lupus and I agree awareness of the disease definitely needs to be raised. But it was a very sad video. Maybe that's the angle you wanted, to make people feel sorry for people with lupus. But I'd also like people to know that we are fighters because we need to be.

[catali3]

your video said it all, I have lupus and have been a strong advocate for making people aware....so thank you.

[dridri052]

I will be using this on some of my sites. Thank you for making this...I have lupus