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From: BrownEarth12
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  • I am starting a channel to bring people with&without illness together so they can help eachother and share experiences, also i want to show that you can be positive even if you are disabled, life is tough when you are ill. Youtube helps me connect to the world as i cant go out and do much for myself but theres so much negativety and arguing. I would like to make people laugh and raise awareness about the hardships of disability&bring people together, i can speak personally about fibromyalgia.

  • my mom's ill, shes having work 4 different jobs on minimum wage and cant afford all my older brothersand sisters lifestyles. half of them are old enough to get a job dont bother and regulary take her money or card wasting it on games then complaining about lack of good food. this is what has to deal with as well, no wonder she broke down.

    stuped GP's...

  • Bad disease. Good song.

  • I have most of the symptoms shown in the video, Im pretty sure I do have FM. Luckily for me my GP is an ass and pretty much tells me to suck it up and quit being a crybaby.

  • @TearsInYourEyes i been told the same thing too.. i just feel like rippin their heads off but that would be too much effort n apin for people like us.. i just walk away n shake my head n diagnose myself n tryna cure myself....

  • fybromyalgia isn't real, your all full of shit and need something else to complain about.

  • @popcornbebop Thankyou so much for your comment. I'm sure that everyone who, in your eyes, pretends to suffer from this will be greatly helped after reading your words of wisdom. Let us all hope that you may live a healthy life where you do not have to put up with such "phantom" illnesses - may i, on behalf of all other commentators leaving comments on this subject, please accept our humble apologies for wasting your, i'm sure, precious time reading about this drivel. 

  • @MrSteevieboy apology accepted

  • @popcornbebop i hope someday you get it... you have no idea! it's real n it exists.. the least you coulda done was just not leave a fuckin comment! i know cos i have it with every exhale n inhale i do my chest hurts n tightens so cut us some slack n get a bloody heart!!

  • @hotmessmissy you need help, you are clearly a Hypochondriac.

  • @popcornbebop I am diagnosed with fibromyalgia....am i a hypocondriac aswell?

  • @popcornbebop hypochondriac*

  • @LifesMyWife yes, and have you noticed how fibromyalgia is the only "disease" where commercials for its medication have to insist that it is a real disease?

  • @popcornbebop Well maybe if you used that little brain of yours you would realise that the reason that is done is because there is no blood test that can be done to spot it and people can be seen as lazy, who wants to do alot when ur hurting? Fibromyalgia could be a bunch of illnesses just thrown into one.People wouldnt take painkillers&try any medication for relief of pain for nothing. You are just a troll and your life must be shit to try and piss off people who are suffering :P

  • @popcornbebop (2) and i have not once seen an advert for fibromyalgia, i live in the uk and i went to the doctors for years&had stupid amounts of tests done and found nothing, i never stopped working, i still work a small number of hours till this day.All the doctors did was bump up my medication evrytime i went back.I went and saw a specialist and i explained it to her and she said "fibromyalgia" and it was a blessing to have a name for it&to get taken seriously. It isnt nice.

  • @LifesMyWife this "specialist" didn't happen to be regularly called a quack would they? Having your medication bumped up would have been nice I bet, was that why you kept going back?

  • @popcornbebop troll...looking for an arguement. Like i said i had loads of tests so the pain killers were welcome. Constant painis a misery. She(the spcialist) is a full fledged doctor specialising in the nervous system and pain. you must of had a hard life too if you get your kicks out of tormenting sick people or did your parents create a child of apathy?

  • @LifesMyWife little of column a, little of column b

  • I have fibro, and although I found most of this video very informational, I found the end irritating. Is this something we are doing to ourselves? Come on...I know what caused my fibro...years of physical and emotional abuse, and a car accident that totaled my car and gave me whiplash. I went through almost 4 years of listening to my primary care physician telling me it was all in my head, and there was nothing was wrong. I don't need to have someone tell me it was my fault. How stupid!

  • I can' see the vídeo with cell :(

  • I too suffer from fibromyalgia and have for so many years. Sometimes the pain is too much to bear and I can’t imagine going on another day feeling this way. But then I found a comforting scripture in the Bible. Revelation 21:4 says “And he will wipe out every tear from their eyes and death will be no more, neither will mourning nor outcry nor pain be anymore. The former things have passed away.” This is a promise from Jehovah God.

  • So frustrated having this constant pain, but your friends or family not believing you hurts more.

  • Fibromyalgia: when a hug hurts..

    I was diagnosed last year, after 9 yers being told "it's all in your head". Someday the question was "Is the pain real, or am I just cray?".

    I'm 18 tomorrow. Meds don't work on pain, I only feel adverse effects and sleeping pills never work.

    Yesterday my boyfriend tried to hug me to calm me down, and I found myself crying while telling him "please, don't touch me", that's something real hard to say when you really need a hug...

  • i have horrible pain when i watch this :(

  • It took several years before I was "officially" diagnosed. Meds take some of the edge off, but it's only temporary. I tried holistic approaches, but none worked (I HATE having to take pills!). On top of it all, I periodically have to get epidurals and other types of injections in my spine. People don't think anything's wrong because there's nothing visible... they don't understand why you can't just "get over" the depression or tiredness.

  • I'm always depressed because the pain, dimotivation and exhaustion won't let me act like a normal teenage. I see teenagers running, jumping, going here and there all day long while for me, just making the bus trip from home to class already proved crippling. My friends don't understand. They call me a grumpy old lady. They don't get that when I say my arms hurt, when I have to sit down because the pain in my legs almost makes me fall down, when my bones ache, that the pain it real.

  • ATTN MASSEFFECT2795: i was diagnosed when i was 14 and i'm only 17 now im a junior in high school and i feel like there are no teens who have it!

  • @Starbound810 i have it and i'm only 18. no teenagers where i'm from actually have it

    

  • got diagnosed with it last year at 15 it help to have some meds to help sleep

  • If this wasn't real I don't think doctors would dedicate their entire careers to it. I have it and at first I thought it was a cop out as well. but the more I learn about my body the more I'm realising that it isn't. People don't know what its like to have to stand up on the train for someone a bit older than you, and to stand there in so much pain you feel like your going to vomit. Silent diseases suck

  • When there is a commercial that says it hurts to be hugged, people need to believe that. You want hugs, but it literally hurts. I believe I have had it all my life also and I am 56 yrs old. None of the medications for Fibro help me. I live on pain medications but they only take the pain away for a certain amount of time. My main complaint to my doctor is also feeling like I have the flu all the time. He looks at me with a puzzled look. He does try to understand though.

  • hi im 25 and have bean suffering for with this most my life but with in this last year it has goten so bad i sleep all the time when i can and its so hard to do any think just thinking abought like taking the trash out it gets so hard to even do that and even thinking abought geting dressed its so stress ful i do is mutch as i can and now one under stands what im going threw my family just thinks its in my head and i thry to tell them how it afects me and i need suport from them its hard.

  • I'm a 16 years old that suffers of Fibromyalgia! Most of the people would say what would you know about pain? Well trust me I do! And I have one thing to say to the people that suffer of it! Live your life like you dont feel anything. If you feel tired take a break, Tell the people around you so they can educate and know how to treat you. And Always pray that a cure is discover! You're not alone! :')

  • Hi! My name is Katheryn. Im 16 y/o. When I was 11 y/o I was diagnosted w Fibromyalgia. Sometimes when I wake up... well I cant get up of the bed cause I feel extremely tired! Sometimes when my friends hug me.. it hurts! :( I feel I have fatigue a lot of times, maybe 5 times a day! My mom suffers of it too! A lot of days my mom cant get up cause the pain is WAY TOO MUCH! I know what is it to live w this! And I know its extremely painful, but my key is to NEVER LET IT TEAR ME DOWN!

  • Sewing & crafting with fibromyalgia...no one understands the pain...but you keep on going.

  • @relindesigns haha yeah I know what you mean!! and I've chosen my career in fashion!!

  • Imagine being able to go any where you want because you dont have to work

    Imagine having a made up reason to be on welfare

    Imagine not work ever again

    Imagine thats the key work "IMAGINE"

    you people are just sick in the head.

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  • Started using fiorecet for chronic right chest/armpit pain that rdiates through out the right arm muscle tissues. My joints & hand seems ok. It's purely muscular pain to the touch. Disabling pain at the least. Makes me sweet heavily & want to black out. It comes in gradual episodes peaks in 5-10 mins. lasts 20-30 mins & gradually fades away & reoccurs sporaticaly through the night & daytime. So far so good. the intensity of pain has dropped, but i still suffer with it. I Hope this helps.

  • Doctors say that it's not real either they are just not educated or they know that they don't feel like looking into it and trying to fix it cause it's too hard, it's bullshit,

    My dad has fibromyalgia and it hurts him everyday, every minute of every hour and I cannot begin to imagine how that feels.

  • they showed pills and pills in medicine.... Why don't they show Hemp? (Marijuana)

  • I started having that stabbing pain in either side of my chest as a freshman in high school around winter time. I had to stop what I was doing to control my breathing. I started to get pain in my knees when I bended my legs. I go to sleep at 8am every day, no matter what time I woke up. I usually eat once. After taking on an extra job, I got pains in my shoulders and neck. I have irritable bowel syndrome, insanely powerful cramps that make me want to shoot myself. Could the answer be so simple?

  • Thank you for posting this beautiful yet enlighting message. Many of us suffer alone with no hope of ever feeling better. I've had fibro all my life and can remember the stabing pains in my ears as early as three years old. Many of us loose jobs, love of day to day living...it's a very sad way to live misunderstood by everyone you meet, having to feel like no one cares or believes you. I wish I had known sooner...I had TMJ surgery back in 1989 and have never been the same.

  • Thank you so much for making this and sharing it!! It's awesome!! As a fellow sufferer and survivor it really hit home. Hope you don't mine that I honored you by posting it to my blog.Thanks again!!! Gentle hugs!!

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  • It's germs. Find a doctor who practises functional medicine. The rest of the medical profession has no idea. One of the worst germs: Chlamydophila pneumoniae. It has been described as “the cause of the profoundest pain, morbidity and chronic suffering experienced by humanity”. Go to Cpnhelp, and decide for yourself.

  • Thanks for this. My life is ruined by this problem. Chronic burning pain in muscles that never goes away, wakes me up, tired all the time, constant back ache, headaches, memory loss, depression. I don't know how much longer I will be able to go on, doctors are little help. Everything to do with movement is a problem. people tell you you look great. You're a malingerer etc, etc, Walk a fucking mile in my shoes!!!!!!!!!!!!!!!!!!!!!!!!!­!!!

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  • This is amazing. Thank you , thank you...so many shed tears, so many hours of silent suffering, so much covering up, fighting alone, struggle......God kept me going through it all........again, THANKS

  • Thank you is all I am able to express.........

  • WHY Does it say at the end...could we be doing this to ourselves???? don't get it.

    If I had any choice I would chose not to have it any time.It isn't fun and it isn't in my head either.I suffer in silence and have done so for years.Due to my bodybuilding background I am used to push past the pain barrier and kinda cope....and being alone I have to........otherwise what will become of me?

  • Im tired of people telling but you look good, are sure you are sick. I have lost over 50lbs and I think the worse is not been able to sleep. Im sick and tired of been sick and tired.

  • This is by far the best video I have ever seen for fibro awareness including the end suggesting the causes. I do believe this is something we're doing to ourselves. Not intentionally on our ends but all those with fibro should research toxic fluoride poisoning. The symptoms match ours. Just my two cents... Thank you for this vid and sending out my prayers for all of us who suffer. (Just of course, don't bother the with ad--there is no cure for fibro)

  • @aerayna I have hopes I believe GOD have something special for us. Everything happen for a reason. Praying helps. I know that this is a terrible thing to live with but we got hopes.

  • Thank god my balls make me immune to this disease. How you ladies tried testosterone pills or something? I mean there could be something to that. Maybe the constant surge of testosterone that is produced by balls regenerates the nerves or makes them impervious to whatever causes fibromyalgia. I mean when chicks roid up like flojo or Marion jones they see really huge improvements in speed and strength so maybe you should roid up too.

  • @Atralis Men get Fibro too.

  • @Atralis You are aware that many men also have been diagnosed with the illness, are you not?

  • for the last couple hours I have been all over the internet looking at the relation between Cipro and Fibromyalgia.  I am so convinced that I have taken notes and printed many articles to give to my doctor to consider. I am pretty sure that I was "floxed". LOVED your video!!

  • fibromyalgia goes misdiagnosed all the time. simply apply Dr. John Sarno's Tension Myoneural Syndrome and your muscles will start to relax. Other names for the syndrome are Mindbody Syndrome (Dr. Schubiner) from Michigan, and Autonomic Overload Syndrome (Dr. Scott Brady) from Florida.

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  • @aerayna i suggest reading healing back pain (dr sarno) and also maybe the divided mind (dr sarno), plenty of information on the fibro patients that eliminated there excruciating muscle pain. Also, read "molecules of emotions". scientifically proven that our emotions are molecules and when we repress our emotions to much and to often they get stuck in our nerve and muscle tissues, which causes oxygen deprivation which rheumatologists (sp) have considered the culprit for fibro, but most likely

  • @aerayna about it. i would highly recommend learning about what your mainstream doctors are reluctant to tell you. there is plenty of hope for you

  • @krauty86 I never said I have no hope. I said some days the pain is better, some it's worse, but it's always there. I don't see mainstream doctors for this so please don't assume. There is certainly hope in God and prayer. My point was that many don't understand what we go through. And, after a while, it gets very frustrating to not be listened to, that it starts to show. My apologies for allowing my anger to show, and also that I refuse to continue this, but it is what it is.

  • Fred Wolfe, the director of the National Databank for Rheumatic Diseases and the lead author of the 1990 paper that first defined the diagnostic guidelines for fibromyalgia, says he has become cynical and discouraged about the diagnosis. He now considers the condition a physical response to stress, depression, and economic and social anxiety.

  • I was diagnosed with Fibromyalgia last year after months of unexplainable pain. No medicine has worked for the pain. I AM finding help through Alternative Medicine. 50% of Americans suffer from chronic pain. This is not normal and doesn't happen in other countries. If you would like to see my journey to wellness and view videos of different alternative treatments please visit my blog:

    joyswellnesstrip.blogspot.com. I FOUND NO PAIN RELIEF UNTIL I TURNED AWAY FROM WESTERN MEDICINE.

  • Imagine having the Flu all of the time.

    Imagine not being able to sleep.

    Imagine Not wanting to step out of bed in the morning, because without a doubt as soon as your foot hits the floor a pain will shoot through your body and the feeling won't stop all day.

    Imagine feeling like you are comming apart at the seems and your Doctor tells you "It's all in your head"

    Just Imagine!

    Fibromyalgia is real!

    I know because I have had it all of my life!

  • @SojournFive Fibromyalgia is just a silly name used by doctors who are too fucking stupid to diagnose your condition. I have lived in pain for many many years and these stupid cunt doctors told me it was Fibromyalgia. Well to all the people on here I'm going to do you a fucking big favour. More than any cunt doctor has ever done for me. Do your research like I did. I have found the cause of my issue is eggplant foods. Cut out tomatoes, potatoes and anything containing Solanine. Google it.

  • @SojournFive Doesn't typing/browsing make it worse?

  • I like this video... I have recently been diagnosed with Fibromyalgia.This video helps people to see and understand what we go through on a daily basis.

  • TYSVM for making this video. I use it a lot to try and explain Fibro to those who don't know what it is. xo

  • Got fibro? Do yourself a favor and check your medical records to see if you'd taken Cipro, Levaquin, Avelox or any other quinolone antibiotics in the weeks or months prior to your symptoms arising. Doctors give out these terribly poisonous drugs like they're candy, and they are known to cause DELAYED REACTIONS that mimic fibro symptoms nearly perfectly. Because of this delay in reaction time, many people never make the connection between the drugs and their new mysterious health problems.

  • Really? Do you have a reference for this?

  • @joyarigel Yes, I'm a living reference. I was horrifically poisoned by Cipro and have been in chronic, debilitating pain ever since. Doctors have tried telling me I have fibro, which I do NOT. I was chemically poisoned. So are countless others thanks to these drugs that docs pass out like Halloween candy. I made the connection, but many others do not thanks to the delay in reaction time. Google 'quinolone poisoning' or 'quinolone toxicity'...almost all the symptoms are the same as fibro. 

  • Last, is there a lawsuit going for this? If not, there should be!!! Pharm. companies should be held responsible.

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  • @joyarigel There's a class action against J&J I believe for people who took Levaquin, but none that I know of for Cipro. You would not believe the horror stories these drugs create. All I know is that if I hadn't made the connection, I'd be going around thinking I have fibro today because that's what one idiot doctor tried diagnosing me with. I'm sure there are countless others out there who have been told they have fibro when in fact they've been poisoned by their docs with these antibiotics.

  • @papatoony thanks for the info. If you find anything that works for you, would love to hear about it. And if you would like a recommendation for what might work...panchakarma cleanse. Good luck

  • @papatoony I suffer horrbly with fibro, but reading your response to this youtube video mentions a problem with Cipro. All my docs & specialists have not been able to find my trigger for my fibro, but I was prescribed Cipro many years ago when I had pneunomia & pleurisy that would not respond to other antibiotic. I am sure you know how it feels when you can look at something else that MAY give you some kind of explanation for this living hell. I wish you peace & wellness.

  • @3cfoss3 I don't know exactly what your comment means, but I know for 100% certain that Cipro caused my severe and crippling health problems. There is no question. There is no test to "prove" quinolone damage, but the effects are very, very real. I'm not saying everyone with fibromyalgia is floxed (aka poisoned by these drugs) but I know for a fact many people out there have been diagnosed with having fibro when in fact their issues were brought on by quinolone antibiotics.

  • Were you being treated for stomach related issues? There's a growing body of evidence that shows the connection between an unhealthy gut and FM. I have been battling SIBO for 3 years now. I believe my FM was a result of this. My SIBO is mos def from being treated with too many antibiotics. I am off all pharmaceuticals and have started a blog detailing FM and my Ayurvedic treatments and my outrage w/ western med. joyswellnesstrip.blogspot.com Would love for you to share your experience,

  • @joyarigel i've been doing alot of research and it seems antibiotics are the only way to beat sibo (even if only temporarily).. have u found another way to beat sibo?

  • Really? Do you have a reference for this?

  • You ignorant piece of shit, what do u know anyways...

  • I have been recently been diagnosed with Fibromyalgia after living for almost 3 years with SIBO. I have found many people with FM also have stomach issues. Drs don’t know what causes FM b/c they are trained to look at/treat the part of the body they specialize in. If one system in the body messes up, (digestion/systems in the gut) other systems in the body follow. To find a cure doctors need to see the patterns! Please visit "joys wellness trip. blogspot. com" to read and share experiences.

  • I have been recently been diagnosed with Fibromyalgia after living for almost 3 years with SIBO. I have found many people with FM also have stomach issues. Drs don’t know what causes FM b/c they are trained to look at/treat the part of the body they specialize in. If one system in the body messes up, (digestion/systems in the gut) other systems in the body follow. To find a cure doctors need to see the patterns! Please visit joyswellnesstrip.blogspot.com to read and share experiences.

  • I have been recently been diagnosed with Fibromyalgia after living for almost 3 years with SIBO. I have found many people with FM also have stomach issues. Drs don’t know what causes FM b/c they are trained to look at/treat the part of the body they specialize in. If one system in the body messes up, (digestion/systems in the gut) other systems in the body follow. To find a cure doctors need to see the patterns!

  • Thanks for posting this and it's all SO true! I deal with fibromyalgia pain everyday and no one really knows the extent of it unless they have it.

  • ALL THIS IS SOOOOOOOOOO TRUE... AND PEOPLE THINK YOUR NUTS WHEN YOU TELL ThEM YOUR SICK..

  • Hi Brisbanette! Thank-you! My sentiments exactly! You would not believe how many e-mails on here I have received. Some of these people are trying to sell me on their bs..ha ha. Thney picke dthe wrong person. I know people that have gone into remission, but then of course, The fibro monster came back. There is no cure; just hopw we learn to live with it and how to find our own ways for relief, etc. There is karma for thos escammers ou there!! Gentle hugs...

  • Have you taken Fluoroquinolone Antibiotic Toxicity (Cipro, Levaquin, Avelox, Floxin) and it caused your fibro?

    facebook page...

    Fluoroquinolone Antibiotic Toxicity (Cipro, Levaquin, Avelox, Floxin)

  • Always look into balancing out nutrients and vitamins in all-natural foods. Remove processed everything! Pain Killers and pharmaceutical drugs are like pulling the Fuse out of your Car when your Check Engine Light turns-on. It may make the light go away, but it does not solve the problem. I have helped a growing number of people to solve problems from Joint Pain, Poor Sleep, to losing and keeping off weight...as well as getting off of heart medication in less than sixty days time!

  • Tks for Posting this Video, I have this condition & struggle each day.

  • The picture at around 0:42 seconds, where can I find it on the web?

  • @Multifarious222

    it's called the nightmare by henry fuseli i think..but not certain

  • We all live in our own worlds within ourselves..... Some live with serious problems and conditions, some don't. Those who don't usually are presumptuous. I hate this world, can't wait until it's finished.

    This video is good but wth (what the hell) it's too fast, I can't read that fast.

  • Theres something that helps me with my pain is cold water, i fill the bathtub up, pour some ice in (not a lot) and lay for 3-5 min, then warm up with towels and it takes some pain away, i just discovered that, my doc said that it can actually help relieve CPS and fibro :D, but sadly theres no cure...........

  • @xSimplyAmusedx When no one knows the cause, of course there is no cure. It is sad. For all those who suffer, and not only with fibromyalgia. I believe us sufferers would be the best scientists, having going through so much, knowing the experiences of true affliction, as well as what ramifications there are.

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  • @xSimplyAmusedx Well Fibromyalgia is just a term given, as you study, learn, understand and grow you can easily work that illness into your profession, not as a reumatolgist but my point is, you are not limited. You and anyone can learn as much as they want and as much variety as they want and later begin your own career with widespread purposes and practices. Lone businessman/entrepreneur is my dream. As long as I reside here in the world, I wish I could fix my health and begin my own practices

  • @xSimplyAmusedx I wish they would find something that really took away the pain. You can't even explain the pain, it is all of what is in the video and so much more. But no one understands, and they just say "well, deal with it." And I feel like screaming at them. Does anyone understand, even the people I see everyday?? And with 2 car accidents that destroyed my spine, upper and lower, I feel ancient physically and mentally like I am very young, but the pain stops me from feeling totally human.

  • @xSimplyAmusedx If you mean that, you may want to look into into following in the footsteps of Dr Jacob Teitlebaum

  • @Multifarious222

    youtube dot com/watch?v=AhYs1AIodBk

  • @MrSuperfood1 I don't know what that link is for, looks like for another video if it's youtube.com, but anyway I found the picture already, it's a painting called "The Nightmare" painted by John Henry Fuseli.

  • @xSimplyAmusedx .......bloody hell!-if i go near anything cold-my fibro is absolute agony......i would just seize and lock up if i did that.....and to get moving again-i'd be screaming.....

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  • Thank you for this video. Very well done. I sent it to someone who complains that I can't visit, and to others - they said "this is great" - send it to somebody who doesn't understand. I just had to laugh - in fact - laughter is the only thing that helps me. Gentle hugs for all who live with this and left posts.

  • This is NOT a disease! It's a God damned illness! A disease is what you die of! illnesses are not! I have had Fibromyalgia for 15 years now when I was 24 right after I had my 4th seizure. Everyone hates being in pain, I hate being in pain, having migraines, arthritis, chronic fatigue & all that garbage but I have a son to raise & I can't complain about it to him, I just hope he never get this illness, my two brothers have it, my whole family has, my mom has had it since I was 3 but was called RA

  • @marciear1971 you and you're family probably have some sort of virus that was passed on by your mother and it hurts me to say this but probably your son will got it too.

  • This is so true it makes me wanna come out of my skin with frustraition i fuckin hate this disease i'm so damn i tried of it taking away my life taking away the ease of everyday tasks I just want to break down and cry but there's no sense in shedding tears knowing its just another day pain i must i get through so i just get mad rather then cry i'm glad people are starting to reconize this disease because when i got diagnosed i was 14 and they knew nothing! at least now they know somthing

  • @lillmissbaaadasss I understand how you feel. I hate what it does to my family and friends. Everything has changed. It is so hard to work. I pray there will be a cure or something more the Doctors can do to help us.

  • @lillmissbaaadasss you were 14? thats when i was diagnosed with chronic pain syntrome, not fibro but its as destroying as fibro

  • @xSimplyAmusedx

    Yes I agree very similar and just as destroying as you said....Im sorry you were also diagnosed at a young age....Its a exstremly hard thing to go through and hard for other's to understand such pain it ages you in alot aways taking away before you get to begin...But it also makes some very strong people indeed....

  • I don't think there will ever be a cure for this because this just means you're addicted to pain killers... It sounds like the symptoms would get you on all of them.

  • This is so true. No one know what we go thru ~~ unless they have this terrible disease !!  GOD Bless all of us...

  • Who's video is this? I am confused. I have seen this video MANY times before. Now I get a message from Valerie Lumley with this video. I am sorry Valerie BUT I am not new and naive to Fibro. If there was a cure I am sure millions of us would have know baout it. HOW can ther ebe a cure when teh medical profession and researchers do not even know what casuses it? I believe you are spammed for a damn good reason. There is NO CURE for fibro. DO NOT prey on the suffering anymore!

  • @energyila Look up "The Gerson Therapy" or go to Gerson dot org.

  • @energyila I completely agree. FMS is NOT curable. It's not fixable. It "can" be helped...but that is only going to happen when the sufferer finds a way his/herself, not from anyone on the internet selling crap and making money off people's vulnerability. Like energyila said, the cause is unknown. Therefore, the cure is unknown. It's as simple as that. The only thing CLOSE to a cure is "learning to live with it". I hope nobody falls for any scams because they are desperate.

  • @energyila why would you be mad at the video maker?

  • This made me cry thank you for sharing,much love

  • @ValerieLumley im not buying anything youre selling. stop spamming

  • i urge everyone who watchs this and other other fibro videos to report this user for spamming youtube! she is a complete liar!!!

  • @Bluequotations you are right how dare this person give people false hope for monetory gain I would gladly give anyone a cure for this mad condition for free if only I had the result. Till then keep going and don't looser hope!!!!

    My name is Colin.

  • Thanks and Shalom

  • Everyone with fibro/ME/CFS please (like me) keep informed about XMRV.

    XMRV is a retrovirus (another retrovirus is HIV) that is found in most patients last year, while hardly in healthy people. This is highly suspected to be the MEDICAL CAUSE of fibro/me/cfs, so everyone with these conditions, look up sites about XMRV (or youtube), because there's FINALLY HOPE FOR US.

    Please thumb up this comment so it will appear at top &other patients can see there is finally some reason for HOPE for us !

  • @PowerRedBull I am a recovered fibromyalgic who left the medical profession to discover the cause and a cure for this horrific disease, and am living proof that this condition can be cured! After 15 years of failed treatments, I found my own way back to health and through exhaustive research and alternative methods of care. Please do not give up from failed hope. View my video "Curing Chronic Fibromyalgia - Choosing What Works", follow it to my website, and keep going!!!

  • whats the name of the song??

  • This is an amazing video. It captures FMS completely in every way. Never give up! Do not settle for less than a cure!!!

    Valerie Lumley, Recovered Fibromyalgic and

    Author of Curing Chronic Fibromyalgia - Choosing What Works

  • i am 27 male and have this condition. It affected my career, relationships, family, and all aspects of my life. I am in so much pain while typing this. I am in pain on a daily basis yet I cant get use to it. My pain threshold doesnt seem to change. The insensity of pain is same if not higher each day. I no longer try to explain people what I am going through. They wont understand. I dont know what to do. I used to have positive look at life but this pain is so intense and real..

  • @vefabuyuk I am a recovered fibromyalgic who left the medical profession to discover the cause and a cure for this horrific disease, and am living proof that this condition can be cured! After 15 years of failed treatments, I found my own way back to health and through exhaustive research and alternative methods of care. Please do not give up from failed hope. View my video "Curing Chronic Fibromyalgia - Choosing What Works" and keep going!!!

  • depressing......

  • if you have migraines this is what you take...can get at gnc 100mg vitamin b2 500mg magnesium and a herb called feverfew take 1 pill each daily. it cut my migraines down by 90% cost less than 30 dollars for a 90 day supply. i would much rather prevent a migraine than treat one good luck

  • I believe that fuits and vegetables can reduce inflammation in joints!

    I started taking Mona Vie Active for my shoulder pain and now I don't have to take Vicodin before I go to bed!

    My wife has fibromyalgia, she feels a lot better when she drinks it as well!

    If you seriously want the Monavie Active, go to juiceberg's channel! They will hook you up!

  • I've been having fibro symptoms lately, and while the pain currently isn't bad, it's growing more nagging by the day.

    Thank you so much for making this video. Now I know it's not in my head.

  • Thought i got well from fibromyalgia, for Cryptomonadales work wonders for me... till lately, the pain is back. I have to care for my 1 year old son... It's a terrible struggle! Why me??? Really like this video, express everything that it is suffering in me!

  • Thought i got well from fibromyalgia, for Cryptomonadales work wonders for me... till lately, the pain is back. I have to care for my 1 year old son... It's a terrible struggle! Why me???

  • Wow. I don't have fibromyalgia but i know someone with it. it must be terrible.

    is it like RPD?

  • Please read about biological effects of x-rays ... primary ones are inflamm'n and fibrosis of every tissue and organ in the body. X-rays (and antibiotics) destroy enzymes and good bacteria in your stomach, causing digestion problems. They damage your skin (burn), thyroid, lungs, kidneys, eye lenses, nerves, blood chemistry, marrow, DNA, etc. even your hearing. Try to eliminate meds and refined foods; eat raw fruit/veg (enzymes), EFA's, plain yogurt. MRI and u/s can be used instead of x-rays.

  • @julanenova I am a recovered fibromyalgic who left the medical profession to discover the cause and a cure for this horrific disease, and am living proof that this condition can be cured! After 15 years of failed treatments, I found my own way back to health and through exhaustive research and alternative methods of care. Please do not give up from failed hope. View my video "Curing Chronic Fibromyalgia - Choosing What Works" and keep going!!!

  • Very good video/song. I was diagnosed w FM and a host of other auto-immune disorders following MVA (motor vehicle accident) ... very puzzling because most of the symptoms were not related to my injuries. After five years I discovered that they were consequences of x-radiation (had four sessions of x-rays after the MVA).

  • This is an amazing video which captures the impact of fibromyalgia beautifully. It is the one I recommend to people around me who want to try and understand what it is like for someone living with Fibromyalgia. Thank you

  • You should of used Massive Attack's "Teardrop" as the BGM for this :)

    Very informative, thank you!

  • I got this 2 weeks before my 60th birthday in November..'07..I could barely get out of bed in the morning and dress myself. What I once called a lovely fresh b