It would be so nice to have you stand up and speak for those of us who struggle from chronic pain. Your 1st 10 seconds said it all. We are needing your help more than ever right now. We love your talent and am so proud of you for fighting as hard as your do for us...thank you
Really, isn’t it hard enough to just get by every freaking day? She is struggling herself AND she is bringing joy to the entire world with her talents. She is a silent inspiration to those of us with fibro and who know what she goes through. NOW you want to add on having her be a spokesperson too?!?
Yea I think I have it, first it was my left arms, then it’s my right, then it was both my legs, like it dosent hurt on the outside, it hurts like the tendents, like I be doing normal things, then I can’t move my legs or arms, cuz if I move them, it shoots up a pain, but I never got checked so idk if I have it,
@@BrianKim-cz1jxYou can find out if you have it by doing an extensive blood work. You need to see a rheumatologist for that. The extensive blood work is to rule out any other type of joints disease like rheumatism, arthiritis, gout etc.
i have cptsd and fibro and am a aspiring sing & songwriter so she gives me real hope that i can attain the career i want as a performing artist , blessings to her beautiful soul 🙏🏻
Lady Gaga is so on point. Living with chronic pain,can be so shameful and embarrassing. At some point I almost began to feel like I wasn’t even human anymore. 😔. But I’m ok now 💪🏽
That’s why i love her so much! I am also suffering from chronić pain and i am afraid everyday but this person is giving me a lot of hope. True artist ❤
I've only recently heard of Gaga's film and can't wait to see it! I'm sitting here reading the comments and am dumbfounded at the negativity. How do you judge what you don't understand? Personally I get a kick out of people telling me," But, you don't look sick! Why can't you go do this or that today? You look fine." Just so I can say back, "Well, You don't look like an asshole but there you are!" There are good days, there are bad days. And then Really bad days and great days that may take 3 days to recoup from. Everyone is different. I was diagnosed with Hoshimotos Thyroiditis and Fibromyalgia 41yrs ago when they still called it Myofibrocitis. I was 19 then and they've only added on more Autoimmune diagnosis since. Whatever helps one, may not help another. They used to prescribe low dose Antidepressants but they sure didn't work for me or many, many others!! Now the new trend is Epilepsy meds. I had brain surgery for Trigeminal Neuralgia 2 and a half yrs ago and those meds do help in my case bc I also do have seizures and most likely from P.O.T.S. I went to stand up today and almost went, Timberrrrr. Saddest of all I had to leave the teaching job of my Dreams in 96 when I became so ill and the seizures started. Felt like I Died the day I walked out of that school! And yes, it's true, Gaga can afford massage and treatments most of us can't. But Please Don't give up! There are Many things to try. Even good ole Vicks Vapo Rub comes in a cream now that's like a lovely lotion and Not greasy!!! Dried Lavender flowers, Chamomile flowers and Nettle make great bath tea bags. You can also make a tea to drink. Always check with your GP re: allergies first though. I know she pushes herself and I know how hard. One of my old students was her Fitness Trainer. He was taught then he taught, Don't Give Up! So to Gaga I hand you one of my spoons, and one for you reading this, one for you suffering in sorrow today, one for you having a day of joy, one for you in tears thinking you're alone, you're not! One for you sitting in judgment and i 🙏 you or nobody you love Ever is diagnosed with Autoimmune or Invisible illness. Hold onto your spoons, just in case you need the smile and I 🙏 you all ✌&❤ 🕊
Don't be discouraged by youtube comments... Most of the time... On most topics, you'll find a large amount of negativity. Those are either chatbots or some sorry arse old dude sitting in the basement of his mom's house, feeling sorry for himself. 😅 But for people suffering from this pain.. Keep going and keep positive and treat yourself kindly❤
❤! In my humble opinion: People who don't live with chronic pain in any sort will never understand how it is and will never do, not even a doctor, they might have know it and know the studies and patients but they do not know how it feels and what other struggles it brings in life, only when you have it yourself you will fully undestand. Of course a lot of people will care for you and do their best to help you and try to understand. But it is so energy consuming to try to explain how you feel, to people who make you think they understand but actually they don't or even won't. I am happy that a lot of people with these conditions talk about it. That is when I really feel understood. And I share the feeling that I feel guilty, ashamed, whining etc... while I actually am f*cking brave and get through each day as a f*cking warrior. Life is 10 times harder for me because of those conditions, but it goes on. No more shame, no more taboos... I am proud that I can deal with the daily struggle, All of you reading this should be proud too❤❤❤
She needs to advocate for chronic pain patients and getting treatment and tell the truth of what is causing the real epidemic of illicit drugs not prescription drugs
Mental health, pstd, panic attracts, anxiety, OCD, IBS, fibromyalgia, got to the point living this life in constant pain, so many times I've wanted to but and end to it all...I sing manyly just post on RU-vid don't make no money from it I just work part time as kitchen Assistant..I have 4 children and lost my 5th due to Edwards syndrome, (EastEnders is now covering in story about Edwards syndrome 💔) Some days are so bad I can't even hold my mic to sing, now trying to claim pip but made out that I have to prove how much pain I'm in 🤷🏼♀️ and provide evidence.. doctor had also put in evidence to support me but still isn't enough: this life is one big fight!
Do you live in the US? In 2006 I couldn’t work & used the company called ALLSUP to help me get Social Security disability benefits. When I was getting it back in 2006, you could not have any job and try to get disability. You had to be totally off work. I’m not saying that’s how it is now, because I don’t know. That’s how it was then.
I have had FM for 43 years. I can attest that it will be the worst thing that is so debilitating in every aspect of our lives. I wish I could talk to LG to teach her everything I've learned so I can pass it on to help her get my knowledge out there. Ive been researching, studying and investigating Fibromyalgia, CFS, & ME since 1982. I need to tell people what I know and through LG my help might begin to make a hugh difference.
The trouble is you look alright but it's killing you inside you have to try and carry on in pain because you have no choice. You you clean the house you go to work you do this you do that. Then you pay for it the next day when you can't get out of bed because your so tried and in pain if you don't have fybromyalgia you will never understand how it feels
Omg. So true…..once they don’t know what to do with us, they just wipe their hands of us. I am so grateful, though, that I have had a few doctors, out where I live, who actually cared. They over-shadow the ones who don’t..
im suspected to have this illness. can someone tell me how you got the illness or what you think triggered this illness and what makes the pain worse? im so scared.
You gradually have more pain points in your muscles, typically bilateral (shoulders, lumbar area, buttocks...), lots of stiffness, even in the morning like you slept on a Stone mattress... Some suggest It is linked to huge anxiety, having been bullied (gay people at school, shy people, etc.), being hypervigilant, stressful Jobs you hate with toxic bosses, ... It's really not known why It happens.
No. It’s chronic IBS. That’s the reason she doesn’t wear pants or underwear. Besides it’s acceptable today with rock stars to not wear appropriate clothes. 👍🏻
Pior. Repórter. Interview, not. Know. What. S. Question...ir,, contrato. If. It ../ lace?// Stupid,Quest../// world. Is. A. Beast,,,,/// see. Script s. About,,,Tell. Aboutworld///🥰🐝🐝
Well we hide it in public because we don’t want to burst into tears sobbing because of the intense pain. We would be judged even more so of course we have to hide it but I assure you we do have those moments at home where were are done and we just let it all out.
I agree with the others in that you've made an error in judgement. When you hear her words those are the words that describe how I feel. Who else knows of the shame we experience. I am so impressed with anyone who is able to do anything with chronic pain. Getting out of bed sometimes is a triumph for many. of us.
