Jan Hansen
Jan Hansen
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Stuart Murdoch about ME/CFS and #MillionsMissing on CNN
"Stuart Murdoch was an active, vibrant young man enjoying college life in Glasgow, Scotland, in the late 1980s. He was studying science and had completed the Glasgow Marathon in less than three hours.
But over the course of a summer, Murdoch felt his energy start to fade.
"It was like a battery dying in a car," he said.
Murdoch was eventually diagnosed with myalgic encephalomyelitis, more commonly known in the United States as chronic fatigue syndrome. (Researchers refer to the disease as ME/CFS.) Although he had a diagnosis, his doctor didn't have a treatment plan and told him, "You just have to rest."
edition.cnn.com/2018/10/05/health/chronic-fatigue-stuart-murdoch-belle-sebastian-turning-points/index.html
มุมมอง: 1 305

วีดีโอ

Jen Brea and Charles Shepherd interviewed about Unrest - CFS/ME
มุมมอง 81K6 ปีที่แล้ว
Jennifer Brea, film producer and dr. Charles Shepherd are interviewed on BBC about the movie "Unrest". The documentary follows Brea, a sufferer of the chronic disease ME. ... “Unrest,” by Jennifer Brea, demonstrates just how debilitating chronic fatigue syndrome, also known as myalgic encephalomyelitis, can be." - New York Times Brea's debut, Unrest, premiered at the 2017 Sundance Film Festival...
Fighting for the recognition of CFS/ME - UNREST
มุมมอง 3K7 ปีที่แล้ว
Jen lives large from her bed. She's the director of Unrest, a documentary about ME that premiered at Sundance 2017. unrestfilm unrest.film Much more research on ME is needed. Millions of sufferers around the world are without treatment. This can't go on anymore. www.washingtonpost.com/news/to-your-health/wp/2015/02/10/chronic-fatigue-syndrome-is-a-real-condition-not-a-psychological-illne...
The real answer to Donald Trump's hilarious accusations on FOX NEWS
มุมมอง 2.9K7 ปีที่แล้ว
Right wing former british MP and former editor of "Heat Street", Louise Mensch appears on Fox News. She tells us how Breitbart "misunderstood" her report and others, and somewhat managed to imply that Donald Trump was tapped. That was just fantasy. The "Facts" according to Breibart first. Then the solution at the bottom from all this nonsense. Short solution: There was no wire tap of Donald Tru...
BBC: Interview with prof. Simon Carding on ME/CFS
มุมมอง 8K7 ปีที่แล้ว
BBC: Interview with prof. Simon Carding on ME/CFS Researchers in Norwich are teaming up with researchers from Norway to collaborate on ME/CFS research. The researchers say that they believe ME is reversible, and that treatment could be available in the future. More about the story here: th-cam.com/video/tF3jZWVc8F8/w-d-xo.html Check out my profile for more on ME research.
BBC: Research in Norwich could offer ME/CFS breakthrough
มุมมอง 24K7 ปีที่แล้ว
Researchers in Norwich are teaming up with researchers from Norway to collaborate on ME/CFS research. The researchers say that they believe ME is reversible, and that treatment could be available in the future. www.investinme.org/ce-news-1611-04.shtml
Interview with dr. Øystein Fluge on their latest research on ME/CFS
มุมมอง 19K7 ปีที่แล้ว
The interview with Fluge starts at 3:50. Update: French, Spanish, Dutch, German, Icelandic in addition to English subtitles are now available. Press the CC button to turn captioning on. If you have a TH-cam account you can upload your own subtitles by your own. All subtitles are welcomed including, but not limited to: French, Polish, Mandarin, Hindi, Arabic, Portoguese, Russian and Japanese. Go...
Norwegian Institute of Public Health applauds new ME research
มุมมอง 3.7K7 ปีที่แล้ว
Norwegian Institute of Public Health says that the Norwegian ME research done at Haukeland is important. They add that the work done by the Norwegians confirm what researchers from abroad are already seeing. The findings can be important since they can make it easier to diagnose and possibly treat the patient group See also this clip from TV2 about the research done at Haukeland University Hosp...
New study on pathological mechanisms in ME from researchers in Norway
มุมมอง 19K7 ปีที่แล้ว
Update: Subtitles available in Spanish and English. Press the CC button to turn captioning on. If you have a TH-cam account you can upload your own subtitles by your own. All subtitles are welcomed including, but not limited to: Dutch, French, German, Polish, Mandarin, Hindi, Arabic, Portoguese, Russian and Japanese. Add your subtitle here: th-cam.com/users/timedtext_cs_panel?tab=2&c=UCDLzNae5E...

ความคิดเห็น

  • @SonneMond-y6m
    @SonneMond-y6m 4 หลายเดือนก่อน

    Hallo, ich bin aus Deutschland und meine Tochter ist schwer an ME erkrankt. Sie ist 18. Gibt es denn mittlerweile neue Erkenntnisse in Norwegen? Gibt es ein Medikament, welches verabreicht werden kann? In Deutschland steckt das alles noch in den Kinderschuhen. Es gibt kaum Ärzte und Studien, die relativ neu erst laufen. Ich würde mich wirklich sehr über eine Antwort freuen. Ganz ❤️liche Grüße nach Norwegen und vielen lieben Dank 🙏🏻❤️

  • @elliecohen3805
    @elliecohen3805 7 หลายเดือนก่อน

    I have pots! I’m so glad she mentioned it!

  • @Mcfads999
    @Mcfads999 10 หลายเดือนก่อน

    That poor man in his bedroom 💔😢

  • @giseleschmutz7770
    @giseleschmutz7770 10 หลายเดือนก่อน

    J habite en Suisse et je suis atteinte de cette maladie et point de traitement pour le moment ,j epuise car je fais infections virales a répétitions

  • @jkcliff2956
    @jkcliff2956 ปีที่แล้ว

    Thank you Jennifer Brea. I first came down with CFS in 1982 and have been living with it ever since. It is very hard to describe to people, and it was great for me to ask my loved ones to please watch Unrest.

  • @45Thesecret
    @45Thesecret ปีที่แล้ว

    This is so heartbreaking. I hope they find a cure and these people get their lives back and no longer have to suffer😢

  • @tallwomenresistence1473
    @tallwomenresistence1473 ปีที่แล้ว

    But this video is old! Rituximab I think failed. Is has been rulled out! You should take this video off. I thoght it was the real cure! When I first open it. Oh my God!

  • @tallwomenresistence1473
    @tallwomenresistence1473 ปีที่แล้ว

    I have now a lot of balance coordination problems. I have been about to fall many times.l'm worried about😢 But there's nothing I'm afreid but a stick maybe!

  • @debmansbridge3923
    @debmansbridge3923 ปีที่แล้ว

    What a absolute let down of an interview BBC 🤦🏻‍♀️ totally rushed and such a lack of empathy. Shame on you I hope none of you ever get this debilitating disease

  • @needles1975
    @needles1975 2 ปีที่แล้ว

    So follow my 50 yr Odyssey of Discovery ... remember doing so is irrelevant until it becomes relevant Blue Planet determines our destiny a thousand years from now males will certainly hide this information for the future of humanity and guess what that's not my problem ... doing so almost killed me no one cares about you me or children ... moms and dads have willfully chosen to work for money must slaughter their children to pay the price of ignorance dogma negligence so c'est la vie!

  • @needles1975
    @needles1975 2 ปีที่แล้ว

    We're "human beings" 1 double helix DNA, 1 genus, 1 Species, 1 Family, 1 Purpose 3 parts MAINTAIN & GUARD THE INTEGRITY SANCTITY VIRGINITY CHASTITY PURITY HOLINESS GODLINESS of Children from parental negligence ignorance CRUELTY COLD-HEARTEDNESS COWARDNESS COMPASSIONLESS CLOSE-MINDEDNESS per ten Commandments seven deadly sins .... impossible to get males to agree to agree to be nice and kind to their mothers and children it's all free fun to pursue happiness unfortunately doing so is "boring" so c'est la vie Hysteria will continue until females males children break the stalemate and guess what compromise is irrelevant, doesn't matter because we're not here in totality we're literally ghosts 👻 so Boo! Blue Planet determines our destiny! 🙏🏽

  • @needles1975
    @needles1975 2 ปีที่แล้ว

    blows my mind me only human as an old school neighborhood public Health service family doctor in the history of humanity figured out PREGNANCY is fatal to females sexually transmitted disease neuromuscular metastatic malignant cancer ... thank Mother Nature God the cures for pregnancy are already built in working perfectly miraculously no human intervention required once a 9-year-old is impregnated by her father! she is obligated to carry that child through Labor and delivery and forced to nervous that child until she falls over dead of malnutrition vitamin mineral depletion copper zinc selenium lithium magnesium iron postpartum depression anxiety Neurosis psychosis hallucinations complete neuromuscular collapse organ failure which is equal to that of shell shock battle fatigue combat stress ...

  • @needles1975
    @needles1975 2 ปีที่แล้ว

    Once more ... medical alert ... we are Earthlings exactly like all other placental mammals procreate by inbreeding incest except impregnate females our own mothers by COERCIVE HATE INTIMIDATING RAPE so too baby killing cannibalism ... HEALTHCARE WARNING BEWARE 💯 OF WHAT MALE DOCTORS HAVE BEEN DOING playing Medical Doctors Physicians specialist neurologist pediatricians obstetricians gynecologist orthopedic surgeons neurosurgeons in costumes white coats stethoscopes WITH FEMALES HAS BEEN 💯 CRIMINAL CRUELTY BARBARISM SAVAGERY BRUTALITY BULLSHITTERY CRACKERY DEMONISM SATANISM DR FRANKENSTEINISM ... it's impossible for any Male to cure cancer heal fix repair mend diagnosing treat with our hands with knives bone saw meat cleavers amputations eviscerations disembowling exactly like what men do when we Slaughter animals for sustenance with needles and thread Staples glue opioids fentanyl lethal vaccines immunizations 💯 cannibalism ... males medical doctors have licensed to Kill and get paid very well not go to jail just like police officers soldiers preachers pastors popes professors legislators presidents hahahaha 🤯

  • @KiroRocks
    @KiroRocks 2 ปีที่แล้ว

    The biggest problem is actually that you have to pull yourself together on a good day to even see a doctor. They never see you when it's the worst! Only when it's best, in comparison. Actually there is only the way of filming to make others see you at your worst.

  • @travis2318
    @travis2318 2 ปีที่แล้ว

    This shit is so fake 😂

  • @teagunn
    @teagunn 3 ปีที่แล้ว

    4 years later... Has there been any update to this research? I have heard nothing more about this research and wonder if anyone has any updates? I have been a sufferer for 13 years. I lost my job, my home and my whole life. Also lost friends and family who have become frustrated with me and have had years of battles with the DWP. This is not to mention depression and suicidal thoughts due to the feeling of hopelessness. I would do anything and try anything to get my life back... the life that ma stole from me.

    • @SonOfFurzehatt
      @SonOfFurzehatt 2 ปีที่แล้ว

      Unfortunately, the trials failed to replicate the results of the Norwegian study, so we cannot say that it works. If you're looking for the latest research and would like to contribute, check out DecodeME - they are collecting DNA from patients and sequencing it to see if they can find a genetic cause.

  • @catc2926
    @catc2926 3 ปีที่แล้ว

    I did hard time with this mysterious illness for over 20 years, My biggest break through was having a deliverance and learning spiritual combat.

    • @mariaseidi4023
      @mariaseidi4023 3 ปีที่แล้ว

      Well by me i Always think it was Depression

    • @TSeeker1
      @TSeeker1 2 ปีที่แล้ว

      Amen, I also learned this after being born again of Jesus' Holy Spirit! I Immediately felt amazingly better after 10 years of being bedridden. Demonic oppression is real. Stay close to the Lord Jesus Christ, don't open doors, and don't have fellowship with unbelievers. We can't lift them up (other than sharing the Gospel), but their demons will torment us and drag us down. The Bible says have nothing to do with unbelievers. For what has darkness to do with the Light? Put on the full armour of God daily. Msy God Bless you and keep you. ✝️🙏💖

  • @customsongmaker
    @customsongmaker 3 ปีที่แล้ว

    Maybe they should prescribe TV interviews to all the patients so they can out of bed and get dressed.

  • @SeigoSaiga
    @SeigoSaiga 3 ปีที่แล้ว

    Cringe, get a job and stop being a bum

    • @lysas781
      @lysas781 ปีที่แล้ว

      I hope you get it hunt.

  • @milesbodega2853
    @milesbodega2853 3 ปีที่แล้ว

    CFS is fake, it’s a bunch of women who want to be lazy and their spouses bring home enough to allow them to

  • @margottfon330
    @margottfon330 3 ปีที่แล้ว

    Lost 26 years

  • @margottfon330
    @margottfon330 3 ปีที่แล้ว

    Connecting Cancer, diabetes and CFS...huh, whether they want or not, Dr. T. Marshall has connected these dots long ago. I hope they arrive to an answer, whatever it may be.

  • @olgap3765
    @olgap3765 3 ปีที่แล้ว

    The cause of this illness is chronic psychological stress

    • @lysas781
      @lysas781 ปีที่แล้ว

      How do you know, do you have it? Obviously not.

  • @mikekram2199
    @mikekram2199 3 ปีที่แล้ว

    She has ME so badly she cant ever uncross her legs whenever she's being filmed.

  • @chiaro2299
    @chiaro2299 4 ปีที่แล้ว

    This illness needs 100 times more funding for research then what it gets now.

    • @Karuna221
      @Karuna221 3 หลายเดือนก่อน

      👏💯 Especially since 2020 when such cases or similar have at least doubled. I am now part of the chronically ill club with little diagnoses or help. Thus far I likely have one disease that I cannot find a doctor to help with in 4 years, and another that is written off by the medical community because there is so little understanding of it and no one told me I have it. I had to find it in my test results and was shocked. It is unconscionable.

    • @Truerealism747
      @Truerealism747 2 หลายเดือนก่อน

      ​@@Karuna221 diagnosed 27 years then neurosthenia diagnosis then pots now it's more fybromyalgia are you hypermobile? Found out I have autism ADHD causation after a trigger😊 father has CFS to but better than myself at 75

    • @Karuna221
      @Karuna221 2 หลายเดือนก่อน

      @@Truerealism747 I'm so sorry. I'm not hypermobile but feel I'm a good candidate for EDS though no doc has mentioned it. Fibromyalgia gets thrown around as well as MCTD in my records. They can't decide. "Likely dysautonomia" with no help (definite POTS symptoms) and self-diagnosed Tarlov Cyst Disease as I have "hemangiomas" all throuhout my spine on the nerve roots. It's rare to have them and 95% are found in the sacrum yet I have them everywhere else. Docs dismiss them and I'm symptomatic. It's hard to not give up hope. I wish you all the best. 🙏💗

  • @rainbowbgood
    @rainbowbgood 4 ปีที่แล้ว

    Don't take this poisonous chemo for ME/CFS. Science that goes from proving something is real to recommending a treatment with terrible side effects in a heart beat does not seem like its going through the proper methodologies. Olive Leaf Tea is amazing, works for malaria for thousands of years and also has reversed aids diagnosis in some. Dr. Josh Axe online helps in understanding complimentary issues like SIBO and proper diet detoxes you can do to help rebalance microbiome like 'Elimination Diet' and idenitfy food sensitivities (mine are sugar, wheat, caffeine, alcohol). I don't eat strict all the time but like to do periodic 'clean eating' where I stay away from foods that cause inflammation. Spirulina can cleanse out heavy metals which effect the brain as well as Bamboo Extract which contains silicate (good for teeth/nails/hair and pulls out toxins as well). Vitamin with high iron and B12 is energizing. Ginseng/Astragalus tea ( I make it in iced Hibiscus tea with honey) is a good TCM remedy (relieved my sharp stomach pain) and increases energy. Coconut water in mornings helps with electrolyte balance (good for light headedness/dizziness). Good protein and fibre in diet - especially breakfast is key. I take oatmeal with fried onions/mushroom/tempeh (high in protein) every day for breakfast. Bone broth is key for amino acids for muscle regeneration. Protein for muscle fatigue after excercise really helps. Trampoline/Rebounding is great for lymphatic system as well as massage, and for relaxation, nerves are too tense. Also Tai Chi (reprograms the brain which is why it is used for stroke recovery) and Dance. IF tired, best to rest but pay attention to low circulation from too much rest and add movement gradually to increase blood flow but stop before its too tiring.

    • @janhansen9340
      @janhansen9340 4 ปีที่แล้ว

      Think you need to read up on this subject. The researchers in Norway did a major multi-centre phase 3 study and the results showed that Rituximab yielded no effect. The studies have been done extremely thoroughly, and they were published even though the conclusion was negative. That is how science is done.

  • @dynamitedave1438
    @dynamitedave1438 4 ปีที่แล้ว

    Little miss twist, America is welcome To her!

    • @kiernanist
      @kiernanist 4 ปีที่แล้ว

      America loves Louise. Putin & Trump hate her. From March 2017 and her reporting was spot on. Brietbart and Trump twisted the narrative.

    • @dynamitedave1438
      @dynamitedave1438 4 ปีที่แล้ว

      Good to hear it ! Your welcome to her !

  • @shaniashrafza
    @shaniashrafza 4 ปีที่แล้ว

    Anyone here that knows of any possible cure?

  • @dirkkatz172
    @dirkkatz172 4 ปีที่แล้ว

    Dear, now the cause of Chronic Fatigue Syndrome is found: radiation of microwaveoven. To stop you have to eliminate the oven out of the house. The plug out of electricity net because the oven has also radiation when it is not in use.And out of the house because the oven has a high voltage capacitor. The distance between an oven and a person is very important.After a 2 weeks without microwaves health becomes better.

  • @sibelyldrmak5274
    @sibelyldrmak5274 4 ปีที่แล้ว

    Hikayesini Netflix'te izledim. Kendisine nazar değmiş olmasın??? Allah şifa versin

  • @andrewstrakele6815
    @andrewstrakele6815 4 ปีที่แล้ว

    The myriad persistent Symptoms of the Long COVID Patients or “Long-haulers” appear similar to the descriptions of those who suffer from Chronic Fatigue Syndrome/ME, Fibromyalgia, or Lyme Disease. Typically, these diseases, as well as many Autoimmune Diseases, begin with an initial High Stress event, such as a severe illness, physical injury, divorce, job loss, etc. I can easily imagine how the loss of income and lockdown from COVID-19 could provide such a Stress. There are often “Triggers”, such as certain foods, arguments/conflicts, sounds, and smells that precipitate an “Episode” of Symptoms. Cortisol, the Body’s “Stress Hormone” appears to be intimately involved with these afflictions. Systemic Oxidative Stress, leading to an Overreaction of the Immune System, producing Inflammation are also common features. Viruses reactivated and coming out of remission from Stress have been suggested as a Root Cause Cause for these Diseases ( th-cam.com/video/zgBJiQbV30k/w-d-xo.html ). Inflammation of the Brain has also been proposed for Chronic Fatigue Syndrome ( th-cam.com/video/rxdzaWD5wfU/w-d-xo.html ), affecting the Autonomic Nervous System ( th-cam.com/video/xINZnfAB5G8/w-d-xo.html ). Alzheimer’s, recently termed “Type 3 Diabetes” ( th-cam.com/video/vBMOZfGY6uc/w-d-xo.html ), also points to Brain Inflammation, as does Chronic Depression & Anxiety ( m.th-cam.com/video/1-caioklUbQ/w-d-xo.html ). Other Neurological Disorders, such as Bipolar Disorder, Schizophrenia, Parkinson’s, Multiple Sclerosis, and Epilepsy may also involve Brain Inflammation. The extent and area of the Brain affected may determine how the Inflammation presents in various Neurological Disorders. Systemic Oxidative Stress and Inflammation from High Insulin and Blood Sugar affects other parts of the Body (Liver, Circulatory System, Heart, Kidneys, Pancreas, Thyroid, Bones,etc.) These present as Fatty Liver Disease/Cirrhosis, Hypertension, Cardiovascular Disease, Chronic Kidney Disease, Pancreatitis, Hashimoto’s, and Arthritis. Collectively, these Chronic Diseases are all part of Metabolic Syndrome ( th-cam.com/video/ceFyF9px20Y/w-d-xo.html ). Metabolic Syndrome results from consuming a Diet TOO RICH in Carbohydrates TOO FREQUENTLY. Amazingly, The Solution to ALL these Chronic Diseases is mostly DIETARY! 🙀 Stress Management (proper Sleep, Meditation, Exercise ) to reduce the chronic generation of Cortisol (which will thwart any Dietary Efforts) and a Low Carb Ketogenic Diet to manage Insulin and reduce Oxidative Stress/Inflammation from High Blood Sugar, as well as Support the Immune System, may be helpful in reversing these cases. Such a Diet should incorporate Fasting (both Daily Intermittentt Fasting as well as occasional Prolonged Fasts) to reset the Immune System (thesource.com/2018/11/21/fasting-for-72-hours-can-reset-your-entire-immune-system/ ). A good place to start your own research is 👉 th-cam.com/video/vMZfyEy_jpI/w-d-xo.html . Supplements that provide Vitamin **D3, Zinc**, Iodine, and Selenium - nutrients essential to proper Immune System function- should be incorporated into this Diet/Fasting regime. People deficient in Vitamin D3 and Zinc typically experience more Complications for a Longer Period with Infections. The Immune System will use up these Essential Nutrients to fight Infections and Systemic Oxidative Stress. 👉 NOTE: Both Exercise and Fasting are Stressors on the Body. It is important to break into them S L O W L Y to allow your Body to Adapt. You cannot get up off the couch and run a Marathon OR start a 3 Day Fast without first taking smaller steps. Excess Stress only will produce Cortisol and Negative Results. If I were in a Long COVID Situation, I’d probably ignore exercise to start and focus more on eating the Low Inflammatory Foods of the Ketogenic Diet and taking Vitamin D3/K2, Zinc, and NAC supplements. The intent is solely to reduce Inflammation and Support the Immune System at this point. Next, I would try easing into having Breakfast later, moving it closer to lLunchtime. I’d then try to eventually combine Breakfast and Lunch into a Single Meal, eating only 2 Meals a Day, continuing with the supplements. I’d then try reducing the Feeding Window of Time down to 6 Hours, leaving an 18 hour period during every day when NO Eating takes place, only Hydration with Water or a NO SUGAR Electrolyte. The 18 Hours of Intermittent Fasting every day will really help to allow the Body to Heal. Once comfortable with that Fasting Schedule, I’d try a more extended Fast of over 24 Hours, eating something if I started to feel anxious. The longer Fasts induce Autophagy, the Body’s Recycling and Trash Removal Process, which will greatly accelerate Healing and Reset the Immune System. At this point, I’d start with very limited exercise during the Fasting Window. You’ll KNOW if you have more Energy to begin exercising at this point.

  • @danashannon8234
    @danashannon8234 4 ปีที่แล้ว

    We need a cure

  • @danashannon8234
    @danashannon8234 4 ปีที่แล้ว

    And what came if it? : (

  • @heavenlymilano
    @heavenlymilano 4 ปีที่แล้ว

    It looks like this thing starts after an infection which clears from most people as they recover. But with ME/CFS patients, the infection changes something with the immune system for good. I admire Jennifer Brea for being outspoken about this condition.

  • @marcysiaxxx
    @marcysiaxxx 4 ปีที่แล้ว

    Im not sure but there is a woman who have wrong diagnosis.... firstly cfs but then doctors change her diagnosis, women had few surgery of her neck/spine and she got back her health. I remembered she couldnt stand noise or loud talk... - Jennifer Brea's Amazing ME/CFS Recovering Story: the Spinal ...

  • @OlderWomenRock
    @OlderWomenRock 4 ปีที่แล้ว

    Thank you Jennifer and Charles Shepherd for speaking out . It’s been incredibly tough living with this illness. It’s also been terribly painful to not be believed let alone given support or empathy . I dream of a treatment . I lost so much life due to this illness .

  • @freespirit6209
    @freespirit6209 4 ปีที่แล้ว

    Unsung heroes of the modern world. "Celebs" eat your hearts out!

  • @p47rr
    @p47rr 5 ปีที่แล้ว

    So much I guess for a break thru. Two year old show.

  • @ebradley8057
    @ebradley8057 5 ปีที่แล้ว

    I have CFS and POTS as well. I fight through every single day praying that one day I’ll miraculously get better. Doctors know nothing about it and they’ve given me no treatment. I am done pretending to be a normal functioning working adult. I am disabled by this illness, period.

  • @lionrence
    @lionrence 5 ปีที่แล้ว

    Omg I've been sitting that way for years! It helps with the back pain... I rarely see anyone else sit that way

  • @heatherhartman6474
    @heatherhartman6474 5 ปีที่แล้ว

    I love my doctors but even they don't know what to do with me anymore. Me neither😢

    • @Jorg-ug3ie
      @Jorg-ug3ie 5 ปีที่แล้ว

      Xxx hang in there

  • @wearitlikeadiva
    @wearitlikeadiva 5 ปีที่แล้ว

    Cfs survivor 19 yrs. I got help through Clymer Healing, the first cfs clinic ever. I am 60% functional. I will take it from being bedridden

    • @lbllk99
      @lbllk99 10 หลายเดือนก่อน

      Hello how are you currently feeling?

  • @o0xst
    @o0xst 5 ปีที่แล้ว

    Farmvillemyalgia

  • @robinblair7854
    @robinblair7854 5 ปีที่แล้ว

    One of the best parts of this interview, in my opinion, is toward the end when Dr. Shepherd is discussing diagnosis. Everyone says that ME/CFS cannot be formally diagnosed with tests, and perhaps that's right. But Dr. Shepherd describes very well the patient who presents with classic ME/CFS systems. He articulates them beautifully -- one, two, three, four, five, six. He lays it out clearly and says THAT patient should be diagnosed with ME/CFS. Maybe the patient's physician doesn't know how to treat it, but the criteria for diagnosis ARE clear. That alone will help with the "legitimacy" of the disease.

  • @PaulKitching11
    @PaulKitching11 5 ปีที่แล้ว

    Exactly Doctor it is actually NOT fatigue. It’s just the easiest way to say it.

  • @PaulKitching11
    @PaulKitching11 5 ปีที่แล้ว

    The presenter looks like Myra Hindley.

  • @lioradvir2253
    @lioradvir2253 6 ปีที่แล้ว

    nice to see that overall Norwegian doctors do not call themselves as -doctor so and so -they present themselves exclusively by their name , like joe doe and not dr. joe doe , all doctors should drop the name dr because it only shown the repulsive thought that doctors think themselves as God , repulsive repulsive repulsive

  • @lioradvir2253
    @lioradvir2253 6 ปีที่แล้ว

    nice to see the humbleness of doctors in Norway they do not think themselves as being God as it is in Israel , no humbleness here , shame on them , medicine is not mathematics

  • @anniebalsbaugh735
    @anniebalsbaugh735 6 ปีที่แล้ว

    Hey CNN, why don't you talk to me sometime about what it's like to care for someone with ME, maybe I could help others in my place, no one seems to have a clue or care what caregivers live with every day. I'm worn out after 15 yrs. It's heartbreaking being her mom, and nurse. Our daughter will 25 this weekend. She will spend it alone of course. No friends, parties ect or even cake, not for severe bed bound house bound people like her.

    • @anniebalsbaugh735
      @anniebalsbaugh735 6 ปีที่แล้ว

      ...but yeah it seems famous people or successful people are the only ones heard.

  • @Mario-kp8mj
    @Mario-kp8mj 6 ปีที่แล้ว

    ❤️❤️🙏🙏✊✊❤️❤️💪💪❤️❤️Dankeschön für dein Mut, Kampfgeist!!!!!👏👏👏 großartig!!!

    • @carlac.3629
      @carlac.3629 5 ปีที่แล้ว

      Ich glaube viele dieser Behandlungen kannst du machen wenn du viel Geld hast. Leider gibt es viele ME /CFS Patienten die am Existenzminimum leben, da hat man keine solche Möglichkeiten. Aber es ist schön zu sehen das es ihr besser geht.🙏😊