A new understanding of fibromyalgia

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  • Опубліковано 8 лип 2017
  • Fibromyalgia is a difficult condition to diagnose as symptoms take many forms, ranging from chronic widespread musculoskeletal pain to fatigue, anxiety and mood disorders.
    But researchers at the University of Colorado Boulder have discovered a new way of testing for the neurological condition that uses brain scans. www.colorado.edu/today/2016/10...

КОМЕНТАРІ • 18

  • @seannewoods2296
    @seannewoods2296 6 років тому +7

    I have had FMS for 40 yrs now. They called it Fibrositis may yrs ago and that was my original diagnosis. I have been researching and watching my symptoms and others who have I to try and find a cause by elimination. One of the things that I have found is that I remember my dreams vividly. Like I just left the movies but was the person that I was watching on the screen. I watched cars hit me, Jumping and falling and being attacked, anything that was traumatic that I dreamt, I felt in the morning when I woke up. These painful effects lasted until I returned to bed, and the cycle started all over again. I am convinced that the sleep disturbance is caused by a faulty adrenal system that overworks and pours on the juice to protect what the brain thinks is an attack. I don't know if this makes sense to anyone or not, but it should be looked into. I also believe that it has to do with the level of magnesium on the body. If magnesium is not available or the pituitary is not functioning properly, the body will suffer symptoms of a magnesium deficiency or a pituitary malfunction, depending on how you look at it. I have had Drs shrug this notion off, but I would love to try a magnesium supplementation without the risk of hurting my self or to be under a Drs' care. I did notice a difference when I had to prep for a colonoscopy with a magnesium cocktail. I did feel better but didn't enjoy running to the bathroom every fifteen minutes. Maybe you can do a study on the effect of magnesium on the pituatary gland or a the effects on it of magnesium depletion.

    • @01karlie
      @01karlie 6 років тому +2

      SeAnne Woods I have the same experience with vivid dreams and how hard the bad dreams hit on me everyday. I feel my body sore from the adrenaline I live every night.

    • @italiangirl2440
      @italiangirl2440 6 років тому +2

      SeAnne Woods I have fibromyalgia and I just recently started taking 500 mg of magnesium a day cuz I heard that cholesterol statins medicine deplete the magnesium in one's body. The only difference I experienced was my hot flashes went away due to menopause

    • @kellsmum1
      @kellsmum1 3 роки тому

      I have fibromyalgia and have adrenal insufficiency that need to take replacement steroids for. This comment makes sense. This condition needs way more study!

    • @sarahmarshall2474
      @sarahmarshall2474 2 роки тому +1

      I have fibro and my dreams are incredibly vivid, to the point where sometimes I'm half awake and think it's real, which is so strange because my dreams are really out there. I often have this reoccurring dream where I am being chased by some overpowering force. I'm not sure if it's a person, or a group of people, or just some kind of intelligent entity, I've never been caught or seen them close up. Im always running away from them, and right when they are about to catch me, I jump really high, all the way above the earth. It's like I'm almost in space, looking down at the whole world, and then gravity brings me back down on the other side of the planet, and I immediately start running again, because I know they're still looking for me.... i was put on endep for my fibro over a year ago, and it's made my dreams even more intense 🙃

  • @TheNaiv69
    @TheNaiv69 4 роки тому +4

    more on this please, maybe a follow up

  • @lollol-ef1zr
    @lollol-ef1zr 3 роки тому +7

    Please help who has fibromyalgia. It is so painful everywhere body is broken already can't do nothing no hope

    • @grantlawrence611
      @grantlawrence611 2 роки тому +1

      Terrible pain

    • @5ebrambila
      @5ebrambila Рік тому +1

      Nothing helps mine either. :(
      I read that a study from King's College in London has found evidence that it is possibly autoimmune. I'd love to see more studies being done. We need answers. I hope you are doing well.

  • @ashwininarkar9988
    @ashwininarkar9988 10 місяців тому

    Which tablet

  • @tamites450
    @tamites450 6 років тому +3

    Do you have any studies going on now? Nothing helps my fms.

    • @seannewoods2296
      @seannewoods2296 6 років тому

      Try a good dose of magnesium for a few days. See if it helps. It helps with energy.

    • @5ebrambila
      @5ebrambila Рік тому

      Nothing helps mine either. :(
      I read that a study from King's College in London has found evidence that it is possibly autoimmune. I'd love to see more studies being done. We need answers. I hope you are doing well.

  • @annaburns2865
    @annaburns2865 5 місяців тому

    “It’s not all in your head, it’s in your brain.” What’s the difference? 🙄
    It’s not in your brain, it’s in your neurons.

  • @user-eo9qd8zx4w
    @user-eo9qd8zx4w 7 місяців тому

    Dr emuakhe is an epitome of good treatment,the doc has every criteria to human health