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The only way I have survived fibromyalgia for 35 years is antidepressants. Without them I cannot function at all. I was happily surprised when my new Dr asked me if I take them for depression or for pain? So there is some understanding happening, at least in the sense of validation from the medical community. I've had Lyme disease for 35 years so I'm used to being treated like a hypochondriac. Funny thing is, I've become far less reactive to my pain over the years since I've had so much of it. My family now understands when I say I'm in pain, it must be bad. If I'm getting to the point of crying well then something better happen quick. I've told my sister many times over the years when she's not feeling well or this hurts or whatever, buck up woman that ain't nothing ! She has learned I am right. Before being diagnosed with Lyme my Dr at the time thought I might be drug seeking. Though I always said no to any pain meds he would offer. When I was diagnosed by a specialist, he threw down his Rx pad and said anything you want you got it. I said you don't get it, I can't take pain meds they me sick. It was like a light went on behind his eyes. He was finally seeing me as I was not with whatever his stupid preconceived notions were.

I have the opposite! How? Why? 😭 I want my curls back!!! I went from spiral curly to straight. Loss of melanin is no joke and linked to Alzheimer’s.

So true. 3 weeks ago I had a muscle spasm behind my right knee and it took 3 days to heal. It limited the ability to move my leg and my ability to walk. Diagnosed Fibromyalgia/Osteoarthritis. 😩

Fibromyalgia for 35 years almost bedridden now. Considering nerve spine stimulator to help with pain

Our rheumatologist in our city will not see fibromyalgia pts saying gps can treat w drugs approved by fda

I noticed that the woman in the blue and white shirt was not relaxing her muscles as much as possible. I've had severe fibromyalgia since the early 90s. I received injections in my lower back for the severe pain, and after years of very painful shots I decided to completely relax my muscles one day, and I never had a painful injection again. This might be why the woman in the dark shirt had a 19 reading, her body did not seem to be tensed up while having the saline injected. I see that it has been 3 years since this video was made. Let's hope the Australian scientists come out with their pills that will help with fibromyalgia. I do not know the name of the medicine that they are working on, if you know more please let me know. Thanks.

Thanks

When people are helped to understand and become convinced that they must curtail the silent accumulation of Uric Acid crystal deposits in their joints and critical organs or suffer life altering consequences they will be more likely adhere to ULT.

Im excited about this. Now people know how fibro pain feels . It feels like someone is pinching/twisting your muscle and not letting go.

Its muscular ,brain, nervous system and brain and spine and inflammation is a big problem for me blockages and a build up of poisons causes more illnesses while we wait for treatment mercury is a problem for me and floride

🎉My pain is muscle, joint and bone pain. Fibromyalgia is a hideous disease which lives to the first 4 letters: HIDES. Very well so and it's so frustrating and utterly debilitating. 😢😢

none of these people can ever be trusted again.

I would be interested in the difference between the pressure in the muscle knots vs the muscle areas of a FM person in an area where there is not any knots. I know that when I have RFA on my nerves that about two weeks after the knots start to dissolve and come back when the nerves regrow.

This is what I try to explaine to my Doctors, how it feels. But they cant give me meds so, they say there is nothing they can do and a leave with nothing and in more pain then it was worth to get out.

i have been having severe upper back , shoulder and neck tightness and pain ( Fibro pain) and I could hardly function, I took one of my Atenolol 50mg tabs I had left from a script I used to take and I was pleasantly shocked when I woke up the next morning. I had a much better sleep but I also found that the muscle pressue was prob 80% improved from the night before. could fibro possibly be an issue with adrenaline?

How many here have undergone a deworming protocol with pyrantel and ivermectin?

If I step on anything hard it is excruciating!

Did this test turn out to be effective?

Let me starting as a former nursing educator. Why are you touching a sterile needle close to injection insertion length? Second recapping the needle awwwwwww😂 Now as a fibromyalgia patient. My neck has been so stiff for a couple weeks now. I get shoulder pain the chiropractor relieves by stretching my neck. It stays gone too, about 6 months. He said I’m very tight in my neck, traps and area. I couldn’t figure out why. I was thinking my years of bending over a patient’s bed, but maybe not. I’m learning so much between here and Dr Giverna(sp?)

Side effects side effects side effects!! For gosh sakes! And allopurinol doesnt address the CAUSE of gout….and the reason why everyone produces Uric Acid or the fact that just under half of people with high UA have gout, the rest do not…UA is correlated with Metabolic Syndrome….most docs dont even test UA unless there is a flare which ignores the red flag the presence of UA has been providing…the UA score most docs shoot for is still way too high….. sigh

But what is the cause of the muscle pressure... I've been on muscle relaxants for a long time, it rebounds, it's a bandaid.

Cannabis has been a game changer for me. It doesn’t seem to affect me like it does friends I’ve been around who are high. I don’t get goofy or any other typical sigh. Just relief of pain. But to hear there’s an objective test proving fibro feels like a relief in and of itself, really!

@kristinewalberg2938 - I have had a wonderful Rheumatologist for 32 years, of the 34 years I have had Fibromyalgia (FM). The first two years, I was misdiagnosed by a different doctor. I'm sorry you haven't been able to find a wonderful Rheumatologist like I have. He diagnosed me on my first visit and began treating my widespread body pain and the sleep disorder that came with it. There is no cure for FM, and doctors can only treat the symptoms until a cause is found. I was notified last week that my doctor is retiring and closing his office on December 19, 2023 after 46 years of practice. He is entitled to retire, even though it breaks my heart.💔 He had 3 other Rheumatologists working in his office suite, so there are hundreds of patients if not a thousand scrambling to find another FM doctor, not to mention the patients with Rheumatoid Arthritis, Osteoarthritis, Osteoporosis, Ankylosing Spondylitis, and other Rheumatology related diseases. There is a laboratory in Los Angeles, CA that is researching for a cure or a method to reverse it. EpicGenetics, Inc. There is a FDA approved blood test for FM, called the FM/a blood test, and if you have had a positive test result, you are eligible to volunteer for FDA approved trials for better treatment or a cure. fmtest.com.

Also tunning forks vibration and sound frequency really helps! So relaxing it takes you to another world of pure bliss.

We also have to many emf electricity around us all. Read the invisible rainbow a history of electricity and life by Arthur Firstenberg.

You are definitely on the right track doctor! Look into vegus nerve degeneration, there’s many connections to fibromyalgia, and this is one I would ask doctors to look into!

My fibromyalgia started in my neck muscles 15 years ago, it’s always been my muscles and ligaments pain. Every muscle in my body is affected with severe spasms that I felt I needed emergency room treatment. I get this everyday and night. Magnesium helps. Also ice pack for instant neck pain relief. Hurts so much to do this but it works. Tried acupuncture but was to painful in wrists and ankles, made me scream out in agony, they had to be taken out, I’ll never try that again. Vitamin injection helped, gave me a burst of much needed energy!

My muscles go like concrete stones. Absolutely frightening. I use MAMEDICA cannabis proscribed to me by qualified doctors in England, it has helped me so much, I recommend it to help with muscle spasms and chronic pain

Vegus nerve deterioration, many symptoms of fibromyalgia connection to vegus nerve. See Ros Hauser m.d webinars begun nerve degeneration

this technique is helpful for diagnosis. I have fibromyalgia and have suffered all the conditions of pain, trouble sleeping and brain fog. I have seen a lot of the comments here about how different treatments help the pain and sleep. They all help, Magnesium spray and supplements help, drugs that treat neurological issues like gabapentin, and muscle relaxers all have helped. However, the sleep component is very important and no one here has mentioned CBN, cannabinoids found in the cannabis plant. It has no side effects, is not addictive, and gives me a good night's sleep. My doctor knows nothing about it. I had to research it and determine my personal dose on my own. But works it for me.

I even get muscle pain in my face and head. Weird feeling like my head is being pushed, pulled and twisted. I’m a 20 year sufferer but noticed muscle problems since I was 7 years old. Lately I wake up after two - three hours feeling like I have deep bruising across my back and horrible pain throughout my body.

😅 P r o m o S M

I'm just seeing this video now and it's 2 years old. Why didn't my rheumatologist mention this? I've had Fibro for 40 years!

Have there been any links between ehlers-danlos syndrome and fibromyalgia?

After I have interacted with normal life, my muscles feel pulled at both ends. Like wrist to elbow area and elbow area to shoulder. The ends of my muscles are very sore, burn, feel on fire and are extremely pulled. Is this normal? Is this a normal for fibromyalgia? Or am I experiencing something else? Thank you for any insight.

culprit: microwaves: it can last a few years before it disappears

Proper electrolytes, hydration and massage, dilute and move toxins out of the muscle tissue after a couple weeks. BEEF JERKY DOESN'T STRETCH WELL. I have helped dozens of people with massage, castor oil heat packs, essential oils for pain, and gentle ROM stretches. Also probiotics and Epsom salts baths helped with the fatigue. I owned a therapeutic treatment clinic in Carnation Wa for a dozen years, had a six month waiting list to get in the door.

Good luck finding a Dr that works this hard to understand. Most don’t care, your to difficult of a patient, they label you as hypochondriac, drug seeker, depressed, on and on. Tell you to see a cognitive therapy Dr or mindfulness. Ok Dr. Let’s see how well that works for nerve pain. It’s doesn’t

But what causes the increased pressure in the first place? Otherwise we are just treating the symptoms, not the disease.

Gracias

What anbout robaxin?? Instead of flexerile? Is robaxin addictive?

So what can be done to lower muscle oressure?

What all does that indicate, the the muscle pressure is 3 times higher??

Wow... this is amazing.

This sounds interesting, I can find no further information about this.

It is my greatest joy that I discovered about Dr Aluda on RUclips who cured my Fibromyalgia with his herbal medicine. I highly recommend him and a trial will convince you. he cures HSV I&2 and HPV too,,

I take Cyclobenzaprine 30mg and Nabumetone 1,000mg daily and I do this consistently (not as needed). After I had been taking this level daily consistently, after about a month or so my pain was much better. Not ALL better, but much improved. I had bad reactions to the typical fibromyalgia drugs like Lyrica, Cymbalta, Savella and Gabapentin so can't take those. fibromyalgia diagnosed 2011 after MVA. vasovagal syncope diagnosed 2021. small fiber neuropathy diagnosed 2021. autonomic dysfunction diagnosed 2022. I have tons of autoimmune symptoms but no diagnosis in that arena (YET).

Makes sense why cyclobenzaprine helps

One oxy gives 5 to 6 hrs of pain free and reduced inflammation. Been on it for years. No addictive problems. Also used because of massive back fusion with rods and pins up back. The brick I carry, as I call it causes pain. Icing whole body helps. Can’t tolerate any of drugs you mentioned. Had severe drug induced reaction to metoprolol which caused drones of problems in all systems

Yeah but what causes the muscle pressure?