Видео

Suggestion. Do not use white letters on a yellow background. Your message is for eye issues. So people like me with fibro and eye issues cannot read white letters. Back to black.

Why are they doing yoga and having a good time when this disease makes me want to die I don’t understand. Do they have no experience

Sleep apnea for one.

Hello thanks for your video ! (( I've also had this PGAD syndrome since 2021 and the cause of my genital syndrome is neurological. Certain nerves are affected = peripheral polyneuropathy. )) I just give some information to help people who like me, have persistent / permanent genital arousal. Here are the main causes of PGAD, the solutions and the examinations to be done to obviously cure it ! Either the cause of PGAD is psychological: Big emotional shock or trauma following an accident or a physical aggression, rape, recent or even very old touching = during childhood for example ! Follow a good therapy => hypnosis or the EMDR technique which is effective! (avoid if possible the antidepressant drug treatments !...) Otherwise often the main causes of PGAD are => A Tarlov cyst or a hernia or a disc protrusion which compresses or irritates certain nerve roots (nerves) coming from the Sacro-lumbar vertebrae of S1, S2, S3 and S4 which go to the genital organs! Or often a cyst that compresses (pinches) a part of the Pudendal nerve which is the great nerve + its 3 branches of the genitals ! It is enough that a root (nerve) is irritated or compressed for that to cause a permanent genital excitation ! Other causes: Sometimes it is due to a neurological disease => Polyneuropathy (lesions) of the pelvic nerves or at the level of the pudendal nerve ! (Especially at the level of the dorsal nerve of the clitoris, root coming from the pudendal nerve !) Genital pelvic varicose veins are the most common cause of Pgad, accounting for around 55% of cases, especially in women who have had children, and sometimes also in young, childless women. Another cause is vulvodynie Or sometimes pudendal/perineal neuralgia ! => Consult a Urologist or Neurologist. Examinations to be performed: Irm Abdomino pelvic and or a perineal Phleboscanner. Or sometimes an inflammation of the ligaments of the large gluteal muscle, the Piriformis ! The ligaments (canal d'alcock) of this large muscle are very close to the pudendal nerve and can touch a part of the pudendal nerve and create a PGAD! Consult a good physiotherapist or osteopath ! Perform a perineal electromyography to detect whether a nerve is affected, compressed by a cyst or protrusion, or an injury causing neuropathy. Examinations depending on the case or symptoms of PGAD: an MRI (magnetic resonance image) of the thoracic spine and a pelvic MRI or pelvic Doppler ultrasound. It is best to consult a good pelvic urologist or a good neurologist. For Doppler ultrasound or pelvic ultrasound see an angiologist or your doctor. Do not be discouraged ! There are solutions to cure and stop PGAD ! Sincerely 💚

My main problems, apart from disabilities and severe pain, is being unable to sleep nights. Drs won’t prescribe sleeping pills now either. Tried just about everything herbal too. Nothing helps.

An awful lot of pain in the right side of the neck ,back and shoulders too.

GABA for many years. I have every chronic symptom in the short video. I’m 65 and have suffered for over 20 years. I haven’t driven my car in five years. I go out several times a year. I’m just laid up like a caged convict In bed. I’m either sitting or laying down in bed. Our son is 28, an engineer at Boeing in St. Louis. He’s the reason why I’m holding on. I do hope I get older and of course, my illness will never go away. My deep desire is to the death with Dignity or Dr assisted suicide. They give you second all that you mix in some juice and go to sleep forever I keep flaring. I get IBS where my bloated gut is pressing up on my heart and lungs. Throwing me into a panic attack because I’m taking shallow breaths Due to the compression of the lungs I also have Hashimoto’s auto immune thyroid disease. This condition causes fibromyalgia. I’m burning as though someone just sent me on fire 🔥

Take magnesium glycinate it help some. This is disease that that we fibromyalgia patients should get together and ask for funds to find better care of this unbearable pain that the government should research special doctor together and find a cure. We don't have a normal life. I pray for everyone 🙏 amen. Ty

Giving it a psychiatric definition seems completely pointless, just a way to medicate those people back to normal so they satisfy the demands of neoliberal society. Must work, must produce, the planet is only a ball of resources waiting to be exploited. Eco anxiety is based on stuff that is actually happening, diagnosis can do nothing for that. Feeling scared of bad shit that is actually happening is what those feelings are for. Especially when it is human society that is causing the harm, emotions can potentially resteer the boat. Enough people feel hollow about hyperconsumption and working their lives away to feed infinite greed and maybe it will change someday.

I had dry eyes well before my fibromyalgia diagnose, I find that interesting. I have to agree with every one else, there’s no way I could read all that information, the colour was all wrong, it was all too fast. Good luck with sleep and trying to rest your eyes. 🤷🏼‍♀️

I’m in so much pain I can’t stand It. Doctors just say there’s no more they can do to help me

If you want to help yourself, just google Weedborn. I know you will find good solutions for all your ailments there.

Thanks for being awesome!

The standard of care stopped recognizing trigger points as a diagnostic tool in 2010

..in the UK at least it is not possible to access all these 'experts'...the most one gets is medication which triggers more suffering!

Theres no doubt that pain n tenderness comes n goes but cognitive dysfunction is always there. I never knew this happens in fibro until now.I have struggled through horrible memory issues in the past few years and could never figure out its part of fibro and kept on attributing them to my extremely high persistent stress level. They were scarier to me a lot more because I was someone with extremely high learning skills n excellent memory and suddenly am getting all confused and lost progressively.

💯🤍Raelan Agle has over 150 videos of persons interviewed from all walks of life who have purportedly recovered from Chronic Fatigue Syndrome , Fibromyalgia and other challenges, including her own recovery stories. Worth serious investigation?

29 years of agony took everything from me. Just want to never wake up again..

Suffered for so many years insomnia and the huge list of symptoms have caused other conditions

Insomnia is not the cause but a neurological symptom of fibro and ME/CFS

I have been suffering for years😢

The pain keeps you from sleeping , I A HORRIBLE PAIN THAT NEVER GOES AWAY .

I have had Fibromyalgia since 1986. My two biggest problems are blank spots and dislocation. My ribs and vertebrae move in and out frequently. Has saved me from severe injuries many times. I am unaware a blank spot has happened at the time they happen.

I have good nights and bad nights, but I always get broken sleep and I wake up exhausted.

I wake every night, the duvet feels like a lead weight

I guess what i needed to know will go unknown. The music was highly irtating, the white (small) print on blue background was unreadable for me. Is being grouchy a symptom of Fibro ?

Hello Dear, I hope you’re doing great. I researched your RUclips channel for a few days. Your videos are awesome but due to some problems your videos are not ranking on RUclips's top and you don’t get more subscribers, views, and engagements. As a RUclips promotion expert, I have a big plan to grow up your RUclips channel organically. Can we have a short conversation about it? It will be for the betterment of your RUclips channel to grow your subscribers, views, and engagement 4x faster. Thank you for your time and waiting for your positive response.

The font is tiny and the background color makes reading the text difficult. Also the speed of exposure is too brief.

Clothing feels like barbed wire. Wind is extremely painful. Touch from my hair hurts my head, neck and shoulders with subtle movements. Extreme sensitivity to heat and cold. Spiraling to anxiety, depression and isolation. It is much, much more than just this short list.

ALPHA LIPPIC ACID IS GREAT FOR. FIBRO ALSO NEURO MAG. ONEGA TGREES AND B COMPLEX ITZ A LIFE SAVER.

Clickbait crap.

Fibro a nightmare you never wake up from

Wish I could afford all that treatment. In USA that care would cost a lot of money!

1:02 1:02 1:02 1:02 1:02

I am 79 and have had fibro for 30 yrs ugh😢

Much talk - would have appreciated a brief sommary

Is asthma spreading one person to another???

Can't read a word of this, posterior uveitis!

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

I don’t have those problems

Never tried that before

I don’t sleep at all

I don’t have any hormones anymore

I have burning pain everywhere

Had it for 15 years, for me light exercise , meditation every morning and evening and going plant based on food has helped a lot. Takes time but still improving. Meat, dairy, sugar and white flour creates inflammation. No drugs pills or alcohol.

culprit: microwaves. it can last 2 years before musclepain goes away

culprit: microwaves, so eliminate microwave-ovens

Tender points are no longer a diagnostic criteria for fibromyalgia

Ridiculous. I can't read a word. Could you make it any smaller.

Why this disturbing distracting music. Letters are not clearly visible to viewers. What is use without explanation. Wasting viewers valuable time.