Thank you for this presentation😀

Great webinar! Thanks for putting together so much value in one video. From the inmunologic perspective, it’s great to see how it works. Thanks Dr. Nigil. It would be good to to have more information about how exercise affects our inmune system in such a way that reduce inflammation. I have AS and when I do 1h of grabbing, walking or what ever, I can experience improvement in my joint mobility even in those I didn’t practice. It feels like a general reduction of inflammation. It would be great also to understand better how inflammation in joint happen. I never really understand what type of Rosie’s are really inflamed: the bones, tendons, entesis, liquids, liquid inside bones or all of them. Also why inflammation increase during the night, even before going to sleep if I haven’t be inactive yet? I will contact some of you to have and interview if you wish. I have a community of 40 AS patients in Spain. Where should I contact you? Thanks so much really ❤️

I.m 45 years and I have both crohn's and ankylosing spondylitis and very difficult to to explain to the people around you.

It is important to keep this disease in check. Yoga is an amazing way to combat Ankylosing spodylosis and recover from it. I have seen many patients effectively managed by Planet Ayurveda’s herbal combination of - Bone Support, Boswellia Curcumin, Yograj Guggul and Coral Calcium Complex.

AS have been passed down to me genetically (maternal roots) living life with AS is super hard as it fuck you up mentally more than physically…. I have big aspirations and I want to manifest them but with AS things are not simple at all. I stay strong pushing myself everyday and everyday it’s like day 1 no matter how much I try AS gets me down by the end of day. Idk this comment section made me feel secure to open about this struggle of mine with myself. I’m certain that I’m going to achieve everything that I aspire to be or to do! Will not give up💪

Merci pour ces informations précieuses !

'Promo sm'

Due to sound quality I was unable to follow the seminar.

I am just getting diagnosed after 10 years of chasing different subspecialists. I'm tired. And I really hope I find the same relief with these medications. I miss.... Me.

Watching from country with the worst health care in the world, the UK

Instead of showing a good looking guy who is about to get married, show me. No? Okay.

Jane from Ìreland ❤

I am so frustrated. 😭 I've had skin issues my entire life but not plaque psoriasis. I had unexplained rashes as a child. My father and sister have severe plaque so i always thought thats what psorisis was. At 33 i had a SLAP tear in my shoulder which they reattached. At 34 i had 2 major spine surgeries for ruptured discs in my neck that flattened the cord and caused cervical myelopathy. From that point on... I have had a never ending cycle of health issues and have seen multiple specialists. Colonoscopies, endoscopy, allergy testing, cardiovascular tests. Heavy metal tests, bloodwork over and over. Everyone kept blaming the myelopathy and hardware in my neck for the overwhelming fatigue. Then i saw an immunologist and he did allergy testing and told me i had a severe contact allergy to textiles and fabric dyes, so i had to eliminate dyes and synthetic fabrics. I have swelling in my fingers and toes and sometimes when i flare up i have swelling in my ankles. I am SO tired. The fatigue is killing me. I also have nail involvement (pitting, lines and flaking nails) and a patch of dandruf at the back of my scalp. All of these doctors and tests and it took ME figuring this out and realizing this is what i have been dealing with all along. Im 44 years old and i feel like im 60. I hate my life. This is a nightmare.

Thank you very much for all the fantastic and clear information ….watching from Adelaide in South Australia

Watching from Australia

Iceland

am currently awaiting a rheumatologist for evaluation for this disease

Bonsoir. Depuis plus de 3 ans je souffre de spondylarthrite ankylosante, diagnostiquée d'abord par l'ostéopathe de ma commune, confirmée plusieurs mois plus tard par un hôpital parisien. J'utilise des huiles essentielles (HE) pour soulager mes douleurs. Par exemple HE de gaulthérie et d'eucalyptus citronné diluées respectivement à 20 et 10%, avec huile végétale de calophylle inophylle, en massage selon besoin. Depuis plus d'un an, j'ai amélioré mon état en adoptant le régime hypotoxique du Dr Seignalet, ce qui ma permis de m'agenouiller et de réduire la fréquence des douleurs. Ce régime permet de neutraliser les symptômes dans 91% des cas.

Very difficult for me how can I bend my backbone left to right

i have severe arthritis in my neck and it really is horrible and scary

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at 16 gps would excuse it as gout it was mild at first just the big toe then to other parts of my body there medical treatment was drugs if one did not work then try another then the flair up would go away a month or 2 never more than two i first seek a rummy 45 by that time he put me on hurriar never did work hopt to 50 years old i know now that it is AS with bow backed they had me walking with a 4 wheel walker some time i couls to big box store and use a shoping cart and lean on the cart now i am at 62 useing only a walker and to get to my mobility scooteer and use that every day in spring and summer can not walk 20 feet before losing my breathing

I wish i could tal to someone, because cette maladie me détruit ca mepuis et mes ado pence que ses rien et que jdevrai travailler temp plien il comprend pas ma douleur,, et je ses pas quoi faire pour quelke comprendre, peut-être si quelqu’un d’autre leur expliquerais ca pourais nous aider , jem’appelle chritina Bélanger des uveite la spondylite et les hernies a losophage a cause des 14 pilule pas jour et des épidural de cortisone chu découragée 😞

Very gud exercise for As 👍👍

Bonjour je souffre de douleurs intenses au niveau de la colonne vertébrale des vertébrés cervicales depuis des années. Sa me réveille la nuit et je suis très fatiguée, du fait que ça me réveille la nuit.

I think I'm in this club now. High friends. "Feeling like your back is 90" exactly.

can you have AS without the hla-b27 gene ?

😢 This is so miserable. I had the biggest flair up of my life last week, and it’s so hard.

Hii hdb 27 positive who is this doctor the Ayurveda. And my hp fuse help me the my country India the middle class family 🥺🥺🥺🥺

Thank you very much I found that very interesting. Good luck best wishes

I have AS an UC and I get you man.

So glad i found this. I have been for a few blood tests, i had test done for rhumatoid arthiritis it came back false negative, my test for imflammation came back positive, my vitamin D came back low. I had xrays in my back/hip and hands they came back as nothing showing, my neck and back came back saying i have arthitis. Its so confusing as my worst pain comes from my back and hip, although my full body aches, i wake up 2-3 times a night with my forearms, elbow and shoulders aching, my hands ache, wrist, ankles, hip and lower back, And my groin. Also have plantar fascitits in both feet. I have been referred to a rhumatalogist but going to be a long wait. Dont know if i can wait months i have been trying to get this sorted for years this is them just doing these tests. I am so down about my day to day life, my pain on a good day is a 7 out of 10 on a bad day 10. So tired and fed up. Take meloxicam and dhyrcodiene, vitamin d, and onzeprole. Does anypne expierence snapping noise pinging sensation in joints at anytime?? I have not been diagnosed and i know i am probably self diagnosing here but everything i have saw about AS is basically the symptoms i have had for years just over the last 5-6 years its got worse but the last 2 years have been a living hell, like being tortured at times, knowing u can hardly move but know you need too. One of the worst parts is nobody knows how much i am suffering

Great stuff. Love the wall exercises, bird-dog, and seated hamstring stretches!

I have severe symptoms except nothing to see on x-ray.

😝 þrðmð§m

Great info❤️

I’m 44 was diagnosed at 18 but started at 15. You can take all the meds you want or need but take care of the mental side of this. It’s overlooked and often, the worst part about it.

I finally got diagnosed with ankylosing spondylitis at least I know what is destroying my life

I have this disease, it is absolutely horrible. I send my sympathies to all. For... those who are ignored and called paranoid, those who are told it is all in your head, those who are alone, those not alone but still feel alone because nobody understands and accuse you of 'asking for sympathy' or 'feeling sorry for yourself', those who are not super sexy and therefore are not only ugly, but also diseased and a deadbeat.

I hear that so much with myself even about how people are so athletic and then it just dies

Je suis attente de spondylarthrite ankylosante... j'ai su en 2019...en suite j'ai tombé enceinte... C'est un journée difficile...mais le fait de bouger, ne pas se arrêter aide. Vraiment ! Faites du sport, travaillez votre élasticité...allé à la piscine. Faites ce que vous pouvez pour continuer à bouger.

p̷r̷o̷m̷o̷s̷m̷ 😌

Quoi attendre d'autre d'une "Canadian Association" qu'elle EFFACE l'unique commentaire à son vidéo YT? ...

Diagnosed with AS at 43 last year, I'm still going through a grieving process of lost mobility and adjusting to daily pain. I've done quite a lot of investigation into managing the inflamation through diet and it seems possible. I'm still in discomfort daily but that's down to damage unfortunatly occoured undiagnoed over the years, I'm not having the flair ups, my energy continues to improve, I'm sleeping a lot better and there's the stiffness in the morning has diminished. I strongly suggest anyone with AS, or any other auto immine disease looks into a carnivore diet, just eating whoefood animal products. It sounds crazy, unhealth and unsustainable but that's because we're generally misinformed but it truley is not, and it will all make sense once you realise how nutrient dense meat and animal fats are and the corralation between leaky gut and autoimmune conditions are connected. Big love to all AS warriors out there xxx

Merci pour cette vidéo. En complément, je soigne ma spondylarthrite en suivant un régime sans amidon car les symptomes sont en rapport avec la bacterie Klebsiella. J'ai fait une courte vidéo de mon expérience pour vous aider : kzbin.info/www/bejne/o2eqgKinett8gLc

Merci pour cette vidéo. En complément, je soigne ma spondylarthrite en suivant un régime sans amidon car les symptomes sont en rapport avec la bacterie Klebsiella. J'ai fait une courte vidéo de mon expérience pour vous aider : kzbin.info/www/bejne/o2eqgKinett8gLc

More enlightenment need to be made because without that people won't know the truth about the existence of true cure for herpes virus from #drmadida. It's does works for real.

Yesterday i find out i have as I feel you bro

Beautiful video, thank you. 🙏✨👍👍