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Autoimmune awareness month - Pain & Fatigue symptoms  

Ankylosing Spondylitis Man
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Autoimmune awareness month - Pain & Fatigue symptoms #disabilities #health #reel
As part of the Autoimmune Disease Awareness month, I talk about the two big symptoms of pain and fatigue.
Let me know what these feel like for you, and how they affect your day to day life.
#awareness #pain #ankylosingspondylitis #hack #arthritis #disability #asawareness #axialspondyloarthritis #axspa #spoons #spoon #spoonie #lifestyle #life #energy #level #health #condition #chronic #chronicillness #chronicpain #back #backpain #spine #mentalhealth #mentalhealthawareness #theory #autoimmune #autoimmunedisease #depression #anxiety #anxietyrelief #anxious #treatment #psychology #psychologyfacts #psychiatrist #medication #biologic #anti-inflammatory #inflammation #sleep #sleepdeprivation #effects #symptoms #insomnia #instagram #youtube #tiktok
#tiktokvideo #viral #warriors #warrior #struggle #disorder #rheumatoidarthritis #thyroid #HLA-B27 #hlab27 #hlab27positive #positive #negative #dwp #application #departmentofworkandpensions #sunflower #lanyard #claim #reapply #pip

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27 мар 2024

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Комментарии : 16   
@davetherave597
@davetherave597 4 месяца назад
The people who need the awareness are the doctors it baffles me how little they know about AS and the symptoms that come with it
@AnkylosingSpondylitisMan
@AnkylosingSpondylitisMan 4 месяца назад
It certainly seems that there's massive inconsistency from doctor to doctor, and country to country.
@silvermoonuk
@silvermoonuk 4 месяца назад
I've got fibromyalgia/scoliosis/restless leg syndrome....even on a good day, I feel crap. Even with medications, I still feel crap. I might have the odd day where my symptoms aren't as bad, but I'm never symptom free. I don't like the chronic pain. But I find the fatigue/stiffness horrible. My type of pain is different on each body part. So my feet feel like they are burning. My arms feel like someone is pinching them. My other parts of my body feels more dull and irritating can a pain. I constantly feel heavy in my body. I always walk slow even on a good day, due to the symptoms. It's not nice having a chronic disability/health issues. But what I find harder is the lack or minimum amount of support from medical and social services for ppl with chronic health issues. I also struggle with the stigma disabled ppl face whilst they are on disability benefits as well. As a disabled person myself, I always worry what others think of me: for example, if I have the odd good day, and I want to do something positive or productive (such as go for a gentle walk) I often feel other ppl would assume I'm faking my issues. I feel ppl like myself cannot win, as if we just lay in bed all day, then we are seen as lazy but if we try to be productive with our day, then we are seen as not that disabled or that we are faking our issues. Does this make sense? Big hugs 🫂 🤗 🫂 🤗
@AnkylosingSpondylitisMan
@AnkylosingSpondylitisMan 4 месяца назад
Totally agree, and understand your situation, especially the stigma of people with disabilities and benefits. There seems to be quite a hatred online. 😞
@davetherave597
@davetherave597 4 месяца назад
@@AnkylosingSpondylitisMan it's not just online you are treated differently by doctors if you don't work ,the last GP I seen said to me "you should get a job you don't want to be sitting around all day"
@SacredOwl
@SacredOwl 3 месяца назад
I could have wrote exactly everything you did. Chronic pain makes you not able or feel like doing anything, even when you might not be feeling a lot of pain at that moment, it's like you are in recovery mode for that short window. What time is the worst pain? You get hit just before it gets light out? I have the burning feet also btw. I notice that sugar makes my pain so much worse, but I don't do anything about it.
@SacredOwl
@SacredOwl 3 месяца назад
I have adheasive aracanoiditis and no disc at L5 S1. The pain flare-ups are severe and no medication can touch the pain, even morphine. I discovered that the pain flare-ups have a correlation to solar flares and a few other space weather factors. I built a shielding box and now I can go from 10 pain level to 0 pain and inflammation in less than 5 minutes with this shielding box I made. I have been using it for over ten years and shared it with a lot of other people who found the same relief. Except one person it didnt work for and that was someone who just had surgery. My wife uses it for her seizures. Migraines and it works really fast for her Fibromyalgia. Apparently this space weather acts on damage and triggers pain and inflammation. You may notice that there are random times and times that pain flare ups occur; i found that there are windows and it so happens to match up to something called magnetic reconnection. At bed time, 2am 3am and just as the sun is coming up. 3pm os another bad time. Magnetic reconnection tomes are not always strong enough.
@AnkylosingSpondylitisMan
@AnkylosingSpondylitisMan 3 месяца назад
What did you make the shielding box from?
@SacredOwl
@SacredOwl 3 месяца назад
@@AnkylosingSpondylitisMan I made a few differnt ones. 2 inches thick of foil faced Polyisocyanurate. Make sure you use half inch or thinner sheets so it is in layers to make 2 or.more iches. Use aluminum tape to put together. Add several layers of extra foil on outside, i use heavy duty roll from cost co . Cut in a fan. Better if you draw air through several feet of metal duct and put copper scouring pad inside, also ground box... but it will work either way with grounding and extra duct. Depending on the problem, the box needs to have door closed. For back pain and some other issues you will find the door can be open. For geo magnetic issues like migraine and seizure, the box needs to be sealed well and where the duct and grounding may be better, depends on how sensitive someone is to geo magnetic activity (Induction), like my wife is. The vornado 8 inch fan is the best, they last a long time...a fan with air going in and one going out is best. I have tested and used for over ten years. I can walk you through anything. Alternative materials that cost more are HDPE and stainless steel. Geo magnetic activity is very low frequency, I was supposed to find out that stainless is best for this, but cost a lot. I did build a box with HDPE, it cost me a lot of money but I think it was overkill. I tested for over ten years thousands of times with measly every medical episode, some more and some only a few times. I can tell you which ones it worked for and some it had no effect. There are some surprises like a no. Stop cough (like we experienced during lockdown days) and Fibromyalgia takes about 30 seconds. I believe the space weather Activates epithelial and inflammation because in a study from July 2022 they showed solar flare activates endothelial and inflammation. The implications of endothelial I feel is really big becaus it lines out entire body, vascular system and some organs, may explain why space weather is such a primary trigger. Just my thoughts.
@SacredOwl
@SacredOwl 3 месяца назад
@@AnkylosingSpondylitisMan excuse the spelling errors .. I wrote fast while having lunch. Lol. I tried to leave a link to my yt that shows the box, but yt didn't let me
@SacredOwl
@SacredOwl 3 месяца назад
@@AnkylosingSpondylitisMan You can also use Galvanized Steel Roll , it is an excellent metal. It is important to use the foil faced polyisocyanurate (unless you use HDPE) because very few materials strip a muon or HZE high energy particle. We are mostly blocking two different things that occur opposite half the time and trigger specific types of episodes. If you use the roofing roll of galvanized metal, the edge is razor sharp, so be careful. If you ground the box woth a plug in the wall, please buy a cheap tester for 5 bucks and test for a hot ground.
@SacredOwl
@SacredOwl 3 месяца назад
@@AnkylosingSpondylitisMan if you are doing an entire room, it's easy just to use foil and polyisocyanurate. Don't worry about all the other stuff. Also, Best to not have metal facing inside the room as the last layer, you can also paint it if you have the metal facing against the wall. Using the anti wifi 5g paint at H depot would be awesome, you would be covering a wide range.... very peaceful, sleep is awesome either way.
@MissMoToYou
@MissMoToYou 4 месяца назад
Mine is always between 4-9 constant. The lower back doesn't give me problems as it's fused now. But the rest of my body is all affected. Ribs are the worst at the moment, and i have a lung function today 😢 i know it's going to hurt so much. I couldn't sleep very much at all for all different reasons, but cbd and the thc oils really helped. Still have the odd bad nights. Im on cosentyx 2 every month. I also have fibromyalgia, do any of you? Xx
@AnkylosingSpondylitisMan
@AnkylosingSpondylitisMan 4 месяца назад
Did the fusing of the lower spine hurt?
@MissMoToYou
@MissMoToYou 4 месяца назад
​@AnkylosingSpondylitisMan Yes, that was one of my first signs. I was in a wheelchair for about 2 years......back in one now, tho after fractured T11
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