#Arthritis Support

[waywardpostartisan]

[drrestoknee]

Eating Right for Osteoarthritis (OA) of the Knee

Managing osteoarthritis (OA) of the knee isn't just about medications and therapy—your diet plays a crucial role in supporting joint health and reducing inflammation. Eating the right foods can help alleviate symptoms, maintain a healthy weight, and slow the progression of the disease.

[eathealthy]

A Game-Changer for Joint Health: My Experience with JointEternal Supplements

As someone who has been dealing with occasional joint discomfort for years, I’m always on the lookout for effective ways to support my joint health. After coming across JointEternal Supplements, I decided to give them a try, and I am thrilled to share my positive experience.

Why I Chose JointEternal

I chose JointEternal Supplements after doing extensive research on joint health products. The blend of scientifically backed ingredients, including glucosamine, chondroitin, and turmeric, immediately caught my attention. These are known to support joint flexibility, reduce inflammation, and improve overall mobility. The promise of a natural solution made this product stand out, and I was eager to see if it lived up to the hype.

Noticeable Improvement in Mobility

Within the first few weeks of using JointEternal, I noticed a significant improvement in my mobility. Previously, activities like climbing stairs or going for long walks would leave me feeling stiff and sore. After incorporating this supplement into my daily routine, these tasks became much easier. I felt a newfound lightness in my movements and was able to engage in physical activities without hesitation.

Effective Pain Relief

One of the standout benefits of this supplement has been the relief it provided from occasional joint pain. Before trying JointEternal, I often experienced discomfort in my knees and lower back, especially after a long day. Since using this product, the discomfort has noticeably reduced. I attribute this to the anti-inflammatory properties of turmeric, one of the key ingredients in the formula. It’s clear that the product is designed with care and attention to detail.

Easy to Incorporate Into Daily Life

The convenience of using JointEternal is another factor worth highlighting. The capsules are easy to swallow, and the recommended dosage fits seamlessly into my routine. Unlike some other supplements I’ve tried, these didn’t cause any stomach upset or side effects. The company also provides clear instructions, which makes it hassle-free to follow.

Backed by Quality and Trust

I appreciate that JointEternal is made from high-quality ingredients and adheres to strict manufacturing standards. Knowing that this product is created by a brand that values transparency and customer satisfaction has given me additional confidence. The packaging is also sleek and professional, reflecting the care that goes into the product.

Overall Results and Recommendations

After two months of consistent use, I can confidently say that JointEternal Supplements have made a positive difference in my life. My joints feel stronger, more flexible, and less prone to discomfort. I now look forward to staying active and pursuing hobbies I had previously avoided due to joint issues.

If you’re searching for a reliable supplement to support joint health, I highly recommend giving JointEternal a try. It’s a game-changer for anyone seeking a natural, effective solution to joint discomfort. This product has exceeded my expectations, and I plan to continue using it to maintain my improved joint health.

[disabled-bug]

Reminder at all, someone with a disability/chronic illness might be capable of completely different levels of activity from day to day. You can’t hold yourself or others to the best version of the physical self every single day. That goes for able bodied people too! Energy levels fluctuate, and for people with a disability/chronic illness that difference will be even more extreme.

Be patient. Be gentle with yourself and others.

Just because the other day you did a workout, went grocery shopping, and/or washed your hair, it doesn’t mean you’re less valuable today while you’re stuck in bed.

Be kind to yourself.

[twilightkitkat]

HEAR ME OUTTTTT YALL

Logan's bones are made of metal, right? And while adamantium is a fictional element, metals tend to follow a set of properties.

One primary property is that the majority of metals are conductors. This is reinforced in The Wolverine movie wherein the adamantium sword conducts heat extremely well to be able to cut off Logan's claws.

Therefore, Logan's bones are conductors (for both heat and electricity).

Most human bones (like Wade's) are insulators. This makes bones more resistant to electricity as compared to the rest of the human body, which is an electrical conductor because it's composed of water and ions.

I know the dark matter is different, but from how we see it flow through the veins and transfer we can assume it's conducted as well.

THEREFORE, THE REASON LOGAN WAS ABLE TO ALMOST INSTANTLY FORGE THE CONNECTION WAS BECAUSE HIS BONES CONDUCTED THE ELECTRICITY EASILY. AND IT WOULD ALSO MEAN THAT HIS PAIN WOULD BE SIGNIFICANTLY WORSE THAN WADE'S. BECAUSE HE LITERALLY FEELS IT RUNNING THROUGH HIS BONES, JITTERING HIS VERY SKELETON?? BUT HE STILL KEPT HOLDING ON JUST TO SAVE WADE.

Also, this means that his bones would retain heat. If he sits in front of the fire and gets heated up, he'd feel it in his bones. This means the human heater headcanons are 100% true, because he'd literally be hot metal wrapping around Wade if he's kept warm.

Inversely, however, this would mean his bones become cold due to a lack of heat. Metal oftentimes expands in hot conditions and contracts in cold conditions (which is why they leave gaps between train tracks to accommodate for this without them breaking).

So Logan would 100% get aches with cold weather because even if his body was more resistant, he can feel the chill in his bones and how they don't sit quite right and everything is too stiff and doesn't fit. (And Wade would need to heat him up instead because of this.)

Plus his thermal regulation would be compromised because it seeps into his bones instead of just his flesh. Imagine you get in front of a fan and your skin feels cool but your bones are hot. Logan would be temperature-sensitive, but he'd try to hide it because he's used to it (having lived in the mountains for years) and doesn't know what to do. (And so when Wade comes along and cares and tries to help him regulate, he nearly chokes up because it's so much easier to cope.)

[funyiipp]

I'm in an art block period, ho-hum.

This is all I could muster.

[himegyaruo]

why is literally everything so draining , skincare is draining , brushing my teeh is draining , taking a bath is draining , drying my hair is draining , walking up&down the stairs is draining , making food is draining . id ask for help but im home alone pretty much everyday , and thats draining

i sit in bed all day & feel bad & lazy about it

[johnnyiscaged]

happy disability pride month to every disability! remember there is no such thing as disabled enough use the aids you need

[wheelchairbarbie]

[burythecarnival]

hi hello, well met my sweet tumblrites 🖤

i am having such a bad fucking time. any help with meals today & tomorrow would be incredibly appreciated.

an antipsychotic was added to my endless list of medications; i am having a bit of a dangerous reaction... like, i thought i was going to have to call an ambulance in the middle of the night because i felt like i was having a fucking heart attack then came too close to fainting.

i will be off the antipsychotics for today & tomorrow but, am trying to rest as much as possible. standing & cooking sounds like some sort of hell. nothing is expected, everything is appreciated 👻💋

cashapp: $dryboneslive / venmo: dryboneslive

[crazycatsiren]

You are not too young to have arthritis.

Do you hear me?

Disabilities are not ageist!

[calicobeesblog]

A little life update:

Earlier this week me and my boyfriend went to a shopping centre we’ve never been to before.

I was hoping I’d be able to walk around fine but we went and had food and walked around for 25-30 minutes before I started feeling feint and exhausted. Luckily the centre we were at had a shop mobility so we could rent a wheelchair.

(It was silly because I felt like I needed to over explain why I needed that wheelchair to the person there, but she was genuinely so polite about it)

We were able to have another 3 more hours going round before we called it a day. We also went to the arcade and played air hockey and my boyfriend won me a plushie from those claw machines (genuinely impressed with him I can never work out how to get something).

Visual evidence of me in a wheelchair whilst my boyfriend was trying to work out what shops we could fit in with it. And “Noodle” the Dino plushie he won for me.

Also I have a doctor’s appointment tomorrow that I’m STRESSING about. I just hope I get some sort of an answer.

I keep on forgetting that I’m still learning what my body can and can’t do right now which isn’t great but I’m thinking of investing in a wheelchair that I can just keep until I need it for long days out.

[inseparabiles]

observing that there might be a connection between significant levels of pain and poor mood

[talkethtothehandeth]

*vague posts a fake claim about particular people in mind*

*turns around to say they would “never” want to fake claim someone because they know how it feels*

Gaslighting IS fake claiming, it is literally denying the extent of which a disorder/condition affects a person, and replaces it with “it’s all in your head, you’re doing it for attention”

And it pisses me off so much because the comment section is FULL of people who you know would be sobbing and throwing up and claiming ableism if someone even thinks about doubting the severity of their disabilities.

Get over the Sick Olympics already, no one fucking wins that. You get no trophy for being the sickest, no one automatically cares about you more when your body gets worse, doctors don’t suddenly give a shit if you’re dying from complex conditions. You’re not special, you don’t get a crown. You’re not better than anyone at all if your body is breaking down the most. Why is it so important to you to be The Worst? Ass pats? No one gets that and the worse you are the less people care about you, genuinely.

Get over yourself, you don’t know shit about what anyone else on the internet goes through, and fake claiming anyone is fucked up, regardless if the person is shitty or not. I hate that the internet learned the term Münchausen Syndrome because if someone doesn’t present exactly how they think they should be if they’re “truly” sick, then they’re faking the way their current symptoms present because it must not be “that bad”.

Wait until people start turning against you, then you’ll realize exactly how shitty it is to have people who are supposed to be on your side act against you because you’re not “sick enough” to them to actually be suffering— you’re not “sick enough” to receive sympathy. Imagine how isolating that is, to have so many people against you because they think you’re not as bad as you know you are. People have their own websites and never ending threads dedicated to “proving” that someone is faking, some of my mutuals are on those threads and have posted about it— without them I wouldn’t have even known these threads existed. Imagine how many you’re on, how many people are talking about you behind your back, even in your own circle.

By the way, I would rather believe 400 (“undiscovered”) fakers than deny support to one person who is actually disabled. And you should too, because one day, you will be that one person who is actually sick, and you will be considered a liar, or dramatic— and in some people’s opinion, you’ll deserve that treatment after what you did and continue to do all in an attempt to feel superior to someone. One day you won’t have the sympathy you’re looking for.

[wheelchairbarbie]

[burythecarnival]

well met, majestic tumblrites 🖤 i have been so fucking sick; i am not ignoring anyone! the pain from the arthritis flare, edema flare, inflamed spine & feeling like my tissue & muscles are corroding is making me so tired. my kidneys feel like they were stabbed & i am so fucking nauseous even after max zofran doses.

i need to try to eat, get some groceries & order new arthritis gloves because i have no clue where one of my kitties stashed them 🐈‍⬛

help is not expected but it is immensely appreciated. do not apologize if you cannot help! life is a wretched cock for plenty of people right now 💋

luv, cuddles & cauldron bubbles, the ghost queen 👻

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cashapp: $dryboneslive / venmo: dryboneslive