Originally, doctors thought opiods were useful when treating chronic pain. Richard Rosenquist, MD, Chair of the Department of Pain Management at Cleveland Clinic, discusses how this thought has changed over the years and why a treatment should be directed at treating the underlying cause rather than just masking the symptoms with opioid medication.

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So often we hear about narcotic use and the opioid epidemic in America. I've been on prescription narcotics for years due to chronic pain from a variety of issues, and I thought it was time to share my experience.

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Fourteen years of pain brought me to 2018, when I made the difficult decision to become a twenty-seven-year-old elective amputee. This channel is to document my journey of amputation surgery, recovery, and reclaiming my life.

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There are so many myths and misconceptions about chronic pain – here are eight that I've faced, and how I've handled them.

Kati Morton's Video:
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Fourteen years of pain and failed ankle surgeries brought me to 2018, when I made the difficult decision to become a twenty-seven-year-old below-the-knee elective amputee. This channel is to document my journey of amputation surgery, recovery, and reclaiming my life.

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How do I help reduce my chronic pain caused by endometriosis, EDS, arthritis and fibromyalgia through natural ways? As we know, debilitating pain, cramping, nausea, dizziness all seem to love those dealing with chronic pain. Here's a list of things I do to help myself.

(ps. if you're looking for a text version of this video then scroll down to 'Original article to this video' for the link) 🙂

Also…

Please remember: these are remedies that work on occasion and collectively for me. I am not a medical professional so please consult your doctor to make sure these remedies are allowed for you.

Time Stamp:

01:20 – pain relief method 1
01:50 – pain relief method 2
02:31 – pain relief method 3
03:23 – pain relief method 4
04:23 – pain relief method 5
06:05 – pain relief method 6
06:55 – pain relief method 7
07:34 – pain relief method 8
07:53 – pain relief method 9

~~~~~~~~~~~
Original article to this video:

Endometriosis and Adenomyosis Natural Pain Relief – My Journey
https://allthingsendometriosis.com/endometriosis-and-adenomyosis-natural-pain-relief-my-journey/

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[Closed Captions available] An introduction explaining why I wanted to create The Chronic Pain Tag; when you talk about it so much, the words lose their meaning, when so much time has passed, you forget what NOT being in pain is like, you can get a little lost in it. I want to take the time to refocus and share our experiences, because no experience with chronic pain is exactly the same. Spend some time with yourself and express how chronic pain affects your life. I created The Chronic Pain Tag in hopes of increasing visibility for this invisible disability and recognizing the diversity of experiences within it. I hope anyone who watches these videos are offered some insight as to what it's like to live with chronic pain and for those that do, the uplifting of our narratives and a sense of solidarity amongst those with shared experiences.

MY CHRONIC PAIN TAG: https://youtu.be/RGggA7Rh5IM

#TheChronicPainTag Questions
1) How/when did your chronic pain begin?
2) What kind of pain do you experience? What does it feel like?
3) Is it consistent or on and off?
4) Do you have of any specific triggers for your pain?
5) How does your pain limit you?
6) How do you cope with your pain?
7) When are you most comfortable?
8) How do you feel least supported?
9) How do you feel most supported?

I would love if you shared your experiences as well! Tag #TheChronicPainTag on Twitter, Tumblr, Facebook so we can all find each other!

New Videos Monday-Friday ‪#‎WithCaptions‬ Subscribe!

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ABOUT ME
Hello, hello! My name is Annie, my pronouns are she/her, and I'm a QWoC, body positive, disabled spoonie. I create videos five days a week (as long as my health allows) usually introspective topics, social topics, disability, body image, sex/gender/dating, feminism, etc, as well as a variety of music/artistic media, tags/challenges, and day-in-the-life vlogs.

*Currently working on captioning ALL videos, contributions are welcome!

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This was kind of a difficult video for me to film, if you enjoyed it and it encouraged you (hopefully!) please give it a thumbs up=)

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As the U.S. seeks to curb the deadly opioid epidemic across the country, many of the estimated 50 million Americans who suffer from chronic pain say they can’t get the medications they desperately need to ease their suffering.
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Chronic Pain Sufferers Say They’re Being Harmed By Opioid Crackdown | NBC Nightly News

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Postdoctoral scholar Biafra Ahanonu, PhD, studies the role the spinal chord plays in communicating chronic pain to the brain and the effectiveness of possible medications in treating that pain, in his talk "The Path to Pain: It's Not Only in the Brain."

https://www.ucsf.edu/news/2023/09/426206/wormnado-wiggles-its-way-win-postdoc-slam

#ucsf #ucsfpostdocslam

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In this talk, Trung Ngo proposes an interdisciplinary solution to address chronic pain and pain management. When faced with adversity, why do some people become stronger while others break down?

In the past decade, Trung Ngo has been exploring this question while treating people with complex, chronic pain at Mount Sinai Hospital.

Dr. Ngo has worked with leading clinicians and academics in pain rehabilitation and has published research in peer-reviewed journals. In 2017, he founded Novah Healthcare, a community-based clinic that offers an interdisciplinary approach to pain management. He also speaks regularly at public events in his quest to educate the community about chronic pain.

Outside of work, he is mastering the art of changing diapers. This talk was given at a TEDx event using the TED conference format but independently organized by a local community. Learn more at https://www.ted.com/tedx

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READ DESCRIPTION BELOW– (CW: health, chronic pain, possible motion sickness warning due to sped up shots of movement from 00:58-1:14 and 2:00-2:07)

I was never the tidiest person but becoming chronically ill has kind of worsened my cleaning habits AND made me feel crappy about it.

It gets worse because even if I wanted to (and sometimes I genuinely, sincerely want to. Is that me maturing? Or is that me realizing that I took my able body for granted?…) my body hits some hard limits. It's hard for me to stand longer than a minute or so, standing, reaching my arms up (like to hang clothes in the closet), or even bending down and hanging there or getting back up too quickly can trigger my dysautonomia, sometimes my arms experience more fragility and lifting certain weights can cause me injury or just hurt.

Today's video is the epic adventure of trying to get my room clean within a day, no naps, just a lot of pain levels peaking and having to stop whatever I'm doing in order to attempt to lower the pain enough to be able to function. The pain doesn't stop, it's always there; if my chronic pain were a person, they'd be permanently twisting the skin of my arm (metaphorically… because my pain is more often in my feet, legs, and back), just sometimes the skin twisting isn't enough and the person strikes me with a hard object instead and that's when I need some real recovery time.

At the start of the video I used the wrong language, I said, "whether I want to sleep or want to be awake" I wasn't actually referring to emotional desire but rather where I was chemically. The strange feeling that I was trying to describe before I interrupted myself was that I was physically exhausted because I did not sleep well due to pain levels but I reached the point of spiked adrenaline (from the lack of food/appetite and sleep perhaps. Adrenaline spikes in survival mode). This feels physically like dehydration, exhaustion, derealization, etc. but my body is filled with enough adrenaline that IT; my body, "wants" to keep moving.

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Annie Segarra (Annie Elainey) creates mainly first-person videos on introspective topics, social topics, sharing her experiences and thoughts on disability, body image, LGBT topics, gender equality, etc, as well as creative content; a variety of music/artistic media and short films. Annie identifies as a queer disabled (Ehlers-Danlos Syndrome) Latinx woman and uses she and they pronouns.

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[Closed Captions available, CW: visual text of q-slur at very end of video in "Previous Video" promo"] I created The Chronic Pain Tag in hopes of increasing visibility for this invisible disability and recognizing the diversity of experiences within it. I hope anyone who watches these videos are offered some insight as to what it's like to live with chronic pain and for those that do, the uplifting of our narratives and a sense of solidarity amongst those with shared experiences. For my chronic pain tag I tried to gather up all possible info about the pain I experience, but there is still stuff I managed to leave out, like how high the pain levels can get; how a flare once lasted 10 whole days, 10 whole days of being in so much pain that I couldn't move an inch, I managed to get out of bed for bathroom emergencies but the rest of my time was spend lying flat on my back, staring at the ceiling, perfectly still. Unable to turn my head to watch television, unable to sit up to eat, unable to bathe. I constantly experience a pain that feels more like muscle tension in my upper back, neck, and shoulders, but once again, didn't consider mentioning it because I dismiss it as something "everyone goes through". I am also still in search for a diagnosis and treatment and the majority of my time is spend on bed rest. When someone tells you they experience chronic pain there are so many things that could mean!

The Chronic Pain Tag (Explanation): https://youtu.be/CSFIO0Z_e3c

#TheChronicPainTag Questions
1) How/when did your chronic pain begin?
2) What kind of pain do you experience? What does it feel like?
3) Is it consistent or on and off?
4) Do you have of any specific triggers for your pain?
5) How does your pain limit you?
6) How do you cope with your pain?
7) When are you most comfortable?
8) How do you feel least supported?
9) How do you feel most supported?

I would love if you shared your experiences as well! Tag #TheChronicPainTag on Twitter, Tumblr, Facebook so we can all find each other! Tag #TheChronicPainTag on Twitter, Tumblr, Facebook so we can all find each other!

New Videos Monday-Friday ‪#‎WithCaptions‬ Subscribe!

HELP ME GET TO VIDCON: http://bit.ly/1XI8Ez6

If you enjoy my videos, please consider supporting this channel and/or my medical funds:
Patreon: https://www.patreon.com/annieelainey
Medical Expenses, Pain Relief, and Mobility Devices: http://bit.ly/1U62Kti
PayPal: http://bit.ly/1D7QYW2

ABOUT ME
Hello, hello! My name is Annie, my pronouns are she/her, and I'm a QWoC, body positive, disabled spoonie. I create videos five days a week (as long as my health allows) usually introspective topics, social topics, disability, body image, sex/gender/dating, feminism, etc, as well as a variety of music/artistic media, tags/challenges, and day-in-the-life vlogs.

*Currently working on captioning ALL videos, contributions are welcome!

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Will Humble says it's the way government is supposed to work. A 2018 state law cracking down on opioid prescriptions had the unintended consequence of depriving chronic-pain sufferers of vital medication. Humble, a former Arizona public health director, says a new law taking effect later this year should provide some relief. The sponsor, Republican State Rep. Nancy Barto, said she got the idea talking to residents in her district.


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Alternatively titled: Why Being Called "Lazy" While Chronically Ill Hurts So Much

My entire life I've been the opposite of lazy, I've always been working, I've always put too much on my plate in regards to activities and work because I love doing things! Since my health decline because of EDS, my limits have drastically changed but my drive and my burning desire to create is still there. It feels like any time I am able to accomplish something I'm doing it with metaphorical 50 lb weights around my arms and legs, it's much more challenging now and it leaves me wondering when am I allowed to rest? How long am I allowed to rest? When should I be pushing through symptoms to get things done? What are the possible benefits and consequences of doing so? I try to find my balance but it never feels like enough. And I'm not even talking about economic survival but the work of our passions, the things we wake up in the morning for, our survival in regards to our mental health. How can we do that for ourselves when our physical health knocks us down so hard and so frequently? What do you all think?

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Annie Segarra (Annie Elainey) creates mainly first-person videos on introspective topics, social topics, sharing her experiences and thoughts on disability, body image, LGBT topics, gender equality, etc, as well as creative content; a variety of music/artistic media and short films. Annie identifies as a queer disabled (Ehlers-Danlos Syndrome) Latinx woman and uses she and they pronouns.

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Opioids for chronic pain don't work: here's why!

For more on WHY opioids don’t work for chronic pain and why the repeated prescribing of opioids for chronic pain is a major issue, check out the full video here: https://youtu.be/CtmJN8VmgEM

#shorts

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DISCLAIMER: The Wellness Puzzle is intended for educational and reference purposes only. The videos on my channel, content on my website or on social media are not intended to be a substitute for professional advice, diagnosis or treatment by a healthcare or medical professional. You should always carry out your own research and seek medical advice where required regarding a medical condition. Never disregard professional advice or delay in seeking such advice because of something you have heard on this video or read on my blog or website.

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hi artists! This week I’ll be talking about some of my favorite tools that help aid in living with chronic pain and fatigue. I have psoriatic arthritis and fibromyalgia, so being an artist living with these is sometimes a big challenge. I know many of you have your own diagnosis and thought I’d make a video on what helps me.

Disclaimer:
These tools do not provide medical advice. It is intended for informational purposes only. It is not a substitute for professional medical advice, diagnosis or treatment. Never ignore professional medical advice in seeking treatment because of something I have recommended here. If you think you may have a medical emergency, immediately call your doctor or dial 911.

Products mentioned in this video:
Compression gloves:

https://amzn.to/2Y95mRr
Wrist brace: https://amzn.to/3B3oQFv
CBD lotion: 2021’s 5 Best CBD Creams for Pain: Warming, Cooling, Inflammation
Avexia 1:1 Harmony Topical
SHEIN blouse:
https://www.amazon.com/dp/B08DT4L34H/ref=cm_sw_r_as_gl_api_glt_fabc_NVFKQ0GH950DFN15CQJ9?_encoding=UTF8&psc=1&linkCode=ml2&tag=artistjanebus-20

Makeup:
Halsey’s About Face Fractal Glitter Eye Paint:https://bit.ly/2Y39KBk
Colourpop I Lilac You A Lot eyeshadow palette: https://bit.ly/3B3DIUe
CC Beauty Flash Palette*: https://amzn.to/3l18LKM
LA Girl Line Art Matte Eyeliner in White*: https://amzn.to/3B2bARF
NYX epic ink eyeliner in black: https://amzn.to/3miVoVM
Maybelline Sky High lengthening mascara*: https://amzn.to/3iokqBW
Essence What The Fake! Volumizing & Lengthening Mascara*: https://amzn.to/3CUA7sm
LA Girl Shockwave Neon Eyeliner: https://www.ulta.com/p/shockwave-eyeliner-pimprod2003318
J.Cat Beauty Masterclass Face/FX Neon Palette: J.Cat Beauty Master Class/Fx Color Palette Neon | Ulta Beauty
Wet n Wild Megalast Matte Lipstick: Wet n Wild MegaLast Catsuit Matte Lipstick | Ulta Beauty
Colourpop BFF Lipliner in Jubilee: https://colourpop.com/products/jubilee-matte-liner-pencil

*amazon links are affiliate links.

http://www.janebushartist.com

Follow Jane on Social Media For More Inspiration!

IG – http://www.instagram.com/artistjaneb
Tiktok @ artistjanebush
Facebook page: http://www.facebook.com/touchedbyfirephotos

Jane's Concert Photography Gallery:
http://www.flickr.com/photos/artistjanebush

#fibromyaglia #spoonies #autoimmune

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Osteoarthritis treatment | Osteoarthritis Home Remedies | Arthritis Treatment | Joint Pain Treatment | OA treatment | OA signs & symptoms

Here we have discussed some Home remedies for osteoarthritis.

Hot & Cold Compress:
When it comes to pain, hot and cold compresses may be very beneficial. Compresses can reduce muscle pain or spasms surrounding a joint.
Making a compress can be as simple as using a warm or cold towel.

Epsom salt baths:
Epsom salt baths can provide all-over relief, especially for joint pain. The

Osteoarthritis-friendly foods:
Glucosamine and chondroitin are one of the most popular nutritional supplements.

Avocado-soybean unsaponifiables. This nutritional supplement which is used in Europe to treat knee and hip osteoarthritis. It acts as an anti-inflammatory, and some studies have shown that it can slow or even prevent joint damage.

Omega-3 fatty acids. Omega-3 fatty acids, found in fatty fish and fish oil supplements, might help relieve pain and improve function.

Maintaining a moderate weight.
Carrying extra weight increases the stress on your weight-bearing joints, such as your knees and your hips. Even minor weight loss can relieve some pressure and reduce your pain. Talk to a dietitian about healthy ways to lose weight.

Physical therapy and Occupational therapy
A physical therapist can show you exercises to strengthen the muscles around your joint, increase your flexibility and reduce pain.

Occupational therapist can help you discover ways to do everyday tasks without putting an extra stress on your already painful joint.

#osteoarthritis #osteoarthritistreatment #osteoarthritishomeremedies #jointpain

Medical disclaimer: Medinaz Academy does not provide medical advice. The content available in our books and videos, on our website, or on our social media handles do not provide a diagnosis or other recommendation for treatment and are not a substitute for the professional judgment of a healthcare professional in diagnosis and treatment of any person or animal. We intend to provide educational information only. The determination of the need for medical services and the types of healthcare to be provided to a patient are decisions that should be made only by a physician or other licensed health care provider. Always seek the advice of a physician or other qualified healthcare provider with any questions you have regarding a medical condition.

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Did you know that 70% of disabilities aren't obviously apparent? Because in my experience going to specialists, it seems like doctors don't know that… but anyway, if you're wondering what it's like to have invisible disabilities, this is the vid for you
——————
Autism Resources:
Ultimate resource guide – https://www.disabledautisticlesbian.com/resource-guide
How to support an autistic person – https://www.disabledautisticlesbian.com/im-the-parent-of-an-autistic-kid
Help! I think I’m autistic – https://www.disabledautisticlesbian.com/help-i-think-im-autistic
Unmasking/How to Start Over – https://www.disabledautisticlesbian.com/i-want-to-start-over
——————
Hey! I just had an album come out! You can check it out here – disabledautisticlesbian.com/rewrite-history

Also a new EP you can check out here – https://youtu.be/6pGSdJWO7Bs

If you want to support me financially, you can…
Buy me a smoothie! – https://www.paypal.com/paypalme/sydneyzarlengo
Check out my merch! – https://www.disabledautisticlesbian.com/shop
——————
My Music:
Alive (Single) – https://li.sten.to/alive
Start Over (Album) – https://li.sten.to/start-over
The Confused Linguist (Album) – https://li.sten.to/the-confused-linguist

Find me on Bandcamp – https://sydneyzarlengo.bandcamp.com/music

Check out my #ActuallyAutistic playlist made of entirely autistic artists!
https://open.spotify.com/playlist/3gIiA3ZPsZlx8lZXWdJv6U?si=0mU6TSvXRcmDpn-ff6aq9Q
——————
Hello my dears!
My name is Sydney and I’m an actress/singer-songwriter who writes music about my experiences being autistic, disabled, gay, and in general, a human. My goal is to fill musical gaps and write about things people often forget to make music about. I’m also a vintage enthusiast and disability advocate (among other things). I’ve now released 3 albums and, most importantly, my favorite color is buttercup yellow.
——————
Find me on…
Facebook – https://www.facebook.com/Sydney-Zarlengo-110498164188464/
Instagram – https://www.instagram.com/disabled.autistic.lesbian/
Website – https://www.disabledautisticlesbian.com/
Email – disabled.autistic.lesbian@gmail.com
——————

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Cold exposure can help an individual's perception of chronic pain. Dr. Drew Timmermans, ND, talks about how we can help change our body's perception of stressful stimuli and pain. To put it simply, if we train our body and mind to perceive less pain, we can see shifts in perception of pain in the long term.

Thank you so much for watching! My hope is to create a community where you feel like I provide value to your life. If you feel this is the case, please take a second to introduce yourself, add a comment, or share this video with your closest circle.

// Subscribe to my channel here: https://www.youtube.com/user/dmackayt?sub_confirmation=1

// Sign up to purchase physician-grade neutraceutical supplements here: https://us.fullscript.com/welcome/rp.

// Want to see everything I've got going on at the time you watch this? Check out my TapLink here – https://taplink.cc/regenerativeperformance

Want to connect with me?
// Instagram: http://instagram.com/regenerativeperformance
// TikTok: https://vm.tiktok.com/ZMJP85fKn/
// Facebook: http://facebook.com/regenerativeperformance
// Snapchat: http://snapchat/add/regenperform
// LinkedIn: https://linkedIn/in/dmackayt
// Twitter: https://twitter.com/dr_timmermans
// Website: https://regenerativeperformance.com
// Podcast: coming soon

Bio:
Dr. Timmermans is a licensed naturopathic doctor in Gilbert Arizona with a passion for helping his patients overcome chronic pain to reclaim their life. This passion is what drives him to think outside the box when helping patients who are looking to reduce/resolve pain. and avoid surgery if possible. With a clinical focus in regenerative injection therapies such as prolotherapy, PRP, and autologous cellular therapy, he takes a holistic approach to healing from chronic pain.

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In January I had surgery to correct a bone deformity after being told it was the cause for the chronic pain I had been experiencing for almost a year. The recovery process from the surgery was incredibly painful, but after a final analysis from my doctor, it turns out that my pain is unrelated to the surgery. It's the same pain from before the surgery only it has gotten so much worse, to the point I cannot put weight on it at all. Now we are in the market for a new diagnosis. Until we can diagnose and start treatment, it seems I will need a wheelchair as a mobility device.

Please if you can donate to my medical fund:
https://www.youcaring.com/annie-segarra-470698

OR

PayPal http://bit.ly/1D7QYW2


Let’s be friends!!
http://annieelainey.tumblr.com
http://instagram.com/annieelainey
http://twitter.com/annieelainey
http://facebook.com/annesegarra

PLEASE SUBSCRIBE
http://youtube.com/theannieelainey

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https://www.footankle.com/gout/ If you are having a gout attack learn how to get relief as fast as possible. Gout can cause severe and debilitating pain in your foot. Caused by an excess production of uric acid crystals, gout can be one of the most painful conditions you can experience. Seattle podiatrist Larry Huppin reviews the most effective treatments for an acute and painful gout attack.

If you are in the Seattle area appointments can be made from our website at http://www.footankle.com/

Dr. Larry Huppin has practiced podiatric medicine in Seattle for over 20 years and treats ingrown toenails every day. His techniques allows for virtually painless treatment of ingrown nails.

We are located at:
Foot & Ankle Center of Washington
600 Broadway, Suite 220
Seattle, WA 98122
206-344-3808

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