popularpennysave posted Yesterday 03:16 AM
Item 1 of 10
Item 1 of 10
popularpennysave posted Yesterday 03:16 AM
$21.47*:AccuRelief Wireless Tens Unit and EMS Muscle Stimulator - Includes Pulse Massager - Pain Relief Device with Remote and Mobile App, TENS Machine, TENS Device
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Our community has rated this post as helpful. If you agree, why not thank bluekiwi
Some of my best tools are a heating pad, percussion massager, light exercise bands just to move a bit, and an acupressure mat like this one: https://a.co/d/4wrTbWN
It can feel like torture getting off of it with bare skin, but the pain relief is real. It really does palpably send a flood of blood and endorphins to your muscles.
I'm assuming you also have CFS. Have you heard of PEM (Post Exertional Malaise)? I recently found that there's a name for all my complicated and confusing fibro/CFS symptoms. It's not in your head! Hang in there!! 👍
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I found out that I had endometriosis at 22 and then at 30 fybro, cysts and fibroids.2 years ago I found out I had a pinched nerve on each side of my neck 🤷I just turned 50 a few days ago but I feel like everything is colliding together and the pain has been on another level.
I'm a mom so I have always pushed myself to keep going, even if that means crying,balled over because of the intense pains and still cooking, cleaning etc...I will definitely purchase the mat and I'm not sure if I should order this item post but I will definitely keep looking for something. I'm so sorry that you have fybro as well , I wish they would find a cure for it. Taking opioids when you have fybro is like eating a tick tac or like a fake hug, you know that pat pat hug lol it just sucks.
I'm sorry I'm so long winded my apologies to everyone on slick deals, I truly just needed some help. If I had to take a guess about how many days of a year span that I have slight to no pain, perhaps 65 days out of the year. In person you would never know because I'm always smiling, but if I cry it's a wrap that means I feel like someone is breaking my body into pieces... I truly pray that no one else is going through this and if you know someone who is, be understanding when they break down because it messes with your mind and spirit....
Some of my best tools are a heating pad, percussion massager, light exercise bands just to move a bit, and an acupressure mat like this one: https://a.co/d/4wrTbWN
It can feel like torture getting off of it with bare skin, but the pain relief is real. It really does palpably send a flood of blood and endorphins to your muscles.
I'm assuming you also have CFS. Have you heard of PEM (Post Exertional Malaise)? I recently found that there's a name for all my complicated and confusing fibro/CFS symptoms. It's not in your head! Hang in there!! 👍
https://a.co/d/9PahA8p
But if you're unsure, you could start with the mini unit:
https://www.ireliev.com/products/...91ec&_ss=r
I can only speak from my experience, but I've had a variety of pain issues for years, where I was in so much pain I was snapping at my partner. After one day of using the tens unit about 4 times (30 min each) and it eased the pain approximately 60%? It was enough where it was bearable again. I'm pain free for the most part these days, but I still use it from time to time and it helps me tremendously.
Of course, it may or may not work for you; everyone's different. But my experience was life changing.
By the way, I thought slickdeals used to have a private message system, but I can't find it anymore, so my long reply is here.
Watch this video about Post-Exertional Malaise: https://youtu.be/cGQFGgb_PtA?si=
I stumbled upon it, and I'm not kidding, my wife and I were in tears watching it. It's like the doctor had a window into my life, with all its confusing and chaotic symptoms. This condition has a name, and it's real, and its NOT IN YOUR HEAD!
In a brief summary, PEM explains why you crash for no apparant reason, and then your symptoms skyrocket and you're barely hanging on. Let me know what you think...
Another recent thing I've tried is Cannanda CB2, a targeted terpene in CBD oil that is specifically for fibro symptoms. Not that expensive, maybe give it a try. https://cannanda.com/en-us/collec...438614
If you'd like to chat further, I'm at my slickdeals screen name followed by the opposite of coldmail.com (think that'll fool the bots? 😂)
Another thing I've found that's important, especially after watching the PEM video, is to show it to your loved ones and older kids. Not out of looking for sympathy, but because they NEED TO KNOW what Mom is going through. Our disease is so strange and arbitrary and changes by the minute or hour. It often feels like someone has a voodoo doll of you and some days goes to town and other days forgets about it.
Merry Christmas MsTrinidad, you'll be in my prayers.
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