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Have you ever tried Carnivore? I has seen 2 videos on RUclips that it has put people in remission. Dr. Anthony Chaffee and Dr. Ken D. Berry are good ones to listen too!

Hi

Hi i am indian

Music ruined video.

Wow, you had to put in some work to comeback from your injury…amazing!

I have CRPS type 2. I have had to have my right leg amputated below the knee. I had CRPS before (it was due to shattering my right leg and ankle by falling in my kitchen) and it is worse after along with having phantom pains.

I absolutely love this woman’s gift . Thank you for sharing this.

This was a huge encouragement to me … possibly have CRPS after ankle fracture … I had never heard of it before. Jeremiah 29:11 🇨🇦 ❤

thank you for sharing your story as its brought the light into a dark loney place right now..

Same exact stuff happened to me but it was my ankle and then I became allergic to salt and then Glyphosate and then atrazine and the benzethonium and I had them completely out of me for months but coors light just changed there operations over to using glyphosate for the hops and barley and I’ve spent the last couple weeks trying to get it out and keep it out , I’m on Guinness now and shop with gloves for life ! Wine is next but I hate it . I had this and now I don’t due to not eating processed foods anymore especially the Cereals they don’t use natural gas anymore to cook they use chemicals now glyphosate ………… made in USA used to be a good thing , what you throw out after the meal is the is the garbage the food ! It would be better if you ate the carton it came in there less chemicals. Either you way you die from the food or the suicide disease from the chemicals in the food… y’all have a choice ? Food or pain I hope this finds you in the worst pain so you can listen to the content which is true and my experience and I’m free of pain now rice and bottled water changed my life back happy

CRPS is so intense. Ketamine is the only thing that has helped me.

"every plan I had for my life was just done." So true and so painful. At 26 i had a failed radiofrequency ablation, resulting in crps. It's been three and a half years and it's just getting worse. I know a lot of the time disease comes around at some point in life. but I wish I could have gone through my twenties ans thirty's.

Try pain reprocessing therapy or somatic tracking

Thanks for sharing your story man

The style of this short reminds me of Christmas in July. Some things never change 😊

Gorgeous visuals! A fun sensual story with engaging characters. Thanks for sharing your work with us Myles

I hope you all enjoy this episode on Victor Sanchez from Los Angeles, CA!

Thank you for sharing your story Molly. I was diagnosed yesterday, and my DR said our goal was to get me to the point where I had some quality of life. Going to do all that I can and pray a lot!

Wild story! Have you or anyone had a nuclear medicine bone scan done? If so results? I have been diagnosed with this and truly indescribable from hips to feet after being put in a cast and boot for Achilles tendonitis and plantar fac. 15 months now of the craziest symptoms and feelings…..

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Wow. Very inspiring 👏🤩

Its the most painful unbearable thing I've ever experienced... I think I have PTSD even watching this video

Beautiful video Myles!

Way to kick ass girl. I'll celebrate you all day long. We can party Party PARTY like it's 1999.....and then some

Hollywood best actress Lacy

Best paired with a 2001 Shafer Hillside Select

And this is why I adore and respect Myles Matsuno, and gladly call him my friend! Such talent!! 💙

This is great

A great way to start my day, thanks Myles.

Myles~Wow-that's outstading uploading-see you later,😉

A little somethin’ somethin’ of footage laying around 😎

Very cool and inspirational video. Always great to see anyone, particularly former pro athletes, find another purpose and path after their careers are over

I am presently dealing with crps after a wrist fracture. I am a 72 yr old lady. In 2010 I was in the same situation and doctors told me that there was no cure. I refused to accept that and though it took many months I slowly recovered. Proof that with belief and determination anything is possible. Back to the present- my hand and fingers are frozen and off the scale painful. Don't get me wrong- I have felt despair and depressed, but I have full belief that I will recover . I honestly wish that for you- don't give up hope.

Brittney, your music is a gift from God. Yes you write and sing but by singing you are giving a gift to listeners. A song belongs to all as it has been shared by the loving singer (yes the royalties need to be paid to the artists). I will buy your CD for sure. Always write your feelings and NEVER let people tell you to sound a certain way

Wish you all the best, Sir 🙏

I have been a member of churches of multi racial people. Jesus shed blood was red and we all have red blood. Great power. Billy graham was a while southern man. Early in his ministry he said tear down all the ropes dividing the races. He was having none of it. Remember this was when races were told to be separated but the division was not of God.

I was diagnosed with crps. I was in a car accident in 2002 where I broke my femur in 4 places. But, I ended up spraining my right ankle. I ended up on crutches for 17 weeks. It took me 6 months to get a diagnosis because it was showing up as a leg infection.

Molly! And also anyone with CRPS or EDS! Please look up the Spero Clinic in Arkansas! They are doing pretty amazing things to help improve significantly or even heal from these conditions ! Dr Katinka also has a podcast that’s pretty great too! “Hope for chronic pain” (definitely check it out, it helps give a better understanding of what they’re doing at the clinic) Overall they help calm down the central nervous system and what they’ve seen is people with random conditions especially CRPS really improve because you’re nervous system is not hyper focusing on the pain as much and because the nervous system is calmed down your body starts becoming more efficient at healing itself again even with things like EDS Keep going and keep hope ❤️

This is kind of nuts to come across this in the wild. You probably don't remember me as we only met a couple of times. My name is Bonnie, and my family/members and the Armstrongs have been in and out of each other's lives for almost as long as I've been alive. More out in the last several years, seeing everything that has been going on. I just wanted to comment, ultimately, to say that my heart goes out to you, dearly. I do not have the same conditions as you, but I grew up with several undiagnosed illnesses, a few genetic in nature, and I, too, thought that being alive just meant being in pain. Always "sucking it up" because the people around you say so. Walking through injuries. Continuing to do so because then you have doctors, even with your lengthy medical charts, telling you you're wrong about the the things that you feel every moment of every day. I am horrified each time I see another human being experience this. I see endless demonstrations that a compassionate response is created from blood. My own body collects diseases like they're pokemon. It all finally decided to crash and burn when I turned 19. It's endless pain, endless therapy, endless new treatments, endless treatments that you just can't afford, endless working and searching except for those few moments of escape. Usually with our "person." The one human being that loves you so much that you find true respite. You're strong. You're not a failure. Your pain is real, and your thoughts and feelings are valid. You're right every time you stick up for yourself, and it's okay that you've had moments that you couldn't. Our own agency is borne out of these moments, though I know you do not need me to tell you. I am not a religious person so I can't offer prayers. I can only extend my own love and humanity to you, and express my sincerest hope that you intersect with the medical advances that you certainly deserve. All my best to you, Ben, and your families.

Omg I just discover you on "Today with Hoda n Jenna" morning show. I love your voice, your music and your message to the world...You are an inspiration...Ty for sharing your story!!!👏👍🙏🎵

I was just very recently diagnosed with CRPS, after undergoing ankle fusion surgery! This knocked me on my butt, out of my mind and in so much constant pain. I’ve found a great team of pain management doctors, physical therapists and behavioral health specialist that I feel confident that I will get at least some relief. 🤞 Thank you for sharing your story!

I've had it since I was 17. 5 years down the road it's a unbelievable struggle .I Physically becoming weaker each week. I met people who had RSD but I'd really love the time to speak to someone else with crps. I can't even imagine what life is like without constant pain and maintenance. This sounds so much like me and others I couldn't even finish watching it. It took them 6 months to find a bone floating around in my ankle. They told me forever I should be walking. Trust the Lord.

I want to give a testimony on how I got cured from cold sores and herpes Virus. Few months back with is herbs 🌿 all thanks to #Druromi on RUclips💕

Beautiful story! Keep up the good work!

No more CRPS pain? Please read. About ten years ago I began to experience pain in my left foot that was simply excruciating, I thought it might be gout but after tests that was ruled out. I was eventually diagnosed with type 2 CRPS, no idea what triggered it. I was fortunate because my doctor allowed me to try Tramadol, and unlike any other PK, it was reasonably effective at 200-300mg a day. I was looking forward to living my life in a state of semi zombi-ism, that was the effect Tramadol had on my get up and go. When the pandemic hit I began boosting my vitamin D levels, I was 5' 7" tall and about 19 stone, so I took 5,000 itu's every day, I still do. A few months into my regime I had lost about a stone in weight, I put it down to our being on lockdown, but since then my weight has continued to fall, I now weigh 13 stone, but my eating habits really haven't changed. The real benefit however has been this. About 3 months into my regime, I began to notice, or should I say, not notice, the background pain that always persisted, the Tramadol numbed it well, but it didn't stop it. I slowly reduced my Tramadol intake over a 3 week period, the result? I have had no neuropathic pain worth talking about any longer, I occasionally find there is mild discomfort, but nothing I would describe as pain. I have not taken any Tramadol for about 18 months :). Please try this, please, please try this, it cannot hurt you, most of you are vitamin D deficient period. 5,000 itu's a day for 3 months, maybe I am a unique case, but if you don't try it you will never know. God bless and I hope this helps some of you.

Thank you Molly for your story, I'm glad to know I wasn't the only one who kept telling medical professionals there's something wrong. Back in 2018 I had two jobs on with a pest company and a Firefighter. One day at a big box store a mess of wood feel out and struck my ankle, my foot went numb for a sec but when the feeling returned I couldn't feel the tip of my great toe and pain slowly crept in. I told doctors something isn't right, instead of an MRI I was sent to physical therapy, which later I found out made things worse. At first I was told I had cellulitis which was very painful, but after the infection went away I started to have a burn that just wouldn't go away. At the time I was very active, worked out at the gym 3 times a week, hiked 10 miles with 100lbs of logging chain in a backpack. I'm 6'5" tall weighed 210 muscle I was a stomping tough tree lol, but I kept telling myself I'll get better it will go away, just push through it, as I have a high pain tolerance I thought if I could just ignore it I can still be a Firefighter. I worked so hard and all the training and certification we have to do to be able to be a firefighter is life long really and training and testing never ends. Being a firefighter was my life calling it's the only job I had were I felt whole complete it's where I was meant to be. As time went on I couldn't ignore it the pain is so intense, people can't imagine, I did go to a different pain management doctor who had a great main degrees under is belt and I explained it started in my ankle and it's slowly moving up the calf and back of my knee. He looked me over and touched my leg I jerked back he saw the color swelling the shine of my leg the hair that's missing and ask me some questions did an x-ray and he told me I have a very rare form of CRPS Type 2, rare because mine spreads. He said I'm sorry but it would be a great risk to your life if you went back into a burning house having this in your leg, I can no longer be a firefighter. That was a very dark period in my life, I understand how everything for you went black, I lost everything, had to force retire from the fire department, I did nothing wrong but turning in my gear and cleaning out my locker felt like I was fired for misconduct or something. A shameful feeling. I did after several months and therapy finally accepted it's not my fault, the years I was a firefighter God put me there for that time to help people and I helped a lot of people on their worst day. I got to do things others only dream about I was very lucky, but still I hear the sirens of my engine from the station that's 3 blocks away from my house head out and I know their missing a guy, I pray for their safety. Like a frog who dreamed of being a man to wake up and realize he isn't even a frog! Lol I still have my sense of humor. Speaking things up I was unable to work in 2019, haven't since as I'm disabled. It finally spread to both legs waist down. And it's spreading upwards to where I have pain in my organs I can actually feel my intestines on some days it's shooting it's burn and stabbing pains off and on here and there through my arms face and hands. It's hard for me to walk or even stand long. I now weigh 300 lbs, and that's do to not being able to exercise and the type of pain meds I'm on that slows the metabolism way down. I can eat once a day and be satisfied I actually have very low to no appetite, I know when people look at me and see my shirt that I'm a firefighter as see how big I am and unable to walk well and lol all the sweating pouring off my face they are thinking I just need to exercise, and when I tell them what's wrong they change they're look so I know they were judging me. I keep moving, I even tried the spinal cord stimulator trial but it barely touch the pain. I'm told eventually I'll be in a wheelchair. I no longer fear death, but I have a great family wife kids and support structure that I'll not be another CRPS suicide statistic. It's really a terrible disease, many times I can't even take a shower because the water coming out from the head that hits my legs and body hurts. And the one bathtub we have is a joke when you're 6'5" tall. I pray you keep your head up Molly, and I mean that, it could be worse you could have the variant that spreads like me. But I keep going, and if I can, I know you can too! And to anyone who reads this, you are not alone, my prayers do include others who have CRPS, I may not know your name, But God does, I am accepting hugs, just be gentle. Thank you for reading.

Have been battling RND, a form of CRPS since 2015. The level of pain across my whole body is agonizing. I hate my new limitations, but received quite a bit of relief by balancing life and medical marijuana. It opened my life to more freedom and despite still having a lot physical challenges, I'm making it through college with accommodations. When you get a chronic illness everything changes and slows down, but I know I'll still find a way to live a fulfilling life.

Lovely trailer. I don't remember learning much about this time in school. It was when I was living in a small community with many elders who had been in the camps as children and near to families who had both lost everything and a fortunate few who had their land titles and machinery held for years by neighbors until they were able to return. To hear these stories firsthand touches on a part of history that has been quite invisible until the last few years. I am looking forward to learning more about the Kataoka Family and their story.

Husband was just diagnosed. I want to understand everything I can about what he is going through.

One of the most impressive people I know .... Newton is a golden-hearted soul. Funny, kind, generous. And a real live genius. This video doesn't get into his accomplishments at Cal Tech studying climate science, his musical abilities. .... one in a million.