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Pool misses his full attention, and we miss our average pool player.

has anyone just left it in the car dash to see how well it works over time? IE go into work and leave it charging all day.... etc

It's so heartbreaking to hear about someone so young with this. I have it and the pain is unbearable. My prayers for her

did the climateers get ya buddy? what happened?

this is great, somehow, i think we needed this so we could come to our senses

Sadly there's more. Politicians expanded the borders of St. Louis to include Town and Country, Wild Wood, Webster Groves, and Clayton to name a few. This happens to be expensive homes owned by educated people. I found the rant I thought I saved and lost. Remember, I was tired and angry. Why I LOVE ST. LOUIS A to Z... Whize Cracker Favorites · · I hope "C" isn't CRIME & "M" isn't MURDER. Do you know what an incident is? A car full of gun carriers sprays the front porch of a family enjoying a cool night with bullets, killing 7 people. That's ONE incident. Imagine if they used this ploy in Vietnam when 40 or a thousand die in one day, a MILLION. Well, we had another incident in Vietnam today. If you believe our St. Louis is GREAT, YOU HAVEN'T DONE YOUR HOMEWORK!!!

In the world. 6th most dangerous. St Louis, United States of America Population - 272,673 Homicide rate - 66 per 100,000 inhabitants With the highest murder rate in the US, St Louis is a highly dangerous city that is fueled by gun violence. The city’s limited gun control measures and high levels of juvenile crime contribute to feelings of unease among residents. However, the city’s government is actively implementing public safety initiatives to make St Louis a safer place to live and visit. This includes passing bills to regulate the open carry of guns and providing mentorship programs to aid those in the city’s marginalized communities.

How this guy explain things is hilarious 😂

Lyla, how are you doing now? I se that it has been two years. How I pray you were able to get the help you needed. I also have CRPS in my left foot and leg after an ankle injury. By the time I was correctly diagnosed, my foot and leg were black and the pain was unbelievable. After years of treatment, I am happy to report that I have learned to cope much better with the pain. Between coping skills and a Nevro neurostimulator, I am holding my own without pain medication, which never really worked for me anyway. I still have daily pain, but it’s not screaming at me the way it first did, and I’m much better at ignoring it. How I pray that is true for you as well❤️🙏❤️

Damn man, this is too funny. I'm doing p90x these days and I can relate to this. Keep it up and don't stop man. Ur doing good. Cheers!!

I just know you drive your parents crazy🤣 reddit led me here and I'm glad it did, too funny

As a man with CRPS I couldn't imagine a kid going through this. Does anyone know If she was able to have the procedure? I've had it for 10yrs now my life stopped the day it happened I don't live anymore I just get through the day 😢

How long it takes to charge a bank with the solar panels

I have CRPS and i am 47. I could not even fathom having it at such a young age. Prayers going up for this young woman and her family.

I was diagnosed 22 years ago with Complex Regional Pain Syndrome and it started after what I thought was a sprained ankle and within 1 month it spread to my other foot so I was in a wheelchair then it spread to both of my arms and my head I couldn’t hold a fork and my nurse had to use pillows to hold covers up because I couldn’t be in the wheelchair anymore so I laid in bed screaming every day and night I had my friends and nurses go online constantly looking for a cure I found one case of remission in a man from the UK He only had it in his hand but I was desperate He used a Hyperbaric oxygen chamber in his home daily so I bought one and within 2 weeks I was walking with my wheelchair and I pushed it out the back door and used the walls to lean against I still am not 100% but I can walk and swim It’s the main thing that keeps my pain under control I truly couldn’t live without it I was so sure of it I went to school to become a Hyperbaric technologist when I could barely walk and just started driving again I have treated so many people with this disease and other conditions Everyone is blown away by how much better they got in such a short time A woman who couldn’t walk on one foot wanted to go to the beach She couldn’t believe after 3 treatments we walked on the beach and she cried If you get a stroke victim in within the hour it’s as if they never had a stroke It takes away bruising and cuts overnight Athletes use it Prize horses are put in hyperbaric trailers before they race because it legally dopes them and super charges them after they race they are hosed down and put back in the Hyperbaric trailers so it prevents heart attacks like athletes do also If your in pain it takes about two weeks of going in daily then you can switch to a less aggressive maintenance program like 3 treatments a week Because it’s expensive I highly recommend owning one I use Oxyhealth because when you want to get a new one they give you a huge discount with a trade in If you go to a clinic try to negotiate for 85$ per treatment That’s usually the lowest they will go Always ask them to lower the price because you have not been able to work and when you do get back to work BUY A chamber because you will need it for the rest of your life 🙏🏽❤️

I've had it for 23 years now. It's in both feet and legs. Been in remission for several years now but there's been a few times I thought it was spreading. Thank God that wasn't the case. I just try to keep nerves under control as much as possible. I've had a few flare ups off and on the past few years. Still on gabapentin, muscle relaxers and pain meds. I've been trying to work for past three years now. But also have flare up from fibromyalgia . Still have a lot of allergies to different medications. Still sensitive around areas from where spinal cord stimulator was implanted. I will NEVER recommend that damn thing! After the 5th surgery on it. Wish uns well and stay strong. I know it's easier to say it than fighting this. But there is light at the end of tunnel! I'm still not completely pain free but it's not quite as bad as it once was. I'll keep you in my prayers🙏

The biggest wind turbine installation vessel called the Voltaire is installing the Haliade X 13 MW units off Dogger Bank, UK now. There have been a few delays however. The foundation installation has been slowed by storms as the North Sea is one of the roughest seas in the world and the turbines are 100 miles offshore. There has been a problem getting ships to install the foundations and also a shortage of blades.

200K cases isn't actually considered "very rare". But rather just "rare". And it is incredibly underdiagnosed, which means there are likely closer to 300K cases. Consider that ALS IS very rare, and there are about 10K cases nationwide. And yet nearly everyone knows about it! The lack of awareness of this condition is totally stunning. I know. I have suffered it for over eight years. and it took them 3.25 years to get a proper diagnosis. PLUS, there is NO TREATMENT PROTOCOL for it. We simply get sent home to suffer. And people wonder wy we have suicidal thoughts (on a regular basis. Which is entirely normal for CRPS patients, by the way.). Thank you hugely for posting this video. This is very difficult to discuss. and to impart just how tough and awful it is with only words.

I learned to walk when I was almost 2, and needed a podiatrist and special shoes. My feet and legs hurt all the time; so much so that until I was 14, my Mom massaged and rubbed my legs all night, every night until dawn. I couldn’t partake in gym class all throughout school, but loved weight training and later became a personal trainer to special needs people such as the extremely elderly and the terminally ill. While working with a client who had psoriatic arthritis, I felt the first lightning bolt of pain shoot up my right arm, which was holding a 25 lb weight over my head with one hand. I walked over to a mat and let it drop. That was in 2004. My CRPS has been several years in each place: right shoulder, left shoulder, right wrist, right foot, left foot. My ears just simply went deaf one day in my 30’s at the same moment tinnitus switched on, and it’s been on ever since. I use 2 canes to walk, but that’s really hard on the wrist that had CRPS. I was kicked out of my GP’s practice where I had been going for 28 YEARS when I told my doc what I had. (Diagnosed at Drexel Pain Clinic; Cleveland Clinic stole my doctor/head guy away) It has long since closed. Nerve blocks (2) took the neuropathy completely away from my right foot, (not something I was seeking) and it just returned. It was particularly awful. I hardly ever mention it because compared to the CRPS, well, it’s like bringing up my PE. I can say that the spinal stimulator helped take the edge off the pain. We took a year to crank it all the way up. The Spinal Stimulator is about as long as a business card but many times thicker. Wires are placed inside your spine

Have you ever looked into urine therapy? “The water of life” by John Armstrong is a good book on the subject

Hey, do you have any old examples from the 20th century or earlier? I'm doing a research paper for my college and plan on the topic being this!

I also have CRPS. I've tried literally everything. I did k infusions, dexalog 12, calmar treatment. Not to mention all the meds. Calmar treatment worked the best for me.

If you consume cheese you aren't helping

Hi Good video I go to by a water bottle 🇬🇧😁

I know where she is coming from! I've had CRPS for @25 years. It started on my left foot and has gone into 3/4 of my body. There DEFINITELY needs to be MORE attention to CRPS!

So funny! 😂 Thanks for sharing!

I know this is quite an old video and I never leave comments but I just wanted to say I was really impressed by your accountability. There are very few people/companies/etc that readily admit their mistakes or errors and you did so and used it to further the information provided in the context of the video. It's actually what has made me subscribe, despite knowing the videos you create may not be relevant after my assignment is due. Well done for being not only a great source of information but also for being genuine and holding yourself accountable.

I have crps know for 40 year an it is a monster or dragon the last couple of years it has been hard because some of the meds I can’t take any more because they are doing damage to my kidneys so hang in there

I always send this video when I want to convince a friend to watch the show with me and it's worked *every. single. time.* cheers Travis! people are still watching years later 😀

My son has CRPS 😢and he's struggling 😪

What abt scrambler therapy

Although I just found this and it's two years ago. How is Lyla now? I have had CRPS Diagnosed too and no one knows about it where I am from either. Thank you for posting out of Love for others

I've just been diagnosed with this in my foot after a surgery. The pain is no joke. Can I suggest that they use e-tranfer or another fund raising site a GFM takes a big percentage. There's other fund raising sites that take nothing so all the funds can go to them.

“or 3 years later” being October 2023, I felt attacked 😂

Your video is great! And this product is very cool! I received a lunch pack as a gift and am excited to try it out!

The sun bit is hilarious

Thanks ❤

THANK YOU ❤

theres so many solar power banks with random ass names idk which one is truly the best and trust worthy to buy

Praying for her as I have full body CRPS and can’t imagine a poor child going through this. Gentle warm water exercises are best.. don’t overdo because anything done is felt the next hour or day and you need to recover. Dr Phillip Getson in New Jersey has very informative videos on RUclips and speaks at the RSDSA conventions. He was one of the first to do ketamine and is a believer in as little medication as possible. Pain meds are usually a must. Teach her about God and he will watch over her on her journey always. God gives us the strength only he can give.

oh i love lyla i have crps too and we met at a camp for kids and their families who suffer with chronic pain and we have become friends i love these videos about her because when we met (just a few months ago) i didn't know she went viral she's doing much better and she has given me glimpse of hope that i too might be able to walk unassisted one day

The wind turbine in the video is maybe a ge 3.4 137, but the vestas V236 is bigger, 15MW

I have CRPS, God bless this little girl..... I absolutely feel you, the pain makes you not want to live.... but you have to keep pushing through

Yeah Andrew Tate didn’t recycle them pretty well did he?

Can you check out True Earth please?

I wish to use these in our biological restaurant. But i am afraid they wont keep up the promises

My doctors call my physique: 'Pre-Diabetic'. Id call it: 'Peak Winning Condition'

So good

I was diagnosed with crps when I was 11 and right this minute I am in so much pain. I’m now 16 and I hope Lyla is a bit better now. x

@6:28