Chiropractor Helps Wheelchair User With EDS | Crack Addicts 

At least here in Europe, we never, ever, Ever touch the neck of an EDS patient, I'm in shock. Personally, I would never go through with this.

As someone with EDS I have been to numerous chiropractors and various times in my life. It gives some pain relief for a short period of time but with two days I have always been in much worse pain than before.

My first thought is EDS which is already hypermobility and it seems like adjusting would be contraindicated

After watching this show i want to find someone to help my granddaughter

I was told NEVER go to a chiropractor, especially on my neck.

I have Ehlers danlos syndrome as well. chronic pain is one of the reasons I left my husband. After 30+ years and being diagnosed with EDS he doesn’t believe I have this pain. I think sometimes that’s partly due to our determination to not look sick and the fact that we can fake it for a day a couple hours even a couple of minutes but that will just lead to rebound pain like an exacerbation. When that happens I may need three days to a week to feel my normal chronic pain. I feel for this girl.

It’s what A.T. Still wanted Healing with hands and care for emotions Medicine cannot cure it all! Pain is so hard to live with everyday!

I have hEDS. I had a great chiropractor long before I got my diagnosis at 46 years of age. When he told me there was nothing else he could do for me because I needed surgical intervention, I stopped chiropractic care. Having dr's gaslight you your entire life, tell you that you just need to exercise, lose weight, or that is all in your head. THAT'S what it's like for people with EDS when dealing with the medical field.

I want to know how she is feeling the next day, and then a week after. Remember she said she wanted for the adjustment to last!? Also I have EDS and sure it feels great in the moment but then there are diminishing returns, and worse off than that all the constant pulling and tugging to get that release willl eventually wear down the joints all the same. There is no magic here.

I understand living with severe chronic pain, it is absolutely frustrating & mentally draining!! I don’t have EDS but I have fibromyalgia, neuropathy, spinal disease with fluid on my spine & two herniated disks. I see a spinal specialist for epidural injections but I also see my MD & a chiropractor! I do get temporary relief from getting adjusted but it sucks it doesn’t last but a few days!! They said surgery would be the next step with my spinal issues which scares the hell out of me!!! I’m searching for a holistic MD so I can try something else before going through surgery!!

Like all your vids!🌟

I’m 52 and was dx EDS at 36 after a dx of fibromyalgia. In a week m having my first spinal fusion surgery to correct moving vertebra !! I hate EDS and most medics won’t touch you once EDS if mentioned. 🇬🇧

I have hEDS, last time I went to the chiropractor I thought I had pulled something under my shoulder blade…..nope…..dislocated rib 🙄😂

I used to love watching your show on TLC but I don't see you on there anymore so I'm wondering what happened also I don't really do social media RU-vid is about the only thing that I like to watch and I was surprised you had a channel on here 👍😇🥰🫂💖 So I just wanted to say I am so happy that you do what you do for those who really need you I wish you lived out here in Palmdale California because when I went to see a local chiropractor he refused to touch me said I had too many issues going on😢 So keep blessing those who truly need your help. 👍❤

Lol. Chiropractory is not generally recommended for EDS. "I'm kinda freaking out." Because you're not an effing physician.