Support Community for Amputees

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This is a support community for amputees and their families, to discuss the issues facing those with limb loss in a safe, friendly environment.

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founded 2 years ago
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Amputee Devotees, BID (Body Integrity Dysphoria) and social media addressed by an amputee.

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Project Bike Leg (www.projectbikeleg.com)
submitted 4 days ago by ExtremeDullard@piefed.social to c/amputee
 
 

Learn to create a below-knee prosthesis from bike parts and empower amputees globally. Access detailed guides and videos for innovative prosthetic solutions.

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Healthcare clinicians are already using artificial intelligence to guide decisions related to limb loss. AI is being integrated into prosthesis alignment, socket fabrication, exercise management, gait monitoring, and beyond. For better or worse, it’s also playing a role in insurance approvals, denials, and appeals.

According to a new study published in the medical journal Artificial Intelligence Surgery, AI’s role in limb care is almost certain to keep growing. “Our review suggests that the integration of AI in limb care is not only rapidly growing but is seemingly inevitable,” write the authors, who are based at the University of Colorado School of Medicine. They go on to identify some distinct areas of limb care in which AI is rapidly emerging as an important tool, and changing how clinicians treat limb loss.

You can read the full paper online. Here’s a quick summary:

Prosthesis Use and Design

AI is driving rapid innovation in the development of neuroprosthetic devices. Systems known as convolutional neural networks (CNNs) have been shown to support highly responsive prosthetics that give wearers a high degree of control over joint flexion, a greater sense of proprioception, and some degree of sensory feedback. The study also notes the potential for AI (used in combination with advance imaging) to help determine the optimal placement of implants that connect nerve endings to prosthetic controllers. This type of research has shown promising results at the University of Minnesota, North Carolina State University, University of Wisconsin, Shirley Ryan AbilityLab, and elsewhere.

Management of Nerve Injuries and Pain

Pain is one of the leading causes of post-amputation health complications, the authors note—particularly phantom limb pain. Researchers have begun applying AI technologies to help identify the causes of pain and yield more effective treatment strategies. One of the most promising frontiers lies in the mapping of dense neural networks; AI now allows neurologists to develop highly precise blueprints of nerve pathways (down to the level of individual axon-synapse connections) in 1/50th the time required by manual methods.

Drug research is another area of progress: AI makes it possible to rapidly model physiological responses to thousands of individual drugs, and millions of drug combinations. By quickly identifying the most promising therapies, these preclinical models can streamline the process of clinical testing and approval.

Nerve repair and regeneration represent yet another area in which AI is driving innovation forward. The paper notes that “the application of AI to nerve regenerative strategies has the potential for revolutionary biotechnologies,” particularly in the development of biomaterials such as nerve guidance conduits.

Clinical Decisionmaking and Limb Preservation

“The application of AI in clinical decision making may revolutionize surgical practice through novel patient-centered approaches,” the authors write. AI systems are becoming extremely accurate in modeling the odds of success for limb-preserving treatments such as revascularization, vascular bypass, and minor amputation in patients with limb-threatening conditions. Similar approaches are helping clinicians evaluate limb-salvage options in patients with complex injuries.

In addition, clinicians are beginning to use AI to identify patients who face elevated risk of amputation and intervene before the conditions become limb-threatening. For example, AI can screen electronic health records and flag patients who require targeted PAD screening. It can also refine the results of conventional imaging techniques (such as ultrasounds), leading to more precise selection of treatments.

“AI-based strategies complement clinical judgment and support innovations in …. [amputation] prevention, management, peripheral nerve injury treatment, postoperative outcomes, and prosthesis design,” the paper concludes. “AI as a methodology holds promise in revolutionizing practice.”

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Finally cured! (piefed.social)
submitted 1 month ago* (last edited 1 month ago) by ExtremeDullard@piefed.social to c/amputee
 
 

After 11 weeks, a lot of pills and a whole week in hospital, I finally kicked the infection. My foot now looks normal - well, as normal as residual limbs go 🙂 i.e. not red or swollen - it feels great and I feel great. I haven't been feeling great for a long, long time, so that's quite a novel experience.

Today I went out and did 4 hours of yard work in 15 degree weather. The house is finally getting taken care of, I could undo the neglect and I had no issues whatsoever.

Yeah, it don't seem like much, but that a huge win for me. I just wanted to share the joy 🙂

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Rodney Taylor says detention ‘draining on my body’ as Democratic senator Raphael Warnock lends support to case

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Filmmaker Rachel Handler Wants Your Healthcare Bill Horror Stories

July 29, 2025

Ever had an insurance claim denied for a much-needed prosthesis? Lost coverage due to confusing fine print or technicalities? Got saddled with an obscene pharma bill? Struggled to find an affordable ACA plan? Award-winning filmmaker Rachel Handler is training her lens on disabled people who’ve been told, in essence, that their health isn’t profitable enough to pay for.

Handler is using a grant from Adobe to expand her 2020 short “How Much Am I Worth?” into a full-length feature. The original five-minute documentary, an award-winner in the 2020 Easterseals Disability Film Challenge, illustrated how the US healthcare system had failed four women with disabilities. The feature-length format will allow Handler to get far more voices into the mix. In addition to a telling a broader range of in-depth stories, she’s planning a coda in which dozens of people share brief summaries of their unhappy run-ins with insurers, hospitals, clinicians, government agencies, and other health system gatekeepers.

“Our goal for the end of the film is to feature at least 50 people talking about denials they’ve received from the health system,” Handler explains. “We want to have short clips where people talk about how their insurance wouldn’t cover their diabetes medication, or they got stuck with an $800 bill for a basic service. The ultimate goal is to focus on how people persevere through these hardships with resilience.”

If you’ve got a story to share, get in touch with Handler via Instagram DM; the project’s handle is @howmuchamiworth. We connected with Handler last week to learn more about the project. Our conversation is edited for length and clarity.

There’s been quite a bit of change in the health care landscape since 2020. Will you track those ups and downs in the film, or are you focus on the landscape as it exists in July 2025, post “Big Beautiful Bill”?
We’ll be focusing on what’s going on in people’s lives right now. So in my case—my own story will be in the film—I’m looking for new health insurance on the ACA marketplace. And it’s really expensive. New York State just doesn’t have good options for freelancers. We’ll probably follow my journey into next year to see if any of the changes in the federal bill affect my coverage and the pricing on the marketplace.

Another person we’ll be featuring uses Medicaid for herself and her children, so it will be interesting to see how those cuts affect her. Andrea, who is a nurse in a wheelchair, hasn’t had a wheelchair covered by insurance in many years, and she’s trying to raise money for a new wheelchair through crowdfunding and sponsorships. The ultimate goal is to be able to track these intense situations from beginning to middle to end, so the audience can get a sense of completion within each story.

You’ve had a number of different films do well in the Disability Film Challenge, and you could have applied for Adobe grants to keep working on any of them. Why did you single out this project as the one you wanted to do something more with?
This one seemed like the obvious choice because it is so timely. Ever since I made it, I’ve been wanting to expand it. I’ve been having people come up to me after they see screenings of it, asking for more information. They want to take it to their elected representatives. So I’ve been wanting to expand this since 2020, because health care and health insurance have only gone downhill from there. I love the other films I’ve done, but this one was my priority.

What’s your your timeline for shooting new footage and doing all the post-production and everything else that needs to occur.
I want to use this grant to produce a sizzle reel that we can show by the end of the year. We’re starting to film in August, and we’re hoping to be done with that by October and start post-production in the fall. We’ll use that to continue fundraising from other sources.

I’m in a documentary filmmakers fellowship, and the director of Patrice came in and talked to us. Patrice is an incredible documentary on Hulu. He told us they shot a sizzle reel—like, four scenes—and pitched that to Hulu, and Hulu loved it and gave them a budget to make the film. That’s really unheard of. We’re hoping that once we have some more footage and that start of a narrative throughline, that will help us get more money involved.

Are there documentaries you have admired that you would like to capture some flavor of?
Well, I want to steal everything Patrice did. It’s so well done, and it’s beautiful to watch. I think our approach will be a little more verite. We want the film participants to sort of forget that we’re there and just capture what’s actually like happening in a very natural way, so we can be as truthful as possible. They did that nicely in Patrice. It’s just the cameraman and the two subjects in a room. That’s sort of the vibe that I would love to have for this.

I also just watched Deaf President Now, and I really loved how well they showed the hardships of being disabled, but also the ridiculous amount of strength we have in our community to overcome and persevere and take charge of our own lives. I want to portray that kind of resilience and empowerment in this film, too.

I have the impression that five years ago, when you made the original short for the Disability Film Challenge, it wouldn’t have been realistic to think about pitching a project like yours to Hulu. But today, that’s a real possibility. What do you think is behind this shift?
I think that people are always fascinated by documentaries, specifically when it comes to the disability community. We’ve always been almost hidden in the shadows, so I think that’s been a really positive shift to get more of our voices out there. But when it comes to narrative storytelling, we still have a really long way to go, especially with casting authentically and making stories that are disability inclusive and authentic. The more we can get these documentaries out the better, because then people in Hollywood can see beyond the stereotypes. I feel like documentary filmmaking is getting it right when it comes to being disability inclusive, and it’s getting the recognition it deserves. But that’s not really the case with narrative fiction filmmaking yet.

Tags: Disability Film Challenge film movies Rachel Handler

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This is a good tutorial video showing how the Amputee Mobility Predictor tests with a prosthesis (AMPPRO) and without a prosthesis (AMPnoPRO) are performed in the US, to assess the activity level - or K-level - of a person with lower limb amputation. The tests are easy enough to perform at home with the help of a third party, if you want to assess yourself.

The supporting documents and forms for the AMPPRO and AMPnoPRO can be downloaded here.

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submitted 1 month ago* (last edited 1 month ago) by ExtremeDullard@piefed.social to c/amputee
 
 

Master Ken teaches us how to defeat an armed amputee.

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The moment occurred at 12:34am and took him 15 hours 21 minutes to complete the race.

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You might remember this story. This is the sad conclusion, brought about by terrible racist adults.

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After more surgery and more crazy antiobiotics - seriously, those antibiotics were really rough and my guts still have trouble recovering from them - it looks like I may finally be rid of the MSRA in my residual phalanges. All remaining fingers crossed...

I went see my surgeon today to check on the wound, and I mentioned that, while it seemed to get better, the joints in my foot felt more "frozen" than usual. I mean they're not normally terribly nimble because of lack of use, but now they feel worse, and I was concerned the staph infection might be attacking the joints.

"Well, the good thing is, they don't really matter" he said.
"What do you mean?"
"Those joints are useless now. They don't help you walk."

But that's just not true! I don't have much length left, but they do help some for walking.

Also, I explained to him that, even if something is functionally useless, it doesn't mean you don't mind losing it. There is such a thing a sense of loss, and I wouldn't want whatever is still moving in my feet to stop moving, even if it doesn't impact my walking.

"Really?" he said, "I had no idea!"

The guy is supposed to be an orthopedic specialist. What the hell... Something tells me he spent too much time studying surgical techniques and not enough time wondering how the patient lives with their body...

But hey, at least he admits it when he doesn't know. That's rare enough in MDs. Also, I've had a couple brewskies with the guy and I know he's cool. So although he can be kind of infuriating at times, I'll stick with him.

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Highlights:

  • A night out at a rock concert changed everything for Tommy Hurrell, who made a life-altering decision after years of health struggles.
  • The 20-year-old was attending a Supergrass concert with his father when he decided to amputate his leg.
  • Post-surgery, Hurrell shared his journey of adjusting to life as an amputee and to “redefine his disability” on social media.
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Northwestern Medicine and Ukrainian physicians have now identified another potential use for Botox — relieving devastating phantom limb pain in Ukrainian war amputees.

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I spoke too fast. I'm back from surgery for more bone trimming to try and get rid of the infection. If the new antiobiotics don't work, I'm scheduled for radiotherapy. And if that don't work... I guess I'll be losing a whole lot more shoe sizes.

Funny how life suddenly starts to suck really, really fast sometimes...

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submitted 3 months ago* (last edited 3 months ago) by ExtremeDullard@piefed.social to c/amputee
 
 

A week after this, the diarrhea-inducing course of antibiotics seems to have done its job: my residual phalanges are now healing nicely, the swelling is down and the pain is subsiding - although not the phantom pain: that's still going on and it sucks...

And yeah, the test results came back and I did have an infection. And the surgeon did consider doing more chop-chop if the antibiotics didn't work, and I wasn't all that keen...

I know it's still nobody's problem but mine ultimately, but I'm a happy camper right now. So ya know, just sharing the joy with y'all 🙂

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This group is awesome!

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So I had revision surgery 2 1/2 weeks ago to remove simple bone spurs. It was a half-hour, 5-sitch affair that went well... until it didn't.

The incision isn't healing well. my residual phalanges hurt more and more every day. The pain is going up my foot. The phantom pain is off the charts and not letting up - and now it's waking up in my other foot too for reasons unknown.

The surgeon kept telling me it was okay, just wait until it gets better. But it doesn't. And so I saw him again today and now he seems worried too. He says I might have bone infection and he gave me a horse's course of antibiotics.

I know nobody can do anything about any of this - particularly the phantom pain: it's like tinnitus, it's just your thing to deal with. But... well, I'm scared and my family doesn't really understand. And I don't want to bother them with any of this either. I know they mean well, but there's only so many times you want to hear somebody complain about the same thing.

So, that's my outlook for the weekend I guess...

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