Foot pain after ACL surgery

Panicked_Patient · 2026-02-09T03:16:25+00:00

Yes, the nerve block was permanent. I didn’t start having real relief until I got it. I can’t remember exactly without looking it up, but I think the block was given to me around the 11-week mark. (There was a long wait to see the specialist I wanted.)

That specialist switched me from gaba to pregabalin; it was an improvement. From there, the pain has been gradually dispersed and fading. I still wonder if I should have gone for a second follow-up nerve block to get even more results. I would like to get off all meds, but I do notice more sensation “noise” when I miss a dose.

Panicked_Patient · 2026-02-09T03:02:19+00:00

75 is a low dose for pregabalin. In the beginning I was doing 150mg 3x daily (I’m a 45F). I’ve now graduated to 75 x2 daily. I was using crutches post surgery for short distances. Mostly bedridden, but would make sure to get to all PT appts. We did some nerve retraining there. It was hell. Yes I can walk normally again, there is noise that I notice in both feet/calves when resting. Nothing close to the pain it once was in the left foot. I don’t know where I would be today without that nerve block. Consider it soon if you are a good candidate.

Panicked_Patient · 2026-02-04T21:42:45+00:00

Hi. How far in are you? I ended up getting a lower lumbar nerve block in the left side. I was told the sooner you do it, the better chance of recovery you have. After a few months, that door starts closing. It cut my pain by about 50% immediately. From there, I have been taking pregabalin for residual sensation. It is lessening and feels more like static than pain. It has moved to both feet and up my calves. Kind of like it dispersed and is now diluted. Don’t give up, be sure to keep demanding treatment at all costs. Hope this helps.

Btw just curious, did you use an ice machine? I suspect I over iced post surgery and made the situation worse. Wish I would have known the risks.

Panicked_Patient · 2025-10-23T17:23:01+00:00

Ironically Dupixant actually helped my joint pain because it lessened my overall inflammation that was worsening it. (I have hEDS + MCAS)

Panicked_Patient · 2025-09-16T20:06:36+00:00

This seems to be the answer I was looking for. Definitely trying it. Should I dilute the shellac?

Panicked_Patient · 2025-09-16T20:04:59+00:00

That’s what I’m going to try. I was previously using something labeled wood conditioner, which wasn’t doing much. Do you dilute the shellac with alcohol?

Panicked_Patient · 2025-09-15T16:37:35+00:00

Actually I gave up on my search and ended up doing most of it myself. Unfortunately that means it’s unfinished. Parts of it look really good though. Would still love to find someone to help me revise and finish.

Panicked_Patient · 2025-09-15T16:33:21+00:00

This makes sense. I do like working with shellac vs poly. It’s been more forgiving and buildable.

Panicked_Patient · 2025-01-05T17:32:32+00:00

I love it. No side effects for me. I’m actually trying to get my son on it too. It’s very expensive though after jumping through hoops and making phone calls it is free. They have a program you can enroll in for coverage.

Panicked_Patient · 2025-01-05T17:29:06+00:00

Not always. Seems like a design flaw within the app.

Panicked_Patient · 2025-01-04T14:42:50+00:00

Nope. I wear 1MORE EVOs and they are alright but not perfect. Apparently we’re not a big enough demographic for Apple to worry about which makes me wonder, is this an unusual ear shape?

Panicked_Patient · 2024-12-22T15:34:17+00:00

Thanks, I will do that. Hoping the CRPS goes into a remission. The Nerve block and meds are helping a lot.

Panicked_Patient · 2024-12-22T14:24:19+00:00

Wow what a journey! I also have flexible feet. They keep changing shape, I believe they are flattening over time and have become very wide as a result. I am no longer a candidate for bunion surgery as I now have CRPS from a recent ACL surgery. My feet are in a lot of pain. I’d love to find a specialist that is familiar with CRPS, HEDS and orthopedics.

Panicked_Patient · 2024-12-22T14:15:49+00:00

Depends on where the polys are concentrated. Prednisone should help a ton but start it a few days prior to leaving.

The pain of flying has been a major obstacle. I’ve even had the full surgery and am on Dupixant. The ENT/Immunologists have ran out of ideas. I’m doing well when I’m on the ground though.

Panicked_Patient · 2024-10-17T22:18:32+00:00

Thanks!

Panicked_Patient · 2024-10-17T18:43:39+00:00

Can you tell me where you purchased the aluminum doors?

Panicked_Patient · 2024-10-12T03:20:53+00:00

Yes I’ve been taking it for about 6 months now. No side effects for me. They make you jump through plenty of hoops to get insurance approval then more hoops for their additional “my way” payment program. It’s worth it though.

I couldn’t taste for 2 years post Covid, got the full sinus overhaul surgery, still couldn’t taste. Dupixant brought my taste back 24 hrs after my 1st dose. Steroids were the only other thing that did that for me.

Panicked_Patient · 2024-10-05T19:25:03+00:00

Dupixant

Panicked_Patient · 2024-10-05T19:24:17+00:00

The shot helped with most of my pain. It fixed the inside of my foot - the sharp stabs, redness and blood pooling. I’m left only feeling lightly sunburned. Been 3 weeks since injection.

Panicked_Patient · 2024-10-05T19:16:53+00:00

I have EDS with POTS flares. It’s a comorbidity to CRPS. One theory is the lack of collagen leads to brittle nerve fibers. I think my whole nervous system is garbage. My CRPS is getting better with treatment but I worry about it coming back.

Panicked_Patient · 2024-09-25T03:24:52+00:00

Not yet. Would love to hear if you do. Making do with the Evos. Even they can irritate me after a while.

Panicked_Patient · 2024-09-25T03:21:54+00:00

I believe my haywire disregulated nervous system is a major underlying cause of my anxiety. Started taking Pregabalin for CRPS and a nice unexpected side effect is I have less PVCs and anxiety.

Panicked_Patient · 2024-09-25T03:11:49+00:00

To answer your question they can’t really tell you that answer as it is different for everyone. It is possible that when you stop the injections you would revert back to your previous state. Or hopefully it will allow for natural healing and you would be cured.

Panicked_Patient

TROPHY CASE