r/CRPS • • 2d ago

Moderator Approved Rule: Prohibited Substances & Compounds

16 Upvotes

The r/CRPS moderator team have added a new rule. r/CRPS will restrict discussions of non-prescribed, research, or gray-market chemicals, compounds, drugs, and peptides (such as BPC-157, TB-500, or gray-market GLP-1s) under the following general medical safety and anti-doping/pharmaceutical policies:
- No recommending or requesting suggestions for unapproved research chemicals, drugs not widely approved, or non-prescribed performance-enhancing compounds.
- No sourcing of gray-market peptides, peptide based compounds, or unapproved peptide alternatives
- Restrict discussions to peer-reviewed science or human trial data. Unregulated research peptides without clinical human data are heavily moderated or restricted to keep discussions focused on established science.

Please note, government approved prescription GLP-1 medications (e.g. Ozempic, Wegovy, Zepbound, Mounjaro) prescribed by a doctor, are allowed where relevant to CRPS.

Why? Facilitating the sale, sourcing, or acquisition of unapproved research chemicals violates Reddit’s sitewide terms.


r/CRPS • • 4d ago

Weekly CRPS Free-Talk Thread

6 Upvotes

This weekly thread is for those without the combined karma to make their own posts, and a general location to ask questions or provide support, especially for our newer users. If your posts are getting auto-removed by the subreddit filter due to account age or low karma, you can post your question here.

We ask that our community members regularly check this post for new content, and reply where they can. Please abide by our subreddit rules, and be kind to each other!


r/CRPS • • 10h ago

Advice how do you stay nice on big pain days

24 Upvotes

i’ve realized that i (30f) can become a very very very short-tempered, grumpy old man on really high pain days, especially when i have really high pain days a few days in a row. i’m currently living with my parents as my life has deteriorated (this developed after a brain surgery 11 months ago) and even when i limit the people i interact with on these bad pain days i still interact with my parents and i don’t want to be a bitch to them just because i’m on day 5 of feeling like all my bones are breaking over and over again. it’s not fair to them and i feel worse.


r/CRPS • • 8h ago

Had to pick a flair New Here

13 Upvotes

Hey everyone, I 29m active duty navy have been diagnosed with CRPS resulting from an injury back in February (Lower half of my right leg). 2 xrays and 2 MRIs. Been through Physical Therapy, Orthopedics and now Pain Management. Currently on Gabapentin and Celebrex and as of today adding Cymbalta to the cocktail. Just wanted to do a little about me post because I feel Ill be in here a lot now.


r/CRPS • • 2h ago

Am I overly concerned and just sore?

3 Upvotes

Hello all! I’m new to the group. I recently had a work injury involving an excavator and had to have emergency amputation on my right pinky toe. I completely severed the nerve in the toe, so I felt very little pain in the day I was waiting for surgery. But now, 12 days post op, it’s a different story. I’ve been feeling pretty constant pain and am experiencing hypersensitivity on top of my foot right above where the toe was taken off. I’m also feeling constantly sick to my stomach and have bad burning pains in my foot at night.

I had my first follow up with my surgeon this morning and I did not like the look on his face when I explained the pain I’m experiencing to him. He seemed concerned and immediately said it could be early signs of crps, which to be fair, he did explain was a small possibility before the operation. He ordered me to 6 weeks physical therapy with someone who specializes in crps, and said it’s the best thing I can do right now to try and mitigate/prevent it from getting worse. He said that since I severed the nerve in the accident that the remaining nerves are shocked and swollen, and that I need to constantly touch the area to help my body understand that’s it’s ok to be touched there.

After reading quite a bit about crps today, I’m not convinced I have it. It’s typically explained as excruciating constant pain, which I don’t have. But I do seem to be more sore than I should be and sore in places I shouldn’t be.

So my question is, has anyone else had a similar experience that got better or worse? Do you think I have it or are my symptoms too mild? Am I just extra sore after getting my toe and nerves crushed?

I’ve never been through anything like this and I’m just concerned about the potential long term implications. From what I’ve read today, this seems very serious and life altering for those that have it! I feel for you all and wish everyone the best in their own journey!!! I appreciate any advice or input!


r/CRPS • • 5h ago

TW: Active Flare Photo Anyone deal with weird bumpy nail growth? Spoiler

Enable HLS to view with audio, or disable this notification

2 Upvotes

I’ve had ingrown toenails on my crushed toe before but why does the nail grow like this anyone else had this bumpy texture? I thought it was the nail polish but all other toes are fine even on the good foot so what gives? This is recurring even without the nails coated.


r/CRPS • • 1d ago

ECT curing CRPS symptoms

Thumbnail painphysicianjournal.com
4 Upvotes

I’m pretty interested in trying this. TMS, the brain magnet, has some evidence as well.

https://pmc.ncbi.nlm.nih.gov/articles/PMC7711855/


r/CRPS • • 1d ago

Question What do you even call this?

24 Upvotes

So this particular pain, discomfort or whatever that I can’t put into words for my husband. My hand is burning but it’s cold and aches but there’s still this overwhelming feeling of what? It f**ing hurts and I’m tired, exhausted and I don’t know how to even explain it with words and I’m tired of trying. I’m tired of “how’s your hand today?” He’s tired of “don’t ask” What am I feeling? That gnawing pain that burns but it’s cold, under my skin it’s hot? But on top it’s cold? Am I crazy? I just want to sleep. Is that too much to ask?


r/CRPS • • 1d ago

Spreading Hemiplegic CRPS and severe dystonia

8 Upvotes

Rambling after seeing my specialist today.

Onset was 2016 in my right leg - hip to toes. More recently it's spread up my side, down my arm, into my neck and head.

The dystonia is so violent I've subluxated a rib twice, as well as it continuing to try dislocate my wrist and clavicle.

Half my face is now starting to show the color changes, swelling, my eye gets forced closed and mouth twists on one side. Now having trouble eating and swallowing.

One of the things that happens is I keep punching myself in the shoulder/throat/face. On Sunday I punched myself in the face twice and managed to pull the third - only to think "ha ha, missed!" What on earth is this doing to my mental health?

Specialist is wonderful but obviously not a magician. Medication is being tweaked. Problem is the major thing stressing me out won't be resolved any time soon. Consciously, I'm relaxed. Subconsciously... I can't even do my breathing exercises any more as they set everything off.

Can anyone relate?


r/CRPS • • 2d ago

Celebratory! Small Victory

64 Upvotes

I’ve had CRPS for almost three years now (since 10/22/23) and I can kind of run now. Only for really short distances and I kind of look like a duck when I do lol, but yay! 🎉🦆


r/CRPS • • 1d ago

Title: How do I get started with ketamine infusions?

10 Upvotes

I’ve heard that psychiatrists sometimes offer ketamine infusions, but pain specialists don’t always provide them. For those who’ve tried them for chronic nerve pain, where did you go to get started? Should I contact my insurance first, and does insurance usually cover it? If not, how much do you pay out of pocket per session? How many sessions did it take before you noticed a difference, and how long did the relief last? I’d really appreciate hearing about your experiences!


r/CRPS • • 3d ago

Thank you!

49 Upvotes

Although I hate others are dealing with this hell of a disease, it helps so much to know I am not alone. I am so glad to have found this community! Thank you all for your willingness to share.


r/CRPS • • 3d ago

Peripheral Nerve Stimulator

4 Upvotes

Has anyone had a PNS work for pain management when both the SCS and DRG stim have failed? For context my pain is mainly soles of my feet and a bit further up into my ankles.


r/CRPS • • 3d ago

Medications Too sensitive for most meds, what other options are there?

9 Upvotes

I have been going through trying the medications being prescribed for the intense burning nerve pain and finding my system is just way too sensitive so far. Gabapentin , lyrica, and cymbalta...even at low doses the side effects are intolerable. My pain management doctor said I need to give cymbalta 3 months to work, and their next med to try is amitriptyline. I just don't feel any of these are a good fit for me.

I need to find some relief from the daily burning flare ups as I am stuck in a viscous loop. Central sensitization being constantly triggered by daily activities that flare me up.

Any other recommendations? I'm considering going to an ND to ask about LDN.


r/CRPS • • 4d ago

Question Crps post brain surgery?

11 Upvotes

Hi everyone! I have had 2 invasive brain surgeries and have developed severe central sensitization/allodynia all over my scalp. If anything or anyone touches my head too much or if it’s not extremely gentle, the headache flares to a 10/10 lasting weeks to months among other symptoms. I’ve only been diagnosed with chronic migraine & the treatments from my neurologist haven’t helped. I have tried an abundance of medications and desensitization therapy. Is CRPS a reasonable diagnosis to look into? A medical provider mentioned this condition to me recently, so trying to learn more to (hopefully) make progress in my pain. I appreciate any insight you all may have!


r/CRPS • • 4d ago

CRPS in face

15 Upvotes

Hello all. Terrible morning here. I’ve had facial CRPS for 11 years from a jaw surgery. Long story short- I have almost 30 screws in my face. The screws are shifting now and even sticking out of my gums. I have intense headaches daily now and blame the screws. Does anyone have anything similar? Anyone have any ideas of what to do? My neurologist sucks, and insurance will no longer pay for Botox. I live in Alabama, so it can sometimes be tough to find a doctor. Any suggestions? Thanks!


r/CRPS • • 4d ago

Question Over Exertion & Adrenalin Tax

15 Upvotes

Hey Everyone,

I’ve been living with RUE CRPS Type 2 for five years now. Yesterday, I had an experience that I’m sure many of you can relate to, and I really want to hear how you cope with the emotional and physical fallout.

for the previous two weeks, I considered attending a conference. I closely monitored myself and was doing quite well despite some other things happening in my life, so the day before I had to travel I decided to pull the trigger and attend the conference.

Once I arrived, I had an absolute "hat trick" of fateful encounters in one evening. One meeting was a deep, instant alignment with someone (another cancer survivor). The second was a wild, protective coincidence where I was actually able to warn someone about a bad situation. The third was meeting the exact inventors of a system I’m currently using for a home project.

It was magical, high-energy, and gave me a massive wave of hope and excitement. I felt so alive.

But today, the bill arrived. That intense rush of positive adrenaline completely broke my nervous system, and I had a horrible, full-body flare.

It is so disheartening to get over-exerted not from pushing my body physically, but just from experiencing joy and connection.

How do you handle the mental toll of being penalized for being happy?

Do you have a protocol for pacing your emotional energy when the universe drops something amazing in your lap?

How do you ride out the "adrenaline crash" flare without slipping into depression?

Gentle hugs to anyone else fighting a flare today.


r/CRPS • • 4d ago

Vent Will I ever close my hand again?

14 Upvotes

Hi all. Sorry in advance for the long text and complaining.

Last February, I got tripped while playing hockey and I broke my hand and got operated. After weeks of painful physical therapy I got diagnosed CRPS.

I had all of it: the swelling, the hair growth, the discoloration of the skin, the pain, unable to bend my fingers, etc. But, after months of therapy with a Certified Hand Therapist - i started seeing some progress.

I also just recently started nerve block injections in the neck. Getting my 2nd dose next Tuesday.

But with the temperature getting colder outside, the pain came back almost as worse as in the beginning, my fingers cant bend anymore, it feels like I went back to square one.

Did anyone ever experience this kind of accident/crps where they cant bend their fingers? Were they able to ever close their fists anymore?

At this point ill live with the pain forever if I have to - but my girlfriend is pregnant and I just want to be able to use my hand normally when my baby is here.


r/CRPS • • 4d ago

Airplane ride

16 Upvotes

I have to go to a funeral in another state and I’ve haven’t flown since I’ve had CRPS. I have it in both lower extremities. How does flying affect CRPS? Thanks!!


r/CRPS • • 5d ago

Treatment for those who have had CRPS for a few years..

30 Upvotes

I've noticed that treatment for CRPS, in the first year or so, is heavily physical therapy based. That's all well and good, I suppose, but what if you aren't in the magic first year window?

December is 8 years with this condition, for me. I've had to do this myself for the last seven years and damnit, physical therapy is bullshit to me.

Mine is in my neck and a flare is not going to be fixed by whatever physical therapy they try to come up with.

After being blown off for pain relief yet again, and told I have to find my own provider to prescribe pain meds, fuck you OSU, I finally found relief in ketamine infusions.

It's out of pocket for me, like everything else. But fuck me, I detest being ignored by supposed pain clinics.

Has anyone else found physical therapy to be beneficial after 7 years or so, once you've been dealing with it so long? Or am I just a complainer?


r/CRPS • • 5d ago

My tank is empty. Not sure what to do

23 Upvotes

I’ve lived with nerve pain since I was 23 for 15 years and gradually it’s spread, most recently to my back. I’ve tried everything except ketamine infusions but I’m in the UK and I think they only do low dose here. I literally have nothing left. I’m in agony day and night and struggle to get off the couch. Even lying on the couch sometimes I just cry all day. I do have a support network but I’m really seriously thinking about ending life options in Switzerland. Not sure why I’m typing this I’m just sad my life has gone this way and so tired.


r/CRPS • • 5d ago

Has anybody here had a positive ANA blood test result?

3 Upvotes

I recently had a series of blood tests done, and one of them was an ANA panel that came back positive.

From the reading I've done, it could indicate an auto-immune condition, connective tissue disorder, chronic inflammation, or nothing. I don't think it's nothing for me, since I have pain in all my joints over and above my CRPS sites, which is why I had all these blood tests.

The lab result came in this evening, and so I have no doctor's notes or anything, just the lab result and my friend google. Since I have CRPS, chronic inflammation doesn't sound too far fetched for me. I was just wondering if anyone else has had this kind of blood test result, and what it meant for them. I will talk to my doctor when everything re-opens on Monday, but I'm curious now.


r/CRPS • • 6d ago

Persistent/Late Stage CRPS Good News to Share

45 Upvotes

You never know which treatment is going to help, so keep trying.

I'm a little over 5 years into CRPS type 2 in my right arm (dominant arm, dammit), and this year I finally found a few things that were relative step changes. I thought I knew the territory because I'm also a 22-year rare cancer survivor. I didn't. If you ever get to choose between cancer and chronic pain, totally fucking get cancer. Not joking.

I got CRPS because my appendix cancer came back 5 years ago after a 16-year break. The treatment is HIPEC, a 15-hour surgery, and it turns out the way they position you on the table can injure nerves badly enough to cause CRPS. Nobody mentions that in the consent forms. My career was in healthcare tech, and cancer taught me a lot about fighting rare disease, but CRPS has felt less like a medical journey and more like the time I got jumped in Washington, DC by ten people. It's been a street fight, and I've lost most of what was dear to me, right down to my LTD benefits, which Lincoln Financial cut off after the two-year own-occupation period 🙄 (sorry, I'm fluent in profanity and sarcasm). I'll leave it there.

The point is this year something shifted. In April I did the ketamine protocol (10 infusions over two weeks), and it gave me real, if temporary, relief. That sent me down the rabbit hole on how ketamine actually works, which got me tracking my flares. After a sprained ankle, I noticed I was flaring every four days; extra pain load on an already-sensitized nervous system drives more frequent flares. I kept digging into neurochemistry until CRPS finally made sense to me, and that pushed me to add a compounded pain cream to everything else.

No single thing got me here. Not the cream, not the ketamine, not the meds, Curable, PRT with Dr. Lisa Van Allen, psychotherapy, graded motor imagery, or plenty of social isolation. Each one bought me maybe 3%, and the road here is littered with even more failed treatments. But stack enough 3%s and you eventually cross a threshold.

I still hurt every day, my life has slowed down drastically, and I’ve accepted I’ll never work again. But I now have enough pain-free time that there's finally room to appreciate what CRPS has taught me. I never thought I'd reach that oasis, and the sense that I've grown from this is durable. So keep trying. Even five years in, the next thing might be one that moves the needle for you, too.


r/CRPS • • 6d ago

Muting Bad Vibrations: An Effective, Vibration-Dampening Car Floor Mat --- A Practical Application

6 Upvotes

2.2k words, about 15 min read

A companion piece to last month’s article, Bad Vibrations: Increased Pain from Molecular Compressions. 

Vibrations are often highly unpleasant for those with CRPS, making riding in the car an uncomfortable or intolerable experience for many. People may limit time in the car or avoid going out to prevent being exposed to transit shaking. 

A vibration absorbing seat cushion—such as memory foam or an air-filled wheelchair seat—can be highly practical for reverberations coming up through the seat into the body’s core. However, seat cushions do not help with the vibrations that come up through the floorboard into the feet and legs. 

People often speak of their negative car experiences, so today I offer a practical, effective, and somewhat moderately priced DIY car mat to minimize transfer of rotational movements from the vehicle frame into the person. My personal assessment—which may not translate to your lived experience—is that this mat provides significant reduction for higher Hertz powertrain vibrations and moderate reduction for low sub-10 Hertz suspension system vibrations. 

I have tested this mat for several weeks now in a car with fair-to-middling suspension quality. The bumps and jostlings from road debris and potholes can definitely still be felt, but the harshness of impact is notably blunted. The constant hum of the car itself is much more effectively mitigated and makes a massive cumulative difference in ride quality, especially over longer distances or if making multiple shorter trips in a day. 

All together, this mat will be 2.4” to 3.25” thick, making it primarily oriented towards passengers. Users may need to move their seat backwards or upwards for comfort to prevent knees or hips from being at awkward angles, particularly for taller or lankier individuals. For safety reasons, drivers should not use more than the thin base layer to prevent pedal interference. Let’s begin.

Base layer

For the layer touching the vehicle floor, use heavy-duty butyl rubber matting. This is often advertised as “sound deadening,” “noise insulating,” or “vibration dampening” material. It uses low resilience to absorb lower-frequency structural vibrations and rumbles, turning energy into heat. These are often targeted towards those with large sound systems that tend to resonate through the vehicle’s frame, but they will serve the same function of muting vibrations from the road or engine. 

The most practical and cost-effective choice will likely be a 10sqft, 80-mil [0.08 inches or 2mm] thick option. This can be purchased online for about $20. Cut the pieces to the size of the footwell and turn 2-3 layers into one thick, solidly connected layer through their adhesive backing to maximize their density and ability to mute vibrations. 

The 10 square feet option I selected had nine 16”-wide pieces, which perfectly fit the width of my footwell. Three long covered my full footwell length, overlapping slightly, and then I stacked three high. This became a very solid, fairly heavy mat that filled the footwell quite snugly. Only the stack closest to my chair needed to have a small section cut out of the lower left corner to lay flat. I did the cutting before sticking all the pieces together, as each raised piece needed a slightly smaller section removed to keep a snug fit within the footwell. 

These butyl squares are generally intended to stick directly onto the metal chassis, and their adhesive is very strong. If you do not want the base layer permanently attached to your vehicle, do not remove the backing of the bottom-most layer. Instead peel the backing away by an inch or two in order to overlap the layers together and then smooth the adhesive backing flat again after they are connected. 

I recommend taping over the places where the adhesive backing is loose, so that any shifting during transit doesn’t peel it off and accidentally stick it to the flooring of your vehicle. Additionally, the edges should be secured with something like foil HVAC tape, roofing seam tape, poly film tape, automotive harness cloth tape, or gaffer tape to prevent the adhesive from seeping out the sides onto the floor during hot weather, especially if your car is carpeted. 

If you feel the need to have additional stabilization, you can use some heavy-duty velcro to prevent sliding or shifting. If you have carpet, you can use just the velcro’s hook-side and it will attach directly to the fibers. If the butyl mat is both several layers thick and sized to fit snugly in the footwell, it is likely heavy enough that it will not shift or slide and may not need to be additionally secured.

Middle layer

To help feet float over heavy vibrations that don’t get absorbed by the base layer, choose rubbery, high-density, closed-cell foam; specifically, use thick and flexible NBR [Nitrile Butadiene Rubber] (preferred) or EVA [Ethylene-Vinyl Acetate] yoga mats, approximately a 1/2" thick. Cut to the size of the footwell and stack loosely in 3-4 layers to a height of 1.5-2". While these can be purchased new for about $20, a used NBR or EVA yoga mat will work just fine and be much more affordable. 

Unlike the base layer, do not connect the yoga mat layers together with glue or other adhesives. Intentionally allow the middle layers to decouple with movement, which reduces the intensity of vibrations that make it to the top layer. 

To prevent shifting or slipping, connect only the corners together using elastic bands, silicone grip dots, or small sections of non-slip carpet mesh or cupboard liners, allowing the individual layers to slide just a bit without moving too much when getting in or out of the car. As an additional option for those who feel the need, you can also place a tiny square of non-slip mesh or grip dots in the center of each layer for a bit of extra stability while still allowing the majority of the decoupling movement that dampens the vibrations. 

When to replace?

The yoga mat will need to be replaced in 2-3 years as constant shaking and extreme temperatures will degrade it over time. Cabin heat during summer is the primary threat, but using a sun shield or tucking the vibration mat under the seat can significantly extend its lifespan. If you want your mat to fill the entire footwell, it will not tuck away well and you should pursue the sun shield instead.

Where is the most prominent slip point?

Personally, I have found that—without any form of added stabilization at the corners or center—the most sliding and shifting happens between the top two layers of the yoga mat closest to my feet as I get into and out of the vehicle. The butyl matting is too heavy to shift, the bottom layers of the yoga matting are held in place by the footwell, and the top-most layer grips the yoga mat quite well of its own accord. If you only have a little bit of additional grip to work with, I’d suggest prioritizing the gap between the highest yoga mat layers.

A great deal of the shifting can also be reduced by adjusting how you get in and out of the vehicle, particularly if you are someone who tends to pivot on the heel of your foot, which causes the layers to pivot with you. Redistributing some body weight to a third point of contact—such as the ceiling grab handle or a portable mobility tool designed to be temporarily inserted in the door's strike plate to aid those with stability issues (name brand version Stander's HandyBar)—can be massively assistive in reducing the shifting.

Is there a practical difference between using three or four layers of yoga mat? 

I was able to tell the difference. It is noticeable enough to me that I put the fourth layer back in the stack, even though it raises the top layer above the door sill and significantly increases the shifting risk unless additional measures are implemented. For someone who has long legs or who really struggles with bending their joints or who isn’t able to raise where their rear end actually sits in comparison to the mat via a cushion or seat controls or who has significant stability challenges getting in and out, removing that extra half-inch to increase leg room or drop the entirety of the mat below the door sill may provide significantly more comfort and peace of mind than the little extra vibration reduction the fourth layer brings to the table. 

Top layer 

To absorb ultra-fine, higher-frequency hums, use a 3/4"-1" memory foam mat with a gel-enhanced or high-density polyurethane core and a vinyl or weather-proof outer layer instead of fabric. Too thin—such as a 1/2”—doesn’t offer enough density to absorb the hums, but too thick—such as over 1”—allows for too much jiggling. I found a thickness of 4/5” [0.8”] to be ideal for me. Those with very sensitive feet should avoid deep or heavy texture stamps on the vinyl. 

Cold temperatures will make the top layer extremely hard, so warm the cabin before driving or bring the memory foam into the house during wintery weather when not in use to keep the top layer soft and absorbent. 

To prevent slipping or sliding, get a mat that comes with anti-slip silicone dots or other treaded backing options and tuck the edges under the door sill or the footwell if there’s enough space to do so. 

When to replace?

If the rubbery layers of the yoga mats in the middle layers can be felt against the heels or if the memory cells remain collapsed or pop back up instantly instead of slowly melting back to flat, the memory cells have degraded and need to be replaced. Uncut mats will last for 12-18 months and cut mats will degrade faster. 

For those who prefer to buy a larger mat and cut it in half, use a sharp utility knife to size it to the dimensions of your footwell and seal edges with heavy-duty gorilla tape, HVAC tape, roofing seam tape, poly film tape, or silicone caulk to protect the foam against moisture damage. Keep the spare half as replacement for when the memory core begins to degrade due to "foam fatigue" in 3-12 months, depending on use and driving habits. New vinyl memory foam mats can be purchased online for between $15-20. 

Yoga Mat Testing

Not sure if the yoga mat you’re looking at is NBR or EVA? Firmly press your thumb into the mat for 5 seconds, then let go.

NBR is heavy for its size and feels gummy, doughy, and soft with a dull or matte finish, has porous or foamy edges on the cross-cut, and horizontal ridges or ribs on the surface. A thumb sinks deeply, and the dent stays visible for a few seconds before melting flat. It rolls tightly and easily, and will droop, flop, or hang like heavy rubber.

EVA is lightweight and feels firm, springy, plastic-like, and air-filled with a waxy or sheeny appearance under light, has solid and smooth edges, and often has smooth surfaces or is stamped with geometrics. It resists thumb-pressing, will pop back up instantly, and stiffly resists folding or rolling.

Avoid yoga mats made of PVC, TPE, or natural rubber.

PVC makes for very thin yoga mats that completely compress with a sticky or plasticky feel that smell like a shower curtain.

TPE makes lightweight yoga mats that bounce back quickly like EVA, but they lack shock-absorption and have a velvety or powdery feel.

Natural Rubber makes for incredibly heavy yoga mats that are usually very thin with a fabric-like weave on the back and an intense tire smell.

Additional Considerations for Drivers

Since most of the mat layers won’t work for those who need to operate foot pedals, here are three alternatives to consider in addition to the thin butyl mats. Drivers should aim to keep their vibration reduction methods to under ¼” [6mm] and secured to the floor to prevent safety hazards. 

⅛” to ¼” commercial-grade high-density SBR [styrene-butadiene rubber] or closed-cell neoprene sheets. These do not compress and absorb low-to-mid frequency vibrations.

3mm to 6mm industrial-grade anti-vibration equipment matting made of compressed recycled rubber compounds. These are tough, high-grip, do not compress, and are designed to mute mechanical hums from machines or treadmills. 

Vibration-dampening shoe insoles made of Sorbothane or Poron XRD, which absorb up to 94% of impacts and high-frequency mechanical shocks. This is considered the safest option for drivers as it is in direct contact with one’s feet and will never interfere with the pedal clearance.  

Quick DIY Reference

  • 2-3 layers of solidly connected, heavy-duty butyl rubber matting, about 80-mil / 0.08 in / 2mm thick, seal edges, can use velcro to connect to vehicle flooring for extra stability
  • 3-4 loose layers of NBR or EVA yoga matting, total height of 1.5-2”, connected only at the corners with optional non-slip mesh at the very center for extra stability
  • ¾”-1” memory foam matting with weather-proof exterior, high-density core, and anti-slip backing, if possible tuck edges into sill or footwell to prevent shifting

Closing

This DIY vibration-absorbing mat is customizable to the size of your specific footwell dimensions, easy to replace in sections as parts degrade over time, and can be made as thick or thin as you need it to be for optimal vibration reduction. May you find this as useful as I did and may it greatly expand your quality of life and transit comfort. 

Thanks for sticking with me, I hope you learned something, and I hope to see you next time.


r/CRPS • • 7d ago

Celebratory! Psilocybin Study

84 Upvotes

Just wanted to share that I’ve been excepted into a clinical trial for CRPS type 1, pain management! I am over the moon and will update what I can as I go along for those interested. 🥰😁