Pain in the butt - Can't sit down

Posted by ecalderman @ecalderman, Nov 21, 2012

I have had very intense pain at my sitz bones for over 7 months and am unable to sit down. when I sit, it feels like I am sitting on two hot pokers or rocks and it is really unbearable. So, I have been standing for seven months. I've been to a couple of spine and pain management doctors, an orthopedist, a chiropractor, a neurologist, an acupuncturist, and a massage therapist. The original diagnosis was ischial bursitis but that ha not appeared on any images. I don't have any issues with any of my lumbar disks. I'm in constant pain even when standing or lying down though those activities do not hurt as much as sitting. Has anyone heard of anything like this before?

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@shaytsadik

Hi,
I am 22 years old. Suffering from sitting pain in both sides of the buttock under the seatbones. The pain is also going down to the hamstring. I am sitting on the dount cushion for reducing the pain, but still can’t sit more than 15 min. I have tried all the therapy that you mentioned- Pilatis, injections, noytroliyn, massages. This is the only forum that I found that mentions that kind of pain.
Please help me.

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l@shaytsadik, Good afternoon. I think first you need a three breath hug. I am sending one your way...... You are so very young to have your life so filled with those very negative sensations we call pain. I am 77 and have had it all (13 orthopedic surgeries) and also tried it all.

My routine is quite simple now....Myofascial Release Therapy (MFR) and medical cannabis. Just those two things plus a loving and caring life partner. Throw in my swing at the river and the songs from birds overhead and I am content for a little while. There are such wonderful folks in the Mayo Connect volunteer mentors. Hang in there .....they will give you their best efforts. Chris

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@ecalderman

Your situation sounds very much like mine. You probably don't have the same thing but it would be worth asking your doctor about. I can't sit on my right butt cheek and it's quickly spreading into my left side. It comes up from the bottom of both butt cheeks. I was told that it's part of the pudendal (sp?) nerve. Is that what you're experiencing? Have you ever had a pudendal nerve block? My diagnosis is Tarlov cysts (perinerual cysts). They come out of the spinal cord and are innervated so they cannot be removed. There is a surgery available for them though. They drain the CSF out of them and fill them with another substance. There are only a few doctors in the U.S. that specialize in these.

Tarlov cysts are considered an incidental finding on MRIs, CTs, etc. The radiologist may or may not even document them. It has taken me 16 years to find a doctor that questioned what was seen on my MRI. The cysts were present back in 2003 after my accident. I've found that most doctors won't even acknowledge them and say they don't cause any issues. When they grow bigger they DO cause issues. Most times they are in the sacral area and push on the nerves at the end of the spinal cord and cause cauda equina syndrome.Do you have any of the cauda equina symptoms? It would be a really good idea to request all of your images on discs and the reports that go with them. From now on when you go in for any kind of imaging ask for a disk and that a copy of the report be mailed to you. They will give you a disc before you leave. Read through all of your reports and ask about the things you aren't familiar with. Also, I've found that talking to the tech. that asks you all the questions before your scan helps. Tell them you want all incidental findings documented because they haven't been able to pinpoint exactly what is causing your issue. That's what I had to do anyway.

I hope you find out what the problem is. I absolutely understand the agony that comes with not being able to sit! Best of luck to you:)

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@shaytsadik

Hi,
I am 22 years old. Suffering from sitting pain in both sides of the buttock under the seatbones. The pain is also going down to the hamstring. I am sitting on the dount cushion for reducing the pain, but still can’t sit more than 15 min. I have tried all the therapy that you mentioned- Pilatis, injections, noytroliyn, massages. This is the only forum that I found that mentions that kind of pain.
Please help me.

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@shaytsadik @qball2019 Chris mentioned myofascial release therapy, and I would also recommend it and it has helped me a lot. It is physical therapy and can help a lot of conditions where nerves are compressed by tight tissues, and it can help pundental nerve issues. We have a discussion with a lot of information and links to videos with John Barnes where he explains the process. The pelvis can twist out of shape and cause nerve compression and pain to the legs. Here are 2 links to explore. The other link is displayed below the video.
https://connect.mayoclinic.org/discussion/myofascial-release-therapy-mfr-for-treating-compression-and-pain/
Lumbo Sacral Decompression video with John Barnes


https://trainingandrehabilitation.com/identify-treat-lumbar-plexus-compression-syndrome-lpcs/

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@jenniferhunter

@shaytsadik @qball2019 Chris mentioned myofascial release therapy, and I would also recommend it and it has helped me a lot. It is physical therapy and can help a lot of conditions where nerves are compressed by tight tissues, and it can help pundental nerve issues. We have a discussion with a lot of information and links to videos with John Barnes where he explains the process. The pelvis can twist out of shape and cause nerve compression and pain to the legs. Here are 2 links to explore. The other link is displayed below the video.
https://connect.mayoclinic.org/discussion/myofascial-release-therapy-mfr-for-treating-compression-and-pain/
Lumbo Sacral Decompression video with John Barnes


https://trainingandrehabilitation.com/identify-treat-lumbar-plexus-compression-syndrome-lpcs/

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Like Chris, I have found MFR to be a blessing regarding help in the PN in my feet and chins. With 2 sessions I had very little numbness, pins and needles etc. I’m on therapy number 6 and my therapist had found several areas where I had back surgery that she is working on, loosening the fascia to keep the pain at bay. It might take several treatments, but if you stick with it, and be constant on self treatment, hopefully this can make an improvement.
Good luck. Mitch

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My pain started in the butt crack.It feels like hot pokers. A pain specialist. Injected cortisone in it. It made it totally intolerable. I'm currently taking Gabepentin 300 mg three times daily. It helps a lot but I'm still in pain. I get relief laying on my sides.

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@russy it could be compression on a nerve is causing the pain. Does stretching, exercise (possibly including Kegels - especially while seated) or other supplements (like turmeric, hemp seed oil) cut the pain in addition to Gabapantin?

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@richman54660

@russy it could be compression on a nerve is causing the pain. Does stretching, exercise (possibly including Kegels - especially while seated) or other supplements (like turmeric, hemp seed oil) cut the pain in addition to Gabapantin?

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I haven't tried anything other than the medication. Per your suggestion I tried the kegals exercise and it makes it worse. Does the turmeric supplement come I various strengths? I may try that.

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@russy

I haven't tried anything other than the medication. Per your suggestion I tried the kegals exercise and it makes it worse. Does the turmeric supplement come I various strengths? I may try that.

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@russy there are various turmeric capsules available. I use youtheory brand extra strength available at Costco or on Amazon. You may want to seek out a physical therapist who does pelvic floor rehabilitation. They might have suggestions that help you.

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@richman54660

@vklittle61 Until the sitting pain is better you can buy a: "Hemorrhoid Cushion by Vive - Donut Cushion for Hemorhoids, Pregnancy & Piles Pain Relief".... which is an inflatable donut pillow. Inflate to your liking and use with other cushions, too. You can put it in a black carry bag "Reusable Grocery Tote Bag Large 10 Pack - Black". Search those terms on Amazon and buy them if you like. I still use those on harder seats. The vive cushion gets your sit bones off the surface until it's better. The muscular tension can cause a bursitis which is agonizing to sit on (bursitis is usually a secondary condition caused by something else behind it). Eventually, my sitting pain got better and I just use other types of cushions now like a thinner (bed bath and beyond has many seat cushions you can check out). You may need to keep looking to multiple doctors and multiple physical therapists until you find approaches that work. The standard NSAID's the Drs. push probably won't do it all alone. Also, keep trying different things until they work.

Below was the entirety of my 3 posts I'd replied to someone else: ( @melissahebert ), Stretching and exercise for both glutes as well as hip flexors may help (search the internet (or talk to physical therapists) and do what is tolerable to you). If you suspect an internal trigger point may be responsible (you have evidence of that) you could contact pelvic therapies (Carlsbad, CA) and get an LA wand and try some self treatment. They have training videos on their website. Also, you could try and find a physical therapist that can do internal and external Myofascial release – but they might be few and far between, depending on where you are at. I have tension near the tuberosities, too, with sit pain. Somehow nerves are compressed, irritated triggering tension. It’s a viscous cycle detailed in the book “headache in the pelvis”.

My biggest symptom was sitting pain as well as stiffness (a hallmark of myofascial pain). My lower lumbar DDD probably fuels it for me but proper stretching and exercise (Pilates reformer, TRX suspension for core and do intense psoas / hip flexor stretches, too, and very deep breathing to release tension (while I exercise)) really helped me. In your case, I’d think internal massage is needed along with stretching and exercise. The “headache” authors advocate a whole program including internal massage. You’ve got to get those muscles relaxed and they’re also all connected (as are the nerves).

Post 2: I also forgot to mention that I had piriformis syndrome (buttocks spasms & can cause sciatica) and all kinds of tension in upper legs, too (tight IT bands, tight areas/ trigger points in quads, glutes and upper hamstrings; in my lower back my quadratus lumborum was tight). I learned all this working with various therapists. Again, stretches and exercises for piriformis, glutes, may help you. Trigger points in that area can refer pain and tension to the buttocks and anal area. TRX suspension core routines work glutes well, try the figure 4 stretch against a wall for pirifirmis (or get a piristretcher from miracle stretch). Rollga foam rollers are good, too, for rolling legs and glutes. Electrical stimulation of tight areas might help. Some chiropractors have e-stim or you can buy a TENS/EMS unit for yourself. Try rolling tennis balls or 4 or 5 inch massage balls on the glutes or along the upper hamstrings to get rid of trigger points (you may need to rest on trigger points for several minutes to get rid of them). Try the other suggestions in my last post, too. Yes Myofascial pain and tension is probably caused by some type of nerve compression – but it can be made better or made to go away with the right stretches and exercises (possibly). Mine got a lot better. I still have a little sitting pain is all. Try everything, and listen to your body. BTW, a TRX system, a Rollga roller (these are curved) a TENS /EMS system and a pelvic therapy wand will probably cost you less than 1-2 Myofascial release treatments will cost. My thinking is getting rid of this was a do it yourself project for me – but I actually enjoy stretching and exercising. A chiropractor that uses electrical stimulation on the glutes helped me a lot, too, for a time. However, the MRT approach (mentioned below) worked best of all. Good luck.
This is post 3, with prior ones in this forum – sorry – but I can't edit prior posts – so there is more information, below. I am not a Doctor so this is not a diagnosis. However, spasms, and pain in an area are generally part of myofascial pain. Medical Doctors are notoriously ignorant about muscuar pain and it's consequences. Nerves aren't necessarily always "entrapped" but rather compressed, irritated. This may repeat some of what I said but, you'll may want to google "trigger point massage" and look for stretches for all areas of your hip (both front and back) and do them. That being said, overdoing trigger point massage can cause some pain and often the "tension" is internal – and you have evidence of that. That's where the stretching and exercise can help for the internal (as well as the LA wand).
Also, I found working the stairclimber at gym as well as weights, pilates, TRX (I talked about that in my prior posts). I also use an inversion table as I have some degenerative disc disease. Supplements helped too, maybe, I am taking 1 tsp of hemp seed oil extract orally, resveratrol supplement + quercetin supplement and 1 carnitine seemed to help me, too. At a different time you can take Rutin with the resveratrol (Rutin is related to Quercetin - so beware you're not overdoing some of these). There are published reports that resveratrol + quercetin helps burn more fat and may reduce lactic acid buildup which might be a source of problems in myofascial pain for some people (see Amazon for all these).

For exercise, stretching physical therapists and knowledgeable massage therapists were the most helpful. I finally found a certified massage therapist in the Palm Desert, CA area called MRT (muscle repair therapy) that does intense ultrasound and stretching – that helped me immensely but I had a history of doing tough martial arts including Judo with breakfalls on the legs / hips so some of my issues were due to scar tissue he's remodeling (and it's working). If you can take heat you can lay on jade stone far infra red heating mats, too – that heat penetrates (however, if nerves are irritated and that is the source of your pain it could get worse ((supplements can help that)). Check and see. I personally went away from ice because it tends to cause trigger points and stiffness. However, I bet you'll find stretching and exercise (and very deep inspirations) will help you the most. Try stretching the piriformis and all kinds of other muscles and make sure you don't have weak muscles. Muscle imbalances as we get older can happen and a weak muscle is a tight muscle (i.e. "piriformis syndrome" – stretch it and do "clamshells" with some resistance bands). Glute spasms can be caused by piriformis syndrome; TRX workouts will help with weak back and glutes and weak core). It's all connected but you can get it all to relax. It isn't permanent even if you've had it a long time – but, that being said, chronic pain gets harder to get rid of the longer it goes on. Books to read: Headache in the Pelvis, Life after pain (Kuttner) and Pain Free (Egoscue) – but I prefer more intense exercises than his simple e-cises ("A muscle that does not move becomes a muscle that can not move" -Egoscue). Also, "Heal Pelvic Pain" (Stein) is good. When you get nerve compression and possibly whole regions of tension – like I had. You may have tension you're not really aware of – you just feel the pain/ spasms/ other nerve pain (burning/tingling) and even other parasthesias (altered sensations also including sweating and ciruculatory effects). Good luck. Work hard and you can get your life back! The Headache in the Pelvis authors point that out – everything in the hips and back is so tightly innervated together that often people have multiple problems that are related (i.e. back pain / hip pain / spasms / IBS, diagnosis of IC, (with some diagnoses often a guess), etc.). Those nerves are all connected. Free the nerves! That's a lot of info – and my last post, I should think, but that is what helped me after two long years to get rid of most of my pain in the lower back, glutes, sciatica, and ease IBS-like symptoms.

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Hello, wow so much info to read and understand. The awesome info you wrote does it apply to rectal pain? I have had this pain 24/7 365 for over 7 years and have doctors say its levator ani syndrome to bursitus. The pain is always on the left side. The latest doctor in charge of the pelvic dept said it was bursitus located behind a lot of nerves
She said it's not curable and not one surgeon would operate becsuse the procedue has a very high chance of creating incontinence. I'm still seeking answers. Do u have any advice. Thank you.

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@tjp4

Hello, wow so much info to read and understand. The awesome info you wrote does it apply to rectal pain? I have had this pain 24/7 365 for over 7 years and have doctors say its levator ani syndrome to bursitus. The pain is always on the left side. The latest doctor in charge of the pelvic dept said it was bursitus located behind a lot of nerves
She said it's not curable and not one surgeon would operate becsuse the procedue has a very high chance of creating incontinence. I'm still seeking answers. Do u have any advice. Thank you.

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@tjp4 There is also a pudendal nerve entrapment post and I'm going to reproduce a post from that. I've had sitting pain and it got a lot better with the following. My doctor thought I had ischeal bursitis at first and after two years when a bunch of myofascial pain and stiffness mostly resolved he though it was some type of myofascial pain syndrome. The idea is, tight myofascial tissue may be compressing your nerves, creating pain - especially when sitting. Also, consider looking for a physical therapist who specializes in pelvic floor rehabilitation. In some cases, this my involve treating internal trigger points and this has been described in the book "a headache in the Pelvis" by Wise and Anderson. Did the doctors talk to you about trigger point therapy and since you've been diagnosed with Levator ani syndrome did they suggest seeing a pelvic floor specialist? They might be able to do something about your condition. If untreated, these things seem to be able to go on and on, I believe. With treatment, they can often be made better.

Here was a recent post from me from the Pudendal nerve entrapment post: There were many suggestions for coping with sitting pain in old threads, above (in pudendal nerve entrapment thread). Mine has gotten much better thanks to stretching, exercise, MFR and I found a therapist that used intense ultrasound while he does active release stretching. Recently, I've started taking some enzymes (serrapeptidase (biomedic labs) and Nattokinase (Doctor's best); both from Amazon) and these helped immensely. I believe these help the tissue remodel (compression from MFR isn't the only way to remodel the fascia – electrical (galvanic) stimulation, ultrasound, stretching, exercise can assist this process, too). However, I had a lot of stiffness and I do believe it is from deposits of fibrin in muscles, on nerves, on bursa, etc. My pain level (and stiffness) is way down after taking the enzymes I mentioned (on an empty stomach). If you are not on blood thinning medication already, it might be worth a try. That seems to be the contraindication. Also, for some reason 10-15% of Especially if you have stiffness, too. I believe that now I am mostly dealing with healing of tendons that attach to the ischeal tuberosities – hence I have some small sitting pain (which has been getting better over time). Here is a review I wrote for an enzyme product on Amazon:
Long story short I was having some myofascial pain (stiffness, sitting pain) in the legs, glutes, lower back. It’s been getting better thanks to various supplements (especailly Vitamin C with citrus bioflavinoids, quercetin / resveratrol, stretching and exercise). I also had plantar fasciitis in the feet in the past as well as some sciatica symptoms (which is due to some type of nerve compression / irritation somewhere along the nerve).

This helped along with taking nattokinase (2000 U) and I worked my way up to 2 tablets of the Serrapeptase 3 times daily (one dose with the Nattokinase) Eventually, I’ll cut back to a maintenance dose and maybe use just 1 of the 80,000 U serrapeptase and 2000 U nattokinase.

While speculative, deposits of fibrin may be the culprit in causing tissue stiffness and improper tissue remodeling as you age. This may accompany (or possibly cause) conditions like plantar fasciitis, phlebitis (and some leg swelling), stiffening of the tissue – all things I am encountering. I noticed a decrease in sitting pain (i.e. less glute stiffness) right away within about four days of starting serrapeptase. On higher doses, I occasionally felt tingling in my feet while walking – but not in a painful way. More like the itching a healing wound might have. I had some areas near the ischial tuberosities that had dense areas that possibly were scar tissue-like (many years of martial arts with kicks, plyometric moves, hard landings probably contributed with this as well as possibly abnormal amounts of fibrin that were deposited on top of that as I aged – that was suggested to me by an injury massage therapist who specializes in aging athletes). Over several weeks, these became smoother and less ropey feeling. Prior massages including aggressive trigger point massage could not remove this / smooth this out. I’ve done all kinds of stretching, exercise and massage. These enzymes have been one of the most effective treatments in healing what I’ve got. Once I started on these enzymes I could feel the difference within a couple weeks. I could see some more recent scars that I have that were raised up appear flatter and remodel.

I generally research what I take and also read all the reviews from people taking these products and also scholarly articles. Based on what I’ve read, (and this is speculative – I can not state any of this as a universal medical certainty) it is quite possible that Serrapeptase can assist tissue remodeling, help remove / minimize scars / adhesions / help break up cysts, etc., including those that may irritate nerves, too. For many people, poorer healing may accompany aging. I believe this enzyme helps healing. I had no gastric irritation from either the 80,000 U version of the 260,000 U version of the enzyme. I was not recompensed in any way for this review. At some point, I'll drop down to a lower maintenance dose with the 80,000 U tablets, I suppose. End of post.
These enzymes and the supplements I mentioned may be worth a try for anyone experiencing pain from nerve compression. The contraindications for the enzymes are if you are already on blood thinners or if they give you gastric irriation. I personally believe that, for me, these treatments needed to be done together. That is, upon using the enzymes suddenly the stretching and exercise really made a much more rapid breakthrough (although the vitamin C and other supplements were helping - but it was slow). Maybe you'll make a breakthrough. I just took a 12 hour flight and only used 1 extra thin cushion and was relatively comfortable. For me, that's way better than it had been.

Also, you can search online for terms involving levator ani and such as: "internal trigger point release for levator ani syndrome" or "Levator ani treatment", etc. A Pelvic floor specialist (a phyisical therapist) should be able to help you, I should think. Good luck.

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