I’m not a marathon runner. In fact I don’t really even think I’m that much of an athlete. However I have suffered from chronic exertional compartment syndrome and have since had surgery to correct it. I thought I’d write about my experience here in the hopes that someone might find it useful.
A Little Bit of History
I was very active, mostly with a lot of squash, premier netball, as well as the odd game of touch rugby. I had had a tightening of what I thought were the muscles on the outside of my legs for some time and had asked various people if they knew how to stretch them. I’m fairly au fait with anatomy after studying it at school but even I couldn’t figure it out. They’d been uncomfortable mostly while I was playing netball, but I put it down to not being as fit as I could be and put up with the pain.
It wasn’t until one day I was playing squash when the pain got so bad I had to come off the court. Luckily the manager of the team I was training with happened to be a physiotherapist and mentioned that the symptoms I was describing sounded like compartment syndrome. I was training for squash nationals and playing finals netball so I didn’t want to stop. I’m also fairly stubborn when it comes to pain stopping me doing things (says the girl who walked home one day with two badly sprained ankles!) so I didn’t treat this any differently.
With squash nationals done and dusted, I moved away from the city where I first heard about compartment syndrome a few months later but began to research it online. It wasn’t until one day I left the squash court and ended up on the floor in tears from the pain that I knew I had to do something about it.
What causes the pain?
When we exercise, the body pumps blood to the muscles that are being worked, causing the muscles to swell or expand. The muscles are contained within a sheath. You know when you buy meat from the supermarket and it sometimes has that clear, stretchy stuff on it? That clear covering is the sheath. When people with compartment syndrome exercise, there’s not enough room within the sheath for the expanding muscle, therefore pressure builds and pain arises. A friend of mine once used a great analogy – it’s like trying to blow a balloon (muscle) up inside a drink bottle (sheath). It just doesn’t work.

Doing Something About it
I went to my GP who referred me to a specialist sports practitioner, who then referred me to a surgeon who specialised in compartment syndrome. Said surgeon sent me for tests (which, by the way, aren’t covered by ACC as the ‘injury’ is deemed to be progressive – kind of like RSI which, incidentally, IS covered).
Honestly, if there were a best part about having CECS, it would have to be seeing a medical practitioner about this condition and watching their eyes light up when you tell them what you have. It’s not a common condition and I think they get a little bit excited when they get to deal with something different from the norm. I digress!
By the time I got the appointment for pressure tests, I had developed drop-foot (or foot-drop as it’s otherwise known) which is when your foot makes a distinctive “slapping” sound as you walk because you can’t lift the front of your foot properly. I couldn’t walk more than 100 metres without the pain getting so bad I’d have to stop. Ten minutes after ceasing exercise, I was fine – which was probably the single most frustrating thing about the entire condition.
The Pressure Tests
I will not lie. The tests are not pleasant. Basically I had three injections of anaesthetic (in marked spots) into each leg to numb the areas for when the BIG needle gets inserted. I was then told to do an activity that causes the pain and come back to the room once it comes on. The specialist was surprised that I was back within five minutes, even though I’d continued as long as I possibly could because I wanted to be sure I got the results I knew would come.

The second round of injections measure the pressure inside the compartments of your leg. Anything over 30mmHg is “surgery territory”. As a gauge, my worst compartment was ~90mmHg. No wonder I was in so much pain!
As a result of the pressure tests, it was recommended that I be prioritised for surgery and I was placed on a waiting list. Through a mix of medical misadventure and me moving city again (and therefore District Health Board jurisdiction) it took me a further 8 months before I finally got my surgery. Bearing in mind that this was around two years after I had initially consulted my GP, I was virtually unable to walk and had put on a lot of weight – a horrible side affect for someone who used to be so active.
Finally! The Surgery
The technical name for the surgery I had was bilateral tricompartmental fasciotomies, which loosely translates to having three compartments in each leg released. When I say released… they make an incision, then cut open the sheath that holds the muscle in place. It basically allows the muscle to expand as large as it needs to when you’re exercising.
It was an overnight stay in Middlemore Hospital for me (and I’m thankful it was only one night!). When it was time to go home, I actually managed to stand up with my legs supporting my full weight while I got dressed. The only piece of advice I can give you is DON’T DO THIS. You may think you won’t move, but you will and it hurts! I was in a wheelchair to start of with, but given crutches before I left the hospital.
Healing Time
I have two scars on each leg – one on the outside above my ankle bone about four inches long and one on the inside of my leg toward the front about midway up my lower leg – about three inches long.

The advice I had read and was given was that it should be around 12 weeks until I could get 100% back into sport. This wasn’t the case for me, however. I went back to work two weeks after surgery (I recommend taking longer – perhaps another week) and even though I held a sedentary position, my ankles and feet would swell up enormously after keeping them “down” for the day, even though I had tried to elevate them as much as I could.

My employer at the time was less than supportive, even though I’d requested that I work from home. If you can, I would definitely aim for three weeks to recover. I was walking without crutches after one week but would still get pain and swelling in the week following. My recovery wasn’t aided by a minor infection in one of the wounds either, so I now have a more prominent scar than I would have otherwise.
Getting back into the Swing of Sport
So, after my two years of not being able to do anything, I was finally free to get back into sport! Unfortunately for me, I don’t think my body was as keen as my mind was and I was bogged down with miscellaneous injuries over the coming year (including prolapsed discs in my back and strained calf muscles). It’s now been around 15 months since I had the surgery and I’m finally uninjured enough to get back on the exercise wagon – enough to hopefully start losing some of the 20kg I packed on over the time I was involuntarily inactive.
Even when running now, I get numbness in my toes and feet. Areas of my leg, ankle and foot are still numb due to the nerves being severed during surgery but I’m hoping to get most of that feeling back. I still get some fatigue and soreness in the same areas as before but nowhere near the amount of agony I was in pre-surgery. My legs are also a funny “shape” because the muscles bulge out in places they didn’t bulge before, but it’s purely aesthetic and I knew to expect that. They are though, still a lot more svelt and “spongey” to the touch than they were pre-surgery. My poor legs.. what an ordeal!
Further Information
If you have any questions, you can contact me or leave a comment on this post.
Here are some websites I found useful:
MayoClinic – Chronic exertional compartment syndrome (Highly Recommended)
Wikipedia – Chronic Compartment Syndrome
EDIT: I have now also created a Facebook page. See https://www.facebook.com/compartmentsyndrome/
277 replies on “Life After Compartment Syndrome”
I developed compartment syndrome on July 17 2012 I was found unconscious by my sister I was lying on my bedroom floor my whole body was on my left leg and my left eye was on the floor as well and when my sister got me up she thought that I was having an allergic reaction to something because my left eye was puffy and she asked me if I wanted to to go to the hospital and I told her no so she just gave me some benadryl and helped me get in bed so I went to sleep for a while and woke up around 10 am I had to go pee and so I got out of bed and I noticed that I couldn’t put weight on my left leg and so I hoped to the bathroom and I went pee and noticed that it had turned black and I told my sister and she told me to call 911 my leg had swelled almost to the point where my pants didn’t fit anymore. My eye was also almost swollen shut. My memory from that point is vary hard to remember. I don’t remember the ambulance ride I kind of remember the doctors working on my eye they asked me if I had been in an accident or if someone had hurt me because thats the only way I could have developed my injuries but I told them no. So they continued to work on my eye they had to cut my eye lid and stick a needle in my eye because by the time I got to the hospital my eye was so swollen that it came out of the socket. The next thing I remember is the doctors saying OK YOU ARE GOING TO SURGERY NOW! After that I don’t remember a whole lot. I was in the hospital for a month and I was in and out of surgery almost every few days to remove any dead tissue. But after I was released from the hospital I developed a contracture in my left foot and I was walking on my tip toes for a year and so I had a tendon release. So now my foot is stuck in the position the doctors put it in and my toes are curled under they are stuck like that. But I’m blind in my left eye because of what happened to me that day. If it wasn’t for my cat waking my sister up wanting in my room I may not be here by the time my sister found me my kidneys were failing so he saved my life.
My son also went through a similar situation. He might have been on his right leg for about 8 hours or more before someone found him. Hes been in the hospital for 2 weeks now and they still cant close his wounds due to swelling. His kidneys are still not functioning. How long were you in the hospital? How long did it take your kidneys to start functioning again?
This blog is great. I had my bilateral fasciotomy on both legs last week she they are still swollen and the tops of my feet and the lower 1/4 of my legs are numb 🙁
Weirdly enough, today I got a sharp pain through the lower part of my leg, felt quite nervy. Has anyone else experienced this? Thanks.
Yes, that is nerve pain. I had this for a few weeks after my surgery but it seems to have stopped now.
Yep. I had a fasciotomy on my left leg about 4 weeks ago now. From my knee down is numb, including my foot, except the under side which is normal. Crazy!
I get pains in the top of my foot and in my leg pretty much just in my incisions.
I sure wish I knew when these pains in my foot and the total numbness and tingling were going to end?! I saw the dr. Today and he said 1-2 years!!!! Are you kidding me?!?! I honestly don’t think I can live with this, that long!
I had a fasciotomy in 2013, drywall fell on my leg. The scar on the outside of my leg is a straight line but the scar on the inside of my leg is worse due the wound vac I had for approx 7 weeks, both are 8-10 ” long. I have a lot of stiffness, a lot of little veins showing around my ankle and sometimes pain in my ankle. The stiffness has caused me to overcompensate at times which has caused some issues with the other ankle. I stretch my leg and that can give relief but looking to see if anyone has any other ideas for the stiffness.
My friend had compartment syndrome and had to have a skin graft done because it was so bad that they had to remove most of her muscle from her right leg on out side of right leg on inside of right leg 10″ long scar. On left leg on 4″ scar on both sides . My question is why did they have to remove so much skin if it supposed to only a problem whit the muscles
I had compartment syndrome in 2011 due to an injury and had to have a fasciotomy. My scar is about 8 inches long. I’ve noticed lately that the scar is always warm. There is no pain at all but I am just curious as to why it is always warm. By the way, this is a great site. Thanks.
my surgery was done in two operations, 1st to place vacuums, pump in my leg thenthen 4 days lster to remove it all.
Does anyone else have problem in feet after the surgery? My feet hurt so much even at rest and they get worse after activity.
It’s nerve damage it can take up to a year to heal or maybe even longer I had open compartment syndrome as well and it has been almost 3 months since I had the surgery and I havent been able to run without feeling numbness on the right side of my leg
Hi, i was involved in a car crash, my left leg crushed. compartment syndrome. Now my foot feels so tight ,its going to explode. i guess i need to see my doctor?
Dear CECS;
My surgery was on my right foot that was very extensive. After surgery, ( no cast or boot ) I lay in bed for about 2 weeks in excruciating pain. I have a very high tolerance for pain and being athletic all my life, I just though it was normal and you know you just tough it out. Not so, after two weeks of pain that I seriously don’t think any human words could describe, I had my husband take me to ER, where my DR. performed emergency surgery on my R leg. Due to CS my foot was damaged by nerve issues. There were no words to describe that either.Then I broke my R big toe, then had Achilles lengthening surgery. However, my foot is doing much better, 7 months post surgery. As of today, I still have no feeling in the end of my R big toe. My foot does have tingling when I am exercising, or been standing or sitting for extensive periods. My doctor said it would take 1 to 2 years to fully recover, and then I may still not have total feeling. When I get out of bed first thing in the morning, I have some foot salve that I rub my foot very deep rub with. This helps wake up my foot. My doctor stated a couple of weeks ago, that he thought I would never walk again. He said he didn’t know how I was doing all the things I’m doing now. I told him I know how, it is because of the healing of my Lord and Savior Jesus Christ.
That being said; keep rubbing your foot with oils or foot balms. Make sure you rub it deeply for at least 5 min. At night time when you get still and your foot isn’t, rub it as this will help to calm it down. Keep going and don’t give up. The Lord knows what He is doing, and never forget He has you and will never leave you.
God Bless
I am 10 years post op. I had bilateral fasciotomy all 8 compartments released. I have debilitating feet pain, specifically my left foot. I did have numbness after surgery on that lower leg. I’ve seen 15 doctors and have done and tried everything . I’m trying to get to the Mayo Clinic now. I can’t live like this anymore
I had surgery 11 months ago. All has been well except the bulging of the muscle ( which is normal) however I recently started getting a cramp in my leg every time I stretch. It is a Charley horse feeling and I can bring it on every time I stretch out my leg. Just wondering if anyone else has this problem?
Hi Stacey,
I actually had a very similar thing. Started taking a magnesium supplement and immediately noticed the difference and still get the same thing if I don’t take it for a while. Maybe magnesium will help 🙂
Has any one gotten the botox treatment from Dr. Mcginley from Wyoming? How was the result?
I got the surgery two years and half ago, but nothing worked. Has anyone had second surgery? How was it?
My daughter has been treated by Dr McGinley in Casper, WY with excellent results. She had CECS in 2 compartments in each leg and B Popliteal Artery Entrapment. Artery entrapment was resolved in 2 treatments. CECS required 3 treatments. He is amazing and has pioneered a conservative treatment that is very effective. He treats areas of the calf muscles that are compressing the veins (CECS) or arteries (artery entrapment) to restore normal blood flow. He has a 100% success rate with the artery entrapment problem and I believe 80% success rate with CECS. If you have not ruled out Popliteal Artery Entrapment, that may be your issue. Fasciotomy surgery will not improve symptoms of popliteal artery entrapment.
Oh my gosh I want to hug you all after reading all of these! I am a mid twenties ballerina turned runner (turned barely anything) who has been dealing with chronic compartment syndrome for 7 years in both lower legs. The issue with me is that I also have discomfort and pain constantly not just upon exertion (although intense activity does make it much worse). When I’m extremely sedentary or standing the pain also worsens and feels tighter. Several surgeon consults have advised against surgery even with testing positive for CECS as they’re unsure it would be successful with something else going on. I’ve explored inflammatory diseases, bone scans, MRIs, ultrasounds, neurological issues, have tried acupuncture, massage therapy, physical therapy, foam rolling, nutritionists, orthotics, gait training, holistic doctors etc. Going back to a vascular surgeon next week. Two questions: 1. Has anyone else experienced a non-textbook case of chronic exertional compartment syndrome? What other things were you diagnosed with/did you explore? 2. For those told to “manage” the pain instead of surgery, has anyone tried pneumatic compression devices such as the one from Normatec to help with pain/mobility?
Meredith my story is very similar to yours except I went down the surgical route! I was first diagnosed with CECS at 13 after being a high-level sprinter and had bilateral fasciotomies a year after diagnosis. However my symptoms didn’t improve at all after the surgery and I was re-tested which sure enough showed that my pressures were too high still (above the surgical threshold). I tried everything to improve my symptoms as the surgeon said he wouldn’t operate again; MRIs, 4 different physios, rheumatologists, holistic medicine, accupuncture, foam rolling, re-learning how to walk, orthotics etc.. Eventually 4 years later nothing had been successful and so I had the surgery again at 18. I’m 22 now and unfortunately round 2 was no more successful than round 1 and so I have to find my own ways to manage the pain (and still can’t do any exercise – 50m of jogging and I’m done). Very frustrating and would love to hear people’s suggestions surrounding pain management and alternative therapies!
Hi Bridget – wanted to update you on some things that have helped manage pain this year.. I wonder if you’ll ever look back at this thread, but just in case you do. I cut out dairy in my diet back in February and it has helped curb some inflammation. I’m considering cutting out gluten and extra sugars because when I have them (like during the holiday times) my pain is worse. Also, in addition to self massage and foam rolling which is time consuming and tiring, I am going to invest in Normatec recovery sleeves to help manage when my legs feel really bad. I’ve gone to a local physical therapy spot in NYC to try them out before buying them and I think it would help for ongoing pain management (they’re expensive though.. $1500…) but if I use them at least once a week, they pay for themselves in a year. I no longer am a long distance runner, but have been cycling, playing tennis and boxing instead which cause less pain than cranking out 15 miles. Hope you’re feeling better!
Did you our insurance cover Botox injections? How are your daughters symptoms now? Is she still pain free? My 19 year old had bilateral fasciotomy all 4 compartments 2 years ago with very little success. Recently re-tested and diagnosed AGAIN with CECS.
Hey what was the cost?
Hi Amy,
For me there was no cost as it was under the public health system. Where are you based? Perhaps some of the other commenters can offer some insight 🙂
my total for my fasciotomy was 115,000.00
Susan, what country are you in and if you don’t mind me asking what currency was the 115,000.00