Costochondritis pain and discomfort

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Im 31 and was diagnosed with costochondritis about a year ago. Its kinda lasted the whole year, but recently, over the past few months its been really bad....went back to my gp twice in the last 2 weeks because was convinced it was something more serious.

The main tenderness has been on my left lower rib cage, just under my breast, but now I have pains on my upper right breast plate. My gp has requested ecg/chest xray and blood test to reassure me that there is nothing seriously wrong (still awaiting to have these tests done, but should be anytime soon) hence the reason im on this forum as even tho my gp actually said to me 'I will fall off the back of my chair ifit is anything more serious...I still can't stop worrying as the pain is so bad.

Im getting so anxious about it too, especially at night just before bed, then find it so difficult to sleep, the more anxious I get the worse the pains seems.

Does anyone else find themselves pushing onto the pain when it hurts? This is probably making it worse I know, but can't help wanting to hold the pain!

Im really glad to have read all the discussions on this forum, it really is giving me some reassurance that it isn't just me and that something that isnt life threatening can be so uncomfortable and painful sad

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  • Posted

    Hi all,

    Firstly thank you for all the very useful info and tips! 

    I suffer from mild asthma however following a nasty infection in my left lung it has been exhasurbated (for about 6 weeks now). I finished my antibiotics about a month ago but have continued to have "attacks" of sharp chest pain, difficulty breathing, dizziness (perhaps through panic!) and pain around the back of my lungs. 

    These attacks had been happening almost daily and having had an ECG, bloods, and two chest X-rays the doctors advised me it was muscular pain following the infection (I believe to be Costo).

    Has anyone else had experience of Costo with asthma? Or found CBT helpful with the anxiety/panic? 

    I also wondered about exercise as a trigger? I walked up a rather large hill yesterday (about 30 mins walk) felt v breathless and have had 3 attacks in the 24 hrs since.

    Been taking paracetamol but now on co-codamol! 

    Anyway many many thanks in advance for any advice, always appreciated :-) 

    I xxx

    • Posted

      Hi Isabelle,

      Walking up a hill makes costo worse.  You breathe more deeply and you move your arms which puts a strain on the sternum/rib area.  Even if you keep your hands still, that takes effort as you are using muscles to inhibit a natural movement. 

      What worked for me (and it's not good news, sorry!) was to give up almost all exercise for a three months.  I am 61.  If you are younger it might be less. Avoid load-bearing activities (lifting, pushing, pulling). Where possible avoid hoovering, gardening, shopping (can you shop online?), carrying a heavy handbag, opening heavy doors (say you have a ribcage injury and ask for help).  You might have to go without a bra for a while.  And as another poster said, it's better to sleep on your back as this avoids compressing the ribs.  The alternative is to sleep on your side and support your upper arm with a large pillow. Avoid hunching over a phone or ipad or PC.  And anxiety, if it makes you hunch your shoulders or tense up will make it worse, so CBT might well help.  If you can improve your posture so that your upper chest area is open, then it will help a lot.  I have set a reminder to do this on my mobile as I have always tended to hunch (asthmatics tend to!).  I wish I had a magic wand. What helped me was trying to stay positive, finding things I could do (not so easy) and the support of friends, especially friends who have dealt with disability. All the best,

    • Posted

      Hi,

      Can anyone around my age 59 tell me if they have had costo for more than a year ? I was first aware something was wrong Oct last year - sent for scans etc and nothing was found. I have constant pain under rib cage which has now spread on occasion to between shoulder blades. Breathlessness and sometims my abdomen feels swollen and tight I cant believe all this can be from costo? anyone else have similar experiences. I seem to have a constant dull ache somewhere around the back,ribs, upper chest, ribcage - I could go on and on ! Some days better than others when I think it is going away and then back to square one - so worrying which I think then makes it worse ? any replies/experiences welcomed.

    • Posted

      Hi, I am 52 yrs old and have had costo for 3+ months and my situation sounds similar to yours. Pain started in the left ribs under my breast after I had bronchitis. I had 2 xrays to rule out pneumonia or broken ribs from coughing. I have been on Tramadol for pain and I take ibuprophen daily. The pain is now in my back, shoulder blades, ribs, sternum and also I have the stomach problem you describe every now and then. Stress is a factor and I have been under alot of that as my husband was diagnosed with a blood cancer in late March. I also use heat packs, and other times ice packs. I am at my wits end! This has been the worst condition I have ever had and sympathize with anyone who also has to go through this agony.
    • Posted

      I sympathise with all you guys, but this really seems to be a particular condition that we in New Zealand phsiotherapy have no difficulty treating; however it's just not understood in the UK.  Sure it's irritation, inflammation and pain where the ribs hinge onto the breastbone, but the [u]reason[/u] for it is because the other ends of the ribs which hinge onto the spine are basically jammed.  Medication is only ever going to try and put the lid on the inflammation and pain; it's not going to free up the mechanical problem of the frozen joints around the back causing the reason for the pain in the first place.  That you do with what we see as pretty straightforward hands-on manual physiotherapy - essentially jiggling or cracking the frozen joints back into full movement again.  Otherwise they can just stay stuck.  There is more to it, but that's the answer, and we don't actually find it difficult.  

      Good luck, Steve August (B.A.,Dip.Physio.).

    • Posted

      Hi Stevie I'm 51 and have a similar story to yours.  I'm sorry for your pain and for your stress!  I think we should keep in touch because I'm just starting to address this issue.  I didn't realize something like this condition existed.  I thought I had a horribly pulled muscle and have been stressing out about this constantly.  Best wishes to you.  Please keep us updated and I will do the same.  Feel free to remind me!
    • Posted

      Hi Mr. August,

      I am seventeen and have had costochondritis for over three years now. I am through all the medical options suggested by my doctor without success; I also did physiotherapy for awhile, and have not truly benefited. Since I live in Canada, I am not sure if there are significant differences in physiotherapy practices here compared to New Zealand. Could you give me some information on how costochondritis is cured in New Zealand, and is there anyone you can reference for me, in Canada, who understands how it is done? Or can I treat it myself somehow? Is there literature on this subject that you could suggest, especially physiotherapy exercises or instructions? Any help would be greatly appreciated!!!

      Philine

    • Posted

      Hi, i'm 59 female.Everything that as been describe i feel.

      The  pain between the shoulder blades.

      The feeling of bloated abdomen.

      Constant niggles around ALL the chest area.

      Fluttery, throbing feeling thats there almost 24/7.

      I've had this for 1 year.

      I have had bloods checked.

      ECG.

      xrays.

      Having a MRI this sunday.

      Doctor told me in march it was costo.

    • Posted

      Hi, had this since January, mY GP is surprised that I still have it. I had to tell her that it can be chronic, she had no idea...my chiro is treating it, but as long as I am anxious or stressed, it will not go away. That is my diagnose...
    • Posted

      Hi there,

      I am coming up on 1-yr now too with all your symptoms and more... I have gad the $ million workup showing nothing but blood work does show that I'm fighting something.

      I am now throwing some money at alternative medicine doctors to test for Lyme Disease and other obscure situations... Just thoughts for you to consider. It's awful I know.

    • Posted

      I am having the same symptoms as described started in February with lot of pain around breast bone and right rib pain, have had every gastrologist test done, egd, ultrasounds on every body part, all normal, lead to heart palpitations , and panic attack, ended up in ER, they focused on my heart and said I have afib and need Abalation. Had every test done, 2 electrocardiocagrams, at least 50 EKG, Heart Cath, blood work up, several chest X-rays...all normal.. Been thru several Dr's, no one understands the extreme pain like a band around my upper GI, to ribs, sometimes it chokes me, cannot wear a bra or pants, only lose stretch , eventually had gall bladder removed a month ago, no difference, still get attacks , they still insist it's afib, just started acupuncture treatments for stress and pain, and physical therapy, I'm at my wits end! Nothing makes me better, very depressed and now battling anxiety, have lost 40 in 3 months, eating so little and very bland, no caffeine, no alcohol ,no fried or fat, because everything brings on tremendous pressure in breast bone area , feels bloated and gas very painful to touch, been living on simethicone pills to relieve some of the pressure, no pain meds work, please explain me to me so I can relay to my pt on releasing the frozen joints back into full movement around the back, as he started to work on my right rib area

  • Posted

    I am new to this forum, as a matter of fact I am new to posting full stop! I have suffered from Costocordritis now for the last 3 years, I have found ways to manage it and the associated ‘issues’ arising from the disease.

    Instead of giving you my lengthy back story first (however I will write it afterwards so you can read it if you so chose) I will impart my techniques to manage the symptoms.

    FIRST AND FOREMOST (apologies for shouting) GIVE UP SMOKING (apologies again)

    It is not the nicotine, I know because I have ran a series of tests with e-cigarettes and NRT patches, neither the e-cigarette nor the patches affected me in any way, save as to the typical side effects accompanied with nicotine, however smoking an actual cigarette triggers my Costo off instantaneously.

    Carrying and lifting - unfortunately, if you like I have children (3 of them including twins) then lifting is as innate to you as feeding or sleeping, however you need to cut down on the amount and question the necessity of lifting, as this will enflame the costal cartilage and then back to square one.

    DO NOT JUST LAY IN BED - This is actual counter-productive as you are not evenly distributing the load of your body through your skeletal structure, you are point loading and if you lay on your side, newton and his pesky laws win and you are applying more load through your chest and ribs.

    ANXIETY! - Yep, the gift that just keeps giving! I cannot say you are not having a heart attack, however if I am having a heart attack, then I should probably register myself with Guiness and their book of world records as I must be the only survivor of a 3 year heart attack. We have been conditioned to believe that chest pain=myocardial infraction, that is non-sense, there are clearly lots of conditions that cause chest pain, including hypersensitivity due to anxiety that mimic the symptoms of heart attack, chances are if you suffer from Costo and have the symptoms, it is the Costo, but of course if you are really concerned go to the A&E.

    NSAID’s - Here the old adage “Everything in moderation” is certainly applicable. Most NSAID’s such as Ibruprofen (Nurofen etc) Diclofenac and Aspirin have harmful affects on the digestive system, especially the stomach, they can also cause problems with your liver. Take them in bursts, 3 - 4 days max when it is bad, then rest off for a few days or as long as you can. 

    Muscle Relaxants - I take Bromazepam which relaxes me, but of course you can also create further problems with reliance by taking them. Think long and hard before you do, if you do not suffer from Anxiety then steer clear!

    Light Physical Exercise - It seems to me that a lot of sufferers seem to just do nothing physical, this in itself can cause all kinds of problems including depression, get out and walk, during an attack of Costo, do not walk fast, keep your breathing right down to prevent further irruption of the Costal Ligaments, but you will feel bette for doing it, and it will keep your mind healthy!

    THERE IS NO MIRACLE CURE……. but talking really helps!

    A little about me:

    My humble beginnings were as a child forced into care due to a series of very unfortunate domestic circumstances (my step father had a penchant for beating to within an inch of my life, and had on one occasion, or the day world stood still and I was robbed from my mother, very nearly did). 

    I managed due to the support of my peers and the people around me to get straight A’s at both GCSE and A-Levels, which for me at the time was my magnum opus!

    I joined and served in the Royal Marine (42 RMCDO) until I left in 2004 after a few rotations to Iraq and Afghanistan. I had served 7 years until I left. During which I had also studied and gained a degree.

    Soon after leaving, I had been first on scene to a car accident, to which my friend and I had managed to pull the occupants free from the car prior to it becoming an inferno. It had dawned on me at the time that there must have been over 50 people on scene that day, none of which volunteered their help.

    That very event sent me into a deep and existential journey where isolation was the only way to understand the world…. This was my take on the situation, turned out that the events of that day had triggered some latent form of PTSD and I had actually isolated myself for the past 3 months, become and alcoholic and believed I could well be on the way to becoming the next messiah, problem was I was 32 and died at 33 so I only had a little time left!

    Anyway, after losing my girlfriend and son, (she left and I still do not blame her) and a failed suicide attempt, which thanks to a man walking his dog at 4.30 in the morning, thwarted my cunning plan, I decided to seek help, this is where they tell you real kicker, PTSD has no cure! Brilliant! Very long story short, this is a disease with good days/months/years and bad… Pretty much like normal life for anyone, only problem is, when it gets bad, it gets really bad.

    So, I managed to get back on my feet, 33 came and went, still alive, realise that maybe I was not the messiah after all and that I need to proceed!

    My first dance with Costocordritis…. It was not a foxtrot, more like a waltz! 2011 came and my friend and I decided to go snowboarding in France. Whilst boarding through a forest, a clearing appeared and somebody had quite rudely laid a strip of tarmac with 3ft high curbs which I managed to protect the rest of body by smashing my rib cage into, snapping 2 ribs forcing one through the lining of my chest and cracking 6.

    Rehab was long, but some 6 months later, chest pain, pressure on my chest, numb left arm….. HEART ATTACK! My new girlfriend and now wife rushed me to hospital, at this point I had convinced myself I was fine and it was a panic attack (had never had one up to this point, but now they seem part of my monthly ritual) however the doctor was concerned about my ECG, I then allowed the demons in) Just to digress, I think now if my anxiety as my friend, my old reliable friend that pops in now and again in order to remind me that he is still alive and well, ready to jump on me when the mood takes him, the problem is he is very convincing when he seduces me in opening the door. Back to the point, so I ended up spending a few days in hospital, everything was fine.

    This occurred maybe 3 more times with me being rushed to A&E… There is no dignity in this, but equally no diagnostics, just a “You seem to be fine now, go home”. 

    Who can really live like this? So decided to do my own forensic investigation, had all the blood tests under the sun, all fine with the exception of my ALT levels, and chest x-ray was clear, most likely no cancer. I then looked at the symptoms, there are lots of conditions that mirror my symptoms, but none more that Costo, so when on holiday, (the UK is not the best place for diagnosis) I dislocated my toes, and when seeing the doctor I asked him for his opinion, he examined me and in about 2 seconds said yes, with little doubt in his mind that I was suffering from Costocordritis!

    Then my journey began into the best ways to manage the inflammation (as above)

    Any way, if you managed to read my little essay, then god bless you and I wish you all the luck in the world in living with Costo, everyday is a gift no matter what the circumstance.

    • Posted

      Hiya warren. Not sure if smoking is a factor, though it wont help.

      I have never smoked, ever.

      Not had a drink of alcohol for 12 months.

      This as made no difference to my costo.

      I think my problemm is anxiety, though i dont have attacks, it's just there more or less all the time.

      I would love just one day of freedom from it.....still waiting.

  • Posted

    I have the same problem myself. this is so painful. i swear i was having heart atttack. my doctor had to run all the test EKG,Spiral CT chest, all the blood test for me to stop worry. at nights the pain gets worse. how long your pain lasted for. i am now going into three weeks and still no relief. i am on cataflam.

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