22 years old With Osteomyelitis in my jaw- 8 years of pain -

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It is quite difficult to start writing about something which has been such a big part of my life for 8 years. I will start from the beginning...

It started when I was 14 out of nowhere. The dentist I saw said I had a displaced jaw bone and this was the reason for my pain. I will always remember him asking if I had a boyfriend 'as kissing would make it worse?!' I did not. So at this stage I thought that this was the reason for my pain - a displaced jaw bone. I was given 600mg of Iboprufen and took this every day alongside paracetomal (8 tablets a day).

Over the next year the pain got particularly worse and my face swelled like a balloon. At the age of 15 I did not sleep at all. I had constant pain and was taking as much painkillers as I possibly could. The swelling got that bad on the right side of my face I felt like a monster. I grew my hair to as long as I could and would constantly cover my face with my long hair and a scarf.

Over the summer it would be increasingly difficult to cover my face without a scarf and when I was 15 I could no longer take this pain from my 'displaced jaw'. My mum and dad took me to A&E. Instantly the doctors here realised something was not right and I was admitted. Many tests were done to see what the problem was. I was discharged from hospital with painkillers and had to wait for my results.

I went to see one doctor for my results who I had seen whilst in A&E she specialised in cancer but luckily I was told by her I did not have this.

I had tests such as blood tests, bone scans, MRI scans, CT scans and a biopsy which told me that I had Osteomyelitis in my right lower jaw bone. I was referred to a very good consultant in the 'maxfax' department. He said that the steps that would be taken would be firstly an operation which would be done internally to shave away the acess bone and would hopefully relieve me of some pain. Whilst waiting for the operation I was given the antibiotic Amoxycillin.

I had the operation when I had just turned 16 I think. By this point I had not had a full night sleep for a year and a half. This was very frustrating as I was trying to live a normal life as possible. I was trying to be a good student at high school and not get behind with work. I was in excrutiatiing pain- I constantly felt like I was being viciously stabbed in the right side of my jaw. This pain often went up into my ear and below my eye. Often I was in too much pain to attend school, luckily I had one amazing teacher there that always sent work home and constantly reassured me that everything would be fine. I was particularly worried as this was happening whilst I was preparing for my GCSE's.

After the operation my face was badly bruised and I had very bad swelling. This was expected though as the operation wasn't plain and simple. One part of my face looked as though I had a tennis ball in it. I also had drains coming from underneath my chin that was draining access blood. I recovered in hospital for around 10 days and was given oral antibiotics to take home.

I saw my consultant regularly. Once the swelling had gone down from the operation- the swelling that was normally there from my osteomylitus wasn't as bad at the side of my jaw as this had been shaved away. Swelling of the bone was still there though. My consultant suggested I have hyperbaric treatment every day for 6 weeks. I was just waiting for a space to become available.

A space came available for the hyperbaric treatment - I remember being at school , I was taken out of my class to be told this treatment was going to start. I cried. A mixture of relief that the pain and this horrible swelling might eventually go. Again I missed a lot of school as I went every day to hull for this treatment. I have sworn to myself I would never have this treatment again. Hyperbaric treatment helps to get oxygen to the jaw so there is a better blood supply to the bone. A lot of cancer patients attended this treatment also. I had to enter a tank every day- put a oxygen mask over my head - something I can only describe as something astronauts would wear! For around two hours I was In this tank with a nurse and around 6 other patients- the pressure in the tank is changed and you have to make your ears pop like you would do on an aeroplane before the pressure goes below a certain number- a weird treatment but I can see the logic in it. I don't think the treatment really worked for me to be honest and I wouldn't do it again- but it may work well for others.

For the next couple of years I went on to do my a levels. I was on long term anti biotics as the osteomylitus had not gone away. I found Amoxycillin did not work for me so I was put on long term penicillin whilst on painkillers. I found that stress aggravated my jaw bone and I had episodes where my jaw would swell up more. At this point I had always said to my consultant that it may be my wisdom teeth were making my jaw worse. I was put to sleep and I had these removed from my right side- my pain did not stop so unfortunately this was not a cause of my osteomyelitis.

After my A levels I decided to take a year out and work full time at the job I was currently working part time at. At this point I was 18-19- during this time as I was older I could take stronger pain killers. I am intolerant to codeine so my options were ibuprofen and paracetomals or dicloflenac when this didn't work I would take tramadol which would have horrible side effects. When these did not control my pain my only option would be to go to A&E and be admitted to have stronger pain killers and anti biotics through an IV.

When I was 19 I was admitted to hospital because I was in so much pain. My consultant wasn't around at the hospital in this occasion so people he worked with decided they would operate as they wanted to drain my swelling at the side of my face of fluid as the swelling was getting uncreasingly worse. I have forgotten to mention that most of the time the opening of my mouth is restricted due to the swelling in and around my bone. This is another reason for operating. When they operated there was not a lot of fluid. The IV antibiotics took my pain and swelling done as well as a lot of morphine! And this episode seemed to be over with.

That's what there seems to be these episodes where my face swells and which then leads to a lot of pain. Some times I go months without these flare ups. From the age 19.5 - 21 I had minor flare ups which were bare able.

At 19 I started the studying for my 3 year course for my degree- I didn't want this horrible infection to take over my life. During this time I was given a mouth guard to wear at night to make sure that grinding my teeth is not an aggravating factor, and I also had root canal treatment to make sure I had nerves in my teeth and that a tooth was not dead and the cause of the osteomylitus. All of my teeth are fine.

It is now December 2011 I am 22. I am in the 3rd and final of my university degree. This year I have had many episodes/flare ups of my osteomyelitis - even though I always have it- my face can flare up and swell more and the pain is worse and becomes unbearable. This year I have been admitted into hospital twice.

First in April- the reason for this flare up I believe to be because of stress with work from university as I had 4 exams in a week so lots of intense studying. I had IV of antibiotics and Painkillers in hospital which seemed to work. I was in hospital for 4 days.

August of this year I was admitted for the second time. This was a very different experience for me and not a pleasant one. My consultant was not informed that I was admitted and I had doctors which new nothing about my Illness working on me. I was in for 8 days. I was not happy and did not feel any better from me entering hospital until the time I left. Normally when I am given metrodisonal and clindamycin through IV this reduces the swelling this did not happen and the swelling started to go to the side of my throat.

After seeing my consultant he suggested that we operate again as the anti biotics are not working as effectively. I really want to finish my degree at uni so I am trying to simply power through the pain. My consultant is fantastic and we work together as he rightly says nobody knows my condition as much as me. So I am delaying another operation at the minute. The operation Wil not guarantee that the osteomyelitis will go completely and this time he would have to operate externally which will leave me with a big scar. This is the reason for him not wanting to operate before with me being young he does not want to leave me with a big scar.

At the minute I am in the middle of another flare up it is close to Christmas and I do not want to be in hospital again So I am trying to control the pain at home.

A few things I have forgot to mention: at one point my consultant explained to my mum the pain I was going through like having 10 abcesses under each tooth on the side of my face ( hopefully this will put the pain I go through in context)

Also factors I have found which make my osteomylitus flare ups worse:

Cold weather (the reason for my recent flare up)

The change in weather

Lack of sleep

Cold drinks

Alcohol assumption when I am having a flare up.

Finally, sorry if my story is a bit all over the place it is hard to remember everything that has happened in 8 years. Please anyone get in touch who have this condition maybe we can help each other?!

8 likes, 253 replies

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  • Posted

    Hi,

    I have been suffering with osteomyelitis in my right jaw since November 2012.  I have been through such a similar experience as you; it's incredible.  Believe it or not today is the first time I have google osteomyelitis of right jaw(that's how I found you).  I have always tried looking up my particular bacteria to gain more information and advice.  NEver really helped...and then I read your account.  I am so sorry you have been going through this ordeal.  Thank you for posting because I FINALLY FEEL LESS ALONE.

    Hope you have been doing well and have been able to manage both the infection and the pain.

     

  • Posted

    G'Day all,

    Wow on hearing all your stories.

    I know this post is old, but it is the only post for osteomylitis I have found online that gives an inkling of what it is and what is involved.

    My story is that I've had a few problems over the years from hyperthyroidism now hypothyroidism after radioactive iodine treatment, past facial palsy, White matter lesions in brain possible M.S but not confirmed yet (even though it has been 4yrs of periodical MRI scans) they can't seem to decide if it is vascular or M.S 'sigh'. And now, after an incident (my 3rd incident) of what was thought was ATypical problems with my trigeminal nerve, followed by MRI and CT bone scan, I am told I have possible sclerosing osteomylitis of the left mandible and need urgent assessement by an oral surgical dentist...yayy me! If I could only be as lucky in winning lotto lol.

    They believe it is from two teeth that do not have crowns, and are partially still in my gum, because a dentist said these would not cause me any more problems, I left them alone and went on my way. 7 years ago this area / teeth were painful enough to have numerous antibiotics to clear them up and since then, they have not bothered me for the last 7 years.

    Yes I now want to slap my previous dentist.

    I thought I might have trigeminal neuralgia, so did my neurologist, so the possible (or showing signs on ct scan) sclerosing osteomylitis has been found incidently.

    I am in Australia.. but I think the "G'Day" gave me away lol, and I can not find any information on the condition, or how they treat it here, very frustrating.

    My symptoms have only been trigeminal neuralgic pain, followed by constant dull ache along lower left jaw, some cheek and lip numbness, and my face on that side just doesn't feel the same as the other side, like it is either numb or slightly swollen, me thinks more swollen than numb. I also have painful instances of biting my inner left cheek...OUCH! Oh and riding my motorbike, I have noticed pressure in my jaw when I have my helmet on.

    Lately, over the past week, I seem to notice the dull ache more, and the swelling, but I think that is because I am now aware of what is going on.

    Can anyone tell me what the sergical dentist might do during the initial consultation? I am not a fan of normal dentists lol, so you can understand how I can be very apprehensive with an oral dental surgeon...yikes!

    Am pretty spooked that judging by all your comments, this condition can be an ongoing problem also.

    Ok just posting my story wink will now continue to read everyone elses story

    Oh btw, I'm F 45yrs old.

    Cheers

    Lee

    • Posted

      Hi,

      My name is Mary and I'm an RN in San Diego and I too got my osteomyelitis from a dentist and his poor work. Because this is a difficult problem to eradicate, many people have more than one surgery. My most earnest suggestion as a nurse is that you do a little research and find a head and neck, facial reconstructive surgeon for this. The oral surgeon I went to was supposed to be really good and he was clueless. My NEW regular dentist was the one who found it. My symptoms are more low grade fever, and profuse night and day sweats. I've had 4 surgeries and only have one more to go. But because I had a terrific surgeon, none of them were very uncomfortable or difficult to tolerate. So don't be afraid

    • Posted

      Hi nurseotr,

      Cheers for the reply smile

      I am not really scared, but my previous visits to the dentist have been not only expensive, or should I say, highway robbery, but also been a little traumatic as we had problems with numbing areas when trying to extract two teeth in my upper jaw when the dentist didn't listen to my screams, or to the nurse when she said "I think we need more numbing", so am just apprehensive, and have avoided dentists for years because of this. I have been told by my GP that he trusts this dental surgeon and has used him before. My GP knows my financial situation is a little grim because I only recently had shoulder surgery and am living on workers compensation, so has suggested to the surgeon that I be seen in a 'public' capacity rather than a private, which will mean medicare for me but the initial consultation will be like $180, of which I get $70 back..then the surgeon will treat me through the public hospital, even though he is a private hospital surgeon..so at least that works out in my favour.

      I don't have all the harsh symptoms everyone else is describing, thank gawd! Just slight swelling with no abscess showing, and very mild pain, so hopefully my osteomylitus isn't too bad, or in the early stages.

      4 surgeries? Wow! That's a little daunting to say the least! Sorry you have had to endure that sad

      I am hoping I will not need such invasive treatment, but judging by the comments here, and depending on my prognosis I guess it might be something I haveto look forward to.

      My neurologist and radiographer did state my condition is a cronic one, but I am not sure what that means in terms of prognosis.

      I guess I will find out in two weeks..is all I need, more surgery to keep me off work sigh, I've already been off work for three months and I go back to work 4 days before I see the dental surgeon..my employer is not going to be too wrapped in me taking more time if I need surgery again lol, atleast I have some sick and annual leave left to take if needed, which adds up to like 7 weeks.

      I will post again after my consultation

      Thanks again for your reply, I hope your last surgery goes well for you

      Be well

      Lee.

    • Posted

      My first 3 surgeries were debridements. So they weren't too bad. The last one he had to remove a 4 inch piece of jaw and the nerve. He then put in a new nerve graft. Because the infection has been so tenacious, I have to wait about a year for the bone graft. So I'm the titanium woman.
    • Posted

      Do you know if osteomylitis can spread elsewhere in the body?

      Also, could it cause anemia, cough, sinus problems, numbness in cheek or corner of the mouth, headache or ear problems?

      I have a slight numb sensation in my cheek and also in the corner of my mouth (lips), headaches, and itchy ears and bad sinus, seems also every morning my saliva glands swell and get sore under my chin / neck.. I know this is not lymph nodes cause my GP said they were fine but he has noticed the swelling of my saliva glands in those areas, but he can't see swelling inside my mouth, other than my left inside cheek, where I usually have instances of biting.

      I am a smoker, in the process of giving up by cutting back, and had a chest xray because of a persistant cough, but my DR stated the results were unremarkable and quite normally clear, not even signs of emphesema...(he was surprised as I've smoked since I was 14yrs old).

      Is why I wonder if osteomylitis can cause cough...hmmmm

      I find it hard to find information on these things and this condition that is in laymans terms and not pathological or extremely technical Dr terms...sigh

      I know we shouldn't go to the google gods for information as this can lead to more frustration and worry, is why I figure asking other patients with this condition could be helpful.. I mean, they've been through it ... ofcourse after my consultation, I will be ready with many questions for my dental surgeon, but that is two weeks away lol. A reasonably short time to some, but to me it is ages away lol.

      It's the not knowing that is frustrating

      smile

    • Posted

      I live in San Diego and have been following this thread for a year because I am still untreated. My problem started in late 2010.

      I would like to know which doctors and dentists you are seeing? I sent you a private message! I am having difficulty finding a surgeon who is proactive and who will order the right tests.

      Thanks so much! You're lucky you got treatment so quickly!

    • Posted

      Sorry, I forgot to mention the specialists I've seen are supposed to be top-notch and know what they're doing, but it hasn't been the case for me either! I am so stressed out and desperate at this point.

      Please check your messages and get back to me ASAP!

      I am so happy you've found the right docs to help you!

    • Posted

      Do you mind me asking who you have seen in the past?
    • Posted

      Most of the symptoms you mention aren't usually associated with osteo. Low-grade fever, swollen glands, jaw pain, night sweats,. Fatigue, like with any other chronic infection. Osteomyelitis is an infection strictly in the bone. It may affect some lymph nodes but it won't affect all those other areas that you mention. All your other symptoms sound like you may be allergic person and has chronic sinusitis. Am I close??
    • Posted

      Lol, did I forget to mention the fatigue, sweats, sorry, being hypothyroid, those symptoms are usually present, but lately I have noticed them more, sleeping naps during the daytime but they are not really doing anything for the fatigue, where as the thyroid stuff, if I napped I always woke refreshed. Night sweats are more common with hyperthyroid, so I just figured my meds needed upping, but got my results of thyroid blood test half an hr ago at dr's and thyroid levels are normal, he did say my feeling hot all the time but needing to put a long sleeved top on is a low grade feaver that could be from my infection.

      I had to laugh when I saw your post, cause I just returned from my GP.

      He said he did some textbook reading on sclerosing osteomylitis of the mandible and said it can affect some nerves in the face and lips, generally the corner of the lips, headache can be referred pain from the jaw, as would happen if you had a tooth ache, pain can affect the nerves causing referred pain in other areas. So guess that answered that question lol.

      He has referred me for an ultrascan on my glands, just to be sure there is no stones. He said I should ask the dental surgeon about the saliva glands as he would deal with that stuff in the 'oral' field, but my GP also said he will look into it with some collegues.

      He laughed because I am giving him alot of work to do in regards to research lol, he is good like that.

      I am not allergic to anything but some sergical tape they put on your eyes during surgery, lol weird huh, but we found that out when I had my shoulder surgery.

      I do have the jaw pain but it is very low grade, mainly noticable at night in bed or when I have my helmet on

      smile

    • Posted

      Oh, I forgot, my GP said anemia or low iron can be caused by infection anywhere in the body, my iron is still low even though I am on suppliments, he was going to send me for scans of my bowel and intestines, but now because of the osteomylitis in my jaw, he wants to wait and see the outcome / results of treatment with that first to see if my iron improves. If it doesnt then my low iron has another cause he will look into.

      Am sick of being prodded and poked now yes I am lol

      If I never see a dr again after all this, I'll be happy... but alas...wishful thinking

    • Posted

      Fellow.  I am new to this forum because your post came up in a google search.  I am in San Diego and looking for a doctor to help. I have been diagnosed with many thing from trigeminal neuralgia to dystonia and the list goes on and on. My symptoms and story is very similar to everyone on here. Can you help with Dr. Referrals .  Every time I have asked about bone infection I am excused by my dentist, ent and neurologist. 

      Thank you

      Stephanie

  • Posted

    Hi.

    My name is Mary. I had this 7 to 8 years before it was found in my left lower jaw. I had three debridement surgeries before they finally excised about 4 inches left lower jaw bone and nerve and put in the nerve graft. I wish they had done the excision of the bone and nerve graft earlier and not done so many debridement surgeries first. I've been on IV antibiotics for almost 2 years. And I'm just now starting to feel better and I think I'm going to be getting well. This particular illness takes a long time to go away , So don't be discouraged

  • Posted

    Hi everyone. My osteo is not in my jaw (it is in my cervical spine) but I still wanted to write and comment on how many are saying they never before met someone with osteomyelitis as this is the same for me. I think most of my issues are due to the large debridements I had to go through. Pain from debridements are with me every hour I live. It is a challenge explaining to people that what I am going through is a bit more than just a "stiff neck", people really just do not understand that getting osteomyelitis can become a chronic condition that you are just going to have to live with, it is not something that will be cured (well at lest not in my case).
    • Posted

      I know exactly what you mean! Pain has just become a permanent fixture in our lives and no one will ever understand what its like or how horrible it is unless they actually have walked a day in our shoes. Doctors who can't fix us just pump us full of drugs or say they've done all they can do.

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