For some time now I have thought that my upper and lower set of front teeth were becoming loose. On my last visit to the dentist I mentioned it to him. He said they didn't feel unduly 'wobbly' and that teeth are meant to move slightly, so I shouldn't worry. Still I was concerned as they often move when I chew - to the point that I have to chew more on one side - the less 'wobbly' side.
I have always worried about losing my teeth. From an early age I've had vivid dreams where they would loosen, crumble in my mouth and fall into thousands of tiny pieces on the floor. Apparently these type of dreams are associated with stress, so I'm told. When I visited the dentist a few weeks ago I mentioned again that I was concerned about them as my teeth grinding had worsened. Low and behold, my dear dentist said "Oh, this one is loose!" I wanted to say 'I told you so!' but thought better of it.
He took x-rays of the tooth in question and said that the bone was undamaged but the pocket had 'stretched' somewhat because of the tooth grinding. He said he had never seen anything like it except in text books. I must be kicking quite a punch with my grinding. Fortunately, if I wear a nightguard to protect my teeth during sleep, the pocket should shrink back to its normal size and tighten up again. So I am having one fitted next week.
I have posted a poll on this very subject (which you will find in the introductory section at the top of the blog) please take the time to complete it as it will be very interesting to see just how many of us are having to deal with tooth damage as a result of grinding, something that is very rarely mentioned in the medical books.
Welcome
This site is intended to provide up-to-date, relevant information on the condition Chronic Fatigue Syndrome/Myalgic Encephalopathy and help raise awareness of this debilitating illness. Please help me to do this by sending the link to anyone who is or might be suffering with ME/CFS.
Please note that I am not a medical doctor but a sufferer of ME/CFS; you are advised to contact your own practitioner if you are at all concerned with your health. The information I provide is gathered from my own experience and research and I ask the reader to look into things themselves before embarking on any new regimes. Please be aware that I cannot accept any responsibility for damage arising as a result of readers accessing this website and using the information I provide. Thank you.
If you wish to contact me personally my email address is: wordsworth99@hotmail.com.
Please note that I am not a medical doctor but a sufferer of ME/CFS; you are advised to contact your own practitioner if you are at all concerned with your health. The information I provide is gathered from my own experience and research and I ask the reader to look into things themselves before embarking on any new regimes. Please be aware that I cannot accept any responsibility for damage arising as a result of readers accessing this website and using the information I provide. Thank you.
If you wish to contact me personally my email address is: wordsworth99@hotmail.com.
Check out my Squidoo Lens for more CFS information and my online shop for cottage-style homewares.
WHAT EXACTLY IS CFS?
Chronic Fatigue Syndrome, also known as Myalgic Encephalopathy, Post Viral Fatigue Syndrome, Chronic Fatigue and Immune Dysfunction Syndrome, is a poorly understood condition that is characterised by profound fatigue and exhaustion - with loss of muscle power, pain and tenderness following normal physical or mental activity - and a range of neurological, endocrine and cognitive disturbances. CFS is classified as a neurological disorder by the World Health Organisation (International Classification of Disease 10: G93.3).
Affecting all social classes and ethnic backgrounds, it is estimated that between 0.2% and 0.4% of the population have the illness. It can occur at any age with the greatest incidence being between the early twenties and mid forties. Women are most commonly affected.
Often sufferers are unable to work, with 25% acutely disabled. It impacts severely on the lives of sufferers and carers. Very little support is available and isolation and loss of hope often follow years of suffering.
It most commonly occurs in a sporadic form but there have been epidemic cases, such as the outbreak in the Royal Free Hospital, London, 1955.
Very little is known or understood about the illness and its causes and as yet no universal cure or treatment has been found.
Affecting all social classes and ethnic backgrounds, it is estimated that between 0.2% and 0.4% of the population have the illness. It can occur at any age with the greatest incidence being between the early twenties and mid forties. Women are most commonly affected.
Often sufferers are unable to work, with 25% acutely disabled. It impacts severely on the lives of sufferers and carers. Very little support is available and isolation and loss of hope often follow years of suffering.
It most commonly occurs in a sporadic form but there have been epidemic cases, such as the outbreak in the Royal Free Hospital, London, 1955.
Very little is known or understood about the illness and its causes and as yet no universal cure or treatment has been found.
Monday, 22 October 2007
Teeth Grinding and ME/CFS
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4 comments:
greetings from a fellow m.e. tooth grinder!!
m.e. is a neurological illness quite distinct from cfs or post viral fatigue. the paper by dr byron hyde on the nightingale site or on the site www.ahummingbirdsguide.com-gives the info.
your quilts look beautiful - wishing you every success with your business and for you to realise all your dreams.
Ouch! Don't you hate it when you're right and you don't want to be?
I had a mouth guard fitted 6 months ago. It was an excellent investment!
I noticed I was clenching my teeth a lot when I was stressed and sometimes just when I was very very tired and trying to get through the next hour or two before I could crash. Literally gritting my teeth!
My dentist said there seemed to be some wear from the grinding. But I've (hopefully) stopped it from getting any worse with the mouth guard.
Mine is a soft one (made from some kind of plastic) but they said I can have a hard one fitted if I chew my way through this too quickly!
Mine fits on my bottom set of teeth and it's sort of bendy so it goes in and out really easily. You can just wash it with water - no special soaking or cleaning required. It acts a bit like a cushion and it also helps align my jaw a bit better when i wear it. I tend to stick my jaw in odd positions when I'm tired or stressed.
It stopped the habitual grinding in a few weeks of wearing it. I just got to the point where I felt I didn't need it. I wear it ocasionally and sometimes in bed if I've had a rough day and have tension in my jaw.
It feels a bit weird - I can't talk properly with it in and it looks like I have something in my mouth. But it's clear plastic so I'm confortable wearing it in the car and so on without feeling freaky!
I keep mine in a small tupperware box - as recommended by the man in the sports shop who had sold out of gumshield boxes. He says it's a lot cheaper too ;-)
Apologies for the long comment!!
I don't have ME but have been grinding my teeth too. I have Sjogren's which can cause lots of issues with my teeth. Just now having two crowns done :(
After that the dentist wants me to get the fitted tooth guard but like Rachel I'm trying to cheap and easy way first. I'll let you know how it goes.
I don't have any loose teeth but have pain like I keep thinking I have a cavity except it's on a bunch on teeth.
hi - could you remove my comment -re - m.e. not being same as cfs. i realise it's come across as uppity and abrasive - it wasn't meant that way. i really struggle to get any words from brain to fingers and kind of despair when it comes out not how i meant it and i'm then too brain dead to explain how i do mean things.
sorry!
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