Injuries not getting better

Status
Not open for further replies.

longtimer

Active member
Joined
Feb 5, 2020
Messages
85
Reason
DX FIBRO
Diagnosis
02/2020
Country
CA
State
AB
Hi - About 5 weeks ago I tripped and fell on my knee on concrete and the bruising is gone but the pain is still there. Then about 4 weeks ago I was digging in the garden wearing garden clogs and using a spade. The repeated action damaged my second toe somehow and its been weeks of swelling and pain (but no bruising) and its no better. Does fibro somehow boost the pain for these minor injuries? Normally something like these hurts would clear up after a few days of rest and ice - but these haven't.

I have soo many questions for you guys...
 
I haven't personally noticed that random injuries are taking longer to resolve once I was officially diagnosed with FM, which isn't to say it doesn't happen. It just hasn't happened to me. However, the knee injury, especially, sounds like something you'd want a doctor to check out - maybe with an x-ray to be on the safe side. There is considerable research indicating that fibromyalgia itself is a disorder stemming from a problem with how the brain/spinal cord process the body's nerve signals, with regard to what is felt as painful and what is not, or to what extent something is painful. So logically, it seems that it would be possible for injuries which should not be causing so much pain to be causing it anyway. But I think it's wiser to run it past the professionals who deal with injuries for a living, rather than presuming it's connected in any way to fibromyalgia. If it were me, I'd have my painful knee and toe checked!
 
Hi there,
I too am having pain from a shoulder injury from last November. The pain is just as bad as right after I fell, if not worse, so I can identify with you. That said, I agree with Mirador, that you should get checked out. I am also seeing massage therapists who specialize in injuries, but so far, no decrease in the level of pain. I do agree that fibromyalgia makes pain signals get amplified because of the nervous system being overly sensitive. I wish you the best of luck!
Lori
 
I have not noticed that my injuries take longer to heal, but there is definitely one thing. All my life I have had a very high pain threshold and tolerance; when I was working very physical jobs I would sometimes find a huge bruise somewhere and have no idea when I got it because, while I might have felt a blow in the moment, I would always just keep going and forget about it.

Since I developed fibromyalgia, I am still a person with a high pain threshold, most days. I have often thought that if many other people could feel what I feel on any given day it would bring them to their knees.
But, there are days when, if I stub my toe or bump into something it is more painful that I can believe. On some days, just something touching me, even lightly, especially if it is on my back, will bring a pain sharp enough to make me gasp or even cry out. It's weird, but it's just part of the syndrome. Tends to be pretty embarrassing when it happens around other people because then they get concerned that I have actually hurt myself, and then I feel compelled to explain that I am not actually hurt, that it's an effect of fibro, and I really would rather not talk about fibro with people.
 
Hello, I was interested to hear your question as I had this conversation with my rheumatologist and she confirmed that one of the key traits of fibromyalgia is the body’s inability to heal quickly, if ever, from things that people without fibromyalgia would typically recover quickly from. So, to answer your question, yes, it is very common in those with fibromyalgia. That’s not to say it’s the same for everyone of course but it certainly is in my case. Injuries take a very long time to heal and some of them never do. They keep recurring and I just have to manage them. I have built up resources to manage pain and have become very mindful about how I move my body in space so that I practice functional movement and use the right parts of my body and try not to compensate triggering secondary and tertiary pain patterns. I use a lot of K tape to support painful joints and muscle areas, and also practice Feldenkrais which has helped me tremendously. Feel free to look it up if you are interested. It’s all about empowering people by bringing deep sensorimotor awareness to how we move and how we sense our own movements. It also cultivate deep awareness of unconscious compensatory patterns in our bodies that can lead to further pain and damage without our realising it. The alternative is to become locked down and afraid to exercise or do anything which is very bad for our health. Movement is life and it’s an extra challenge for those of us with fibromyalgia as movement can also cause pain that can last a long time. It’s quite a challenge finding the sweet spot and the right balance, but it is possible with patience and kindness towards ourselves, and a good support system.
I’ve read a lot about the neurophysiology of chronic pain and what happens over time is that the synapses in the brain start to rewire themselves thinking that pain is normal to be on all the time or more often than necessary. Therefore, we become hyper sensitive to pain as our pain threshold becomes much lower than someone without chronic pain. Therefore, even though our pain response to a stimuli may be far greater than that of someone who doesn’t have chronic pain, it doesn’t mean our pain isn’t real. It’s simply means Our brains and nervous systems have become oversensitised to accommodate pain signals. Basically, the pain processing centres in our brain become larger, hyper vigilant and overreactive, like a fire alarm going off all the time. Feldenkrais works with this to help deactivate or lower this level of brain noise. Not a quick fix but definitely one of the most helpful protocols I’ve practised. All the best.
 
Last edited:
Thank you Peachy - I've never heard of the Feldenkrais Method before - and just looked it up and there are practitioners here where I live. I will do more research to see if it is something I'd like to go to (if it is a long drive I may not). I have read a lot about the nervous system and pain as well, and I have been told I have a hyper sensitive system so what you wrote makes a lot of sense. It is in a weird way reassuring to know that this is something that can happen with fibromyalgia. I have noticed that when I get a flare up, old injuries reappear as pain so it seems logical that new injuries impress pain circuits that keep firing. I try to do gentle yoga every other day and stretch every evening and that helps.
 
Hello, I was interested to hear your question as I had this conversation with my rheumatologist and she confirmed that one of the key traits of fibromyalgia is the body’s inability to heal quickly, if ever, from things that people without fibromyalgia would typically recover quickly from. So, to answer your question, yes, it is very common in those with fibromyalgia. That’s not to say it’s the same for everyone of course but it certainly is in my case. Injuries take a very long time to heal and some of them never do. They keep recurring and I just have to manage them. I have built up resources to manage pain and have become very mindful about how I move my body in space so that I practice functional movement and use the right parts of my body and try not to compensate triggering secondary and tertiary pain patterns. I use a lot of K tape to support painful joints and muscle areas, and also practice Feldenkrais which has helped me tremendously. Feel free to look it up if you are interested. It’s all about empowering people by bringing deep sensorimotor awareness to how we move and how we sense our own movements. It also cultivate deep awareness of unconscious compensatory patterns in our bodies that can lead to further pain and damage without our realising it. The alternative is to become locked down and afraid to exercise or do anything which is very bad for our health. Movement is life and it’s an extra challenge for those of us with fibromyalgia as movement can also cause pain that can last a long time. It’s quite a challenge finding the sweet spot and the right balance, but it is possible with patience and kindness towards ourselves, and a good support system.
I’ve read a lot about the neurophysiology of chronic pain and what happens over time is that the synapses in the brain start to rewire themselves thinking that pain is normal to be on all the time or more often than necessary. Therefore, we become hyper sensitive to pain as our pain threshold becomes much lower than someone without chronic pain. Therefore, even though our pain response to a stimuli may be far greater than that of someone who doesn’t have chronic pain, it doesn’t mean our pain isn’t real. It’s simply means Our brains and nervous systems have become oversensitised to accommodate pain signals. Basically, the pain processing centres in our brain become larger, hyper vigilant and overreactive, like a fire alarm going off all the time. Feldenkrais works with this to help deactivate or lower this level of brain noise. Not a quick fix but definitely one of the most helpful protocols I’ve practised. All the best.
Great information here, Peachy, and thanks.
I will beg to differ with you on one thing, though. Chronic pain doesn't mean that a person's pain threshold is lowered. Many people with fibro, and with other chronic pain conditions, have become more inured to pain, as it is there all the time and the body and psyche grow accustomed to it. Therefore, something that would have bothered you a lot before developing the chronic pain is now something you feel every day and it doesn't bother you as much because you are used to it. I know this is true for me.

On the other hand, fibro has a weird thing about it, that is over-reaction to minor pain. some people have this all the time. I have it only occasionally and on certain days. When that is happening, just lightly bumping into something is very painful. But the rest of the time, my pain threshold is probably even higher than it was previously because I am now accustomed to frequent and chronic pain. I think this is true of many people with chronic pain. If other people felt what we deal with every day they would wonder how we cope with it.
 
I have not noticed that my injuries take longer to heal, but there is definitely one thing. All my life I have had a very high pain threshold and tolerance; when I was working very physical jobs I would sometimes find a huge bruise somewhere and have no idea when I got it because, while I might have felt a blow in the moment, I would always just keep going and forget about it.

Since I developed fibromyalgia, I am still a person with a high pain threshold, most days. I have often thought that if many other people could feel what I feel on any given day it would bring them to their knees.
But, there are days when, if I stub my toe or bump into something it is more painful that I can believe. On some days, just something touching me, even lightly, especially if it is on my back, will bring a pain sharp enough to make me gasp or even cry out. It's weird, but it's just part of the syndrome. Tends to be pretty embarrassing when it happens around other people because then they get concerned that I have actually hurt myself, and then I feel compelled to explain that I am not actually hurt, that it's an effect of fibro, and I really would rather not talk about fibro with people.
This is exactly the same as my experience, to the letter! I'd also read that fibro was meant to mean a lower overall pain threshold, and didn't feel that this was really the clear-cut case for me at all. I know it's all pretty grim, but it's comforting to know that others are going through the same strange things. Makes me feel a little less like I'm going barmy - so thanks for that!
 
Hello,

I think we may be speaking of different things. I agree that people living with chronic pain are like super heroes in the way that we managed to keep going in spite of the pain and do adapt to it being the new norm. I completely agree. To anyone else, it would be completely unacceptable. I’m happy for days where my pain is at level three or four, LOL. The bargaining! To someone without chronic pain, a three or four level pain would be unacceptable.

Just to clarify, as I think it’s an important point, I was referring to the science of neuro plasticity which has been empirically documented. One very interesting neuroscientist is Dr Michael H Moskowitz. (Quote borrowed from his website).
“…persistent pain takes into account that this type of pain develops because of neuroplastic change in the Central Nervous System, marking the transition of pain from a symptom to a disease. Additionally, the brain directs changes in the rest of the body based upon the alterations that have occurred due to it’s own changes secondary to input from the periphery.”
DB5D97F8-E482-442C-AF70-EAA992F97E16.png

He has taken brain scans of people with no pain, acute pain, and chronic pain, and they are fascinating. You can see how many centres of the brain are permanently lit up to accommodate pain in people with chronic pain conditions including fibromyalgia. As the brain is plastic in nature, it literally rewires it self to accommodate the pain. It’s hyper alert and on the lookout for pain sensation with pain centres taking up five times the amount of space in the brain that should be being used for other purposes.
These images are fascinating. In a person with no pain, no areas are lit up. Check out the difference between normal appropriate pain to an actual stimuli and someone with chronic pain. The pain centres are turned on all the time.
 
Hello there, I posted a photo and some references to a neuroscientist who specialises in the effects of long-term pain on the brain and vice versa. It’s super nerdy but it’s so interesting and to me, empowering. It means we are not imagining things. The pain centres in our brain are measurable and are in fact taking up a whole lot of real estate that is supposed to be being used for other things. The centres remain on and hypervigilant and on the lookout for pain. With neuroplastic retraining and functional medicine, these faulty neural pathways can be rewired to be healthy again and not be so accommodating to chronic pain. No wonder we have brain fog. Our poor brains are overloaded doing things that should be being used for other purposes.
 
Last edited:
That’s good that you have the option of a Feldi practitioner. It was a game changer for me. At the very least, it’s good to feel we have choices and options even if different things help each of us. 🙏🏻
 
Persistent pain from injuries has been a major part of my Fibro, it's had a big impact on life and I'm not the same person. I happen to have heard of Feldi after seeing a YouTube video about neck and shoulder posture. Not sure what to do for best but I do try a bit of Tai chi each day.

Wishing you well longtimer 👍
 
Hi - About 5 weeks ago I tripped and fell on my knee on concrete and the bruising is gone but the pain is still there. Then about 4 weeks ago I was digging in the garden wearing garden clogs and using a spade. The repeated action damaged my second toe somehow and its been weeks of swelling and pain (but no bruising) and its no better. Does fibro somehow boost the pain for these minor injuries? Normally something like these hurts would clear up after a few days of rest and ice - but these haven't.

I have soo many questions for you guys...
Bit of background / terminology / perspective, taken me a week to get round to this properly, but I think it's fundamental:

The answer of researchers that favour the CSS-hypothesis to @longtimer's original question is: pain boosting/amplification is called hyperalgesia and is together with allodynia (touch felt as pain) commonly found in patients with fibro and should be explained by the neurological CSS-hypothesis that fibro is a form of central sensitization (or sensitivity) syndrome, which @Mirador is referring to.
However whilst this seems to be #1, there are at least 3 further mainstream hypotheses (and 3 or 4 outsider ones) about the cause of fibro, like the autoimmune one that was explained in the Guardian and sciencedirect articles a month ago, based on the study by Goebel. Also we do by far do not all have hyperalgesia and/or allodynia - Mirador, jemima and myself for instance, sunkacola only occasionally. I haven't found statistics about this yet, but CSS / central pain hypothesis-proponents (have to) assume that many have it, but others also do, so it can be phrased "common", "typical/characteristic/defining for".
The further development of the CSS hypothesis can be seen in the definition of a 3rd pain type, which is being increasingly mentioned in research (pubmed since 2019 and in the fibromyalgia controversies convention in June 2021).
The process of nociception is the normal perception of pain (1) nociceptive pain) through threat or damage, as opposed to 2) neuropathic pain due to nerve damage and a new category developing in pain research around the concept of CSS since around 2019 3) nociplastic pain with neither tissue nor nerve damage, to which fibromyalgia pain belongs. (see the newest terminology on iasp-pain.org)

Another explanation for some hyperalgesia is "opioids addiction which can then lead to fibromyalgia problems" (fightfibromyalgia) and "Symptom of fibromyalgia often triggers the diagnosis of opioid addiction, tolerance or dependence." (fibromyalgiaresources)

I agree fully with @Mirador that it's always wiser to check everything. And despite the above I wdnt explain either as pain boosting. Both @longertimer's knee and toe as well as @Hopeful7's shoulder can still have an additional injury (e.g. the toe swelling), which hasn't been resolved yet, I'd think.
Which brings me on to a different idea. Whether nociplastic, autoimmune, small fibre, neuroendocrine, mitochondrial, caused by sleeplessness or low neurotransmitters, fibro is real pain. Plus we get additional pain with injuries. The two together are more pain. That can cause a protective/relief posture which worsens other pains. The three together are even more pain. Not the same "doubled"/"trebled", not imagined, not neurological, not oversensitive, but simply added. The threshold isn't higher or lower, but the injury wdntve been enough to get over the normal threshold, together it is.
Wouldn't that be enough to explain it, apart from the fact that we don't yet know where the fibromyalgia pain comes from?

Now I see an interesting difference in experiences and ideas here, @Peachy's seem to accord to the pain research quoted, whilst @sunkacola and @Jemima differ. What Peachy seems to imply when talking of "different things" is that there is a difference between pain threshold and pain tolerance, but sunkacola is already talking about both, at least in her first reply (the 2nd is only about pain tolerance, hyperalgesia & allodynia). What research often claims is that we have a low pain threshold and a high pain tolerance. I'd chime in here with sunkacola & Jemima that I not only have a very high pain tolerance, but also a high pain threshold. Meaning as sunkacola has already said: Like before fibro I get skin injuries without realizing it. Plus neither pains nor the Ache are things that bother me about fibro. When I think I can carry on thru with some activity after 30-60mins my wife often looks at me and says: you look in dire straits and are greenish-white in your face. So while I agree that pain research says this, favouring the CSS hypothesis, our bodies are different. I don't know why this happens. Maybe the cohort selected for studies is no neutral or a too small a selection.
I also have the same experience als sunkacola & Jemima that my skin injuries heal just as fast as before fibro, whilst tendons / muscles
now heal faster than before fibro, because I'm wary of them and do something about them immediately, whilst at the beginning of my full flare there was just too much to cope with and not enough know-how about how tendons & muscles work & can be alleviated, so that's how they summed up.
Hello, I was interested to hear your question as I had this conversation with my rheumatologist and she confirmed that one of the key traits of fibromyalgia is the body’s inability to heal quickly, if ever, from things that people without fibromyalgia would typically recover quickly from. So, to answer your question, yes, it is very common in those with fibromyalgia. That’s not to say it’s the same for everyone of course but it certainly is in my case. Injuries take a very long time to heal and some of them never do. They keep recurring and I just have to manage them.
We read things like hyperalgesia is a "key trait" too, e.g. fibromyalgiaresources about it, but it isn't a key trait in the sense most have it, more in the sense if you have it then it's likely you have FM, unless you've overused opioids. Maybe this is how 'key trait' is meant here too.
I don't think what the rheum. said about healing is nec. wrong, but out of context. sunkacola, Jemima and I aren't representative of course, but we do exist and do have FM ;-D.
I have noticed that when I get a flare up, old injuries reappear as pain
I had this with clavicle pain I hadn't had for a few years too, originally from breaking it, but everything else seemed "new". Here too I think it hadn't been healed properly and it didn't amplify, but everything added up. Now it's been treated by my acupressurist better than the osteopath before it has disappeared, however much pain I may otherwise have.
certain days. When that is happening, just lightly bumping into something is very painful.
This'd be more hyperalgesia and I don't ever have it, I don't think, everything hurts just as much as it used to. I've had allodynia tho, sensitive to longer touch of my wife, which really sucks.

What irritates me is that hardly anyone ever distinguishes between single, often alternating pains in a certain body part and a general fluey-type Ache all over - fibromites, docs & researchers alike - only my acupressurist asks exactly what type of pain I mean. But the other day it turned out that even what she calls her fibromyalgia pain was only single pains esp. in her thighs, and didn't really realize that I distinguish that, so no wonder she often doesn't really how bad my FM is thru the Ache etc. and thinks we may be thru with it soon.... o_O
Any ideas on this?

(I started a sentence a week ago, I hope if I leave it here I'll remember some day... "Brings me to the idea that the term hyperalgesia is...")
 
Wow. I noticed that areas I have that problems I had that would return again and again - like golfer's elbow/tendonitis for instance - was horrible during my recent flare. Awful! And that was just one spot. It isn't really even bad really now but the flare hit. I am new to this and the flare was my longest - 4 days - and I was afraid it was not fibro but something worse and it would never end. Then the flare went away. I mean, it's not like I'm symptom free but compared to that nasty flare... But it helps to know that this is normal for many of you, too. Luckily all my past injuries aren't doing that. But two that tend to simmer and come back are, plus any I tend to treat all the time.
 
Wow. I noticed that areas I have that problems I had that would return again and again - like golfer's elbow/tendonitis for instance - was horrible during my recent flare. Awful! And that was just one spot. It isn't really even bad really now but the flare hit. I am new to this and the flare was my longest - 4 days - and I was afraid it was not fibro but something worse and it would never end. Then the flare went away. I mean, it's not like I'm symptom free but compared to that nasty flare... But it helps to know that this is normal for many of you, too. Luckily all my past injuries aren't doing that. But two that tend to simmer and come back are, plus any I tend to treat all the time.
Hi DebMarPir,

I have exactly that too, in my neck, my elbows, and my knees - can feel just like tendonitis when a flare gets going, although not always the same. Sometimes, it's more like blinding white flashes of pain if I move, and my neck locks up. Sucks! I know that I had whiplash in my neck, my knees gave me trouble when I used to run a lot, and my elbows took a pasting through years of weight training. None of the damage is bad enough to show up on a scan, but I suspect that minor damage - the kind that wouldn't be an issue for others - can be a demon for those with fibromyalgia in a flare. It's interesting, too, that different flares can ramp up different clusters/types of pain. They can certainly last for very different durations, too. I'd say that's pretty "normal" for fibro, as far as anything can be 🙃
 
Status
Not open for further replies.
Back
Top