Please get a test for Lyme disease western blot. You should try to rule it out since I have random stabbing pains and am confirmed to have Lyme. I got it 4.5months ago, Had two months of antibiotics, rashes went away but random stabbing remained. Not sure how to cure it yet but many people do well with antibiotics and no further problems.
I have been told I have fibromyalgia. I take gabapentine (aka neurotin) which has reduced the attacks greatly. I do not have anxiety issues. The cause is over active nerves but no one can get rid of it just treat the symptoms. Not sure how it gets started.
I have the exact same thing. I'm pretty sure these are anxiety symptoms.
My first memory of these pains is of telling a nurse that I got them. I was about 12 years old when I told her. I explained to her that I'd been getting them for a while, but I couldn't figure out the cause. I told her exactly what they were like: sharp pains that randomly occurred in random places on my body, usually on the tops of my hands, sometimes on the side of my neck, but occasionally it'd be a different place. The pains were sharp, stabbing pains, that would sometimes slightly throb, but they would not hurt exactly. They were just irritating. They would occur in the same exact spots from time to time. On the tops of my hands, the stabbing felt like it might be within a vein. I remember being worried that there was something stuck inside my vein, possibly a tiny clot or maybe a cluster of parasites, like bacteria or something similar. The nurse had no clue. She drew some blood to test. Results came back completely normal. There was nothing wrong with me. I've continued to have these pains throughout my life. I'm 28 years old now. Over the years, their occurrence has fluctuated. Sometimes I would go months without feeling a single stab, other times I would feel daily stabs. The locations of the stabs have changed over the years. Lately, I've been getting these pains constantly. They happen on my chest most frequently and on my forearms and thighs. They definitely don't seem random anymore. Their occurrence seems to be directly tied to my stress level. I'm in college, and as the semester has progressed, they have worsened accordingly. Finals week is next week; I'm positive they will subside after exams and summer break starts.
I've tried to find the answer to these pains for years to no avail. Fortunately, there is no need to feel alone, as this is a common symptom among people. I believe it is stress-related. I found a website today that seems to be describing our symptom. I points to anxiety as the cause:
http://www.anxietycentre.com/anxiety/symptoms/shooting-pains-anxiety.shtml
HYPERMOBILITY SYNDROME.
Statistically some of you will have it and there is a simple set of initial tests you can do at home which will give you all that you need to get a referal to a rheumatologist if you're in the UK - if you're elsewhere I don't know what the deal is but at least you'll now be clued up if you meet the criteria on the beighton scale and it's on the hypermobility syndrome website linked at the bottom.
Officially called Joint Hypermobility Syndrome, but that is a terribly misnomer because it affects vastly more than the joints because it's primarily a genetic excess of collagen and collagen is the most common protein the human body - even our bones are fifty percent collagen. Statistically this is what some of you are suffering from because over a million people in the UK have it but diagnosis rates are depressingly low, with estimates ranging between 0.5 to 3% of sufferers receiving the correct diagnosis - and even then it can take years and years. It's also known as Elhers-Dhanlos syndrome type iii - hypermobility type, which is actually the old name for it.
In addition to random pain of every conceivable type appearing suddenly or slowly, anywhere on the body, lasting from miliseconds to weeks and ranging from barely noticeable to excruciating, it is an utterly horribly condition which totally controls your life if you have it bad. I only have moderate HMS but it doesn't stop there.
around 75% of people with hypermobility syndrome also have some autonomic nervous system problems,and given how many processes in your body are automatic it doesn't take long to realise that there are literally thousands of things that can go wrong: with me it's mainly vertigo and balance problems, a bladder that tells me it needs emptying every ten minutes - which has been the case since before I started school - sudden attacks of blurry vision, spontaneous attacks of fight or flight - i.e. the physical symptoms of a panic attack but in the total absence of any stressor, numerous other annoyances too many to list, but the worst of the lot is excessive sleepiness which necessitates 12-14 hours a day + usually one or two naps and I am nearly always tired. I also have chronic fatigue (not syndrome, just fatigue that was clincally chronic) for over four years but eventually got it under management with vitamin B12 Injections - and it took more than three years to get my GP to give it to me monthly, which is what I need, and that was only through the fact that I'm a professional scientist who had access to all the top medical databases and thus could present my doctor with proper medical papers rather than print-outs from "Doctor Google" and the fact that the British Council for Standards in Haemotology published new guidelines in 2014 stating that the standard test is up to 35% inaccurate.
But that's secondary stuff. In the last hour I've had acute burning pain in my achilles tendon,, throbbing/pounding ache in my left thigh, clenching in my chest - which I used to think was a heart attack every few weeks before I got diagnosed - my jaw currently feels like I've just been punched, my right knee like someone's rammed a knitting needle into it, my shoulders feel like a giant is standing on them, and my second toe on my right foot both feels like it's in a vice and the BONE is itching.
http://hypermobility.org/
I'm very sorry for what you're going through. I have a similar situation but I'm affected to a lesser degree. I want to tell you all about Sahaja yoga, something that can change your life forever and I cannot stress enough on how it's the greatest of all gifts bestowed upon us. I don't know if you're a believer but it doesn't matter as long as you try it out before tossing it aside as irrelevant. It's empirical and has a complex system which is explained by logic and reason and not blind faith. Sahajayoga is meditation where a person in the state of thoughtless awareness causes the residual energy lying dormant at the base of his spine to rise up and travel through a channel where the 7 energy centers lie. As it rises up it aligns these centres or chakras into a perfect form where they resume their proper functions exerting control over the body and powering up the system to ward off diseases. This is the primordial power that remains inactive until recollected in a state of Sahaja meditation. Shri Mataji Nirmala Devi ( Mother) has taught us the practice of meditating in collectivity for the greater good of mankind. Please do not consider this propaganda as this comes from a person who was tied to her bed by her ailments until Sahajayoga came along. It will give you peace, hope and direction if you so much as give it a go. There are many frauds in the spiritual business that exhort money and distort the truth. But Sahajayoga gives you results first and then you see the truth for yourself. You establish its credentials through genuine experience that rids you of your ailments and shortcomings whatever their nature might be. I wish for people to find some reprieve where doctors fail to provide it. Anyone reading this, I want you to give it a try and see your life become better as the days of pain and suffering are left behind for a healthier, happier tomorrow. I want for us to be free of all mental strain and physical suffering and lead a life we all deserve.
Just got it. I Googled Lexapro helps Fibromyalgia and NOW THIS SECOND I will start taking my meds again.
I'm writing this very moment with a lot of pain. I have been weaning off Lexapro but I guess I will never leave them.
These pains make me cry like a child and I didn't have them for sooooo long. Hope I am giving someone a some hope.
I have these same type of pains. They are specific and localized and occur as an attack of some sort. It is not a constant concern, but it does happen more often in recent months. Has anyone found an answer to what causes these pain attacks?
I have this as well and am wondering if it may be Hashimotos or a food intolerance, such as to gluten, sugar or dairy.As I know this can cause inflammation in the body.
I'm 22 female mother one 2 and lately for the past year and half I get shots of pain almost everywhere in my head back of head lungs chest arm lately it feel I might have a pelvic problem or appendix I have been feeling pain on my right side for three days idk does any one exactly know we all wanna kno
i too have a a pain like this, but its short bursts almost a stabbing pain. I did a test where i tried to figure out what this problem is, heres my conclusion:
i figured out that when i ate, and laid down or sat in a funny position, i would have these pains, even hours later. I tried this and have been doing for about a week, i found this helps but doesn't fully cure it. i do hope you try this and tell me what happens, thanks -Rob
It might sound crazy.. but I had all types of weird pain, last month I discovered that I have gluten sensitivity/allergy.. so I stopped taking gluten.. right now, I do not have any more weird pain happening to me..
It feels like I had slime in between my muscle fibers which was causing pain.. also was causing hyper active sinus and I had a cold almost every week! But now I don't have any of them any more.. hope this helps!
I am having exactly what you have described. Random shooting pains in random places seeming unrelated to each other . Can be in my foot for 10-30 seconds then disappear next tone in my thumb. Very strange. Not so painful its unbearable but slightly uncomfortable. Doctors have tested blood for everything cant find anything wrong! Driving me mad. Had it around a year now and Im. 27 . Anyone ever get any answers? Only happens in legs arms and neck
I am a 60 year old male and I suffer the exact same thing. I have for as far back as I can remember and I have a long memory. They can happen at any point in my body. Including my abdomen and thorax areas as well as my face, head or extremities. They come on quickly out of no where and can last from a minute or so up to several minutes before fading away.
The cascading effect you described can happen but seems to a rare event for me. I rarely make a sound when it hits but it does make stop what ever I am doing and wait for it pass. It can occur at the same spot with multiple events. It seems to be happening more frequently these days and can wake me out of a sound sleep. It sure would be nice to learn what causes it.
I have what I call "Sparks" in every part of my body. Even my cuticles and nail bed hurt. After holding my phone after 10 minutes, my hand freezes. It hurts bad. I know I have Lyme Disease. I'm trying to also find out what this is?
I've been experiencing the same symptoms as you but I've never had an infection or virus or really anything. It just started and I'm only 15. I get these throbbing pains and they form everywhere. They seem random though. What could I do to get rid of them. And the muscle spasms, I get them in my face too.
I get these too and my research has led me to the answer: anxiety. These sharp stabbing pains that occur in concentrated parts of the body at random times are from high stress and anxiety levels. I experienced a lot of these before big tests such as the SAT. They are caused by muscled receiving nerve signals that cause them to react in a painful way. Hope this answer helped you :)
I've been an RN for years now & about to graduate to nurse practitioner. I recently have been experiencing similar sharp or burning pain twinges and it's not something I'm professionally familiar with nor know any medical professionals that could give me any good answers but my best guess is that it's some kind of circulation problem, similar to how diabetics get those types of pains in their feet. It's peripheral neuropathy, or nerve pain, caused by lack of blood flow to the nerve tissue. People with this condition are commonly prescribed Gabapentin. I personally noticed that when I am more active, my circulation is better and I get less pain. The pain gives me more motivation to stay active, go figure.
Its built up anger in the body. Go somewhere and scream and yell until you're really hot and red in the face. It also works to balance out ecstacy feelings in the body. A common thread among many of you im sure, is that you are dreamer types, mostly positive, and possible people pleasers. Gritting your teeth allows you a slow, socially acceptable way of concentrating the pain in a place of your choosing. Hope this helps.
I'm probably even younger than you, but I have some problems with random pains also. My issue, though, is that while I do have random pains in random places, I also get twitching, and really bad cramping (I'm a guy). The cramping got really bad yesterday. I hope that I could get some reliable answers on what might be happening
This may not help. But wanted to put it out there in case, when I was having what felt like bad heart palpitations and tightness in my chest it ended up being bad esophageal spasms. I had foods that triggered it but that isn't nearly so bad since I quit pain meds years ago. My family has sensitive digestive systems it seems. Now I only take ibuprofen etc when I desperately need to.
the electric shok I get is in the shoulders in the middle near my spine
Hi every one! I'm 17 years old and I've had these pains for about 3 years now. like many of you I've experienced the sharp shooting pain sensations in random places all over my body. For example I'll get one in my calf that isn't that bad and then 10 minutes later I'll have one in my head that put me on the the ground in tears. I've gone to the doctor about this and have had an x-Ray and a blood test done both coming back completely normal. My doctor is now sending me to a specialist on muscles but of course it's been four months and I haven't heard back yet and meanwhile my pains are getting more painful and more frequent. I'm scared that I'll have this for the rest of my life. If any one knows what cause this please let me know
Hi there
Some of you could possibly have neuralgia. This is caused by a knock to the head or nerve trauma. I get shooting pains in the back of my neck, down the left and right side of my body, pins and needles in my hands and numbness in my head. When it is really bad and I’m out and about ( in a shopping mall for example) I get very paranoid, dizzy, dry mouth and feel the need to be sick.
My doctor said that they can treat it with pills but it should hopefully disappear on its own. It’s been 4 years and I’m 30.
Below are a few tips that have helped me get through it. Hope this helps.
• Drink plenty of water
• Eat something sugary ( I find a biscuit helps)
• Get a hot water bottle and put it on the shooting pains ( really helps)
• Take paracetamol
• Run cold water on your wrists and keep the back of the neck cool
Unfortunately I find the big culprit for me is alcohol. I do find if I have a heavy session with my mates it triggers if off and its horrible. Any questions give me a shout
letter is spiral out of control is a hangover. I’ve had to quit red wine as it seems to a trigger :0(
I have been having the same pains the OP and elle27 been having. I think at this point I am not going to the doctor because it is not going yo do me any good. I have some back issues and perhaps it is related to this. I wil probably go and get my back re-checked since it has bern a long time. The problem started about 6 or 8 months ago. Before that I have been having some paresthesias in my legs as a result of a pinched nerve in my back for the last 20 years. But this is completely different. I might have pains occasionally in the tip of my finger. Another day, it is my arm, or my hip, or my shoulder. It is quite sharp and only lasts a few seconds. Sometimes it comes back a few times, sometimes it does not. I can say that for the e first time in my life I have been doing no exercise. I am going to really try to get off my bum. I always noticed that when I exercise, my back is better. I have noticed that very few people on this thread mentioned exercise. It would be good to know if most of us are leading sedentary ives.