I had an Interstim device and the lead was moved during a different surgery. the lead was move into a nerve root in my lower back and I was electrocuted by the device for more than 60 min. this was over a year ago and I am still in extreme pain every day and have yet to be diagnosed with anything. will an MRI show nerve damage in my lower back and leg area?
View 2 RepliesI have a lump on the outside of my lower right leg towards the front. It doesn't bother me at all until I accidentally bump it. Then it sends a pain like an electrical shock down through my foot that brings me to my knees. Any ideas what it could be?
View 1 RepliesI have a question for all of you, I have had these very strange symptoms for the last year, year and a half and I can't tell my primary care doctor because he is treating, or barely treating me for chronic pain due to a pretty bad car accident years ago, (I was holding on to the steering wheel watching this guy drive right into the back of my car and was hit with so much pressure that I clenched up , went forward and when I came back I actually bent the steering wheel in half. I now have severe pain in my neck and lower back. After the accident I went to a chiropractor for 3 years 2 x a week, but only got worse. My PC doc for 8 years told me my pain had more to do with my emotional problems than anything else (I was continually raped by my father and then periodically beaten by my mother for being a ****, starting very early in childhood, also suffered a lot of physical abuse by both, I am really pissed that I have to apologize to the world that this happened to me and that my doctor would blame my pain on this), and always threatened to take me off all my pain meds if I complained about any other pain and symptoms. At one point 3-4 years ago I had such horrible pain in my lower left leg I thought I had bone cancer, it was the first time he ordered an MRI and when he got the results he sent me to a neurosurgeon immediately who told me if I move the wrong way they will never be able to stop the pain. When I told my PCP he dismissed it, but never put me down as having chronic pain syndrome anymore, but now he is taking my pain meds away slowly because he say the CDC is making him do it??? Anyway, I dare not tell him anything else cause I can't walk and do much of anything without a lot of pain in my lower back.
But a couple years, 1 1/2, I started to have this weird feeling of "something not right" in my head, I can't really explain it. Then I got this strong ZAP, like a strong electrical jolt in my brain. It took a while for the sensation to go away, but I ignored it. I also noticed I was "forgetting how to swallow", weird right? Since the ZAP wasn't really painful, but if it was I would be too afraid to tell my doctor, especially if it was painful, so I did nothing. Every few months this would happen again, maybe 4 times total. Last week, I could "feel" something in my head not right, Like something was going to happen, then I got that powerful zap, like an explosion in my head, and it took a little longer to feel okay again, then I got another one, and felt extremely fatigued after this one, and it took longer to "clear" my head. My blood pressure has been rather high lately too, in fact I've noticed my blood pressure goes up the more pain I'm in and since he's lowering my medication, my blood pressure had been around 164/90 to 175/90 from around 128-138/80 normally. My mother died of a brain aneurysm. I don't know if this is something I should worry about and maybe find another doctor, but then I'm afraid I'll be accused of doctor shopping...
has anyone had nerve pain going down the thigh that comes and goes at any time and it's like an electric shock while waiting for a hip replacement?
View 21 RepliesI went in for my routine physical two days ago and got blood work done. The nurse drawing my blood completely missed my vein and when she stuck the needle in, my arm felt like it was being electrocuted. I waited a few seconds because I thought it would go away but it didn't. She took the needle out after about ten seconds. Anyway, I'm almost positive she hit my nerve. I have a tingling pain that shoots through my arm when I extend it or put it in certain movements. I don't really feel any pain in my hand. When looking at a diagram, it looks like the ulnar nerve is the one she hit.
Anyways, I have read many posts of people not getting better after years, and some getting better after a few weeks. Is there any way to tell how bad mine is? Are they required to pay for any health costs concerning this issue?
About two years ago on Christmas due to high blood pressure I lost little pieces of my right eye it hasn't come back Since then the doctor said it's ocular nerve damage does anybody think surgery or anything will make it come back
View 2 RepliesI have nerve damage in my lower back due to four back surgeries. Now I am beginning to have pain deep within my thigh on the same side where my disks were herniated. Anyone experienced this?
View 1 RepliesI first started masturbating at age 15 where I would watch porn for a while and orgasm a few times. After I realized that I could go on for hours, over the years I had a few nights (once in a while) where I would orgasm every 30 seconds-3 minutes until I was drenched in sweat and had to stop. At 18, I bought a vibrator and used that for pleasure and my orgasms were always so powerful in the beginning and after a while they'd get weaker. Now, I'm 20 and my orgasms have become very weak. I can go 2-3 months without even trying and when I go for it I expect magic, but all I get are weak ones. Lately, I've been bored out of my mind, orgasming for hours every day for the last 5 days and they're pretty weak, but just pleasurable enough to keep me going. Now I've just done some research and learned that over-masturbation is bad and that I could be causing nerve damage to my clitoris. Even when I go months without they're still weak. Have I ruined my chances of having a powerful orgasm again?
View 1 RepliesI had foot surgery 8 weeks ago - quite a major reconstruction that took a few hours.
when the plaster was removed at 6 weeks I was told that I had nerve damage causing partial foot drop and a lot of numbness and pain. I have just had nerve conduction studies and have started on Gabapentin and physio..
They said either the tourniquet or nerve block has caused it. I can't believe that this can happen, surely they know about these nerves and how to prevent problems.
Has anyone else experienced this and what has the recovery been like. I'm just wondering what my life is going to be like from now on.
Ten months ago, I had Achilles' tendon lengthening along with foot fusion surgery. Afterwards, 2/3rds of my foot on the outside edge and bottom of my foot has been numb. I kept mentioning it to my doctor, and he would say that it may take up to two years to fully recover from numbness. He even blamed the numbness on the popliteal nerve block that I had for seven days, but the anesthesiologist said that wasn't possible as the numbness started about two inches above my ankle and goes down into my foot.
Finally, I had a nerve conduction study (from my own insistence) that now confirms the injury/permanent damage to the Sural nerve. My surgeon must have nicked the Sural nerve when he did the percutaneous Achilles' tendon lengthening. It causes numbness that radiates down through my 5th metatarsal or little toe. But, 2/3rds of the bottom of my foot is also numb. Could this be from the Sural nerve or may there be other reasons for this numbness? What types of complications might occur with Sural nerve damage? How often does this occur with this type of surgery? This numbness is making it very difficult to walk. I can only walk very short distances at ten months, which is exceedingly frustrating. I am interested in hearing about others' experiences related to numbness and Sural nerve damage.
3 weeks ago I had a muscle spasm in my lower back that shifted the muscles around quite alarmingly - thought my hip had popped out. I went to A&E and they told me I'd had the spasm as a result of my body protecting the horse tail nerves that are around my spine. The only pain I have at the moment runs from my glutes to my calf, in certain stretched positions. It's definitely improving but very slowly, and I know I need to be patient as it can take weeks.
The main issue I have is strength in my right leg. Since this happened I now can't raise myself using my right foot - going to tiptoe. Left leg, fine. Right leg, it's like there's no signal, no strength. And it's freaking me out. Before all this, I was running, going to the gym, cycling - 4-5 days a week.
My question is this - is there anything I can do? Do I need to stretch it (kind of feels taught all the time anyway)? Perhaps I need to massage the areas?
In 2003 I had really painful headaches so bad I could hardly put my head on a pillow, pretty scary as I do not suffer from headaches. Then as I was eating bowl of cereal I kept missing my mouth and realised I couldn't feel my lips or tongue as though I had been given dentist injection. My sister took me to hospital thinking I was having a stroke, this was the first time I had heard of Bell's palsy and I was given steroids, i was very tired and it was an effort to do anything like eat, speech, it did take three months to go.
february 2014 I got a rash on my stomach which spread to my neck, to my back, to my feet, then to my scalp and then my ears, I was in agony, it was urticaria. Whilst trying to cope with this I then got Bell's palsy again, possibly due to an immune system at a low. However it has taken a lot longer to recover this time. Eighteen months later and I still have a twitchy eye and lopsided smile. I am now considering Botox, has anyone here used Botox to correct any of the nerve damage left after palsy and if so what are your thoughts?
6 weeks ago I had foot surgery (modified brostrom procedure to tighten up ligaments near ankle, and a procedure to correct a calcaneonavicular coalition). I have on incision along my ankle, and another incision on my foot. My cast came off 3 weeks after surgery. 5 weeks after surgery, when I was changing my dressing, I saw some some black stitches from the ankle incision on my gauze pad. I called the doctor's office, and the medical assistant said that that was normal. After that, I noticed drainage for a few days when I changed the dressing. I called doctor's office back, because my foot was feeling hot and I was having a burning pain. They put me on an antibiotic (keflex). And I was told to stop walking and go back to non weight bearing. They told me not to clean the incision. I have only been on antibiotic for 3 days, and it is a 10 day course. In the evenings, especially when I am in bed, I wake up because there is so much pain in my foot, it feels like a deep stabbing pain that is sharp, and sometimes burning. Is this normal of a skin infection from an incision? Could it be a bone infection? Or nerve damage? How patient should I be with this doctor and doctor's office?
View 2 RepliesI have diarrhoea all the time since having my gallbladder removed 30 years ago, i now have sacral nerve damage which has caused my annal sphincter to weaken so i now suffer from incontinence. I have been told i may need a colostomy, does anyone out there have one or faecal incontinence.
View 1 RepliesI was having frequent headaches and occasionally feeling lightheaded with floaters. I went to the opticians and they referred me to the ophthalmologist who put eye drops in and said that at the back of my left eye the optic nerve was sheeted. (I don't understand what this term means and cannot see anything on the internet to explain either) He just said that I didn't have any other symptoms for Optic Neuritis and wasn't sure but didn't think it was anything sinister. I am now waiting for a scan of the eye to see what that shows.
However, the last couple of weeks I have been getting pins and needles all over my body, mainly in arms and legs. I've also had general aching pains.
I have read online about symptoms and they point to all kinds of things, Fibromyalgia, Anxiety and possibly MS. As you can imagine this has really scared me as I have read that problems with the optic nerve can also be related.
Has anyone else had these symptoms or are they too few for me to be making assumptions?
I had a fall on june 17th 2014. Fell about 20 feet onto a concrete floor. I fractured the humerus, fairly simple fracture straight across the midshaft, no surgery. fracture to the elbow, and got radial nerve damage.
It is now week 14 and although the nerves are back and my wrist is fully functional, both fractures are yet to heal, the humerus fracture is fairly straight, and some callous is appearing, but there is still movement in the fracture site. And the elbow still shows a fracture.
I now have an electromagnetic device to help with the healing, 30 mins a day i can use it for.
Just wanted to know if anyones had success with one?
Also seeing as i broke the elbow the arm has been held in a sling this whole time, without straightening of the arm, so the inside of my elbow is getting very inflamed, but not painful yet, anything i can do to help it?
I too have been taking Gabapentin for Femoral nerve damage for about 2 weeks...300mg/3times a day. I went out of town recently and skipped a couple doses by accident. When I realized it I took my next dose. For two days I experienced nausea, terrible anxiety attacks, and now my pain is worse.
View 3 RepliesI am 2 week into my broken fracture in my humerus just above the elbow
The doctors undertook surgery and after the surgery they did say my nerve was damaged in the process as I had a metal plate inserted to put back the broken bones together if that make sense.
Whilst I understand the fracture will take a while to heal I am real concerned about my nerve injury I can't move my thumb freely, I can't move wrist at all I can bend my fingers but I can't straighten
My splint is tight so I do loosen this and try to do exercise with my hand.
I'm 32. It was only detected after suffering 2 weeks of intense headaches which eventually affected my optic nerves in my eyes. I wear glasses and after 2 weeks of intense headaches my eyesight actually became much better which baffled me. I was sent away from GP with the diagnosis of a tension headache (which I don't hold any blame for) but luckily I pursued further and booked an immediate appt with an Optician who found that my visual field was affected in my left eye. I was advised to go to the Emergency Eye Casualty who continued with further tests on my eyes. They discovered the damage to my optic nerves but at this point were unable to find the source and I was seen immediately by a Neurologist who at first thought it was benign cranial hypertension. He arranged a CT scan and said that he did not expect to find anything but was very surprised to see the clot on the CT. I was admitted immediately and underwent a lumber puncture. I spent 5 days in hospital and was discharged on Warfarin medication for 3 months. I have since undergone a repeat CT scan. I believe I was very lucky as any longer I could have had a stroke. I was advised to stop the oral contraceptive pill immediately as they said this may have been the cause but also that I have recently underwent a breast reduction 3 months before.
View 44 RepliesI went today to a doctors appointment, he placed a headband on me hooked to a device. The device was then hooked to a computer, he said the device reads my energy and my vibrations. He said he detected many things. Like an allergy I did not know I had to bread. He also said I had blood in my urine. Also, he said that I consumed too much sugar, which I found strange since I drink mostly water and eat very healthy to my knowledge. After he was done with the test, he placed some pills, with no information on the bottle, on top of the device. He claimed that the device gave frequency from the reading in his computer into the pills, and that the pills will now work with the problems I had. I know about the placebo effect.
View 5 RepliesHello I live in the U.S. and I have been reading these discussions for information because I have Molluscum. I have had it since I was 25 and I'm now 31. I was initially told by a doctor the classic " it will go away on it's own in 6 months to a year. Don't touch them, pick them or put anything but soap and water on them." I went to another doctor a year later and a biopsy was done on one of the lesions to confirm it was actually molluscum because all the previous doc did was look at them. Well the test came back positive...of course. She also said "they will go away." well it has been six years and I still have them and they have spread. I have them on my arms, back, buttocks and I have also had them on my face. It has been devastating to my self esteem and my relationship with my fiance. I recently went to a dermatologist and was prescribed RETIN A micro gel 0.8%. I've been using it for 2 weeks and it seems to be working but time will tell if they return to those spots. It's terrible because even though they leave one spot they WILL return somewhere else. Why isn't there a way to attack the virus from the inside like with the herpes virus? I encourage you all to not take "no" for an answer from your doctor. make them give you something to treat the molluscum. If you do decide to dig these things out yourself, which seems to be just as effective as burning them, make sure you wash your hands well and cover the site after. I recently found some evidence of colloidal silver being effective on viruses and bacteria. I found some colloidal silver on amazon and I ordered it. I will update everyone soon and let you know if it has worked. Thank you for listening.
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