Cervical Spondylosis :: Freezing Cold Tingling In Legs And Arms
May 4, 2015
Just wanted to know if anybody has this strange sensation as I have. A very cold tingling going down my legs arms and face more so on right side. Keep getting fobbed off at drs and hospital.
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I was a raving hypochondriac, have suffered cs for 5 years,had mr scans,ct scans,myelograms and lumbar punctures,see my specialist regularly and just given different medication,vi suffer neck pain, headaches,numbness in arms and hands,but also have severe numbness in legs and feet,my hands and feet are permanently icy while the rest of my body burns up,feel permanently dizzy and nauseous,i have vision problems and incontinence problems,for past few months i have got steadily worse and not able to walk more than few yards,and cant get outdoors without aid of wheelchair,as pain in my joints and muscles is so bad,the nerves that are trapped have moved down my spine which is causing the leg pain,i have seen 3 specialists and a professor of m.s,i have meltdowns every so often as i always have been so active and cs can just bring you to your knees,i find that the specialists i see seem to think i am neurotic,i asked him to have my pain for a week and then come back and tell me how he feels...i feel people just don't understand how debilitating cs is and because outwardly you look ok and you do your hair and put some slap on your face,but walk a mile in my shoes when at 3am im walking the floor counting the hours till can have another pain killer,my last visit to my specialist i was given morphine patches,but suffering from ibs and gall stones was warned by my doctor that they would have adverse effects and they were so addictive.
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Last month i had a very bad bout with the flu. My whole body was paining. It started with my upper legs. Almost like someone gave me charlie horse in my muscles. Then my feet and bottom of my feet started paining. I could not even walk. I wore memory foam slippers on my feet the few times out of bed. My hands had the same painful sensitive sensations as my feet. a few days later my lungs started to hurt and I had something pneumonia. When i started recovering, the pain and numb sensations stayed on the bottom of my feet, my hands legs and arms. Not to mention the weakness that still exist in my limbs. Also, which is confusing and worrying me most now is the numbness on my face and in my mouth, it feels like dental freezing leaving my mouth. It's been at least a month since i recovered from the flu. I have seen my Dr. and have been scheduled for a CT scan. Has anyone had these symptoms before?
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I have multilevel spondylosis and I have been getting numbness and tingling throughout my body . Does anyone else get this
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I have cervical spondylosis of the neck and top of the spine I have had awful headaches tingling and a numb feeling on the face
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I was just diagnosed as being hypothyroid, Tsh 10.65, my question is does anyone else experience tingling/numbness in your face, arms and legs and also have head pressure?? I've had some anxiety and I think maybe its the cause any thoughts?
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Male age 49, started with pain in my right hand 4 years ago. Gradually transferred to left hand and now is what I would describe generally as a combination of burning, aching tingling and numbness in both hands, wrists and forearms. No other issues, aside from that in good health and do lots of regular physical activity.
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Lived with the pain which has gradually got worse and probably is something like a 5/10 on the pain scale now.
Recent stressful domestic issues seemed to aggravate the pains so finally decided to see a Spine Doctor (I am a Brit but live in the Philippines where medical care is excellent, especially when they see a foreign face with bulging pockets !)
The Dr did all the usual physical tests and none of them replicated the symptoms and her diagnised me with Carpal Tunnel Syndrome in both hands, to which I said "Sorry Sherlock, it ain't CTS).
Ok, he said, go do an MRI, which I just did and have the results (results pasted at the end of this post)
Went back to see the Dr and he said that I need surgery (Fusion of C5 and C6).
So, my quandry now is should I believe him or should I try a different approach.
The first paste below is the original MRI findings and the second paste is a second opinion that I got from an independent on line service.
IMPRESSION: -BILATERAL NEURAL FORAMINAL STENOSIS AT C5-C6 SECONDARY TO RIGHT FORAMINAL DISC EXTRUSION ON THE RIGHT, BILATERAL UNCOVERTEBRAL JOINT HYPERTROPHY WITH PROMINENT SPUR ON THE LEFT. -CORD EDEMA, C5 AND C6.
There is a moderate sized, posterior disc protrusion/osteophyte complex at C5/C6 causing moderate spinal canal stenosis, moderate compression of the cervical cord and cord edema. The segment of cord edema extends from the level of the C4/C5 disc to C6/C7 disc and affects the left hemicord more than the right hemicord. Significant bilateral foraminal stenosis at C5/C6 with compression of both exiting C6 nerves (right more than left) seen.
I'm 48 suffered with cervical spondylosis for around 6 years, in the last two years it's got so painful. I have tried all meds, last year I had an op foraminotomy where they drilled the left side spurs C4 to C7. But the last year has been a nightmare the pain is worse. I have now had more MRI & CT scans more meds and having two injections next week. I asked the long term affect of my neck I was told I have a neck of a 70 year old. What dose this actually mean? Wheelchair what?? I am also on the list for a anterior cervical discectomy & fusion.
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I have a fall time desk job which doesn't help at all but have a mortgage... holiday is taken as sick days.
I am recovering from Anterior Cervical Discectomy, which became necessary to avoid drastic further deterioration.
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I would like to tell you about my experience and what helped me. My problem started quite unexpectedly with a persistent back ache at work (I am an office worker). Within days it was so bad that I was vomiting with pain and had to stop working (I was commuting to London). I was on morphine within three weeks, but it did not help either. I won't list here all the various painkillers I was prescribed, which helped to certain extent, but the pain was so bad that I was suicidal. The doctors communicated with me hardly at all except writing another painkiller prescription. I felt totally abandoned by them. I tried osteopathy, ordinary physiotherapy and Bowen's therapy. Bowens worked the best but nothing would give more than a few hours relief from the extreme pain. My husband then hit on the Tens machine and that was the only thing that really helped. I would recommend it without hesitation. I dropped the morphine, which was a bit of nightmare for me anyway, and managed to live with the Tens machine.
Unfortunately my problem rapidly progressed to me losing strength from my arm and from my fingers and a neurologist recommended the dissection and fusion. It is not an easy fix, but to me it saved my life. I went back to work four months after the operation, seven months after first feeling the pain. I could not say I'm as good as new, but the pain has gone. My neck is stiff, gets tired very easily and a bit uncomfortable. I cannot lift, push or pull anything heavy. But I'm here, enjoying my family and grandchildren. I couldn't ask for more. I'm 63 and now feeling my age, that's all.
Anybody got these symptoms, hot then freezing cold feel like you're going to fall over, heart palps, feeling scared, Anxiety panicking, feel bad, dry hair, sleep problems, nausea, tummy feeling weird let me know.
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I thought I was truly going round the bend after 2 and half days on Metronidazole. I slept for 10 hours last night, have had mega hot-flushes combined with freezing cold spells during the past 2 nights and feel like a total zombie. I am not going to take anymore of them as I'm also on penicillin 4 times a day for a tooth infection. If the tooth is still sore once I finish the pen. then I'll ask the Dr. for something else, but hopefully it won't come to that.
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12 Jan I had a riding accident, hurt my shoulder. It was previously injured (dislocation/fracture of humerus) and it's been weak ever since. Doc put me on cocodamol as of 14th, and then on the 17th I was back at docs because they were making me sick. He put me on tramadol. 2x 50mg tablets three times a day.
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I wasn't warned about any possible side effects, other than they may cause drowsiness.
11 weeks later, I can't kick it. I no longer require the tramadol for pain. They tried a weaning programme. I was given Tramadol SR tablets. I cut from 300mg a day to 200 mg. One tablet morning, one tablet evening for a week. The week after I was cut down to 100mg tablet in the morning, then nothing.
I lasted a day before I used some left over regular tramadol.
The effects were horrific when I initially changed the dosage, but I thought it would be okay with cutting down and then coming off completely. I was ready for some side effects, but not what happened in reality.
Headaches, nosebleeds, sickness, sweats, freezing cold, aggressiveness, exhaustion, tearful, restless, insomnia.
I had some very very dark thoughts that I haven't had in years. I took the tramadol and felt ten times better.
I have a doctor's appointment today, but they tend to be as much use as a chocolate teapot.
A nurse over the phone expressed she thought that the time frame for coming off them was too short, and the leap from 100mg to none was too much.
I know I have a problem, but I'm scared to come off them and become the horrid, nasty person I was at the weekend. My rational thoughts tell me once I stop for good I'll be back to normal, but I don't have those rational thoughts when I try and come off them. I need them to cope with the most simple of tasks.
I was diagnosed with cervical spondylitis when I was 27 ( had a severe fall when I was 16 yrs old...fell 2 stories), am 48 now and moved to Wales almost 2 yrs ago from South Africa and since being here, my pain has increased in intensity. Used to get steroid injections and am aware that I won't get that here in the U.K. I now suffer extreme nausea due to the pain and can only dry retch, as the valve below the oesophagus was tightened yrs ago and now prevents me from throwing up. I would appreciate if others with this condition could tell me what the maximum dosage of Ibuprofen one can take. Taking the normal dosage (2) does not alleviate the searing pain or spasms.
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I am also very confused. After x-rays, all dr,s have said cervical spondylitis and not cervical spondylosis. Been told that I don't have arthritis and yet this is not ankylosing spondylitis, which 1 dr said it was..(he never saw the x-rays)...really confused even after numerous x-rays and dr,s. I am almost on the verge of giving up hope of getting effective painkillers from dr,s here. Do the exercises, use heated neck bags and nothing much helps, especially when I get a flare up.
Need to know if increased dosage of Ibuprofen would help.
I dont know i have cervical spondylosis , but MRI said i have a cervical spasm < now even after eating food my heart rate increase some times and there are weird feeling all day long in the chest ,pain in arm .. i feel tingling numbness, in legs ,arms , shouledrs some time. disbalance when i just stand up
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Mty Doctors are sending me to neurologist,Cardio , Rheumatologist,Internal medicine .
nothing solved . Heart is ok , ECG is ok, x-ray of heart is ok.Blood test was ok ...
Has anyone tried reiki?
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After a fall at tennis, I am 71 y old lady, very fit normally walk 5 km each am. I thought that it may be due to my balance. feel a little dizzy when stretching to pick up the ball. has anyone had any help with spondylosis. exercises or medication.
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I have cervical spondylosis and I am suffering really bad headaches
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I am due to have cortisone injections on 7th November but am feeling a bit anxious about it.
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I'm 28, work in IT, sit 8h (With 5 min smoking breaks/h) in front of the pc and a few more at home. Exactly a month ago, while on vacation in the mountains, one morning after eating breakfast and sitting down to drink my coffee I started having slight dizziness. I panicked because I was never dizzy in my life and it was new to me, except after nights of drinking. The whole day was scared and worried. The next few days were ok again. Then I had days with light dizziness at work a few hours, then sleepless nights because of panicking that I can't sleep and what is wrong with me. Meanwhile I feel very light tingling in left arm fingers and sometimes in left foot as well. One day at work I panicked because of feeling a little dizzy again and went to the company's onsite nurse. She took my blood pressure and it was at 160/85. I started worrying more. She thought it could be a calcium or magnesium deficiency so she gave me a Berocca tablet. After I left her office and before taking the tablet I returned to normal. Next days again I was confronted with light dizziness, tingling in left hand and foot at random times, mostly at work and very bad sleepless nights. So I went to my GP. She sent me to take blood and urine test. The results of those were PERFECT. Every bit. Blood pressure was once 140/85 and 130/85. Next, I went to a neurologist. After 10-15 minutes talking to the neurologist and going through some exercises she told me I have cervical spondylosis and sent me to an x ray. Result of the xray is that I have deformed neck from siting to much at the pc and small lower osteophytes. The neurologist said its absolutely nothing to worry about, the dizziness and tingling will go away, especially if I change my lifestyle. This was 2 weeks ago. Since then I go every other day swimming for 1h, daily neck, back and shoulder stretching in the morning after waking up for 20-30 mins and will soon exchange car for bike, and go walking as much as I can. I am not sporty at all. I am 187cm and weigh 90 kg constant for the last 3-4 years. This is my story.
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Now, because I was NEVER in my life sick (only the occasional cold) I am very sceptical about doctors and would like some advice from other people, because I am bit scared right now. I still experience light tingling in left hand and sometimes feels like it will go numb (but never did), can't remember when I last time felt it in the foot. Dizziness appears for a few minutes in the morning when I sit down at the PC at work, goes away shortly after. I now quit smoking (it's been 4 weeks and don't miss it), instead stretch around in the work breaks and after lunch I go walking for 30-40 minutes. But being scared about the situation I tend to "feel" different symptoms including being weekend (probably all in my head). Bottom line: is it possible to be affected by cervical spondylosis ? If I keep up with the lifestyle changes, will I have it under control and will the symptoms go away ?
I am 63 and have been suffering with neck pain, stiffness in the neck and pain in back of head for over a year now, I also have trouble sleeping as can't turn over without pain, I have to physically lift my head with my hand to turn over. Initially my Dr said it was muscular and gave me Codeine Phosphate which did nothing for me. I gave it a couple of months and went to see a different Dr at tlhe practice who gave me stronger painkillers....Nefopam and also Amitriptyline to help me sleep. She tried to refer me for a scan but couldn't until I'd had physio which I am still having at the moment. The physio I get is about 15 mins every 2 weeks which in my eyes is not nearly enough. However apart from that I have been managing at work fine, I work in a dept store and am a bra fitter and general sales assistant. Any heavy lifting there is to do my colleagues would help and the rest of the time I have been managing fine. This week however I have been moved and put in the cafe, my first day was yesterday, I found it really heavy....carrying loaded trays of food, clearing tables and carrying loaded trays back to the kitchen. every part of the job involves some sort of lifting, carrying, pushing and pulling and scrubbing! Today was my day off and I have had so much pain and stiffness in my neck and pains in the back of my head! I am really concerned that this is going to make my condition worse. If I am feeling like this after one day I dread to think what I'll be like after five days in there. How do you cope at work, do you have a job that entails lifting or heavy work?
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At age 42, I'm starting to notice some loss of hair on my arms and legs. I'm a male, and of Mediterranean ancestry, so I've been quite hairy in those areas since I was a teen. My hair remains very full and thick on my head, so it seems odd I should be losing it in other places. Is this normal? I don't like the way it looks - like the skin of an old man, all bare and plain.
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