neck pain
Posted , 6 users are following.
Does anyone know whether this is a side effect or not? Think im going mad. I keep getting pain in the left side of my neck which means that when trying to sleep I have to try and put a pillow between my neck and shoulder when on my side. Tramadol isnt touching it and its there all the time but worse at night.Im having every other side effect going so wanted to know is this one too
thanks
2 likes, 146 replies
jean34329 michelle95405
Posted
A good link is the Vitamin D Council.
christine1956 jean34329
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jean34329 christine1956
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You are welcome.
Jeanx
diane94845 jean34329
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terry74787 michelle95405
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diane94845 terry74787
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jayneejay diane94845
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is your neck pain at the back of neck
mine is .. Okay when laid down..
mines stiffness - when moving up and down ..
😟
diane94845 jayneejay
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michelle95405 terry74787
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jayneejay diane94845
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😟
jean34329 diane94845
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Have you had a ctpa scan of your thyroid. If a goitre it may be pressing on the trachea causing a problem.
jean34329 michelle95405
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Pls see my response to Diane. Have you had a ctpa scan of your thyroid?
jean34329 terry74787
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diane94845 jean34329
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diane94845 jean34329
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jean34329 diane94845
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The sign and symptom of breathlessness needs investigating. That is why a CTPA scan was ordered by a hospital. As I keep saying that showed as an incidental finding qa multinodular goitre. I had previously been told by hospital drs that my breathlessness was due to anxiety. The old cop out.
sleep with several pillows propping me up . Perhaps you could explain in more detail about your breathlessness especially when lying flat and keep waking up.
You may have a goitre which is pressing on the trachea. I do not intend to worry you but the breathlessness cannot be dismissed.
My CTPA was done using a contrast medoium otherwise the goitre may not have shown up. However I am not an expert in nuclear medicine or radiology so cannot speak with any certainty. I had had a VQ scan whereby a radio isotope was used one hour preceding the CTPA scan. Sorry to keep going on and on about it.
jean34329 diane94845
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jean34329 diane94845
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Also google Thyroid, flouroquinolones and their link to thyroid disorders.
Try floxiehope.
The signs and symptoms of antibiotic toxicity are remarkably similiar to those of thyroid disorders. I am not an expert so please excuse my loose
terminology.
jean34329 jayneejay
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terry74787 diane94845
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jayneejay jean34329
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oh nooo.. i have 3 bulging disks .. lumbar ... they were awful in Feb couldnt move hardly ... ooooooch' then got shingles too..
had a scan etc ..
have an extra fused disk & vertebrae too .. long tail bone like a monkey..
oh the joys 😟
jay x
jean34329 jayneejay
Posted
Bulging discs can account for neck pain and painful muscular spasms and peripheral neuropathy . I went to physio privately after having an MRI scan which identifid the bulging discs and also an annular tear between L4/5.
Physios assessed me then did some gentle stretching exercises as I have the dreaded osteoporosis.
Another physio said that the neuropathy was due to medication as well. Several drs including consultant endo has said the same. Namely antibiotics, statins, phenytoin, valsartan and a beta blocker.
I was advised to have Pilates, hydrotherapy, physio, TENS machine and to pull in my umbilicus very gently. All these were recommended in order to build/strengthen the core muscles. My feet were and still are in spasm just like plantar faciitis. I understand that all this is due to lack of vit D and a severe Vit D deficiency disorder. I also have tetany spasms of both feet and ankles periodically where it feels like my feet are being severed.
I am just hoping hope against hope that this new diagnosis of multinodular goitre can be successfully treated,
Jean
jean34329 terry74787
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I am in a similar position except I did not sleep for five nights in December 2013.I will look the website up. How are you now?
Jean
jayneejay jean34329
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oh arent we a right pair ..
i had PHN with shingles ... pain was awful all over body for weeks, not been right since this was February ..
i have stiff ankles too, achilles .. if i sit and get up i walk like a penguin for ten minutes ..
i am only 113LB ( 8st 11 ) 5'6 so not at all due to weight, or anything ..
cant put weight on...
i use to be so active, 300 sit ups twice a day, rowing machine daily etc.
now ... i havent the energy.. or the interest...
for last 2 weeks i have been having hunger pains, i always eat little and often and eat healthy, fruit, and good diet etc.. dont drink alcohol, dont smoke .. this hunger pain thing is a nightmare.. even after eating it starts, but being hypoglycaemic can cause that and fatigue, hot flushes etc and hot flushes returned last summer after none for years.. ( i was having 20 plus a day) and they are beginning again ( summer beginning ) heat never bothered me before ..
i been painting the house, normally love it, but have to do abit at a time now, crazy, feel like i am falling apart at the seams ..
' we need quality of life '
going back to thyroid , mines being monitored .. my mother has underactive thyroid and has been on thyroxine for 30 years ..
jay x
jean34329 jayneejay
Posted
I would like to know so I can work out if I have left things too late and if it is worthwhile even starting any treatment. This illness is one of the worst imaginable. I FEEl as though I am sitting on rocks all the time. I dread going to bed but for about six weeks have been worn out and staying in bed until 9am when previously I was up at 7am.
These spasms are literally driving me mad. I lost interest in life itself but
this is improving slightly. I spoke to a nurse practitioner today who assured me that all these signs and symptoms are due to thyroid disorder. I do not yet know whether it is hyper or hypo or a combo of both.
I am unable to make sense of hwich blood tests nneed doing.I do not mind paying frot them to be done.I just want to feel better. This has been going on for years but worsened since \\\\dec 2013. I will be glad when it is all over.
jayneejay jean34329
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its hard for me to say when it started for sure ..
at first i thought it was just peri menopause ( was an early peri gal) had a 9-10 year peri .. and now 19 months post meno age 50 .. ( 51 in June)
i put it all down to that until i feb when i had severe back pain and shingles a week later ( blisters on the butt cheek)
i had a couple of spots blisters on same butt cheek at christmas. but ignored it, thought something ( mozzy) had bitten me, then i had the 3 bulging disks after twisting one day, then these blisters came back, same place, showed doctor and he said thats shingles and said that explained the severe all over pain.
as you may know, we all have shingles laying dormant in our nerves, and it just takes something, stress, trauma, illness to trigger it off ..
so i actually had two attacks of shingles in two months ..
anyway long story slightly short, after this then all the other has come to light after tests.. thyroid, B12, Vit D
i did have an Adrenal check, Cortisol etc .. but one test has to be redone as my blood was too thick. i got the cortisol checked though.
i blamed menopause, but not the case ...
i dont take HRT ( cant and wont ) so just thought it was that menopause as symptoms so similar ..
jay x
jean34329 jayneejay
Posted
Do you feel as if you are sitting on rocks?
I had physio which helped. One of the exercises was raising each ln turn whilst lying on top of the bed.
This pulls bit on the back but stretches the nerves presumably the sciatic nerve which can become traapped due to immobility.
Obviously you had better check all this out with physio first.
Another useful exercise was to pull the abdominal muscles in gently by pulling in the umbilicus but very gently. Physio said this would strengthen the core muscles in the back which in turn would then act as a naturaL splint to support the vertebrae.
Another exercise I was told to do was to stand up then bend over bqaackwards slightly several times but not to overdo it. No chance of that!
I was also advised re posture. To sit upright, not to lean my head forward as the head puts about three stone of pressure on the spine leading to back,neck and shoulder pain.
I was also told that watching tv , using a laptop were aggravating the back and neck problems.
I also have the signs and symptoms of plantar faciitis but I feel sure that this is due to vit D deficiency dosorder which has possibly triggered off goitre disease. In 2009 I was also diagnosed with hyperparathyroidism and prescribed ergocalciferol My Vit D was NINE. It is now 58. My anas are 1 in 80 positive as well. When the vit d level falls the parathyroid hormone-pth- rises.
What a nightmare.
Jean x
jean34329 jayneejay
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I was very interested in what you wrote because your history of some uncertainty when it all started fits in with mine and what I have been told today by a nurse practitioner.
I had an early menopause following a hysterectomy aged 24 then being left withone ovary. Ten yearrs ago the other ovary was removed as a prophylactic measure and HRT was commenced. This caused blood clots hence being discontinued but not for eleven months despite chest pains.
Then about seven years ago legs were numb and gait unsteady. No answrs.
n Dec 2013 everything went worse very dramatically following prescribing of thtree anibiotcs for an unibestgated chest infection.
I started with heaviness and coldness of the legs just three days after being prescribed the abs.
The rest is history. Hopefully this goitre can be treated.
Jeabx
jayneejay jean34329
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we are very similar in our symptoms and ailments ..
what do you think to magnesium supplements..
i mean chelated magnesium - not the laxative Citrate and Oxide magnesium.
Chelated doesn't upset the stomach .
i shall start mine again before bed tonight - good for aches and relaxes you too - i am an insomniac, takes ages for me to nod off then always wake .
sometimes need help with the numerous sleepless nights it wears me out.
also magnesium oil spray is great for aches .. ( used by athletes for pain and football players etc ) i use that on occassion in the arch of my back ..
i dont have physio or anything.. never been suggested.
i did have it years ago for the extra fused disk and vertebrae but nothing helped that - learned to live with it..
i can never get comfy, always moving to get comfy, when i am a passenger in the car i have to sit with legs on one side ... cant sit normal.. doesnt help the matter but its more comfy for me..
and queuing at a checkout, oh nooooo i feel all anxious like i am going to pass out, need to lean on something .. back starts aching, go all stiff ..
jay x
jayneejay
Posted
What are some Signs of
Magnesium Deficiency...
So lets see what these magnesium deficiency symptoms look like:
Constipation
Hypertension or high blood pressure
Anxiety
Depression
Insomnia
Fatigue
Sound like anyone that you know??
It's practically the definition of all of the Symptoms of Fibromyalgia!
Even high cholesterol, diabetes and osteoporosis are related to low levels of magnesium.
Even some so-called 'Side Effects' of substances are actually due to the Magnesium Depletion that they cause- and are not really 'side effects' in and of themselves.
For instance, you should ALWAYS take Magnesium and Vitamin D together to avoid any of the Vitamin D Side Effects That are (almost always) due to low magnesium!!
Pain is One of the
Signs of Magnesium Deficiency
Painful conditions can be due to magnesium deficiency. Especially conditions that are due to tenseness and tightness- even if you don't know that you are tense or tight, if you have these pain conditions, it's likely that you are. Conditions like:
Muscle Cramps
Chronic Back Pain
Magnesium for Migraines
Muscular Pain
Tendonitis
Fibromyalgia
ANYTHING that makes you tense and tight could potentially be due to magnesium deficiency. Even anger, aggression, ADHD, insomnia and obsessive compulsive disorder are Signs of Magnesium Deficiency until proven otherwise. If you can’t relax or you can’t stop, then it is likely that this is a symptom of magnesium deficiency.
chelated magnesium is the best type, easily absorbed, and doesnt have laxative effect
magnesium oxide and magnesium citrate has laxative effect and can cause tummy upset ..
jean34329 jayneejay
Posted
Yes magnesium relaxes muscles as you say best to take the form that does not cause diarrhea.
However check out any interactions with any other drugs you are taking.
I cannot take the citrate due to warfarin but can take the other types.
PHYSIO.
I would review the situation as physio techniques and ideas change with time so may help you now.
Magnesium oil is good for aches.Another good idea is to have a soak in Epsom salts whuich I believe contain magnesium.
Regarding muscle pain and stiffness when standing. I have this but my physio said if you don't use it you will lose it. I think exercise in moderation plus walking to strengthen the core muscles. This will hurt at first until the muscles that went into spasm due to the pain learn to work again.
This was the explanation given to me by my physio who I have not seen since January due to my having chest pains due to this goitre.
Jean x
jean34329 jayneejay
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jean34329 jayneejay
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Just seen your e mail re magnesium.
You are spot on. Low mag and potassium can also cause Long QT syndrome.
Endo said to have bone profile done, this is calcium , phophate, pth and vit D level.
May need injections of vit D if an absorption problem is suspected.
Jeanx
jean34329 jayneejay
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jayneejay jean34329
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If anyone reads magnesium info always check with current meds they take.
I dont take any meds so no fear there, only vits and supplements.
( normally)
Had a break off them as you know, but sure chelated magnesium helped me personally so just had one 😃
Hope you get some answers on the goitre
Jay x
jean34329 jayneejay
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Jean x
terry74787 jean34329
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jean34329 terry74787
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Nothing surprises me anymore where these dr are concerned. I have been through at least twow years of sheerhell with drs not being able to make what should be a relatively simple diagnosis in a hospital setting.
I have been told that my signs ans symptoms were due to anxiety. I pointed out that the physical signs and symptoms were causing anxiety due to drs not being aware of what my diagnosis could possibly be due to.
It was not until very recently when an incidental finding of a multinodular goitre was foun ona CTPA scan that I had evidence that I was not a hypochondriac or insane and that at long last a reason had been found for these horrendous signs and symptoms.
Good on your psychiatrist for senduing you to PT and I bet he or she also had a quiet word with the quack who referred you to the shrink because the medical dr did not know what was wrong so rather than admit his or her ignorancee chose to refer you on under the erroneous guise of a psychiatric patient.
Glad you are now much improved. I know exactly where you are coming from especially in terms of the shoulder problems and spasms. Keep in touch.
Jean
terry74787 jean34329
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jean34329 terry74787
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What did the PT consist of. My shoulder pain and spasms are debilitating. I avoid certain movements but it is very frustrating and I wish to try to get my life back.
terry74787 jean34329
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terry74787 jean34329
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jean34329 terry74787
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I will search round for a physio who does kenisiology taping.
I fully undertsnad where you are coming from when you write about getting courage if the spasms go. I think it has something to do with getting some control back in our life.
This thyroid disorder is really weird. It is quite true that one feels disconnected from life. Until I was told about the multinofdular goitre I had lost all interest in everything. I was like a zombie and sometimes still am.
The aches and pains are horrific. I had a bad back about 15 years ago but did not suffer any depression or anxiety with it . However the advanced nursing practitioner told me today on the phone that these signs and symptoms are typical of a thyroid disorder and that someting can be done. I can honestly say that I have never experienced anything remotely like this in my life.
At least it proves that depression caan be part and parcel of a physical/hormonal disorder.
Jeanx
jean34329 terry74787
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jean34329 terry74787
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Did you have any peripheral neuropathic pains or burning sensations or spasms in your legs, feet and or ankles?
terry74787 jean34329
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terry74787 jean34329
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jean34329 terry74787
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I too have a vit d deficiency disorder and also secondary hyperparathroidissm treated with ergocalciferol which actually was the wrong type of vit D as I needed D3.
Do you know what causes the tingling and pulling sensations of the scalp?
All these sgns and symptoms were blamed on codeine toxicity even though I was only taking 3 to 4 tablets each WEEK for a dislocated shoulder.
I was advised to seek cbt for support and to avoid codeine, caffeine, stress and to exercise.
My theory is that my immune system was compromised due to an infection and that the three antibiotics that were prescribed for this uninvestigated chest infection attacked the dna and caused damaged cells to produce even more damaged cells resulting in tendonitis, ingflamed muscles, throbbing knees, ankles and the signs and symptoms of plantar faciitis.
also had been prescribed perampanel for eopilepsy which caused the pleuritic pain plus severe headaches,
terry74787 jean34329
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jean34329 terry74787
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Here the NHS copied a model of care called Managed Care imported from USA from a well known insurance company. This involves getting bums off beds asap whether the patient is well enough for discharge is irrelevant. Jean
jean34329 terry74787
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terry74787 jean34329
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terry74787
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jean34329 terry74787
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I googled teracane and just saw the ad. I will research this again and order one.
I was a nurse but never had these spasms with back pain in the past.
Thanks for the info.
jean34329 terry74787
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What causes these spasms?
Was it your previous occupation or accident/injury/
jean34329 diane94845
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This happens to me too. Do you know why?
I can have this pain then all of a sudden it will go . But why?
It causes some shortness of breath which in itself is worrying. jean
jean34329 terry74787
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I can't find the website you are referring to.
Jean
jean34329 terry74787
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Jean
terry74787 jean34329
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jean34329 terry74787
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Jean
barbara98940 terry74787
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To save me writing it all here, have a look at the new discussion I've started on Hypothyroidism and muscular skeletal problems and see what you think. Barbara
barbara98940 diane94845
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barbara98940 jean34329
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jean34329 barbara98940
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jean34329 terry74787
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I think I have now found the website for the pressure pointer device.
These spasms have been very bad today and so have the throbbing and burning sensations in both legs.
Sitting down is horrendous but I am scared of staying in bed due to the possibiity of re occurring blood clots. How do you pass the time if you don't mind my asking.
I keep changing my posture every so often and walk from one room to another or up and down the hallway to try to keep muscle tone.
I got a painful spasm in the right scapula following a meal. I assume that using aa knife and fork was enough to induce a spasm.
This is all sooooooooooo cruel. I just want a normal life again.
Jean
Jean
jean34329 terry74787
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I am having a bad day with stiffness and spasms in my knees and legs. Any advice would be welcomed.Just had a hot shower, washed my hair moved around to avoid postural stress and still feeling rotten and stiff muscles.
I am scared of drinking milk as someone said ona forum it can worsen thyroid disorders.
Have you ever heard of that before?
Jean
terry74787 jean34329
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terry74787 jean34329
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barbara98940 terry74787
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jean34329 barbara98940
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jean34329 terry74787
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It was based on a posting saying that milk intolerance is common in hypo. I wondered why.
Are you mobilising as per normal/
Jean
jean34329 terry74787
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Just to let you all know that I have started a new discussion on cough, breathlessness in hypothyroidism. Jean x