Thyroid :: Severe Pain And Tiredness After Parathyroid Surgery
Sep 22, 2014
I had parathyroid surgery 3 weeks ago, apparently i had a rare type of disease as my vit c and calcium were normal but pth off the scale, they removed 2 glands one had a tumour attached to it, so had lymph nodes removed to be sure it was all out, i now have severe hip pain in both hips and thigh bones and most days struggle to walk yet calcium is normal, awaiting lab results on the tumour, my concern is the severe pain and tiredness, any ideas ?
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I don't know if anyone else has experienced any problems after parathyroid surgery. My surgery was 3 weeks ago. I am experiencing on and off again periods of severe weakness and nausea. My labs have all come back normal. I almost feel bedridden at times. Very unpleasant.
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I ve been operated of parathyroid cancer in March 2015 in France. It seems very rare. I m looking for people with the same disease ? I am still in hypocalcemia after 8 months even with 3 g of calcium per day and vit D.
Have you ideas to go out ?
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Recently have FINALLY gotten a diagnosis of PARATHYROID HYPERPLASIA?… After many years of fainting, blood pressure issues, kidney stones, ureteral stunting, a complete hysterectomy at 34 after ovarian cysts reoccurring….I had hoped it was HYPERPARATHYROIDISM…but my PTH wasn't high enough and the sestamibi and 3d scans and ultrasounds showed very thick glands? Does this sound like anything any of you have gone through or experienced, or should I be seeking another opinion?
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My parathyroid hormone is 98.1 intact, the reference range is 14-72. My calcium is 9.7, reference range is 8.7-10.4, my vitamin D level is 50, reference range 33-100.
My parathyroid hormone has been elevated for a couple of years now, but usually my vitamin D levels were a little low, so the doctors seem to think my parathyroid was elevated because of my vitamin D level. Now that both calcium and Vitamin D levels are normal my parathyroid hormone is still elevated. Not sure if there is any correlation to why my parathyroid hormone is elevated, but I have multiple nodules on both left and right lobes of my thyroid. My left lobe has 3 nodules under 1 cm with one measuring 3.1 x 1.3 x 1.6 cm and my right lobe has one under 1 cm with the other 1.0 x 0.4 x 0.6 cm.
December 2013 I had a biopsy on the larger one on left lobe 3.1 cm and was benign.
I haven't been feeling well for more than two years now, doctors just tell me to see a psychiatrist, I am on a antidepressant but it really hasn't helped me that much.
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I am being referred to a surgeon to discuss a parathyroid operation. I am waiting to go for a scan. Can anyone tell me what the scan entails? I know dye is put into you. How long does the scan take?
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I have had a raised parathyroid hormone blood result recently also a raised calcium in the blood result. I had raised calcium levels several years ago but after a scan of my parathyroid glands which showed no growths it was put down to lack of Vitamin D and called secondary parathyroidism
I was told to increase my Vitamin D levels which I did and my calcium level dropped. I have continued on the supplementation. I have severe sleep problems, am tired and grumpy, my hypothyroidism been under control for the last 8 years. I am borderline diabetic. Almost 73 years old.
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I'm a 44 year old female. Earlier this year I went to the doc with lethargy, aches and pains, headaches, Backache, feeling sick, amongst a heap of other basic symptoms for a menopause check to which it came back as positive but they also tested me for low vit d which came back as deficient so checked my parathyroid hormone which was elevated. My Calcium they said was fine so iv been treated with a high dose of vit d pills for three months. Recent testing has shown my Calcium is still stable but my parathyroid has increased further but the doctor said she will have to do and enquires as to what to do next as she expected my parathyroid to balance out but as it isn't I haven't a clue what that all means if my Calcium is ok as I know they are all linked. Is there any clues or experience you can offer as to what it all means.
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I am 48 years old and been suffering many years with pain all over my body, my hip pain is the worst, closely followed by shoulders, wrists and hands, then buttocks, more recently knees. My history has been a bit of a nightmare - diagnosed first as fibromyalgia, then early RA, then back to fibro, abnormal antibodies (autoimmune disease). Years ago I complained to my gp about mouth ulcers and was discovered I was low in vitamin D. Two years ago I started suffering extreme head sweats and a few weeks ago I realised that I was still getting mouth ulcers even if I was just a few hours late taking my Calcium Vitamin D and told my gp, adding that I was concerned that I was still low in vitamin D. Blood tests revealed that I am, even though I never miss the tablets, get lots of outdoors when able, eat loads of fish, eggs etc. So, doc thinks its a parathyroid tumour and according to the website the only 2 reasons you would have low vitamin D is 1- if you don't actually get any and 2 - you do have a tumour. So its looking pretty much like this is the reason and I am guessing surgery will be necessary. My concern is, my muscles and bones ache so much, I walk like a very old woman.
My life has really been mostly bed bound for the last few years with pain, having to use a stick a lot when I do go out - on good days I will be out as much as possible and walk as much as I can-yeah the consequences are usually the next day in bed, but I try to push it as much as I can. I have put so many things on hold, work and social and missed out on so much. Now, I am wondering - if and when this is sorted out, the tumour removed (if the doc is right and I do believe he is) will my aches and pains go? Will I have a better quality of life? If osteoporosis has set it - can it be reversed? I have also noticed very recently things becoming much worse. If I move my hand in a different way the pain is unbearable and feels like something has just broken - my index finger has started moving involuntary, kind of jumping - is this related to anything?
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I had a lesion removed from my back on Wednesday afternoon by local anaesthetic. All was fine..I felt nothing, only pressure but no pain. But my query is this..it's now Friday morning & I'm still absolutely exhausted. The anaesthetist did say she gave me a lot of anaesthetic as they had to go in deep I think. I'm not even in a lot of pain but I didn't expect to feel so terribly tired still. Anyone any experience of this after a local?
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Any one else experiencing the same? & any answer of what it could be?
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had my THR on Jan 25th. The op went well but when I came home the slightest thing i did made me feel faint and dizzy. I ended up back in hospital as my doctor said i was dehydrated. I am fully hydrated now and home but am wiped out all the time and still feel faint . I could cope with the mobility problems and pain if i felt better and had some energy. Did anyone else have this problem? How long did it last? Also sleep is impossible due to a stabbing pain in my lower back. I'm worried now that all the pain i had previously wasn't coming from my hip but some from my back. I feel miserable and tearful all the time, just hope this is normal .
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20 Years ago I had My thyroid partially removed now they tell me one side was never removed and the other side that was, grew back they want to do a 2nd removal what are the risks
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Help! In 2001 I had a thyroidectomy. Immediately, my blood pressure, (which had always been remarkably low), shot through the ceiling and I've been on BP meds ever since. But I digress...
I was always super active. I skied, ran, kite boarded, hiked, biked... all a healthy and important part of my life. I even had booked a trip to climb Kilimanjaro for my 60th birthday in 2010 when I came down with Swine Flu, followed by a couple bouts of pneumonia. When I recovered, I tried to go back to skiing about three months later and found that I had lost muscle strength! I couldn't make turns (and that's a bad thing...) I got weaker and weaker. My doc had no clue. We checked heart, lungs. I was at low end of thyroid and adrenal levels, but "not a problem", I'm told. I'm not a drama person at all, but I really began to believe I was dying because I was getting weaker and felt like my energy was draining away.
At wit's end, I went (for the first time) to a brilliant naturopath who drastically improved my already good died and put my on Chinese meds. It took about three months, but I eventually stopped getting weaker and became stable. That was HUGE! Since, however, I've remained pretty stable and we keep trying other things but nothing has put me even close to where I was.
The best guess is that its related to thyroid or adrenal function. I dunno...
I can now make between 6-10 stairs before I have to stop for a few seconds to regroup. I can swim very short distances but never alone because when I run out of energy, its GONE and I have absolutely nothing left. This has drastically impacted my life and I want to be strong again!
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If anyone has dealt with this or know anyone who has I would love if you would share. I'm just curious about how the operation goes (its preparations, and after). I have 2 thyroid nodules and they are pretty big and is causing phlegm, voice changes and other stuff.
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I have had lower back pain for years. It always gets worse when lying down for long periods or bending over for long periods. I've also had sciatic pain in my left leg for years. It comes and goes. Recently I have started to get the same pain in my right leg. The sciatic pain as gotten severe. I also have some other new symptoms. One new symptom is searing pain in my knee sometimes when I'm standing or when I bend my leg all the way in. The other is sharp pain in my pelvic area. Are these connected? Can you please possibly tell me what is going on? The only notable health history I have is ovarian cysts.
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My 50 year old husband has been a Type 1 diabetic since he was 21. It was a late presenting of juvenile diabetes or so they said then. He has always done well managing his diabetes, wearing a pump for the past 15 or so years. In the past week or so, he has begun to have severe pain/tingling in his feet/ankles - mainly at night when he is trying to go to sleep. He usually has to get up and walk several times before he can finally sleep - he is only getting about four hours of sleep per night. He has an appointment with his dr - but not until the week after New Years.
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Before I start I'll just state that I'm 19 years old, slim and generally healthy. I've been suffering with a cough for 3 weeks now, and it only seems to be getting worse. It is a constant violent cough, dry, but wet if that makes sense? I cough up clear mucus. It seems worse at night, I can't lie down without having a coughing fit and the pain in my throat and my ribs is unbearable I also have awful pains in my upper back, and weird shooting nerve pains in my arms. I've been to the doctors twice, first time he listened to my heart and lungs said they were clear and said I had Costochondritis which is causing my pain. Didn't say anything about my cough. So I went back to see a different doctor, by now I was also having pains in my left leg and googling this and as always it comes up with the worst case scenario... Blood clots which got me really worked up. She told me I didn't have blood clots, just by feeling my leg and saying it was soft, and said I have acid reflux which is causing my cough and all the other symptoms. I still can't stop worrying that my cough is something much worse and I have been misdiagnosed and there is something wrong with my lungs I also keep worrying about the pain in my leg, which is getting worse... I feel as if it was just brushed off but when I read online about others who ended up having blood clots their symptoms were just like mine and I'm so scared of this happening to me
I realise I have really bad health anxiety, but it makes it worse that I haven't even had proper tests or anything done to rule out the worst things!
I'm finding it so hard to deal with this, I feel like this anxiety is taking over my life Thanks to anyone who reads this essay of a post, I feel I just needed it off my chest.
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Ok. So i have broken my fifth metatarsal and have been put into a non weight bearing air cast for two weeks.
Due to the break, the doctor has given me a blood thinner Innohep 4500 UI to take everyday to prevent a blood clot.
My problem is: For the past 3 days my calf (same leg as broken foot) has felt like it's been cramping. Elevating it relieves the pain a little but i am required to attend my courses at University - meaning i'm on crutches all day. Sitting/standing makes the pain increase. The pain has gone from mild to severe; i can almost cry from the pain coming from my calf.
It is extremely painful when trying to stretch any of the muscles in my right leg now, Should I be concerned about a potential clot? (I do not show any of the typical signs i.e. the swelling/heat/redness) Or is this muscle related? I have trawled through the net for similar cases but cannot find anything!
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So this is an embarrassing topic to touch on. But due to my amount of pain and the lack of clinics open due to tomorrow being new years day. I will turn here for support.
Yesterday, I woke up with severe rectal pain. Today it has gotten worse. It burns, aches and is unbearable to sit, walk, or move in any way.
I just recently had my first look at it and I do have a tender lump on the outside. The pain spreads to the inside but most of the pain seems to be coming from that one tender lump. I cannot stand the pain. My only relief is a hot bath, which sucks to get back out of and Vicodin or tramadol which I have had left over since my kidney stone attacks but that's another topic.
The lump is not discolored or anything, it just severely hurts to touch and I have tried everything I have seen on the internet to provide no relief.
Preparation H, no relief.. Also have been alternating between Ice, heat and hot baths with epsom salt. Also have been using triple antibiotic cream, witch hazel and coconut oil..
I am really hoping this doesn't turn into an emergency room visit.
I just don't know if it is a hemorrhoid or a fissure or what the difference is between the two or how to even treat this issue and earn some relief.
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I have had moderate to severe joint pain since April, and was recently diagnosed with Parvovirus B19. Apparently the virus can cause severe Arthralgia that lasts upto 9 months.On good days my pain level is at a 3. On bad days it will go upto a 6/7. Yesterday I stepped on a metal wire and it got stuck in my foot. The urgent care center recommended I get a tetanus shot, since I have not had one in over 10 years. I asked what the side effects were, and they said my arm would be a little sore.
Well, " a little sore" does not quite describe it. My arm was in excruciating pain all night and still really bad today. I can't even lift it more that a couple inches. Also, all my joints on my left side ( side I got the shot) were in excruiating pain 8-9. I just sat in bed and cried last night. I took 3 tylenol arthritis's and an extra Meloxicam that I have for joint pain and it did nothing, My arthritis continues to be really bad today. I called the urgent care and asked if I could come back in to get some medication to work until the pain stops. They said they could not do that, and that the tetanus shot would not aggrivate arthritis.
Let me know if anyone else has experienced worsened arthritis symptoms after a vaccination or shot. I wanted to get the flu shot soon, but I am scared now. Can the Flu shot make me hurt this bad as well? Let me know If I should tell the doctor and ask for additional pain medication. Or if the doctor will just tell me " No".
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