Burping? ADCAL -D3 For Osteoporosis And THYROXINE For Underactive Thyroid


May 24, 2015

When taking ADCAL -D3 for Osteoporosis and THYROXINE for underactive thyroid, there should be a space of at least 4, yes 4 hours between these medications as side effects could be upset tummy, wind and constipation etc.

So tomorrow I will leave off the ADCAL-D3 for a few days to see if this is the problem.

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Thyroid Is Underactive Due To Lithium

I have complex PTSD and Bipolar Disorder 1.  I was diagnosed in September 2013 during a manic attack and started medication regime:  Lithium (225+450) and 300 mg Seroquel.  Now, 2 years + later, my Thyroid is underactive due to Lithium and my Psychiatrist wants to change Lithium to something else.

My challenge:  I start a new job next week (after being unemployed for 7 months and really need this job!) and a few weeks ago I went low on my Lithium (skipped a few morning doses and ended up in mixed episodes and had a spider-related psychosis!)

I am really anxious about one day changing my Lithium.  I was wondering how long can I be on it before it will damage my kidneys like it is affecting my thyroid now?

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Hypothyroidism :: Levothyroxine For Underactive Thyroid

During a routine blood test in August I was diagnosed with underactive thyroid. I wasn't feeling ill so was quite surprised when I read the symptoms. I've been on Levothyroxine for 3 months now and I feel terrible. I'm so drained and exhausted, angry and frustrated, bloated, fat, stomach pains and unhappy, I keep going back to the doctor but she just pops me more pills and I don't feel she is very understanding or sympathetic. I didn't feel this bad before I started the medication so I'm going to stop it. I was placed on 50mg and two weeks later my blood tests were normal and have been since so for such a small dose does it really matter? I'm so low, sometimes it's all too much I want to have a paddy and a tantrum and smash the place up and if anyone gets in my way then they'll get it too.

The doctor wants me to try CBT self help courses to understand what troubles me. When I'm not having some kind of flip out I know what troubles me - things are a struggle and I hate being ill and I want to be better.

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Have been on L-Tyroxine probably 30 years. When I weighed 120, cholesterol was 190, now that I am 68 and 30 lbs more, 150 at 5'4", my cholesterol is 416 (LDL in 300 range). I eat clean, no breads, cereals, carbs, etc (except only once in a while) eat wild game, game hen, fish, chicken, loads of fruits, veggies, etc., every thing super lean, fresh. take loads of supplements. I lift weights, do yoga, stretches, heavy gardening. Therefore, I find it absurd that my LDL is that high! I have absolutely no health issues except high cholesterol. Would Armour be better?

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On last testing I was under active again and only on 5mg of carbimazole, so as no endow appointment for another 8 weeks was advised to make arrangements with family doctor, as it's been christmas peroid I couldn't get to doctor as booked up and also couldn't even get a telephone call so I decided to go with 5 mg every other day to I arranged something, I still feel underactive tiredness, cold and puffy lips and tongue, the main concern is the appearance of my eye and face swelling has went extreme in last week , I am so depressed with this puffy face I don't know if it's as my throid is underactive or because I have cut down the medication, I find endo doctors useless , this diease has left me I don't want to leave the house, I also have dry very spotty skin which has got worse all over christmas I do not recognise the person I have become anymore

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Hypothyroidism :: Thyroxine Makes Me Feel Worse?

I have regular blood tests and have been given Metformin for Type 2 for the past six months. I often feel the need for a nap mid-afternoon but I put that down to the after effects of lunch! I have been morbidly obese for years and considering that, my energy levels are good. I am 65 this month and still work full-time and intend to continue. I also take Tamsulosin for an enlarged Prostate. Recently I was summoned by the doctor after routine blood tests and told I had mild Hypothyroidism for which I was prescribed 50g per day of Thyroxin. They made me feel terrible - every day for two weeks so I've stopped taking them and feel fine again. Seems like the Thyroxin gives me the symptoms of Hypothyroidism - loss of sex drive, tiredness, headaches. What's the likely outcome of not taking these awful pills? Any advice gratefully received.

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Pain In Right Side Of Neck After Reduced Dose Of Thyroxine

I am a 50 year old woman who was diagnosed with an underactive thyroid 18 years ago. I have never been right as the Dr keeps changing my dose every time I have a blood test. He says this sometimes happens, but I constantly feel lousy, tired spotty, overweight, high blood pressure (now medicated) and IBS. I work all week and spend the weekend in bed.The mood swings are also awful. Since another reduction I am now on 100mcg and have developed an unusual pain in the lower front right hand side of my neck (can't feel a lump or anything) but get aching through shoulder and side of head.

am really getting a bit fed up now as the Dr just doesn't seem to understand how I feel and has offered anti-depressants. I have seen a specialist in the past but he was a diabetic man rather than thyroid and actually commented on the wrong set of blood results!

i guess my plea is twofold first is there anyone else out there who has had similar symptoms and 2 can anyone recommend a good specialist? I'm thinking of going privately now even though it's so expensive and thought about the Birmingham Thyroid Clinic?

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I am on 150mcg Thyroxine and have a fasting blood test on Friday.  I take thyroxine at night as it makes me feel better the next day - like my thyroid is already working/functioning as it should be. Lots of speculation about whether to take meds before a test - fasting or not and if it could give a false reading. Wish doctors could be consistent with their thyroid diagnosis, and have not published their findings on whether or not to take meds before a blood test.

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Reverse Osteoporosis?

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Omeprazole Contributing To Osteoporosis?

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I'm 45, I started suspecting early menopause at the age of 37,which is when my symptoms started started including depression and anxiety, I have been on and off (mainly on) anti depressants since i was 39,I  was 41 when my periods stopped altogether.

After 2 years of doctors advising me to go on hrt especially as i am early menopausal, i gave in 6 months ago and went on elleste duet. It has stopped my hot flushes, night sweats, joint pain, dry skin etc: which is all

good but I'm still not convinced i am doing the right thing,I am very concerned about the cancer risks so I am thinking of coming off them as well as my mini pill (which i take to control my endometriosis) I am mostly concerned about osteoporosis, and my question is surely if i take Vit D and Calcium every day I can protect my bones in the same way ?

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 I can't find ANYTHING that removes the pain!  Co Codamol doesn't, the 'so called' pain relieving gels don't (I've tried 3 different types).  Can anyone suggest anything else?

Yesterday I twisted my hips somehow as I got out of the chair, the pain was excruciating.  Since then I can hardly walk (how does excercise, excercise fit in then?)

I had been doing so well, 20 mins walk per day (and I've always disliked walking!) - physiotherapy, etc.

 

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I have osteoporosis and fibromyalgia for the three weeks when bend down filling shelves i have a sudden pain in my left knee and it's the same walking down the stairs its very painful i could cry

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When I met with the gynaecological oncologist, and decided that to be safe I should have a hysterectomy to get rid of the rapidly growing, funny looking (on MRI) fibroid, he said "we'll take out the ovaries, too." At the time, I didn't say anything.

However, after I went home, and I did a lot of research and found that it would be a bad idea because having my ovaries removed increase my risk of heart disease and osteoporosis, and my family has a strong history of both, but not of cancer (which I didn't think to mention at the consultation - finding out that there was a slight chance I might have cancer in my uterus put other thoughts out of my mind.) So I sent a very long, detailed email to the gyn/onc, explaining why I thought removing my ovaries would be a bad idea but never got a response. So I called the gynaecological nurse, who was present at my consultation, and she reassured me that I didn't have to have my ovaries out; I have to consent to the surgery.

Well, I was all relieved until I had my pre surgical assessment on Wednesday, when I was given the paperwork to fill out and on the top of the first page it said TAH/BSO (The BSO part means removal of Fallopian tubes and ovaries.) I wrote on the page that I did not consent to BSO and told the assessment nurse, who said she just go that from the doctor and it had nothing to do with her.

So when I returned home, I spoke to the gyn/onc's secretary, who said that she must have mistakenly wrote TAH/BSO on the form and not to worry, the doctor knows about it. I said that I wanted to make sure that he was aware of it prior to my surgery, which is this coming Wednesday, and she said she would speak to him on Friday (today) and would call me back.

Well, I never heard back so called around 4:50 and spoke to a woman (not sure if it was the same person) who, after I gave my name, immediately started reassuring me that my operation would go on as scheduled. I explained that wasn't why I was calling, I wanted to make sure that the doctor wasn't expecting to take out my ovaries when I didn't want him to. She then tried to reassure me that everything was as expected and something about an email being forwarded to him (not sure if she said she forwarded an email or my email). I think she also mentioned something about getting in touch on Monday.

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We obtained a new orthopedic surgeon who deemed that another surgery would be necessary. He did an internal fixation with synthetic bone graft. After about a year that has failed. Now we have total failure of the arm …. (looks like two elbows), x rays reveal floating screws, wire wrap coming undone from the plate, and most recently painful surges from the shoulder all the way to the tips of her fingers.

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Is there any new technology regarding 'profound osteoporosis bone fixation'?

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