Thyroid :: RAI For 5.3 Cm Multinodular Goiter That Is Benign
May 9, 2014
I have a very large 5.3 cm multinodular goiter that is benign. After my ultrasound my Dr. recommended a Thyroidectomy. He received my Radioactive uptake scan results and now he can recommend the RAI. I have an appointment next week to discuss my options further with him. Anyone that has been hyper with a large goiter and had the RAi, would you recommend it?
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For the last year I have not been feeling myself tired fatigue muscle aches hair falling out small weight gain. I have just contributed to me being around the age of 50 and having a hysterectomy in the last couple years. My job is a little bit stressful as well so thought the symptoms were because of the stress. Last week I went for my annual checkup and the doctor noticed that my thyroid was enlarged especially on my left side. I went for blood work and I went for a ultrasound my blood work came back with in normal limits and the ultrasound came back saying I have several nodules on the left lobe. Because my bloodwork is normal he wants to send me for a thyroid scan at the hospital which I go in for next week. My question is has anybody had any side effects in using soy products and your thyroid? I have read that soy products specially in protein powders will affect your thyroid. In the last four days I have not used my regular protein powder in my smoothie in the morning and I have noticed a considerable shrinkage in my thyroid. Has anybody else had this experience?
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I was diagnosed with a goiter in 2010 and have suffered with severe depression, and anxiety since then but now it seems to have gone away. I went to my endo and she said she doesn't feel an enlarged thyroid and I don't feel it when I swallow anymore and I feel better with the depression and anxiety. What could have caused it and what could have made it go away??? No one made any connection to the goiter and the depression/anxiety. I was not diagnosed or medicated with anything. I made the connection which scares me because I knew something was wrong, but no one helped me...so I'm glad its gone at least for now.. I started probiotics about a month ago, could that be it?
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I have had an enlarged Thyroid since 2004 I have had regular blood monitoring and visits with my local GP who said it was quite normal and dismissed it quite a lot. I became pregnant in 2011 and a good midwife referred me as she thought it was quite large to an Endocrine. They done my bloods etc and picked up an underactive thyroid with antibodies. I began treatment on levothyroxine 50mgs and have been on it ever since. I had my last ultrasound review three weeks ago and got a letter through from my referring doctor today stating my thyroid was quite large and radiographer had suggested a chest x ray to check for substernal possibility? I am a little nervous.....I am waiting on additional appointment with endocrine to discuss treatment options. As I have been have a swelling and shrinking sensation of gland through day I am very active run two miles per day, and am gluten free etc. My last bloods where T4 15.1, TSH 3.59, Antibody level 34.
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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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I suppose a little history would be fitting first...I've been hypothyroid since birth (born without thyroid function), and was placed on a regimen of Synthroid for years. From there, my thyroid grew nodules and became a goiter, and at the age of 23, had to be removed completely. Since then, I struggled on the Synthroid, and finally found a doctor who agreed to try me on Armour. At first, I seemed to do well on it. I've been on Armour for about 2 1/2 years now.
Over the past year, I've developed migraine- like headaches that completely incapacitate me. For the most part, these would come on a frequent basis but I could go about my daily routine without disruption...until about four months ago. The headaches became non-stop. There is no break in the pain (the doctors don't understand this concept- they keep calling them "episodes"). The intensity changes, but the pain is ALWAYS there. I've been treated for migraines, but the medication for it doesn't work, and the pain isn't quite the same as a migraine. It's very hard to describe...almost like a twisting sensation in my skull and across my forehead.
That's not all of it. The pain gets worse with exertion. If I try to go out and run a few simple errands or do some household chores, my body heat goes through the roof- along with a lovely fever and I'm done. I can't do anything else for the rest of the day because I'm in too much pain (from the headache AND body aches from the fever).
I'd love to say I'm making this all up. But would I really put myself through all the blood work, a lumbar puncture that went awry (yes, it was downright awful), and bounce from doctor to doctor? I finally found one who had a brain in his head that said "it could very well be your thyroid!"
The biggest problem I've had is that every doctor I've seen has said "your thyroid levels look fine!" But they've only tested my T4 and TSH...shouldn't they be testing my T3 as well? I know I'm no doctor but...
I know I should be under the care of an endocrinologist, but they are really hard to find around my part of town (at least one that's any good). I just want some other points of view here before I subject myself to more poking and prodding.
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So for the last few weeks or longer I was sporadically feeling a lumpiness in my throat, especially while sleeping. I thought it was how I lie in bed while reading. Then this lumpiness, this weird feeling that isn't exactly painful just awkward and uncomfortable is a daily annoyance. So bad in fact I felt nausea from the feeling in my neck. Sort of like something is rolling up and out; of course nothing ever did. So now this feeling his constant I feel like I'm either vomiting or choking. Lovely! So I also have asthma so my breathing is not 100% in the first place, add tightness to my throat and what? Full blown panic attack sure, lets not sleep tonight. So I finally drag my feet to a Dr. guess what PA says I have an enlarged thyroid, i.e. Goiter. So now I am to have a thyroid ultrasound blood work. Now this goiter is extremely uncomfortable, borderline painful; especially when I swallow, cough or yawn (oh yawning *****). Is this simply because I am now aware of this enlargement in my body. The pain and discomfort seemed to become more acute during a 24 hour fever spike, which is what motivated me see a Dr in the first place.
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Just recently I was diagnosed with a small goiter & nodule on the left side. The doctor ordered all of the tests (TSH, T4 and TPO antibody level) and everything came back normal. The biopsy on the nodule is normal as well. Benign and no signs of cancer. My concern now is regarding my goiter & nodule. If my test results are all normal, what caused it to enlarge? What do I do to shrink it? My doctor will not give me anything because he said there's nothing wrong with my thyroid. The functions are normal. It just enlarges for a reason sometimes.
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i have been taking for over a month 20mg of carbimazole (5mg 4 times a day) the edno said i have hyper and a quite big nodule which is toxic.
i have been suffering the last two years with weight loss and tachycardia,agony and had that worrying feeling all the time.
After taking carbimazole for one month i start to feel BETTER but yesterday i had hyper symptoms again.how is this possible the blood test have showed that I AM NO LONGER HYPER!!!!
i know that eventually i have to choose between RAI or surgery but i m scared that the symptoms will come back.Does carbimazole stopped working? is it normal to have symptoms while taking it?
the edno prescribe me also propranolol but i took it once and it scared the hell out of me!
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Does anyone have information about this type of angina? Mine is quickly getting more aggressive in nature and my most recent episode two days ago caused me to nearly pass out with the pain. I do know that it is caused by a spasm and it is generally considered a benign condition, but it is not feeling that way anymore. Please share any real knowledge you may have on this topic with me. I really hate to call the emergency services if there is something else I can do to alleviate my pain beyond using my nitroglycerine spray and chewing the aspirin.
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I visited my neurologist a few days ago with widespread fasciculations and generalized fatigue as my main symptoms and he diagnosed me with BFS - which, after looking up, I believe is an accurate diagnosis.
However, one symptom I may have downplayed with him is a droop on the left side of my face. It started two months ago with my left eye watering more than normal, air coming out of my left eye whenever I blew my nose (this had never happened to me before), and occasionally when I talk I get this weird sensation of not being able to hear properly out of my left ear that goes away on its own. Now, I have a minor but still noticeable lip droop that has given me a crooked smile and has resulted in me occasionally slurring words.
The neurologist suggested it is a minor form of Bell's Palsy, but when I looked up Bell's Palsy most people seemed to suggest it had a sudden onset, whereas mine came on over months.
So I guess what I'm wondering is, could this be something more serious than BFS? He didn't give me an EMG although I did pass the strength test fine, I do work out, and I am 19 years old, but should I consider revisiting him or a different neurologist and greater stress the severity of my facial droop? What do all of you think it could be?
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Has anyone taken Viagra to help with BPH issues? I take finasteride (Proscar) and Uroxatral for BPH issues and these drugs help immensely along with herbal remedies. I am sexually active and when I take Viagra to help my performance I notice that my urinary flow improves immensely. As a test I started this week to take 50Mg of Viagra daily and I noticed the best urinary flow I have had in a long time and was wondering if anyone else had similar experiences?
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I was diagnosed, by my GP, with BPH about three years ago although I have been having symptoms for way longer than that as I kept putting off bringing it to his attention.
My question is can BPH lead to prostatitis, nonbacterial? I ask because over the past several months I have been experiencing a lot of 'discomfort' after urinating such as stinging, burning, which extends the length of my penis way back up between my legs and 'deep inside'. Along with this is the constant, and I mean constant, feeling of wanting to 'go'. Sometimes the stinging seems to turn to a dull sort of ache which is difficult to describe. Along with this is an intermittent feeling that I am going to wet myself as it feels a 'spurt' of urine is making its way down my penis but only one one occasion, thankfully, has anything actually leaked.
I went to my GP about a month ago now and he did a urine test but it was clear. He has referred me to the hospital to see a urologist as I also had another instance of difficulty in urinating but my appointment is a month away.
The 'discomfort' comes and goes over several weeks or months, or so it seems, but when it comes it drives me to despair.
I take Tamsulosin and Finasteride
Just wondered if anyone else is suffering similarly.
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My only sister has just being diagnosed with BIH which tells me surely its genetic.
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Age : 42
Initially I was urinating 2-5 times a night.
Thought I had BPH. Began taking Saw Palmetto. Now urinating 1-2 times a night.
Not been to a doctor yet.
Tests I have taken:
PSA : Results were normal, Free PSA was .9
Urinalysis : Bilirubin level was high.
I assume I need to go to a urologist. What tests will he request?
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wanting to contact others who have the same condition. Sometimes it is genetically related or not.
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Went to dr last Thursday, he always maintains that my dizziness/off balance problem is due to anxiety. I told the dr I have been speaking to others on this forum who have similar symptoms and problems with their balance and it has to be recognised as part of meno.
After a good chat with the GP, he read through my blood tests which were done in July this year, he said that my estrogen was so low that he would consider me now menopausal, estrogen was less than 70 (whatever that means) fsh 76.
Anyway, he said that the menopause sometimes causes some women to develop benign positional vertigo and that it should settle with time. He said normally by the age of 55 things would be better....I'm only 51, will be 52 in Feb don't think I could suffer this for a long period
Dr had taken more bloods as I asked for progesterone to be checked as well as estrogen
I've made another appointment to discuss the results but another dr told me briefly over the phone that the estrogen and progesterone have both came back low even though I've been taking livial HRT for 3 months.
I went on the internet last night browsing looking at hormone levels and was redirected to another website as I typed in dizziness and OMG I've been in such a state since
I'm wondering if any of you ladies can help if you Google MdDS, it's a balance condition and please tell me that my balance problems will be hormone related
I'm staggering around today balance terrible and feel woozy just unbalanced.
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Have just come back from doctor who has signed me off for a month because of my continuing vertigo which he says is BPPV. (have has symptoms since November). Being signed off for such a length of time has, I have to say, taken the wind out of my sails a bit. When I asked if there was anything I could do to help with the symptoms he said to continue the exercises I was given following Epley treatment and continue taking the medication (Stemetil). Otherwise nothing but wait it out. I've had a CT scan and have been referred for physio and to an audiologist but I was just wondering if anyone out there has found ways that seemed to alleviate their symptoms or are happy to share their ways of coping. I find I'm able to do very little at the moment without feeling dizzy and cannot walk at a normal pace or operate at a normal level for everyday activities. Sometimes I get dizzy even just sitting.
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So after my discordant biopsy that showed only benign fibrocystic changes, surgeon scheduled me for a lumpectomy! I have never been more scared or confused, and she seemed to dodge all my questions about why I need a lumpectomy. So my question is to the people on this board- what is your lumpectomy experience was and why you need it also, is lumpectomy same as excisional biopsy. I read different things on the internet , and frankly it all doesn't make sense to me.
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Six week ago one day I laid down to do an AB exercise, it triggered my BPPV Vertigo. I tried twice, finally managed to stand up and go to work with a heavy head. Next day, I had 45 mins walk under the sun, and tried to fix my toilet at night. When I laid my head on my pillow to sleep, it triggered my Vertigo again. The next day, I couldn't get up because of dizziness.
During this six weeks, BPPV came and went a few times. Then it went away. Now I can tilt my head up, down, left and right. I don't know if it is because of the EPley exercise I have done.
HOWEVER, the sense of unbalance and lighthead kicks in, accompanied by exhaustion fatigue. On 15th of March, I called Ambulance due to a panic attack (suddenly increased heart rate, panic, short breath). The hospital told me that it is BPPV Vertigo and my panic attack could come from anxiety.
I have done Brian CT, neck CT, full blood count, chest X Ray, ECG for my heart, all negative.
Now I get confused. Is it a Vertigo now or a BPPV vertigo? Or it is changed to a Chronic Fatigue Syndrome?
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I had an ultrasound today and it says that there is "a homogeneous appearance to the echotexture of the thyroid gland. Bilateral thyroid nodules are observed. There is evidence of a complex cystic and solid lower pole right thyroid nodule measuring 1.8 x 1.0 x 0.9 cm. Within the left thyroid lobe there is evidence of a hypoechoic midpole left thyroid nodule measuring 0.6 x 0.4 x 0.7 cm. Bilateral thyroid nodules. Dominant nodule is a complex cystic and solid lower pole right thyroid nodule measuring up to 1.8 cm. what does this mean?
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