When Hypothyroid Symptoms Show Up? Total Thyroid Lobectomy
Sep 24, 2014
i had 2 cold nodules in my thyroid and had a total Thyroid lobectomy on 16 sep (8 days ago) and still waiting for the results if the they were benign or malignant so that i start take the hormone replacement in case if benign or start to go into 6 weeks hypo in preparation for the RAI treatment in case if malignant problem is, i fear the result will take more days to finish, and my body is completely without thyroxine now if benign than this wait & deprivation was pointless, and i fear i will need many weeks to fix the damage the hyop state will impose on me so my question is, when will the hypo symptoms start to show in my case (no thyroid at all) ? considering my TSH levels were normal at 2 before the surgery i'm feeling really anxious about this whole thing, and i need your knowledge, i can't even get in touch with my doctor before tomorrow.
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I have recently been experiencing symptoms of raynaud's so I'm wondering if there's any link.
Last check all my thyroid numbers were good and been feeling good with that.
My thyroid antibodies were in the normal range when diagnosed, so not sure if that means mine is not autoimmune or if Raynaud's is auto immune?
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I was diagnosed with Hashimoto's postpartum about a year ago. I was complaining of excessive fatigue/inability to return to running, and pretty bad carpal tunnel. At the time my TSH was 6.893 and Free T3 282.1 pg/dL [230-420] and of course high antibodies. My primary care put me on NatureThroid 32.5mg (25 mcg T4/T3). I felt better within the week and my carpal tunnel completely resolved in about 2 weeks. I felt great on this for a year. I had my TSH tested once during this time and it came to 2.785. I trained for a 50 mile race, including hard training with back to back long runs on the weekend. I then started training for a marathon in January with a goal time of 3:15-3:20. I was training hard but felt great. I did a half marathon March 20th at a 7:04min/mile pace. I felt on top of the world and was on track to run what I had termed my "comeback marathon". The next week I still felt good, but then the following week I came down with a minor respiratory tract infection. I was completely better in 3 days and just thought it was a small blip. I went out for a long run that weekend and felt good for the first 6 miles, and then got progressively worse and felt like I had no energy, completely flat, defeated. It was not normal but I just chalked it up to a bad run. The following week, I had a strange inexplicable flair of wrist pain/carpal tunnel for about 3 days, but then that resolved, so again I kind of dismissed it. I was able to do my weekly workouts and hit my paces although they did feel a little bit harder than normal. But every time I tried to do a long run, I crashed after just a few miles and finished feeling like complete crap. I started to get worried about my race but again just figured I needed a good taper and I would feel better. Well, my race came it was one of the worst experiences of my life. I ran the first half at my goal pace but after 8-10 miles I started feeling sort of ill, dizzy, and had no energy. Again, I have run several marathons and have had bad marathons, and this was above and beyond anything I'd ever felt. I am not prone to cramping, and by the end I could barely walk and my muscles were just spasming uncontrollably.
Ok, fast forward to the following week. The next day I called my doctor and moved my 6 month follow-up to the next week, and got blood work done (unfortunately he only tested my TSH). That week, I developed progressively worse carpal tunnel. I decided to double up on my thyroid dose, and after a few days of that, I then tripled it (so now I was taking 97.5mg (75 mcg T4/T3). I felt fine energy-wise (although was not running), but still had carpal tunnel. Then I went in to see my doctor. My TSH came to 2.94. He saw that and said my symptoms were probably not thyroid-related but that we could increase my dose by 16.25mg to see if that would help (I knew it wouldn't because I was already taking more than that but I didn't want to say that, and I started second-guessing myself that I was hypo). So I dropped my dose down to 65 mg, then back to 32.5mg. Well a few days later my carpal tunnel got so bad I was waking up in excruciating pain even wearing my braces. I was having shoulder impingement pain as well. I couldn't use my right arm in the morning for 30 mins after waking. I called my doctor asking for further testing and for him to test my free Ts. I did that bloodwork and it came out to TSH 2.58, free T4 0.71 ng/dL [0.6-1.6], free T3 3.59 pg/mL [2.39-6.79]. Seeing that my T4 was on the low end and T3 not super high, I figured that confirmed I was having hypo symptoms, even though they were technically within normal. So I started taking the 97.5mg dose of thyroid again. That weekend I upped my dose, I still felt terrible. I had a horrible run, couldn't move after, my whole body ached, and by Saturday evening I couldn't lift my right arm due to the shoulder impingement. I felt the same Sunday. But Monday (day of three of higher dose), I was SO much better.
Well my doctor looked at my results on Wednesday and said, "Your T3 is excellent." When I protested, he said rather condescendingly, "I've been doing this 30 years." Mind you, he's not an endo, he's a naturopath MD. I argued with him until he agreed to up my dose to 81.25mg. I knew this would not eliminate my musculoskeletal issues, but figured it was at least a move in the right direction. (note: he also tested for RA antibodies and sed rate and that was normal, and I don't have any joint tenderness)
I've still been taking 97.5mg dose this week, but won't be able to continue this once I run out of the extra Rxs from dosage changes. Still have carpal tunnel and morning stiffness, but my arm got better throughout the week, and then Thursday, I had a great run. However, today (Friday), I suddenly developed this shoulder impingement really bad again where I can't lift my arm. I'm thinking somehow running is triggering it, but I've never had a shoulder problem before.
Ok, so now for my question. I cannot think of any possible thing this could be other than hypothyroidism. I've scoured the internet and scientific papers for anything at all. But I'm just confused by how suddenly my symptoms worsened, and how my levels are not super low, but even tripling my dose hasn't completely alleviated my symptoms when I was great on a low dose for a year. I'm seeing a new primary care soon and am going to make an appt with an endo instead of continuing to see my current doctor who I'm really p*ssed with. But this will all take time (the endo I'm planning on takes months to get into), and I'm just curious if anyone has any insight into this or has experienced something similar. I'm nervous that I'm going to have to drop down to 81.25mg again and that I'm just going to be miserable, and that when we test my levels again they will be higher, but that I will still be having symptoms, and so my doctor will not listen to me. I know people say that it takes time to have symptom relief with dosage changes, but in my experience it seems like it happens very quickly. Like when I first started on the NatureThroid, I was almost completely better in a week. Is it normal to feel changes so quickly? And does anyone have experience with exercise worsening symptoms - like maybe free Ts are lowish and then exercise is an added stress that sort of depletes the body if it's not able to compensate with normal thyroid function? I'm not completely sure of the biochemistry (I don't know that anyone is actually), so I'm just kind of postulating.
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i had TKR 26/02/15. All went well, been back to near normal for 3 months or so. Had fantastic holiday where I swam, did all exercises in the pool, had 2 weeks no pain in any of my useless joints. Woke up on Monday this week with terrible pain just below kneecap, thought I had turned funny in bed, I was in so much pain today I saw my doctor. She thinks I might have an infection in the replaced knee, bloods and x rays will tell her. I have just looked up what this means, not good possible the replacement will have to come out to get rid of the infection and then start again.
I did not realise that at six months plus this could still happen? Also have had xrays on my good knee, this is not as good as I thought, it will need to go. At the moment I am in a turmoil.
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I took Cytotec 17 pills total over 24hr period, after 8hrs.i had small amount spotting over a 12hr period i have nothing since, 48hrs has now passed. what should i do now , will i begin a new cycle of cytotec , or will i wait three days ?.
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TSH and free T4 were in range and free T3 was high at 4.35. I have some symptoms of hyperthyroid. Heat intolerance, anxiety, stress, hypoglycemia but no weight loss. I attribute the no weight loss to eating all the time to keep my blood sugar from getting to low and I have actually gained some weight over the last few years. I started getting these symptoms 5 years ago and they can kind of come and go but the heat intolerance is always there. If I go out in the heat and work it just zaps my energy.
Also my red counts are just a tad high and liver enzymes are always elevated and in the 70-80 ranged. Non drinker and non smoker.
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just wondering if anyone here has a reverse T3 problem and if so, how long did it take before you saw an improvement in symptoms after taking medication?
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I am 33 years old and have just been diagnosed with having OA Thyroid, but have symptoms of UA Thyroid. I have always struggled with my weight and bloating (from having food intolerances), but have recently gained a lot more weight than normal, despite eating sensibly, walking everywhere (as I don't drive) and swimming.
I have days where I feel really thirsty and have to drink lots and lots of water, unable to concentrate, have a husky voice and morning coughing/ gunk on my chest, rapid heart rate, anxiety, feel achey and exhausted all the time. I also have Fibromyalgia (was diagnosed in 2005). I used to work full time for 17 years, but recently had to reduce my hours to part time, where I constantly felt ill...and I have now had to leave work altogether.
What I don't understand is how I can have the symptoms of UA but be OA. The Doctor has prescribed me 5mg of Carbimazole to take 3 times a day. No Propranolol yet, but I have taken these before as I used to suffer with high blood pressure.
I am worried that I am going to gain even more weight on this medication, when I have already gone up nearly two dress sizes from being so ill. Is this medication usually only given for people with OA? Will the effects be reversed in my case, where I have UA? Are there many of you out there who have the same symptoms as me and who are taking this medication and if so, what has happened in your situation?
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Usually people with hypo are cold but I'm always hot & sweaty even when the temp is chilly. I'm 37, have PCOS and hypothyroid. Since having kids I've gained a lot of weight and can't lose a pound no matter what I do. I'm on Synthroid but I feel like nothing helps.
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Hello All- I have so many symptoms of hypothyroidism and my mother and grandma are as well so I asked my Dr. to test me. She said everything came out perfect, but I still have so many true Hypo symtoms after doing some research on here. Can anybody tell me how normal these ranges are:
TSH- 2.16 (0.3-5.0)
FT3- 3.2 (2.3-4.2)
FT4- 1.02 (0.8-1.8)
Vitamin D- 18
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I've been told I have post surgical hypothyroidism (left side, 2010) but TSH is consistently low (0.1) or low normal (.396), I don't understand the hypothyroid diagnosis with a low TSH. Can someone explain? I also had left temporal lobe brain tumors (cancerous) and gamma knife radiation. Could this be affecting the TSH level. I have many hypothyroid symptoms, basal body temp is on avg. 96.5, weight gain, tiredness/fatigue....blah, blah, blah. My endo doesn't do too much. Currently taking 50ug of levothyroxine 6 days/week and feel horrible. There are also 3 nodules in the right side now that continue to enlarge. Any answers? Thanks.
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Has anyone heard of a special hypothyroid diet?
I would be grateful for any information please as to what foodstuffs to avoid and which ones would help.
Gas anyone heard of any medications that can cause or worsen hypothyroidism?
Many thanks
Jean x
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I have hypothyroid and am taking 175 mcg of thyroxine everyday. I eat low fat diet and exercise regularly. But still my cholesterol levels are rising especially triglycerides.
Is there a connection between them? My blood reports show that my thyroid levels are normal with the current medication. Then why is my Cholesterol increasing?
What measures should I take to stop this?
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hi, my gf is under treatment for PCOS and hypoThyroid and take Harmoni - F (Cyproterone Acetate, Ethinylestradiol & Folic Acid) and Femella tablets from a week. We had sex last night with protection (condom) i ejaculated outside but i found that the condom was punctured with 4-5 holes . will she get pregnant? Should she take any contraceptive pills to avoid pregnancy?
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I've been hypothyroid for a long time. I've been taking Synthroid also a long time. I'm confused by my recent blood test. My TSH was 1.180 within normal range and my Thyroxine free 1.81 . The range should be 0.93-1.70. What does this mean. I'm I hypothyroid or hyperthyroid?
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Wondering if anyone has Hashimoto's disease? I saw a specialist a couple of weeks ago who told me I most likely have this. I went from extreme hyperthyroid to hypothyroid. Skinny and energetic to sluggish and heavy. I'm pretty miserable with it. I've just been sent a letter with my levels:
8 May - TSH .03, free T4 29.3, WBC count 5.1
15 June - TSH 15.95, free T4 9.9
6 July - TSH 12.38, free T4 8.3
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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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I am pregnant with #4 currently 39 weeks. My ? Is did any of u have a bloody show? If so what was it like? I had mucus plug with other 3 but this time I have what they called bloody show but seems a bit much. Almost as like the start of period. Anyone else experience something like this?
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As a kid I think I was 11? I was once pooping and had wurms at some occurrence I even pood out something weird and round that at the time I was sure was an organ. The last thing I never knew really what it was. But as a kid I thought it was my kidney haha!
Anyway moving back to the wurms I have had some worms in my poo at that time. I never paid it attention and as I got older I kept checking but couldn't find any wurms! The thing is I don't know if this has healed itself or if the wurms are still active and if so what to do.
I read you can get some medication take that and after two weeks take it again (because of the eggs.) I also read putting petroleum jelly on the buttocks can kill the eggs. What should I do?
Let's say I have no wurms can it harm to take that certain medication? I am quite disgusted by it and my memory is not as good anymore I am almost 22 now. So I would like to put an end to the wurm infection if I should have one.
Can you have wurms? Even if they do not show up in your poop and can I then with 100% certainty say that I have wurms and what medication should I go for then?
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I have 3 thyroid nodules and 1 cyst. I have been advised to have a thyroidectomy. I do not want to go this route yet and am searching for some natural remedies. I have heard of using iodine but to be careful do to the fact that that might enlarge the nodules. I recently found out that I am very iodine deficient from a lab result. I have heard of iodine trapping, whereby the iodine taken in when their is a severe deficiency is immediately 'trapped' and held in the gland in order to preserve some iodine for the use of the thyroid. I would like to proceed with caution and try the iodine therapy.
Does anyone on this board have any experience with successfully dissolving or at least reducing the nodules/cysts?
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It wasn't long after I moved to an area within 10 miles of a nuclear power plant that I was diagnosed with an enlarged thyroid with nodules. And after a surgery I had, I became extremely depressed and I still am, this was three years ago. Also a feeling of not being myself.
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