I have had Hashi's for over 30 years and I can tell when I am hypo and when I am hyper with alarming accurateness! LOL. I can even say to the doc..."it is time to test, I am off.." sure enough. When I am hyper I am exhausted, mind spins, heart races like waves off and on, dizzy. Bursts of energy like I am moving in fast forward yet extreme fatigue. When I am hypo I hurt all over, legs swell, hurts to move, exhausted, hurts to sleep at night. The only two things in common with both ways are my mind races causing sleep disturbances and I am exhausted. In the last 3 years I have had 2 blood tests come back in the normal range for my TSH. My T4 stays normal most of the time and my T3 fluctuates. I have been tested every 8 weeks for the last 3 years because I have not been able to maintain a normal range for very long. Before that it was just every 6 months. I have developed some nodules and pockets of thyroiditis so I get an ultrasound every 6 months now too. They told me the thyroid gland itself has atrophied and is very, very small. I guess the disease is eating it away. I just want to feel normal too but it happens so infrequently that it does become harder to recognize. I guess I forgot to mention weight as well. When I am hyper I am famished and want to eat all the time. If I am not careful I will gain but most of the time I just find I can eat more and not gain as much. When I am hypo for get it...everything I eat packs on pounds even though I am not as hungry. My weight can fluctuate by 20 lbs or more in the course of a couple months. I have bottles of left over meds because they change my meds so much. In the last 3 years my TSH alons has gone from the highest of 66 to the lowest of .0050 and everything in between. 8 weeks ago I was in one of my 2 normal times and my TSH was 2.1. Got a call today and it is 22.86 and T3 is 224. So now my 150 mcg is no good and I just got a refill last week.....One thing is different this time. Usually my doc only adjusts my meds by 25 each time. This time he is adjusting by 50...I am nervous about that. I sense a med induced hyper coming on. BUT what do I know right????? I have only had this for longer than some of these docs have been alive. They are always asking if I am takikng my meds correctly. I wake up at 6 every day...on weekends too and take my meds. If I don't have to get up and I want to sleep in, I still take the med and go back to sleep. I eat 1-2 hrs later. Up to a year agao I was taking it at 5 am but my schedule changed. Sorry to rant on and on but answering your one question about how to describe what you feel turned into pouring out my frustrations!! Good luck with your situation!
Hi, very new to all of this, just been diagnosed hypothyroid, my lab results as follows : tsh 36.46 T4 5.57 and T3 2.3 started on 25mcg levothyroxine, one week in now, how long will it take for me to feel any benefit? Feeling a little worse, tired beyond belief, night sweats, weight gain, anxious, weepy, irritable, the list goes on.......muscle pain, joint pain, headaches, disturbance in my vision......think I just need to re assurance!!
Nticed something interesting. Yesterday I felt fairly well. No big issues. Then today I felt horrible. I seem to flip to hyper every other day or so. Yesterday was tired, calm, felypt like I needed caffiene. Today my hands are shaking, bad diareah, hot and sweaty and my thryroid hurts like mad. Also ears buzzing, nauseas, eyes hurt. I've realized now I'm flipping back and forth. And what is even more disturbing is that when I take thyroid, the hypersness is so extreme I have to lay down for it to pass.
I think my plan is this:
I am going to see endo on thurs. Will have a sonogram, frees tested, adrenal suppression test (never had).
I am going to stay on .50 of tirosint through the rest of this month and then next month as well. If I do not see a marked improvement, I am going to make a decision to chunk or kill the thyroid. My financial situation is that I am hanging on by a small string. I have tried to be conservative in my treatment but im not quite sure what to do anymore.
I also want to see what happens with danni in getting hers out.
I still think the thyroid is shooting out trying to fight off the antibodies. I am trying to be patient and suffer with dignity, however I keep reading about people who have gone through this for 4 years without any success.
Those labs are pretty irrelevant at this point. You've been on meds, so they've obviously changed.
You can feel hypER when you increase too fast. Your body isn't used to having that much thyroid hormone floating around.
I think, "Everyone i meet that has their thyroid out always feels fine." is a tiny bit of a broad, sweeping statement. Some people have a TT and never skip a beat, but we certainly hear from plenty for whom it doesn't go all that smoothly.
It's a big decision (so is RAI). Also, post-TT, you would still be faced with all the probems with getting to a stable dose that you face now, especially if your difficulties have more to do with meds intolerance than Hashi's.
those were before i was on anything.
whats weird is I feel HYPER but my labs obviously show HYPO
I dont understand.
I am going thursday to an endo to have a re-check of everything. I am going to explore removal or RAI to possibly get this under control. Everyone i meet that has their thyroid out always feels fine. I dont understand it.
You'll adjust.
Your FT3 looks fairly good, but your FT4 is pretty dismal. Are those labs current or from before you started ont he 50 mcg Tirosint? I interpreted them as before...you have to get these guys to test FT3 and FT4 every time.
Great idea!
May I ask a question, at some point will my body just get used to all this wackiness and adjust?
Also, my frees didn't seem that bad at 20.1?
Correct, you are still feeling the effects of the 75 mcg. 13 days is right where I'd expect you to feel it...10 days to 2 weeks.
I know Tirosint doesn't have as many incremental dosages as levo, but when you are ready to increase again, you might ask your doctor about adding 13 to your 50, rather than going directly to 75...unless there's another interim dose available in Tirosint.
When I was overmedicated, my endo suggested discontinuing thyroid meds for 3 days, then resuming at my previous dosedose...you might ask your doctor about that approach. It got me back to "normal" pretty fast.
Here was my progress
NO THYROID SUPPLEMENT (felt horrible)
tsh 20.1
t4 free 0.9 0.8-1.8
t3 free 3.4 2.3-4.2
So then i did .50 for 34 days. I went and got retested and only had tsh.
TSH 5.8
So I bumped to .75 for 13 days. After about 5 of them, felt progressively worse with the ear ringing, hot all the time etc.
So yesterday i backed down to .50 and this is where I think I will stay for a while.
I am suppose to go see my other endo next week and am going to request a full panel, sonogram etc.
today was horrible, so in theory i am probably feeling the effects of the .75 despite being on .50 for 2 days, correct?
bruce
Then I went and got checked but they only did tsh this time.
They really need to understand that FT3 and FT4 are more important to test than TSH. TSH causes no symptoms. It is only an indicator of the levels of mainly FT4, and somewhat of FT3. Plus it is affected by so many variables that statistically it correlates poorly with FT3 and FT4, and even worse with symptoms. The test that correlates best with symptoms is FT3, so don't let them get away with that. Insist on being tested for FT3 and FT4.
That increase in your meds may not sound like very much, only 25 mcg, but think of it as a 50% increase, and you are very sensitive to meds.
How long after you made the change was it before you noticed those bad reactions and reduced back to .50?
Ok now I am very alarmed.
I was on .50 tirosint for a month. Didnt feel any better but really didnt feel any worse. Then I got my tsh checked and it came back at 6 so they increased me to .75. I went totally hyper. Diareah, shaky, ears ringing off the hook, disoriented, more diareah, and misery.
So I went to see my other endo (mr. harvard grad) and he thinks that i should of stayed at .50 for a little bit more as he feels it was moving the dial but I didnt not give it enough time. So he backed me back down to .50 where ive been for two days.
Whats bizarre is that i feel worse than ive ever felt ever. I feel like i have an electric current going through my head, im shaky like crazy, again very hard to think, very testy, caffienated feeling all the time.
I thought maybe this was me going hyper and hoping that it would just go away. OR maybe ill feel this way for a week or so and eventually even out.
I felt much better not on anything at all, but we all know that is not an option.
any advice?
I dont have free labs on my last test. they wanted to get tsh down a little and then they would re-test my frees.
bruce
if your noticing improvements that's good. takes a while to level out. I'm a little hyper now. dose was reduced. i don't sleep well. still have some ringing in my ears not too bad. but i know i'll start the new dose tomorrow. and it will take at minimum a month to re-level. hopefully symtoms will reduce as the levels drop and level out. plus you probable are still healing in-your body now as you get you thyroid levels back up into the normal range so that will take some time. what was last tsh free t3 ? all that? was it still low, it takes time. mine was (TSH)0.09 last time it will take some time to slowly reduce just as your will slowly raise . so all im saying is is good that your feeling better and you'll feel better as time goes on. your on the right road. just a pain in A@@ slow road .but it gets easier and easier to wait as you feel better and better. so hang in there. Kevin
Chronic back pain was my first symptom. When I get really bad my back hurts. I've had two rhizotomys.
I am new to all of this. I was just diagnosed with Hashi's in February. But I do want to ask, Can anyone even remember what normal felt like. I can't. A lot of the problems I have been blaming on my back and I am now thinking it is my thyroid causing them. I have been in and out of several doctors over the past ten years and just kept getting told your back is fine we don't know why you hurt or what is going on. I am hoping, thanks to some great advice from people on here, that I can at least get some relief. I think all of my friends are sick of hearing about my thyroid. Every time I learn something I tell them and they just kinda get a blank look and my husband has flat out told me at one point that he thought my doctor was a quack and there was nothing wrong with my thyroid. I then had to go explain my test results to him but I still don't think he understands. Sorry about the rant lol. I just got to where I tell people I've been better but I've been worse too. That covers most of my problems and I no longer get the glazed look. Good luck to you all!!!
you get that too? You are right as i notice it more because my job is sitting in front of my computer all day in a quiet room. Its still not normal kevin. Something isnt right. Before you kept telling me to take thyroid. Now im on day 46 and taking .75! The stupid ear ringing is worse and then so is the anxiety issue. Its nothing like before when i took it, but still pretty bad.
cold just be the morning , i know its not scientific , but i think your full of energy inthe morning and as you get going burn some off you level out a little bit, i feel the same way most days, but im up and running most days so i don't notice it so much any more.
Question for everyone -
I take my tirosint in the morning and for the first part of the morning I feel very anxious as if i drank too much coffee.
I know that the theory is that T4 pools and that if you took just one t4 it wouldnt do anything, but i disagree to some extent.
Before i started the treatment i had this weird deal that I always felt crappy around 2:30, felt better as the day went on. Now it seems to be worse as im on t4.
I want to start testosterone eventually but im still afraid there is something being overlooked.
bruce
I finally take .50 tirosint but it makes my ears ring and I feel like I drank 89 cups coffee. I'm on day 20,,,
Are you still only able to take a small dose of the thyroid medication or have you been able to increase it?
Ive. Had every test known to mankind.....I've been on thyroid for 19 days Now and feel much much better. My tsh was 22. It's a long hard road out of hell
My endocrinologist said that my primary care physician has to test for my iron and cholesterol so I have to make an appointment with him.
Have you ever had an MRI and MRA of your brain? I don't have the feeling of stars going around my head (I'm sure that's annoying) but I do have dizziness so I had an MRI/MRA and I have to get a second opinion because it showed some abnormality. It sounds like you have hyper symptoms like I do. I've read that with Hashimoto's when you're having an episode of thyroiditis you're more likely to experience hyper symptoms. Is your TSH still high?
I cant even imagine the PMS on top of this. coco, i think you had an iron issue, are you taking steps to get that taken care of?
Remember the cartoons that when people got bonked on the head it would show stars going around in a circle above them? That is how i feel. ALso i feel like someone turned up the power in my body. I shake so bad sometimes I have to take a xanex to relieve it.
Crawling out of one hole and falling into another one....
Once one symptom is gone like tachycardia then the dizziness starts, that stops then I get anxious but I don't get a break once the anxiety stops because my stomach wants to start bothering me....oh, and when I have PMS the Hashimoto symptoms like to get worse.