Hello, I also have <.03 TSH and my T4 and T3s are within normal range. I was 200 mcg and now down to 137, ut I am way to tired, constipated and muscle pain, and the doctors not sure what is happening. Any suggestions as to why the TSH levels are not moving?
It was a gradual decrease with every 6 - 8 week blood works. Each time I went in to get blood work they decreased my dose. I am going to get the FREE T4 T3 done this weekend, so hopefully sometime next week I should have my counts.
Yes the doctor is basing my meds on the TSH and he was going to bring me down to 100 mcg, but I am wiped out. No energy, dry hair, dry skin, and my leg muscles ache. The say that the TSH cannot stay My last visit I had a breakdown and they put me back on 150 mcg until I go and see the endo doctor.
My TSH is a 0.04 - way below what most doctors find acceptable. You know what? I feel great! My endo is smart enough to treat my FreeT3/T4 levels and my symptoms, not my TSH.
Find a new doctor! You are hypo because your doc is basing your meds off of TSH, a pituitary hormone. The frees are thyroid hormones. Find a doc who knows how to treat thyroid disease, not diabetes, like so many endos.
The below website is where I found my endo. Make sure the doc specializes in thyriod, not just diabetes:
Your FT4 is way up in the top quarter of the range. However, FT3 is near the bottom third. The rule of thumb is that FT4 should be near midrange and FT3 should be in the upper half to upper third of its range.
It looks to me like you are not converting T4 to T3 properly, so your FT4 stays high while your FT3 remains low. I'd ask your doctor about adding some T3 meds to your regimen to bring your FT3 up. For every 5 mcg of T3 med that you add, you should reduce your T4 meds by about 25 mcg. This is because T3 is much more potent than T4. Your body can only use the hormones when T4 has been converted to T3. So, even though your FT4 looks fine, you are still starved for the usable form of the thyroid hormones (T3).
Sorry for butting in they just told me T4, I am in the UK and my dr told me that these levels are ok according to their lab. I am always tired but have always been a good sleeper. I can also get quite stressy at times, its better than it was but do sometimes feel my blood boiling!!!
update, I have seen one endo and another one write my doctor and they both have said that I need to come off of my meds. From what they figure I did not need to be on thyroid meds? My question is, has anyone ever heard of this or done this and of so any suggestions? The doctors have instructed me to get blood work every 6 weeks and then go in so they can drop my medication 25mcg. Is this safe?
You can follow the doctors and reduce by 25 mcg every 6 weeks. Make sure the testing includes ft3 and ft4. See how you feel. You may have to do this to prove a point.
Let's say you really don't need the thyroid meds and your pituitary is working fine.... Then the current meds are suppressing your own thyroid function (as demonstrated by the very low TSH). So, as your levels of meds drop, this should be detected by your pituitary as a drop in thryoid hormone, and then your TSH should come up and it would stimulate your thyroid to produce hormone. I think this is the theory the doctors are working on.
However, if they are wrong, and you do need the meds, you are going to go very hypo. Your TSH may or may not rise, but your FT3 and FT4 will drop. Hopefully, if this happens the doctors would be able to pick it up before you feel so bad and put you back on meds.
I had my doctors try the same thing on me. They were wrong that I wasn't hypo and it took me about 3 months to start feeling ok again. And my TSH did eventually start going up, but my FT3 and FT4 dropped. I still kind of hope that if I could get my TSH up it would stimulate my thyroid to work..... anyway, that's another story. My TSH is currently undetectable, with 'normal' upper reference range FT3 and FT4 (target as I am trying to get pregnant again).
Alternatively, get a second opinion, if you can....
wen i went to the endo the doctor said that my tsh was <.01 and my t4 was 31. so he is the first one that said i need to come down on my meds. The second endo was the referal and she felt that since 2002, tat was as far back as she could go, my blood tests came back normal and that I didn't need thyro med. In december the doctor raised my meds to 150, due to my crying as i was sooo tired and my legs hurt so bad. Since this past thursday my family doctor saidwe need to get u off the thyro meds and lowered my dose to 125. So, yes the docto is lowering my meds every 6 weeks, as per my blood tests, and then lower my dose 25 mcg, until I am completely off.
suoer sally are u totally off your meds? and if so what dose where u on?
I still don't understand, I'm afraid. The second endo checked your labs back to 2002 (any you've been on thyroid meds since 2002???), and your labs all came back "normal"? Am I interpreting this correctly?
Has anyone addressed why you are feeling so hypo as they cut your meds?
Your doctor seems to be treating on TSH, which is not a good sign at all.
Your doctors aren't making a whole lot of sense to me.
From what I gathered, the referred endo that did not see says that she went back all the way to 2002 and my tests showed that my levels were always showing to much thryo medication?? Without seeing me, she figures I was taking them for weight loss and need to get off. Not sure where she as going with this as I have always had to work hard at keeping my weight down. Way back then, I think 2002, I was always cold and had lots of shivers, so the doctor put me on thryo meds. When I asked my doctor about the results, he went back to 2006 and he mentioned that my tsh levels were always .03. Nobody has said anything other than I have to come down on my meds. I asked why I am so tired, and they said to take vitamin D.
From what I gathered, the referred endo that did not see says that she went back all the way to 2002 and my tests showed that my levels were always showing to much thryo medication?? Without seeing me, she figures I was taking them for weight loss and need to get off. Not sure where she was going with this as I have always had to work hard at keeping my weight down. Way back then, I think 2002, I was always cold and had lots of shivers, so the doctor put me on thryo meds. When I asked my doctor about the results, he went back to 2006 and he mentioned that my tsh levels were always .03. Nobody has said anything other than I have to come down on my meds. I asked why I am so tired, and they said to take vitamin D.
I was diagosed with Graves disease in 1999 and have been on/off medication since then. Most of the time I've felt fine. A little run down at times. More recently I've had problems concentrating and have had the tremors, palpitations, etc.
I've been reading this website and others with respect to thryoid hormone levels with great interest to determine what is normal so that I can take control and manage my levels. When having a thyroid function test my Dr only does the TSH (which is 0.07), Free T4 (15) and Free T3 (4.7). My Dr tells me this is the great and well within normal ranges..although still having the symptons mentioned above. When reviewing the websites the normal ranges I've found were considered to be:
FT4 - 0.7-1.9 ng/dl (apologies not sure what the measurement units mean);
FT3 - 230-619 pg/d (again not sure of measurement units)
TSH - 0.5-6 uU/ml
My first thoughts are that the range above are based on different measurement units. Does anyone know if there is a universal standard that labs must use when reporting the results of thyroid hormone test.
Unfortunately there is no universal standard. Even when using the same units of measurement, ranges are lab specific. I'm not sure if this is because they get different results when they run standards to calibrate their own testing, or if they just think there is a need to have a slightly different range. Since they won't talk to me, I can't find out the specific answer.
In addition, you will find that different labs use different units of measure. for example, I have seen FT3 ranges expressed as 2.3-4.2 Pg/ml, .23-.42 ng/dl, 230-619 Pg/dl, 230-420 Pg/dl, and 3.5-7.7 pmol/L. All of these are fairly close when you convert to the same units of measure. Best thing to do is to always get a copy of lab reports and keep for reference. The doctor is required to provide a copy upon your request.
Pg/ml is picograms per milliliter. Pg/ dl is picograms per deciliter. Ng is nanograms. Pmol/L is picomoles/ Liter. I think. LOL
Hi , i too am in the UK, i find reading these posts very interesting as when we go to our GP or Oncologists we are never given the results, we are only ever told that they are normal, or below/above normal.
I am due to go for RAI next Monday the 15th but have not had or been scheduled for bloods to see if the TSH FT3 FT4 or at the correct plece before i have it.
I will be putting a call into the DR to see if i can have the bloods done before Monday. Will let you know
My last TSH was 0.01
My T4 was 46
niknak have you still got your thyroid? I had mine removed due to Papp cancer. i have just come off thyroxine in preperation for the RAI i was on 275mcg this time last year i was on 225mcg when i came off they 6 weeks ago.
TSH is a pituitary hormone that is affected by so many variables that it is inadequate for use as a diagnostic, by which to diagnose and dose a thyroid patient. Unfortunately many doctors still cling to the "Immaculate TSH Belief". At best TSH should only be an indicator, to be considered along with more important indicators, which are symptoms and also the levels of the actual, biologically active thyroid hormones, FT3 and FT4 (not total T3 and total T4). Symptom relief should be all important, not just getting TSH to a level that the doctor thinks is okay for you.
In my opinion the very best way to treat a thyroid patient is to test and adjust FT3 and FT4 with whatever type of medication is required to alleviate symptoms, without being constrained by resultant TSH levels. Frequently we hear from members that this requires that FT3 is adjusted to the upper part of its range and FT4 is adjusted to at least the midpoint of its range. When medicating a thyroid patient enough to alleviate symptoms it is not at all unusual for TSH to be suppressed to low end of range or below. For example my TSH has been less than .05 for over 25 years. This did not make me hype. You are hyper only when you have hyper symptoms.
Just getting FT3 and FT4 somewhere within their ranges is not adequate. The ranges have never been adjusted like was done for TSH 7 years ago. As a result, the ranges for FT3 and FT4 are far too broad. This link might give you some good info on this.
Well, I really still don't understand how anyone can look at labs that were done while you were medicated and make the proclamation that you never needed to be on meds at all. If you're medicated properly, all your labs should be "in range". How do you then make the assumption that you never needed them to begin with???
However, I have not seen any of your labs, so I can only say so much. It appears to me that your doctor is reacting to TSH only...a very bad way to adjust thyroid meds. Can you get the actual FT3/4 results and ranges? That would help.
If your doctors think you are overmedicated and reduce your dose, they should be much more concerned with return of hypo symptoms. The doctor who never saw you and diagnosed on numbers alone is a loser. This is a symptom-based treatment...numbers only help you to achieve symptom relief...they are not an end in and of themselves.
Have you had vitamin D tested, and are you deficient? (Sorry if you stated this above, but the thread is getting pretty long, and I couldn't see it.)
I think you have to go in there and make it very obvious that you feel hypo, and the dosage reductions keep making you feel worse.
Hello, my latest tests results which were done in Calgary came in as
free t3 4.6 range 3.5 - 6.5
free t4 31.4 range 9.0 - 23.0
tsh <.01 range .20 - 4.0
As for my Vitamin D, no I have not been tested but my doctor felt that it wouldn't hurt to take some.
Oh well, I was wondering if anyone else had to go through this before. I am so worried about lowering the dose and what my mental state will become and will I ever feel normal again? This is what happens when you go and see endo specialists, you get no where. At this point my doctor does not care about how I feel as he told me that I need to endure this and eventually I would feel better? I need togo through withdrawal in order to feel good once again.
Well, your FT4 is way too high, way up above range, so I can now see why your doctors want you to cut back your levo. However, your FT3 is too low, just barely into the middle third of the range. The rule of thumb for FT4 is midrange and for FT3 upper half to upper third. Your FT3 is not only low, but extremely low when compared to your FT4. Usually FT3 is higher in its range than FT4.
There are a couple of possibilities here:
1 - You could be a slow converter and need to add some T3 (Cytomel) to your meds. T3 is the biologically active form of thyroid hormones. If you are not converting T4 to T3, you will not feel well no matter how high your FT4 is. Your cells cannot use T4, only T3.
2 - You could have reverse T3 dominance. Your liver is converting more RT3 than FT3. RT3 is inert, but can bind to T3 receptors in cells and block FT3. RT3 builds up, causing a kind of "dam" that the FT3 can't get by. The treatment for this is to go on T3-only meds temporarily until the FT3/RT3 balance is restored in your body.
RT3 can be tested. If your doctor will order it (some of them "don't believe" in RT3 dominance), be sure to have FT3 tested on the same blood draw since its the ratio of FT3 to RT3, not the raw numbers, that's important. This is the route that I'd want to go. However, if that fails, you obviously need to at least add some Cytomel. Another approach would be to try just adding Cytomel and see if it does the trick for you. If not, you can then get more insistent on RT3 testing. Just be aware that if you do have RT3 dominance, adding T3 will not cure it...you have to eliminate all T4 meds at the same time.
On the vitamin D, I have to agree that it most likely won't hurt anything. However, if I were a doctor, I'd certainly have a hard time telling a patient that they were tired because of lack of vitamin D when a deficiency hadn't even been established. I think if they're going to use it to explain your symptoms, then they darn well ought to test it.
One more point...when you add T3, you have to reduce T4 meds by about 25 mcg for every 5 mcg T3 added IF you want to stay on an equivalent dose.
I just know that your doctors are not going to be able to "fix" your problem by adjusting your T4 meds alone. You have to get Cytomel into this picture somehow.
Thanks for the information, and about Cytomel, but at one point my regular doctor was going to get me on Cytomel, but then came back and said that it seems that the theory is only theory and as far as statistics go, it didn't seem to work so he decided not to have me take them. For now, unless I can find another doctor I have no choice but to come down to ZERO with my thyroid medication.
Thanks to everyone for all their feedback. It is much appreciated. I will try and post my progress every couple of weeks as well as my blood work. Until then take care:-)
Is finding a new doctor a possibility? I don't mean to discourage you, but if you have to get to zero meds by decreasing 25 mcg every six weeks, that's going to be over 30 weeks of thyroid he// (that's over seven months), and that doesn't include the time it will take to re-stabilize afterwards.
Yes, please keep us posted. It will be interesting to see how your labs go and if their "theory" about taking you off meds is working. Good luck...
Excuse me for being late to the party here, but I just wondered what in the world gives the doctors the idea that you may not need thyroid meds? To the point that they are pushing you to gradually reduce meds down to zero, in order to see what happens.
Curious here but why not suggest that you STAY on the dose of T4 med you are on and take an anti-thyroid med to counteract the hyper levels for a week or 2?
This would bring the FT4 down and you would then see if it IS the meds causing the high FT4 .
As for getting you down to ZERO..forget it!
I have gone meds induced hyper before and I only stopped for 4 days then felt like cr@p as I went HYPO.
Ask about anti-thyroid meds and also ask for a beta blocker to help with any hyper symptoms.
Just a thought......
All I know is that the doctor does not think that I need to go on thryo meds and neither does the two endo's. So on my last appointment, I asked him if their was anything else and he said no, it will like withdrawl but I would have to do it. I feel like crap right now as I am so foggy brain and soooo tired. When I go in in 5 weeks, I'll ask him about the block and replace and see what he says.
the reason is that my tsh levels are reporting low <.01 and my t4 is 31.4 and that was at 150mcg. A 137 mcg my results were as follows:
free t3 4.6 range 3.5 - 6.5
free t4 21.4 range 9.0 - 23.0
tsh <.03 range .20 - 4.0
The endo that I was referred to said that I was <.03 since 2002 and feels that I should have never been prescribed thryo med. She actually thought I was using them to loose weight?? I was put on thry way back as I was tired, and very cold, and at sometimes at night when I was sleeping my body would shiver, I was so cold that my teeth would rattle. So question to ask is my tsh low or high? I get so confused especially lately, I feel like I can't comprehend the simplest thing.
Those ranges look fine to me if you are on a T4 med.
There is no way I would come of the meds with an FT3 at that level.
IF and I say stipulate ..IF......you dont need the meds, then your levels would be sky high and they arent.
Do you still have your thyroid?
And if so.....have you been tested for antibodies?
Normally someone WITH a thyroid AND antibodies...their TSH can stay at ZERO, especially if you have Graves Disease.
Its a well known fact that those with Graves Disease AND a thyroid will very raely get that TSH up.
These are some of the questions you need answers too.
1. Do you have Graves Antibodies? (Test TSI)
2. If you are overmedicated then why isnt the Ft4 out of range?
3. If you are overmedicated then why is the FT3 lower than it should be?
These are all questions I would be asking or .....
I WOULD GO SHOPPING......
Get another Doc/Endo because this one obviously has his/her head stuck in the sand.
Just my opinion, but I think that goolarra's post of 3/9 is right on the mark regarding your FT3 level being too low and contributing to your symptoms. Remember it should be all about symptom relief, not TSH level. In order to get symptom relief the level of thyroid medication I have been on suppressed my TSH level to less than .05, for over 25 years now. You need a source of T3 added to your meds.
Personally, I would not continue to follow the doctor's direction to reduce your current meds. I agree with the suggestions to find a good thyroid doctor.
Your FT4 came down nicely with the change from 150 to 137. It's back in range and looks good. You just need the T3. Don't let your doctors put you through hypo he// to prove you need meds...that's cruel.
I agree with gimel and goolarra -- my TSH levels stay lower than yours are and we ignore them so long as my FT3 and FT4 stay good.
Your FT4 is quite high, even though in range. You might want to cut back "slightly" on the T4 med and add a small amount of T3 med to bring your FT3 up. I agree that the low FT3 is most likely what's causing your symptoms.
Hello again, it's been 6 weeks, and i went to the doctor today to get my results My TSH is <.03 TSH, T4 is 22 and the T3 is 4.6. So within the next day i will be on 0.1mcg synthroid. I am so tired and fuzzy brain but the doctor still thinks I need to come off. So, stay tune for the next blood work:)
I am not an expert, but I am and have been down a very familiar road. First, I HIGHLY recommend you get a new doctor. Don't assume this doctor will figure things out. Life is too short, and you deserve to feel good!
I had the same scenario as you, major suppressed TSH (doesn't really matter!) I had cancer so this was good, however I still had MAJOR hypo symptoms. Chilled all the time brain fog, you know...the works fun stuff. I found an awesome doctor that really knows his stuff (Thank you Lord!) He did a host of panels hormones, thyroid, lipid, you name it. I was deficient in quite a few things, and also had a high reverse T3. BTW...I was on a Levo T4 for about 6 months feeling well maybe a handful of days.
I am now on a host of Pure Encapsulation supplements along with iodine, and dessicated Nature Thyroid and my body temp has come up, I am sleeping a tad better and think I am getting there....please please.
I really think you need some T3. Whether Cytomel (synthetic, or Dessicated) I think this will alleviate a majority of your symptoms. Please note that I think an adrenal support system should also be done when implementing T3. Cytomel works very fast and will get you adrenals going. Don't be suprised if you feel hyper the first few times.
In summary.... New Doc....some T3, probably slow converter, and adrenal support (pure encapsulation ADR?)
Hello Fuel1212, I agree I do deserve to feel good, but I have two endo's and 2 doctors that are telling me to go off the thryoid meds, and so to obtain another doctor will not likely happen as it is tough to find doctors that are taking on new patients. I asked my doctor today again and he still thinks that once I am totally off the thyroid meds, my tsh will move up. I asked them about Cytomel and he said that it wouldn't matter as that is what the studies show.
To Goolarra, I have been on 125mcg for the past 6 weeks.
Question, it seems that my T3 has not moved at all. When I was taking the 150mcg, my levels were t3 4.6 and t4 is 31.4. When I was taking 137 mcg my results were T3 4.6 and T4 21.4 . Now at 125, my T3 is 4.6, T4 is at 22 and my TSH in all of this is still <.03 . Why is it that only the T4 seems to move?
I have always found that my FT3 "lags" FT4. As I'm increasing, FT4 will go up in six weeks, but FT3 may take a while longer to reflect the rise in FT4. Of course, the opposite for decreasing.
T4 is the "storage" form of the thyroid hormones. No receptors have ever been identified for T4...it has to be converted to T3 before your cells can use it. So, as long as there are adequate supplies of T4, and your body is still looking for more T3, the level has a tendency to remain the same because you are not converting enough (but you are converting as much as you can). Another way of saying that is that you have plenty of T4, and your body is converting as much T4 to T3 as it can, but it's still not enough T3. So, the level is staying the same and most likely will until your T4 falls to a level where your (slow) conversion ability no longer has enough T4 to convert.
However, your FT4 does continue to rise marginally despite the decreases.
You do need a doctor that treats based on symptoms, FT3 and FT4 in that order. I wish I could suggest an alternative, but I think you will not feel well until you find a doctor who knows what he's doing and is willing to add some T3 to your meds.
You can get as much T4 and supress the pituitary (TSH) to make the numbers look hyper and overmedicated. The problem, like I said and these docs need to realize is that if you don't convert to the active T3 you are going to have symptoms no matter what doseage, or no doseage. Do you feel hyper...from what I read, it didn't soundl like it. You body will tell you when you are hyper, no matter what the TSH.
Mine is .06 and I have no hyper symptoms, in fact I was not converting and felt hypo.
Question...if you take a close up picture of your eyes especially the corners, do you see a yellowish tint? I am going to bet that you will see this. This is an indication that your liver is not converting and the T4 is buiding up. It collects as carotene I believe?
If you are from IL I have an awesome doctor. Feel free to message me.
Well, I do not feel hyper at all, more on the hypo side. I live in edmonton, alberta. I do have a yellowish tint in the corner of my eyes. Can you tell me where else I can go to do some more reading to find out more about this?
okay, another 6 weeks have gone by and the results are .07 tsh level, and the T3 and the T4 didn't move from my last test. I am exhausted and tired all the time, and the doctor has agreed to keep me on the .1mcg for another 6 weeks as I am way to tired and I felt that if he lowered my meds again my body would be worse off. Any suggestions on what I can do to give me more energy? I have been getting a vitamin b shot (gives me energy) every three weeks, but this time it's been 3 days since my shot and I am still exhausted.
Has your doctor ever considered that the TSH is frequently suppressed below ref. range when taking thyroid meds. That doesn't mean you are hyper, unless your FT3 and FT4 levels are excessive and you are having hyper symptoms, which is not the case. My TSH was less than .05 for over 25 years and most of that time I still had lingering hypo symptoms, until I learned about FT3 and adjusted my meds to increase the level. Now I feel best ever.
I thought you might like to read through some of these patients' remarks about low TSH.
I'm another whose TSH stays in the basement (latest was less than 0.03) and I'm a long way from being hyper. My FT3 and FT4 levels have been good, so we ignore the TSH.
Since your doctor agreed to let you stay on some T4 med, is it possible that you could approach the idea of T3 med again? Would it help if you print out some info regarding the use of T3 meds and take it to him? Some doctors are open to various treatments if you can show that them it's a good thing. I had a lot of the same issues until I finally got in to see my endo, who immediately put me on cytomel to bring my FT3 levels up.
hello again, i am tired and gained a few pounds even though I am dieting and walking running at least 5 days a week, but lately like 4 weeks ago, i got vertigo and I am still not over it. Does vertigo have anything to do with my meds being lowered?? How can I get my metabolism to work so I don't gain any more weight?? Please and thanks
Hello, I am wondering if I go to the doctors and ask him to give me 5mcg of Cytomel, and how much do I need of my synthroid? I am on .1 mcg. I am hoping by approaching the doctorsw this will help me with foggy brain, tiredness and weight gain.
Hope you are feeling better. It looks like you are on 100mcg of Synthroid. You are wondering about the Cytomel. Synthetic T3 works very fast. If it were me, I would start on 2.5mcg of Cytomel a day. Make sure you don't have major hyper symptoms. Eventually, you could go to the 5mcg maybe 2.5 in the morning and 2.5 in the afternoon to keep you going. I wouldnt take it too late because it may effect your sleep.
If it were me, and I am not a doctor, but feel pretty confident in this being where you are. I would guess you are not converting properly. You also may have some adrenal issues. Being from Canada, I would find a good doctor that prescribes ERFA. Start our with 60mg or 1 grain and get some ADR by Pure Encapsulation to support the adrenal with repair. Do that for about 6 months and see where you are of course testing every 3 months or so.
Hello again, I have gone back to get my blood results and they are:
free t3 4.1 (ranges 3.5 - 6.5)
free t4 16.6 (range 9.0 - 23.0)
YIPPY in one way and Boohoo in the other. So I went and saw another doctor in the office and he said my levels are fine and to stay at the .1 mcg. I asked him about the cytomel as I am tired, foggy brain, and weight gain, and he said "NOPE" that the levels are all fine and there is no need to change anything. He said that the T3's are within range, and maybe I should try some Omega fish oils, and or some stress tablets???? So, I am going to see another doctor tomorrow to see if he will do something for me and hopefully prescribe me some cytomel so that I can feel normal again. Question, what should the are the "normal" counts for the T3 and the t4's? What should I suggest the doctor give me?? Do I stay at the .1 mcg and the 5 mcg cytomel?
You're close to what many find good. Definately in the majority of patients upping that Free T3 level some could be very helpful.
I saw on the T4 level however. You could drop down to .88 mcg while adding in the .5mcg Cytomel or stay at the .100mcg Synthyroid and still add either a 2.5 mcg or the .5 mcg Cytomel
Either way the Cytomel would be good to push with this other doctor to bump that T3 level more. You are hovering right in the middle where most patients find being in the upper 3/4 to even 95% to the top of the reference range makes them feel better.
I don't think adding more T4 - depending on that alone to convert is good here and the "tweek" of adding in direct T3 could definately be your answer.
You will need to test all these levels in 4-6 weeks after you get the Cytomel and definately start a log after you start that script to track your symptoms to show the doctor you goods/bads since you started. Taking your symptoms and the new labs after you start T3 will determine what you should do next if anything at all.
Okay, I am so excited. I went to see an old doctor of mine and I told him what was happening and he left me on .1 mcg of synthroid, and told me to take 3 .5mc of cytomel. However, I am not sure how I am going to feel so I'll only do 1 for now. Am I right?
You are absolutely right. 15 mcg of Cytomel is a relatively high dose. Many people find that 2.5 to 5 mcg helps tremendously with symptoms. I think your idea of starting at 5 mcg (you could even split the dose into two during the day) is an excellent one. Give it a few week at 5 mcg, then increase if it still seems you need it. Your labs are not that far out of range...in fact, it might even be best to start with 2.5 mcg. Better to start out slowly and increase than to go at it too fast. Good luck!
Hello.... it's been awhile, so I thought I could give you all an update. I have been taking 2 .5 mcg of cytomel and still on the .1 levo and I am feeling great. I am not foggy brain, tired, etc but full of life. I just got my blood work back and my blood work is t3 5.5 (3.5 - 6.5) t4 17.00 (9.00 to 23.00) and guess what my tsh is once again <.o3 again.
Wow - your labs look great (those are FREE T3 and FREE T4, aren't they?) and even better to hear that you feel so good. It's wonderful to see someone having success with this roller coaster............ I'm so glad you posted, as your experience may help keep others from getting discouraged............
Hello. Well it's been a long time and not sure what happened. I started to take 25mcg of triiodothyronine and 25synthroid. Things were going good as I was feeling great and got a revile on my trio meds and started to feel great. I was alert and then i started to experience anxiety and night sweats. Got another 20 of the trio meds as I thought it was the compound mixture and now I am tired all day had had one episode of night sweats except for last night it started at three in the morning until I got out of bed at five thirty. Went to the doctor today and blood tests showed free. T3. 4.7. Freet4. 7.2. Tsh. 36.6. I am exhausted, hate my weight as all I need to do is look at food and I gain weight. Can I do something to get my thyroid metabolism working right.
Hi, I am on 25 mcg of triiodothyronine and 25 mcg of synthroid. As for my ranges, my Ft3 is 4.7 and Ft4 is 7.2. I am experiencing night sweats even when I take 1/2 a capsule of the triidothyronine and 25 mcg of synthroid. I am foggy brain and not sure what I can do to feel better.
When goolarra asked for the ranges of your tests, she didn't mean the 4.7 for FT3 and 7.2 for FT4 - those are your results...... on your lab report, there should be reference ranges, sometimes in parenthesis beside the result. If your levels fit inside those ranges, you are considered "normal" by most doctors.. We need to know what those ranges are, in order to see where your levels fall within the ranges.
okay here they are Ft3 range (3.5 - 6.5) t4 (9.0 - 23.0). I am considering on taking 50mcg of synthroid and 2 X5 mcg of citomel. The only problem is that if I take the 5 mcg twice a day, my energy level drops and I am lethargic.
thanks Barb, that is what i was thinking of doing on my own. The doctor wants me to stay with the meds, but i am to sick to stay on. I have 50mcg of synthroid and 10 mcg of cytomel and getting off the triiodothyronine as I think that it is to strong for me. Am I going about this right and try it? If so, when should I notice a difference.
The triiodothyronine is a compound and from what I understand it's suppose to be like cytomel but long lasting. I currently take 25mcg of the triiodothyroxine but because it gave me the jitters, and I thought my head would explode I am opening up the capsule and pouring out half the compound and I still feel sick. If I only take 10mcg of the pill form I wonder if that will drop my t3? Should I take the 10 mcg first thing together with my 50mcg of synth rood?
If I unserstand you correctly, and you've been taking 25 mcg of T3 (sounds like it might be time released), if you discontinue the T3 you've been taking and switch to 10 mcg of Cytomel, you can expect your FT3 to drop.
I agree with Barb, your FT4 badly needs to come up.
As for the T3, have you been taking 25 mcg all at once? Most people who take T3 meds will split the daily dose in two, taking half first thing with Synthroid and the second half sometime late morning or early afternoon. T3 is very fast-acting, and that smooths out some of the peaks and valleys. Most people avoid taking it after about 3:00 pm (on a "normal" sleep schedule) so it doesn't interfere with sleep. You might have to experiment a little to see what works best for you.
How do I split it if it's a capsule? Today I took 50mcg of synthroid and 2 5mcg of cytomel and I am having hot flashes. Maybe I should only do1 in the morning and another one at lunch? Thanks so much for all your replies and help lets see if tonight I get the night sweats
I am taking 25mcgof synthroid and 25mcg triiodothyronine capsule form. My understanding is that this is a compound as it is not found in all the pharmacies I can only go and get it in one place This morning at eight I took 50mcg of synthroid and 2 tablets of 5mcg of cytomel as I still have some left from last year. As for the triiod meds they come in a capsule form and I used to open the capsule and empty half close the capsule and then take it but it felt like my head was going to blow off and lots of anxiety and night sweats.
If the triiodothyronine capsule is all T3 (25 mcg), that's a big dose, especially to take all at once. Do you get it at a compounding pharmacy as a prescription, or is it sold over the counter?
If I were you, I think I'd try taking just 5 mcg of Cytomel in the morning with your Synthroid and taking the other, as you suggested at lunch time. If you feel better doing that (don't have the jitters, etc.), you can ask your doctor about increasing a little if you still lack energy.
Its a compound that is made at one pharmacy cannot buy it over the counter. I noticed that be taking the 50mcg synthroid and 10mcg of cytomel I get hot flashes during the day. Not sure I understand it as I was taking 25 mcg of triiomeds and only had night sweats and jitters and with 10mcg in pill form I get hot flashed during the day and I am tired
You said on April 14: "I am taking 25mcgof synthroid and 25mcg triiodothyronine capsule form"......... Now you say: "I noticed that be taking the 50mcg synthroid and 10mcg of cytomel I get hot flashes during the day".
Did you change your synthroid dosage? Do you I understand correctly, that you now take 50 mcg synthroid and 10 mcg cytomel?
Sometimes, changing a medication or dosage can cause different symptoms. Also, keep in mind that it takes several weeks for the synthroid to build up in our system, so you won't feel effects of it, right away.
yes I decided to figure this out on my own as the capsule pills were going to give me a heart attack. The pressure in my head was to much and even when I only took 1/2 the capsule (over 1 week) it still gave me severe headaches. I have been on the capsules for over three weeks now and not getting better. I hope I have done the right thing.
Hello, its been awhile and I thought I'd give u all an update. I have been taking 50 mcg of synthroid and one 5 mcg cytomel in the morning and then another one in the afternoon. How am I feeling... I am tired and I am still having sweats and my voice is hoarse and can't think straight. I know I have to wait but for how long. I am now experiencing day sweats as well as night sweats. What the heck is going on?? HELP! Do I have to give it more time?
We volunteer our time here, so none of us is online all the time and we can't always respond as soon as comment is posted.
It doesn't sound like you are getting any better, but then it hasn't been all that long since you changed doses and it does take a while for it take effect. Most of your symptoms are hypo, but being tired can be either, hypo or hyper. The sweats indicate hyper. It's really hard to know without seeing another set of labs.
It takes at least 4-6 weeks before a med dose has full effect and you've only been on the 50 synthroid and 10 cytomel for about 10-12 days.
Could you please tell me who the tyroid dr is in IL? I have had nothing but trouble and no luck at all since having thyroid cancer l9 yrs ago and I have been on every mcg of synthroid there is whith only side affects...esp hair loss to show for it.
Hello, I also have <.03 TSH and my T4 and T3s are within normal range. I was 200 mcg and now down to 137, ut I am way to tired, constipated and muscle pain, and the doctors not sure what is happening. Any suggestions as to why the TSH levels are not moving?
Copyright 1994-2016MedHelp International.All rights reserved. MedHelp is a division of Aptus Health.
The Content on this Site is presented in a summary fashion, and is intended to be used for educational and entertainment purposes only. It is not intended to be and should not be interpreted as medical advice or a diagnosis of any health or fitness problem, condition or disease; or a recommendation for a specific test, doctor, care provider, procedure, treatment plan, product, or course of action. Med Help International, Inc. is not a medical or healthcare provider and your use of this Site does not create a doctor / patient relationship. We disclaim all responsibility for the professional qualifications and licensing of, and services provided by, any physician or other health providers posting on or otherwise referred to on this Site and/or any Third Party Site. Never disregard the medical advice of your physician or health professional, or delay in seeking such advice, because of something you read on this Site. We offer this Site AS IS and without any warranties. By using this Site you agree to the following Terms and Conditions. If you think you may have a medical emergency, call your physician or 911 immediately.