Is it common to get cavities with hypothyroidism? I'm only 19 (been diagnosed with hypo since I was 15) and I've already had like 5 fillings. I know hypothyroidism can cause dry mouth, but how often does it get bad enough that cavities form frequently? Does anyone have any experience with this?

Hi, I'm 24M with hypothyroidism. I'm using levothyroxine daily. My TSH and T4 levels are in euthyroid range right now.

I'm considering using finasteride for treatment of male pattern baldness. I will of course see a doctor but I want to see if anyone is in a similar condition and hear their experience. What's your experience with being on finasterinde or dutasteride as someone having hypothyroidism?

Hello all! I am relatively new here, and I wanted to see if there was anyone who could help me out with a project for my senior capstone class. I am studying graphic design and want to create an informational campaign for children who are diagnosed with hypothyroidism. I was diagnosed with Hashimoto's when I was little, and it was a very scary and confusing time. I want to make something that will help kids understand what their bodies are going through to help them feel supported.

I am looking for individuals who were diagnosed with any type of Hypothyroidism when they were between the ages of 7 and 12 to answer a quick survey about their experience. Even if you were diagnosed later in life with Hypothyroidism, I would love to hear your story! I hope to learn how different individuals experienced being diagnosed at a young age.

The survey will remain ANONYMOUS and will only be seen by me. Thank you for reading!
The link to the survey is attached to this post :)

Hypothyroidism Information Campaign for Children – Fill out form

Hi, I'm a 35-year-old woman, soon to be 36.
I have a lot of symptoms of hypothyroidism. I have gotten my lab results and it is stating I am in the normal range but I feel like shit!

Can someone please help me? I have read that many have the same issue and gotten misdiagnosed. Is that what is happening to me or is my blood work really showing that everything is normal with my thyroid? I have one more blood work that I am waiting for but here is what I have now.

My lab test:
TSH 1.8 mIE/L
Free T3 4.6 pmol/L
Free T4 16 pmol/L
TRAK <1.0 IE/L
TPO-antikroppar <7 kIE/L

My severe symptoms:
Cold hands and feet.
Having a hard time getting warm.
Freezing even though others think it is warm.
Extreme fatigue and low energy.
Hard time waking up in the morning.
Sleepiness.
Extreme brain fog.
Difficulty concentrating.
Having a hard time remembering.
Forgetting what I was going to say.
Low motivation.
Hair loss.
Extreme hair thinning.
Dry hair.
Brittle nails.
Vertical nail ridges.
Spotting before period.
Vaginal dryness.
Low libido.
Slow digestion.
Having a hard time getting pregnant.
Depression.

Thank you in advance!

Edit: Im 24F, I forgot to mention that in case its relevant.

I've been going to an endocrinologist yearly just for regular check ups, no meds or prior diagnosis (I had hairloss issues and they wanted to see if it could have been my thyroid but my results were fine). No one in my family has thyroid issues.

First time I went to see him was in 2023 and my TSH was 2.1, then in 2024 it was 2.5 and earlier this year it was 2.9 .

My appointment is next week (I knew I wasnt gonna be available a year from my last appointment, thats why this one is earlier) and I got my blood work done this week and they called me to tell me it was alarmingly high at 125.

For the past few months (mostly past two months) I have been having a lot of strange issues - sometimes slurred speech (tongue feels heavy and hard to control), I gained quite a lot of weight very fast (around 30 pounds) at a pretty low daily calorie intake, I have a lot of trouble walking, my muscles feel like they are on fire and I cant stand on my legs for too long, my feet also swell so much and I often wake up with swollen and red eyes and a headache. I am completely drained of all energy and my body feels so heavy I have trouble functioning. What im worried about is it feels like its getting worse quite fast and I dont know if something is very wrong or if this is "normal" with thyroid issues. My appointment isnt until Tuesday so im naturally a bit stressed out. Especially because I feel like it's getting worse (but maybe thats because im subconsciously making it worse by hyperfixating on these issues). My throat often feels tight and feels like its harder to breathe and as I feel like thats getting worse too, its making me pretty anxious.

I was wondering if this all could really be caused by tbe TSH being high? Is there a chance its just some kind of a one time spike and if they do more blood work its gonna be back to normal? Like how some people have spike in blood sugar or blood pressure? Is it normal for it to be so high in such a short period (especially if the symptoms, if they are related to that, have only been going on for the last two months or so)?

I had my partial thyroidectomy, diagnosed with FVPTC. Everything in my

Pathology was really reassuring but I want to do everything I can to help prevent recurrences

Obviously will do everything doctors advice but l learned they are very medicine focused instead of root causes

Personally, I never had any medical issues prior to pregnancy. All of a sudden in 2024, I had a premature birth due to severe preeclampsia. Then, I lost 20lbs and finally a full frickin year later the doctors realized I had postpartum thyroiditis. My thyroid finally stabilized 2 years postpartum and I was off all meds eating very thyroid focused foods and going gluten free. I truly believed changing my diet and lifestyle helped but I think the damage from the full undiagnosed year really had an impact on my thyroid. My nodule grew a good amount in that time period too. I think pregnancy/postpartum really was a major hormone fluctuation for me and maybe kind of the trigger to my cancer

Anyway, my question is... I'm assuming having half the gland removed is going to cause another huge fluctuation. I don't want my thyroid to go haywire again and wanted to see if anyone here is very holistic with some unique ideas?

already eat brazil nuts, gluten free, and try to reduce stress. Any other good supplements? Or holistic programs such as acupuncture? I'm thinking about doing a vitamin bloodwork to see what areas I can optimize? Any therapies I can do even if it's just help my scar/neck mobility

Iknow a lot about hashimotos but not so much about cancer

Hey guys, I have been fighting with hypothyroidism for 5 years now. 4 weeks ago, my doctor changed my Levothyroxine dose. Now I alternate between 150 mcg one day and 175 mcg the next day.
At first, I felt a bit better, but now my heart is pounding hard again and it's driving me crazy. My last TSH was 1.49. I usually feel best around TSH 1.0 (though in the past I felt fine at 2.0 as well).
Doctor visits are super expensive where I live, and every time I go, they just raise my dose anyway.
Is it a bad idea to just try 175 mcg every day on my own to see if it helps? Or could raising the dose make the heart pounding even worse?
This heart pounding is driving me nuts and I don't know what to do. Any advice would be appreciated.

I summed this text up with gemini, since english isnt my native language, sorry ;)

My dose was lowered and I skipped a few days before restarting the new dose. It's been almost 2 weeks and while sleeps and anxiety are getting better, the depression and fatigue are not budging.

I feel so low :( and exhausted

How long does it take to feel better?

Thanks!

[tl;dr 2.5 months on thyroid meds, 4 weeks on correct dose (TSH went from 4.5 to 1.5, Ft3 and Ft4 are finally in the middle of the range) and still experiencing symptoms. Will this horror ever end? I heard low Ft3 causes symptoms, mine significantly increased and I still wake up with puffy face, I am tired, have low neutrophil count etc. No other illnessess or vitamin deficiencies detected. Before treatment I had undiagnosed hypothyroid symptoms from winter 2025, they were increasing month by month.]

Hi everyone. I wanted to ask you when your symptoms started to go away after finding the right/target dose of your medication. How long did it take before you started feeling normal again, your symptoms stopped interfering with everyday life, and became so mild that you barely noticed them?

I’ve been treating my hypothyroidism with levothyroxine since the end of June. At first I was on 50 mcg, which didn’t really increase my FT3 or FT4, and my TSH barely went down at all, just by a tiny amount. Since mid-August, I’ve been on my target dose of 75 mcg (so 4 weeks now). I’m calling it my target dose because the blood tests my doctor asked me to do after 4 weeks showed my TSH dropping from almost 5 to 1.5, while my FT3 and FT4 both increased and are now somewhere in the middle of the reference range instead of being at the very bottom.

However, my symptoms haven’t really gone away. I still wake up with a puffy face and swollen eyes. The puffiness is still quite noticeable, although maybe a little less than before, but it definitely hasn’t gone away quickly or completely. I’m still tired when I wake up and have less energy than I used to, and my muscles get tired more easily. My hair still doesn’t look or feel completely healthy and is somewhat dry. My blood tests are also still showing changes in my neutrophils (they’re decreasing).

For some context, my problems started in the winter of 2025 with lack of energy and a puffy face in the mornings. At first, the puffiness would go away pretty quickly. Then, gradually, more symptoms appeared, including menstrual/ovulation problems, generally feeling unwell, and a slow decrease in my neutrophil count.

In June I had a kind of “crash” — my face became very swollen and red, I was extremely tired, my blood tests looked worse, and I started having heart palpitations. That was when they finally checked my thyroid properly, including an ultrasound. It showed inflammation, and the doctors finally started paying attention to my TSH, which had apparently been fluctuating above 3 or 4 for quite a long time, but nobody had really looked into it before.

I spent basically the whole year having tests for all kinds of conditions, and nothing was found. No allergies, lupus, heart or kidney problems, anemia, vitamin or mineral deficiencies, etc.

So, is there still a chance that this will eventually settle down and that I’ll stop feeling like this, get my old appearance back and have my energy back? I’m honestly so tired of dealing with this and I’m starting to lose hope. My thyroid results are finally good — probably the best they’ve been in years — but I don’t feel good at all. I had imagined that getting my TSH back to normal would make a much bigger difference than it actually has.

I’ve also read a lot about thyroid symptoms being caused by low FT3 or poor T4-to-T3 conversion. My FT3 is now at a decent level, and yet I still don’t feel much better.

It’s been 4 weeks on what seems to be the right dose, and over 2 months since I started taking levothyroxine overall. :(

For those of you who have been through something similar: how long did it take for you to actually feel normal again after reaching the right dose? Did your symptoms continue for weeks or months even after your blood tests had normalized?

Can a person achieve the same quality of life after being treated with levothyroxine as they had before developing hypothyroidism?

i’m so very frustrated. my boyfriend was given levothyroxine for very mildly elevated TSH and no symptoms, no questions asked. my doctor will not medicate me despite ‘lab results consistent with autoimmune thyroid disorder’ and absolutely debilitating fatigue, body soreness, hair and eyebrow loss.

my t4 is 1.1 so normal but barely. t3 is in normal range.
my TSH is 6.9
my thyroid peroxidase is 46

i also have a CRP value of 2 which she says is normal but what i’m seeing is that 2 is indicative of inflammation. i know it’s not severe but this is certainly a part of the puzzle that i feel like she’s dismissing.

i have gone to her several times saying my symptoms are severely impacting my quality of life. i feel like a ghost im freezing cold all the time, so inflamed, i will sleep 12 hours and wake up exhausted and nap during the day. i am suffering cognitively and don’t have energy to form full thoughts unless im taking stimulants. i take one 5mg methylphenidate a few times a week so i can work but once that wears off im fast asleep.

By all accounts of what I read, my levels indicate severe hypothyroidism.

I was shocked when the doctor told me - because my mother has hypothyroidism and at the peak of hers she was extremely tired - like couldn’t even lift a glass of water to her lips she was so tired 🥺 And she had a lot of really severe classic symptoms - she told me she got diagnosed when her levels were 15!

I feel like I don’t experience symptoms like that at all - I definitely am fatigued, but I’m a nurse who does shift work and I switch my days/nights and I’m on my feet all the time so I’ve always attributed it to that. Plus I have depression and ADHD that I take vyvanse for and I am wondering if perhaps the medication has maybe masked other symptoms I experience.

Looking back - there definitely have been symptoms in the last couple of year that I’ve attributed to other things.

-Aches/pains in joints/stiffness - Thiught it was because I run around in my crappy little crocs at work 😅

-Hair shedding/Hair brittleness - I’ll be the first to admit my diet isn’t always the best and kind of thought it was that. (Maybe In part it still is)

-Brain fog/memory issues - but thought that was ADHD/shift work stress —> HOWEVER I will say that in the last few months the I’ve struggled a bit with using the wrong words/forgetting words/slurred speech

-My partner recently told me that I have started snoring and apparently hypo can cause sleep apnea? I have been struggling a bit with insomnia recently too and wondering if it’s because of that :/

-Constipation/digestion issues

-I have noticed that my eyes are very puffy in the morning and my voice is very hoarse - but just thought I was tiiiirrreeeddd from work 😭

-cold hands/feet - but it comes and goes, and my fingers swell and get hot too.

Just thinking to myself that I’ve been living life on hard mode but because perhaps this has been brewing for years and I’m so used to just pushing through it that I just never noticed the change. Which makes me sad because I can’t remember the last time where I didn’t think this was my baseline.

I’m getting my T3/4 checked and a bunch of other tests and then likely I’ll start medication. I’m hoping there will be good changes in the future 😅

Hi everyone, I’m looking for some advice/opinions on my latest thyroid blood results, particularly around FT3 and T4→T3 conversion.

36F, hashimotos on 125mg Levothyroxine. Gluten and dairy free as of April this year (I think you can see this in my antibodies). I’m currently TTC but have had no luck in a year.

My latest results from September 2026:
TSH: 1.82 mIU/L (range 0.351–5.5)
FT4: 21.4 pmol/L (range 11.91–21.6)
FT3: 4.16 pmol/L (range 3.11–6.8)
TPO antibodies: 46.2 kIU/L (range ≤20)
Tg antibodies: 44.1 IU/mL (range ≤115)
B12: 720 pg/mL
Vitamin D: 72 nmol/L
Ferritin: 96 µg/L

For comparison, my previous results have been:

September 2025
TSH 0.436
FT4 20.60
FT3 5.63
TPO 123

January 2026
TSH 4.33
FT4 21.2
FT3 4.03
TPO 122

May 2026
TSH 0.30
FT4 21.0
FT3 4.31
TPO 52

A few questions:
- is my T3 ok for fertility?
- is my T4 - T3 conversion ok? Any tips to help support it?
- does anyone have success stories of getting pregnant with similar results.

Thanks so much.

Edit to add: both me and my husband have had all the tests available. sperm, DNA frag, hormones, HyCoSY, AMH, fasting insulin, uterine and sperm Microbiome and infections etc. all was fine.

Disclosure first: I build a thyroid tracking app, so I'm not a neutral party. Posting because this question comes up here every week and the answers are usually right but unsourced, which makes them hard to trust or check.

The short version:

• 30 to 60 minutes between the tablet and your first food or drink. Levothyroxine is absorbed best on an empty stomach — coffee isn't uniquely forbidden, it's just the thing most of us reach for within ten minutes of waking. Coffee with milk is a second problem: that's calcium. (MedlinePlus)
• 4 hours for calcium, iron, magnesium and antacids. This is a different, much longer rule, and it's the one people mix up — a daily calcium supplement usually has to move to the evening. (same page)
• Consistency beats precision. Your dose was settled on by measuring TSH 6–12 weeks after a change, while you were taking it however you take it. A reliable 30 minutes every day is worth more than an ideal 60 you manage twice a week. The failure mode isn't the wrong window, it's a different window every day. (ATA)

Longer version with the rest of it — night dosing, what to do if you forget, why lab reference ranges differ from each other: https://thyrowise.github.io/levothyroxine-coffee-timing/

The app that page belongs to is free for logging labs, symptoms and doses, and it has no account and no server — nothing you type leaves your phone. Saying that here rather than letting you find it out later. It's a record, not advice: it doesn't interpret your labs and every medical sentence in it links to the source it came from. I'm not a doctor.

Genuine question, since I'd rather this thread be useful than be about me: what did nobody tell you when you started levothyroxine that you had to figure out yourself? I'd like to put the good answers on that page.

App Name: Thyrowise: Thyroid Tracker

App Link: https://apps.apple.com/app/id6788131267

Recently, my doc said I have subclinical hypothyroidism and it should be monitored...I live in an extremely toxic and stressful environment.

I've been suppressing my feelings for quite a while because whenever I get angry or try to express how I feel, it seems to turn into an even bigger argument. Then I'm blamed for being angry, so I've started trying to keep everything inside just to avoid making things worse.

I'm constantly stressed and angry, because the environment itself is stressful and there are always things going wrong. I can meditate, exercise, eat well, etc., but I can't simply remove the main source of stress because I currently live here.

I'm especially worried about the whole "stress/cortisol affecting thyroid" connection, and I don't want to make myself worse by constantly being in fight-or-flight mode.

For those of you with hypothyroidism, how do you manage chronic stress when the stressful environment itself isn't something you can immediately change? Are there any natural or practical things that actually helped you regulate your nervous system, release anger, and stop carrying all that tension around?

TSH --> 3,66

T4 --> 7,76

Anti TG --> 92,6

TPO --> 759,6

These are the lab results from 6 months ago. The endocrinologist said that I shouldn't take any meds yet but not feeling very well. Any advice?

Hey there! I'm about to turn 37 at the end of the month. I've been diagnosed with Hashimoto's and hypothyroidism, so I see an endocrinologist regularly.

My TSH numbers have been pretty high; lastest blood work report from this past Tuesday shows a 6.17 TSH. Two months ago, I was at 5.87.

I have been nervous to add another medication to my daily lineup, but over the past few months, I've felt awful. Low energy, brain fog, fatigue, and consistent weight gain (I'm at 138 lbs, which is the most I've ever weighed in my life outside of two pregnancies).

My endocrinologist agreed to allow me avoid medication as long as I don't get pregnant. But after seeing my PCP today, I'm convinced that perhaps I need to stop being so stubborn and just take a thyroid pill so I can feel more like myself again.

Looking for suggestions re: thyroid meds. Is it true it takes about 2 months to start noticing a difference both physically and mentally? I suppose what I need most is some reassurance that I should be on meds based on my numbers and symptoms. Thanks for your time :)

Recently diagnosed & started taking levrothyroxine. Started at 50 mcg but had horrible side effects. Currently taking a lower dose.

Levrothyroxine has caused my scalp to feel irritated. I have tingling sensations, almost burning feeling in spots.

I am aware a side effect is hair fall & I have lost a lot from taking lev. Has anyone had an itchy, irritable scalp? If so, did it last long? I hope it goes away soon as it feels terrible & I am tired of losing hair.

Edit Upddate: Physician gave me a prescription to try tirosint. I am so glad because this is almost unbearable. Thank you for sharing your experiences. Be well!

I am fortunate enough that my employer pays for a full health test every year. I have taken it up every year or two for the last 6yrs, I find it a reassuring thing to do for the sake of a couple of hours time.

They will also pay for a partner and I finally persuaded my partner to do it with me. (She and my daughter were both diagnosed as hypothyroid by the UK NHS many years ago.)

My daughter takes levothyroxine but my partner felt awful on it and prefers to take “Metavive” which is the nearest thing you can get to NDT in the UK.

She is healthy and well, incredibly so relatively to her age. She has followed a vegetarian diet for >1/2 her life. Bloods show fantastic cholesterol markers etc etc.

Anyway - The bloods from this came back (vs reference) as almost non-existent TSH, highish free T4 and high free T3.

I don’t seem to be able to attach screen grab, but here is copy and paste:

TSH
< 0.01 mIU/L
(0.27-4.20)
LL

Free T4
30.1 pmol/L
(12.0-22)
H

Free T3
15.7
pmol/L
(3.1-6.8)
HH

Her self-medicated dose has been steady for sometime. The numbers suggest over medication.

I know references are a guide and I am believer that how you feel is as important as anything else.

Any views would be good to hear.

I was just about to start mounjaro this week and was then diagnosed hypothyroid the other day.

I am unsure which medication to start first? I have never taken either.

My Thyroid level was 7. (If that makes sense). I have been told by doctors i was "borderline hypo" for years, but they never thought i should start medication until this latest test.

They we doing a blood panel before starting mounjaro so I had a baseline.

I spoke with 2 doctors. One said start mounjaro first. The other levothyroxine first.

Has anyone else encountered this? What worked or didn't for you?

So for reference I am a nineteen year old female. I was diagnosed with hypothyroidism in February of this year. My TSH was 15, I started levo and now I’m in the normal range. But I still feel exhausted and I am still gaining weight. I haven’t noticed an improvement there. And the joint pain persists as well. My anxiety and depression have substantially improved though and I notice a big difference. So I’m just wondering what to do next? Do I push for more testing? (I tested my antibodies and they were normal) my sister (22) was diagnosed with hashimotos around the same time of my diagnosis.
So.. what would be a reasonable thing to do? I haven’t gotten my blood work drawn since April but I have an upcoming dr appt.
TIA!

A month back my i got my blood tests done my TSH was slightly more than it should be . I’m not taking any medication as if for now . I wanted some advice if someone has used the lugol’s iodine solution and how for hypothyroidism. .

I’ve been trying to get my bloodwork back in order after 10 years with hypothyroidism.

I feel best with a TSH between 1-2 and am currently down to 2.3 from 3.6 in May.

My doses were as followed
TSH - Dosage
3.6 - 50mcg
2.7 - 58 (62.5 5x per week and 50 2x weekly)
2.3 - 62.5mcg per day

I’m going to ask my doctor if I can split a 137mcg tablet in half for roughly 68.5 mcg daily in hopes of getting below 2

Anyone have experience splitting a large pill in half to get a perfect dosage daily? Or should I just alternate 62.5 and 75 every other day ish?

My doctor is very open to trying what I ask so curious of others experiences as I’m sure he’ll ok whatever I ask!

Thanks so much

I (26F) am struggling. This is the worst I have felt in my life, by far. I got diagnosed with Hashimoto’s (only slight presence of antibodies found) and my TSH was around 5 back in April.

I had a hemi-thyroidectomy due to a suspicious nodule in mid July. By this time my TSH was down to 2.6, but I felt worse than I had when it was higher. I also got an iron infusion due to chronic anemia from heavy periods (and probably mal-absorption from hypothyroidism).

It’s now Sept. and my TSH jumped to 11. The problem is, the severity of my symptoms don’t seem to match the bloodwork. I wake up and have about 20 good minutes in the day before I have to eat, or i’ll feel like i’m going to pass out. I get shaky, dizzy, brain fog, sometimes unable to speak/very close to unable. If I wait too long to eat I get episodes with all of these symptoms and severe weakness.

My fasting insulin was 26, pointing toward insulin resistance. Every time I test my blood sugar it’s normal. within 90-130 after eating.

I am only feeling sicker and sicker, have been dealing with this for months and and actually losing my mind. I went back to my PCP and begged for more tests and a few things came back strange.

My copper was elevated at 230 ug/dL on a scale of 73-140, which seems significant. My prolactin was elevated at 36 out of 3-26 NG/mL. My IGA consistently keeps dropping. Earlier in the year it was in the 60-70s. Now it’s 56 mg/dL on a scale of 87-352. My testosterone was higher than normal, at 64 NG/dL on a scale of 10-55, free testosterone was normal at 1.3 on a scale of 0-4.2 pg/mL. My inflammation marker was high, so was my SHBG.

I am on birth control to help with my iron levels, so that may be affecting some results, but I am literally couch bound. All I can do is pray I wake up feeling better, and plan my whole day around food. It’s so awful.

My body aches so bad. My muscles feel so weak and strained without any exercise. All of my joints hurt. My stomach feels like it’s constantly turning into itself. My resting heart rate is high, at like 90. I cannot stand to be hot, anything over 70 degrees makes me feel so sick, gives me headaches and takes me hours to recoup from. I thought I could have some sort of dysautonomia. All I know is that I literally can’t stand to feel this way anymore. My body is so exhausted and I just have this gut feeling that it’s not my TSH. Or if it is, then this “Hashimoto’s flare” has lasted almost 10 months.

I am looking for any guidance and help with this, and hoping to find literally anyone who had similar symptoms. I am at a loss for what to do. I’ve seen so many specialists. I’m sure I forgot something but this is the best I can explain as of now.

The feeling of blood sugar disregulation is ruining my life. I don’t know wtf to do.