Chest pain with even small amount of T3? - Thyroid UK

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Chest pain with even small amount of T3?

jjyankee profile image
40 Replies

I'm new here and have a question/concern that I have not seen posted here. I was NDT and had to stop because of chronic chest pain (at any dose). I then went on straight t4 and felt awful- so now I've been trying to add a tiny bit of T3 to my 50mcg of synthroid and every time I try to increase just a tiny bit ( 2.5 mcg) I start having chest pains. I had a stress test done and doc said my heart looks great (no symptoms on treadmill or with exercise ever). On 3 mcg of t3 (twice a day) I'm ok- on 5mcg the chest pains start. I feel like crap on just t4 and even a smidgeon of t3 helps my low mood and energy. Anybody else have this issue with chest pain on low dose t3? I read about the doses of medication that folks here take and am dumbfounded. Does anybody here benefit from tiny amounts of t3? My integrative doctor also suspects that I am a very slow metabolizer of all meds. I've read 3 books on thyroid disease and just keep trying to get it right! I also take Vit D3, B complex, magnesium, vit C, selenium, and a basic multi.

Last blood test

TSH 4.5 (prior 2.7) 1 year ago - I felt better at these levels but NDT had the bad side effects (chest pain and anxiety/irritability even at low dose)

t4 .7 (prior .9)

T3 2.6 (prior 3.9)

I am very sensitive to medications in general and have never been able to increase my thyroid meds very much without tons of adverse effects.

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jjyankee
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40 Replies
Tristy profile image
Tristy

Hi jjyankee, I have no experience of this but I did see a post about this earlier today by sampydoodle which might help.

jjyankee profile image
jjyankee in reply toTristy

Thanks a lot Tristy - I'll look for it

Judithdalston profile image
Judithdalston

I added T3 to T4 ( 75 mcg) earlier this year starting off with 1/8 th of a 25 mcg T3 pill so little over 3 mcg, and got tight chest / palpitations along with raised Bp/ pulse but over a month gradually increased the dose upto 25 mcg. After about 3 weeks these symptoms literally disappeared overnight to normal Bp/ pulse and no palpitations/ tight chest ... so I personally would suggest be patient. Have you got a Bp/ pulse machine to test yourself at home- might help you introduce T3 confidentially?

jjyankee profile image
jjyankee in reply toJudithdalston

yep- I have a BP cuff- my blood pressure is always great (usually 110/60ish) but my heart definitely has increased some (I wear a fitbit). I will try to be more patient - thanks for your response @Judithdalston

Saggyuk profile image
Saggyuk

Have you had your vitamin levels actually checked - ferritin, B12, Vit D, folate and blood count? What levels were they?

Are you eating enough? I only mention that because personally I have difficulty tolerating higher levels of thyroid meds if I start to eat less as busy or something or my symptoms of deficiencies get worse if i take a higher dose - such as iron on my heart etc? My body doesn't want to work faster or more efficiently when I have either or these two issues so thought just worth a check?

Saggyuk profile image
Saggyuk in reply toSaggyuk

Also I would suggest you actually need T3 or higher meds if neither of those issues apply as you're not on enough medication in general as tsh is way to high and needs to be nearer 1.

I can't say much about your T3 and T4 levels without the ranges (the numbers in brackets after the result)

jjyankee profile image
jjyankee in reply toSaggyuk

Yes- TSH is too high- t4 and t3 is in bottom 25th percentile. However, I've been on meds for years and have never been able to raise much without horrible side effects- I honestly feel like jumping out of my skin and get so anxious and agitated and the chest pains- like I have all the symptoms of going to being hyperthyroid even with tiny increases. But the chest pains are a more recent side effect- I think I need to find the right ratio of t3 & t4- The ratio in the NDT was too much T3 for me and I think that is either 3:1 or 4:1

Thanks so much for responding to my post Saggyuk.

Saggyuk profile image
Saggyuk in reply tojjyankee

Hopefully you get to the bottom of it soon but please get those vits tested and bring the results back as what is in range is often out of date or not optimal for thyroids or treated adequately. Some of them like iron will cause heart issues :-)

SlowDragon profile image
SlowDragonAdministrator

Do you have Hashimoto's also called autoimmune thyroid disease diagnosed by high thyroid antibodies?

Low vitamin levels are very common result of Hashimoto's

Strictly gluten free diet often is helpful

Ideally ask GP for coeliac blood test first

amymyersmd.com/2017/02/3-im...

chriskresser.com/the-gluten...

thyroidpharmacist.com/artic...

scdlifestyle.com/2014/08/th...

drknews.com/changing-your-d...

thyroidpharmacist.com/artic...

jjyankee profile image
jjyankee in reply toSlowDragon

Yes, I do have hashimotos- other tha D my other vitamin levels were all fine

Marz profile image
Marz in reply tojjyankee

Please post your results with ranges - they may be fine but not OPTIMAL. B12 - Folate - Ferritin - VitD need to be optimal for your thyroid meds to work and for you to feel well ...

SlowDragon profile image
SlowDragonAdministrator in reply tojjyankee

So are you on strictly gluten free diet? Many with Hashimoto's find it essential. You won't know unless you try it

Multivitamins are not usually recommended on here, especially with Hashimoto's. They usually contain iodine, which is recommended we avoid

drknews.com/iodine-and-hash...

Vitamin B complex needs to have folate in rather than folic acid

chriskresser.com/folate-vs-...

Essential to have good vitamin levels

Vitamin D around 100nmol (Uk units)

Folate and B12 towards top of range

Ferritin at least half way in range

Other vitamins that may help

Daily vitamin C for adrenal support

Test zinc

Selenium supplements can help improve conversion of FT4 to FT3

Link about high cholesterol and hypothyroid

nhs.uk/conditions/statins/c...

jjyankee profile image
jjyankee in reply toSlowDragon

because I have methylation issues, I always take methylated B vitamins (never folic acid)

Also-thanks for link about statins- that is very useful as I was not aware of connection with hypo and cholesterol

Aurealis profile image
Aurealis

I’m sensitive to meds too. The advantage is that you are able to finely adjust meds to your body’s needs, but the disadvantage is more side effects. When I first took thyroxine I got some chest pain and I used to get it on increasing dose. I have read that it can be due to a speeding up of the heart following dose increase after a period of undertreatment which has led to some furring up of arteries due to high cholesterol arising from hypothyroidism. However, I used to tell myself it was just anxiety as it always resolved in a few days. Have you tried reducing synthroid first?

jjyankee profile image
jjyankee

I do have high cholesterol as well- and yes I have tried decreasing synthroid. Some days I seem to be getting better and then other days I don’t want to get out of bed because I’m so tired and incredibly depressed- but I can see that I’m certainly not alone in my frustration. My pharmacist told me that the therapeutic window for these meds is very small and it’s just a hard thing to treat effectively. I’m just so tired of it 😞

SlowDragon profile image
SlowDragonAdministrator in reply tojjyankee

High cholesterol is often a result of being hypothyroid

As Marz says, vitamin levels must be optimal, not just within range for thyroid hormones to work well

Add actual results and ranges and members can advise

jjyankee profile image
jjyankee

Thank you all for your input- I really appreciate it.

Marz profile image
Marz in reply tojjyankee

Are you on statins ?

HLAB35 profile image
HLAB35

Low iron or high/low cortisol can cause tolerance issues for some on NDT / T3. Read the following article about why that occurs.

stopthethyroidmadness.com/n...

Also, I'm not liking the sound of your 'multi' vits + a B-Complex - you may end up having too much folic acid in them when you add up the totals which for many people is not helpful. Large doses of folic acid given to an individual who has a vitamin B12 deficiency and not a folate deficiency can cause neurological damage. I much, much prefer methylated versions of folate and b12 as they don't require conversion to the usable forms. Conversion issues seem to be a thing for many with an under active thyroid.

wellnessmama.com/12543/foli...

b12-vitamin.com/folic-acid/

Marz profile image
Marz in reply toHLAB35

Great links :-)

HLAB35 profile image
HLAB35 in reply toMarz

Like this section explaining the different types of B12. It's really interesting.

b12-vitamin.com/types/

Marz profile image
Marz in reply toHLAB35

Do hope people read your links. I self inject B12 weekly - sometimes more - having been on my B12 journey for many years. Terminal ileum removed in 1973 - and I live with the consequences of medical ignorance ...

jjyankee profile image
jjyankee in reply toHLAB35

Yes, I've don a lot of reading about these differences as well, my B complex contains both Methylcobalamin and Adenosylcobalamin

Chippysue profile image
Chippysue

I just want to add that nutrition and good gut health is crucial for good health. Sadly the conventional doctors are not taught this. I highly recommend books by dr amy Myers and dr Isabella Wentz

Margiebess profile image
Margiebess

Hi! I have had great success with a compounded slow release T3 (3mcg) added to my ndt.

jjyankee profile image
jjyankee in reply toMargiebess

Does the slow release T3 interfere with your sleep? Thanks so much for telling me this-

Margiebess profile image
Margiebess in reply tojjyankee

Not if I take it before noon. When I was getting used to it I poured out about half of the capsule then worked up. It really makes a big difference in energy and mood. Funny such a small amount.

jjyankee profile image
jjyankee in reply toMargiebess

That makes sense- I take my second dose of t3 around 12:30 (can't take any later either). You are taking a small amount but it's added to the T3 in your NDT. It's strong stuff- some of us just don't need much. I think I'm going to ask doc for the slow release- only problem is that I'll have to pay for it out of pocket : ( but if it works it would be worth it.

Thanks for responding.

Wolfiesmom08 profile image
Wolfiesmom08

I'm in your same boat I'm really sensitive to meds I've tried a few. NDT had way too much T3 for me or at least not enough to T4. I had a lot of chest pain's and anxiety On NDT but then my doctor added 12 milligrams of T4 (Tirosint) and I started feeling better so I added another 12 and up to 25 and I felt OK, except that Tirosint gave me horrible headaches so I switched all together to another T3 T4 combo. It's been four years of not feeling myself. I just keep telling myself life doesn't have to be perfect to be wonderful . I tried to really enjoy the days I don't feel like crap. I add my T3 in 2.5 mg doses and it comes from a compounding pharmacy in it slow release. That has helped me. I've worked my way from 5mg to almost 15.

jjyankee profile image
jjyankee in reply toWolfiesmom08

Thanks so much for sharing this- how much t4 are you currently taking with the t3? I guess I'm just going to have to titrate VERY slowly. I also found the t3/t4 ratio in NDT to be too high for me- finding the correct ratio is my goal.

Wolfiesmom08 profile image
Wolfiesmom08 in reply tojjyankee

I take 112 mg of T4 and 15 mg of T3. My gut tells me if I just add a little bit more T3 I'll be great but my doctor won't let me because of my TSH. So next visit I'm going to try to convince her to at least give me more T3 and maybe lower my T4 since I don't think I'm converting. I still battle fatigue

jjyankee profile image
jjyankee in reply toWolfiesmom08

I called my Integrative doc today and asked him to call in a SR t3 at my compounding pharmacy and he agreed- (5mcg to start but could dump some out if I have adverse side effects) So I'm anxious to give this a try. I'll start low and see how it goes-

thanks again- sharing your experience was helpful

silverfox7 profile image
silverfox7

Your TSH is supposed to be suppressed on NDT, FT 4 can drop down the range but FT3 can be high but never over range. Does you doctor know this?

jjyankee profile image
jjyankee in reply tosilverfox7

Yes, my doc knows this but I’m no longer taking NDT because of side effects- currently trying to find right ratio of separate t3 and t4

silverfox7 profile image
silverfox7

The same applies if you are taking any form of T3

Goodlife1 profile image
Goodlife1

Yes I'm really sensitive to t3. T4 only doesn't relieve my symptoms though, so I have to add t3. I haven't found a perfect ratio yet, it's a moving target I find. Using 12.5mcg or 6.25mcg increases of t4 and 2.5mcg of t3, I've been tweaking for a year. I can either have good sleep, good energy and chest pain with higher t3 to t4 ratio or insomnia, exhaustion and no chest pain with lower t3 to t4 ratio. I don't think supplementing hormones will ever be like how it was having my own hormones produced. I think I prefer no chest pain and lower energy but I hate insomnia.

I'd like to try slow release t3 but getting standard t3 on prescription is difficult enough.:-(

130557Pine profile image
130557Pine

I was on synthroid for 15 years with compounded T3 which was not bad, but I became very sensitive to things I had taken for many years, such as foods and supplements. Then my dr. recommended WP thyroid and it was great! for a whole year I felt I had my life back. Then came the shortage of product, and I was switched to Nature Thyroid ... and 1 days later I began having shortness of breath and it just got worse and worse. Doctors thought I had pneumonia, and I developed this awful bronchospasms.... when i researched the bronchospasms, I learned that it was a reaction to something I'm allergic to .... and I thought again about NT... finally after 2.5 months of being really sick, with chest pains, sporadic heart palpitations, and feeling like I couldn't breath for 3-5 hours a day ... I stopped taking it, and the very day i stopped, it was like a cloak had been lifted off me. When WP was finally brought back, I was so hopeful, and to my chagrin, I started having chest pains etc. I stopped after 10 days. I had to go back to synthroid but I am starting ERFA ... if I have the same chest pains, I will have my compounding pharmacy put togehter a t4/t3 pill. It's probably the new product that is causing the alergic reaction.

jjyankee profile image
jjyankee in reply to130557Pine

Since writing that post I have found a solution- I now take Synthroid (50 mcg) (has to be brand name) with a small dose of Naturethroid (3/8 grain) and this is the best combination I have found- no Chest pain or hyper feelings. It took many months to work up to this dose of meds, and I still need to increase a bit more, but I feel like I'm on the right track. I came to this protocol after reading the book " The Functional Approach to Treating Hypothyroidism" by dr. Kenneth Blanchard- I'd read many thyroid books, but for me, this one made the most sense as related to my experience with t3 reaction.

I also got a script to switch to WP but couldn't get hold of it so stuck with Naturethroid.

Because of all the sensitivity issues that I developed I had to start over with only 25 mcg Synthroid and 1/8th grain NDT- then added t4 in 12.5 mcg and NDT in 1/8 grains verrrrrryyy slowly. Good luck to you- hope things work out better.

Lymeforyears profile image
Lymeforyears

Yes!! I was even lowered to 1.25 of t3 as 2.5 gave chest pains. We may try compounded t3 or a different brand as we are working on iron and adrenals etc as well. I was so looking forward to t3 and hopefully I will find a way to take it. (My t3 is very low).

Daffers123 profile image
Daffers123

F

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