Finally after seeing different Gp am able to increase Thyroxine from 25 to 50, now 2 weeks in- pulse is up and I feel like heart beat is in my neck- i do have horrible cold which is flu like and sinuses are worse than ever-awful! Experiencing some palpitations at random times. Bp is fine no change. Is it just my yukky cold or increase-should i do alternate days on higher dose ? Or will it settle?
Same thyroxine brand, bloods showed me in bottom of range last year, GP i saw then wouldn't increase!! Next bloods in 3 months. Thanks
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Robinface
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Sorry you are feeling grim, a stronger heartbeat feels weird as likely you have been undermedicated for sometime but it is a good sign that your heart is getting what it needs for a change, how are you other vit/min levels as low iron and B12 can lead to palpitations.
I had private tests done last year but the GP i saw then wouldnt look at them let alone act upon them! B12 was low and have addressed with diet- hoping to afford repeat tests next month. Thank you for quick response, will see how it goes- hopefully when cold thing goes i will feel some benefit of increased dose! Thanks
Likely you'd do better on a good Vit B complex.... my daughter was investigating heart palps and it turned out her B12 was within 1 of the bottom range and ferritin low too. Luckily I had primed her to question the 'normal' on her results with GP and they gave her some tablets... pretty crappy ones though so self sourcing OTC often better 🤗
Medichecks often have a 20% offer each week on difference tests so keep an eye on them, if it's for TSH, T3 &4 then Monitor My Health do one for £29 but use the code to save 10% they have a new one which includes (see Below) for £65 monitormyhealth.org.uk/full...
If you're unwell with a cold and possibly more and have been undermedicated for a while then it's understandable that you are feeling changes in your body. 50mcgs of Levo is still a very low dose and likely some of what you are experiencing are hypo symptoms. It's common to feel a bit worse on lower doses as it's not enough hormone to replace what your system was putting out. Hang in there, get bloods done in 6-8 weeks at 9am with 24hrs since last Levo dose and post the results here.
hi restest hopefully next month when funds allow! taking vit D spray see pic below daily but struggled with the B complex- digestive issues left me unable to tolerate so increased diet levels- not ideal but better than nothing! Thanks
thank you, much appreciated! Will have a look- Shall i start them then do test in a month or 2 or longer? Are they recommended to halt before blood tests? Sorry my awful headcold making me dim today!! Thank you
careful adding supplements, only do one new thing a fortnight or you won’t know what is causing what when something gives you a dicky tum or spinny head.
I felt weird going from 25 to 50, took it alternate days for a week and then tried again and was much better. Going to 75 was easier and better still. 125 now and I walked 2.5 miles to work and 2.5 miles back today 💪
Gotta say though on 50mcg I felt worse of all. I used the advice here to pester the gp surgery with my £29 blood test results and insisted on a raise sooner in 8 rather than 12 weeks as my symptoms were so awful. Try it.. 3 months feeling like that is just horrific. The patient leaflets in the pill boxes say 3-4 weeks but that isn’t long enough for me to settle on a dose. Wishing you a smooth titration to good health 🌱🦋🌱
I have had heart palpitations quite bad since before Christmas. Long story but I had a second blood test this week. Text received from GP tonight to say I am low in Folic Acid and a prescription is waiting for me at Pharmacist! Having read about this deficiency it does explain some of my symptoms. I am not over medicated on Levothyroxine, I am currently under medicated!!! Heart palpitations and fast heart rate is awful, hope you get sorted soon.
lots of us have the MTHFR gene mutation that affects our absorption of vitamins like folate. I was recommended to take the methylated version (L-methylfolate) (same with B12) rather that folic acid for better results. I’m waiting on a blood test myself to see if this has helped. Just thought I’d mention it, be interesting to see how the folic acid version work for you 🌱🦋🌱
Hi. I don't think I have the MTHFR gene, well not to my knowledge! I have never heard of that. Never been folic acid deficient before. I eat plenty of green vegetables, oranges, etc so not sure why this has happened. My TSH has inceased in last few months. Blood results show folic acid at 2.6 which is below ref range of min 3.90. I now have 3 months worth of Folic Acid tablets, brand Crescent 5mg once a day. Doctor never asked about my diet and hasn't suggested a blood test after taking meds. Mind you he didn't bother speaking to me just a text!!!See how it goes. Hope your blood test goes ok.
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