Follow up to previous post . TT several years ago with brand Synthroid 125 mcg only as medication.
Added generic cytomel 5 mg daily in March and switched to generic Synthroid 125 mcg at the same time. Generic cytomel 5mg plus generic synthroid 125 mcg daily )
Labs in March before Cytomel was added
FREE T3 = 2.4 Range 2.3 -4.2
FREE T4 =1.2 Range 0.8 -1.8
TSH 0.13 Range 0.40 -4.50
Labs a few days ago approximately 8 weeks after Cytomel was added
FTEE T3 = 2.9 Range 2.3 -4.2
FREE T4 '= 1.4 Range 0.8 -1.8
TSH = 0.01 Range 0.4 -4.50
Any thoughts on these results please ? Do I need to decrease the Synthroid ?
Thanks
Written by
jarock
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Thanks for your input. RAI was not a part of my treatment I had TT due to noncancerous nodules. I would love to try NDT but I have tried several Docs who are against giving me NDT. I had to fight for the T3. I will try your suggestion while I keep looking for NDT.
Recommended on here that all thyroid blood tests should ideally be done as early as possible in morning and fasting. This gives highest TSH, lowest FT4 and most consistent results. (Patient to patient tip, best not mentioned to GP or phlebotomist)
Last Levothyroxine dose should be 24 hours prior to test, (taking delayed dose immediately after blood draw).
If/when also on T3, make sure to take last dose 8-12 hours prior to test, even if this means adjusting time or splitting of dose day before test
Is this how you did your tests?
When did you last test vitamin levels ?
What vitamin supplements do you currently take
Perhaps you need to try adding a second 5mcg dose of T3 and retest in 6-8 weeks
Honestly I feel much better with the added T3 than with the Synthroid alone. I still have difficulty losing weight despite watching my diet and going to the Gym 4 days /week
I had stopped both medications about 24 hrs before testing . Vitamin levels done in March were fine excepting slightly elevated B12. I will increase the T3 as you suggested. Another member suggested lowering the Synthroid with an increase in the T3 .
In my quest for wellness I am interested in NDT because it seems to work for a lot of people, but I have a difficult time getting a prescription. I think I will go back to the brand Synthroid during my next refill even though I will have to self pay. I have read so many negative stories about the generic versions. Thanks for your continued suggestions.
The recommendation when on a T4/T3 combination is a 3:1 or 4:1 basis. Your T3 dose is too low, I think. Besides, seeing that the blood tests were introduced along with levothyroxine alone, it is our symptoms that have a priority. That's how we used to be treated, i.e. given NDT and small increases every few weeks until symptoms were relieved and we felt well again.
Thank You. I was told that high doses of T3 will cause heart problems If I decrease the T4 to 100 and up the T3 to 25 (100/25 ) . Would that 25 mg be considered too high ? My Doc will not endorse this because he was even too scared to give me 5 mg , so I will make these changes on my own .
My next intention is to try NDT but I may have to source that on my own too. Thanks for your continued suggestions.
To my knowledge, you can't get any lower dose of Cytomel than 5 mcg. And I think whoever told you that high doses of T3 cause heart problems might be confused. Having high levels of Free T3 in your blood could be hazardous, but you would know that was happening because you'd have a racing pulse and/or palpitations. To get rid of hypo symptoms, you probably will need a high enough dose of Cytomel to get your blood level of Free T3 up into the top quartile of the range. That would equate to an FT3 of 3.725. You are currently only 32% through the range.
Thank you so much. I intend to try 4 : 1 T4/T3 ratio--100 mcg T3 and 25 mg T4. Starting out 100mcg T4 / increasing T3 by 5 mg weekly until max 25 mg. Then retest after 6 weeks . 5 mg daily is max amount that my Doc will prescribe so I am not even sure where to source the extra T3 .
When on levothyroxine when I was first diagnosed, (I was very unwell anyway due to being undiagnosed and TSH 100) levo didn't do anything for me but we struggle on as it is all new to us.
I was forever in and out of the cardio dept due to severe palps, espcially during the night. I had the usual tests and Cardiologist was puzzled and was considering putting something in my heart to 'figure out' what was going on. Shortly after the appointment T3 was added to T4 - palps stopped and I never saw the cardilogist again. I eventually went onto T3 alone.
I assume that a T4/T3 ratio is 100mcg T4 and 1/4 tablet of T3 as one 25mcg tablet of T3 is approx equal "in its effect" to 100mcg of levo then a 4:1 ratio would be 100 mcg of T4 and 1/4 tablet of T3. If I'm wrong someone will correct this statement. Read safely getting well on thyroid hormones:-
Are you saying that 4:1 T4/T3 Ratio would be 100 mcg levo and I/4 of a 25 mg tab T3 (approx. 6 mg T3.).?
On YOU TUBE there is a video with a doctor who recommends about 80 : 20 ratio for Synthroid to Cytomel . As an example he suggested. 100 mcg Synthroid to approx 20 mcg Cytomel. which is not exactly 80:20 ratio but it is close enough .
25mcg of T3 is equal, in its effect on the body, to approx 100mcg of levo. Therefore12.5mcg T3= 50mcg T4 and 1/4 T3 = 25mcg T4. Of course there may well be variations as most of us don't have identical experiences with thyroid hormones.
I should also state that I'm not medically qualified and also knew nothing about hypothyroidism - neither did any of the doctors/specialists I saw before I diagnosed myself when TSH was100. No doctor or specialist or A&E knew any clinical symptoms which they did before the introduction of blood tests which means many remain undiagnosed.
Due to my Total thyroidectomy it seem as if over the years I have developed poor T4 to T3 conversion , because I have borderline low FT3 on several labs. I have tried a low dose of cytomel but my FT3 remains low. Thanks for your response.
Just to add my " tuppence worth " and sorry I missed your post when recent, some 2 months ago.
A fully functioning working thyroid would be supporting you on a daily basis with approximately 100 T4 and 10 T3 daily.
I am with Graves post thyroid ablation with RAI and am now on Natural Desiccated Thyroid.
I did source and trial myself T3 and NDT, as I found no help or support within the NHS.
Both thyroid hormone replacements worked, but have settled on NDT since it's seems currently to be easier to source and somewhat less " turbo charge " as was my experience when I trialled a T3 and T4 combo.
I had TT years ago and used T4 only until about 5 months ago I added T3 . I will check my FT3 level again within a week . I think I will source and try the NDT if the T3/T4 combo is ineffective. Could you please PM me the source of your NDT. Thank you.
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