I have just received my latest blood test results which, according to the lab and GP, are "normal, no further action". This is brilliant news for me as it means I can now take my thyroid health into my own hands, hopefully with your help and guidance. It has been an uphill struggle with my GP!
I have had three different results on the same dose of levo. They do not differ widely and I am wondering if, at least for the moment, this is a good dose for me.
The results were:
May 2018
TSH 0.29 (0.5 - 4.4)
FT4 18.5 (10 - 20)
FT3 5 (3.5 - 6.5)
GP not happy with this result. Thought treatment too aggressive but agreed to a further blood test to confirm.
22nd June 2018
Medichecks blood test results
TSH 1.7 (0.27 - 4.20)
FT4 16.700 (12 - 22)
FT3 4.05 (3.10 - 6.80)
I did the Medichecks blood test in case I needed extra ammunition to argue my case for staying on current dose. GP talked of reducing.
29th June 2018
TSH 0.83 (0.5 - 4.4)
The GP will, I think, be happy with this and not bother with me for a while.
I have Hashimoto's so realize levels can fluctuate and dose may need to be changed, also my later results are not as good as the first, even though my GP will prefer them.
What do you advise?
Thank you all so much for the support you have given me so far. I would have been totally lost without this site to turn to. I am so grateful.
Best wishes
Caroline
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Caroline888
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Yes I showed my GP Dr. Toft's article but he dismissed it out of hand. That is why I am so glad I don't have to see him again. When I next have to see a doctor I will see someone else. I tried to see another about the thyroid issue but he wouldn't do anything for me without referring back to the original doctor who stuck to his guns. He didn't know much about being hypo but was very dogmatic. I couldn't shift him and he was adamant that my TSH stay in range.
I did comply with all the rules re early fasting tests. All blood drawn at about 9.00 a.m. and no levo for more than 24 hours.
So do you think, based on my blood test results, I should stay on my current dose of levo, at least for the time being?
I totally agree with you, but the symptoms crept up so slowly it was easy to come to the wrong conclusion.
Glad you're doing so well. I will be 69 later this month and feel better than I have done for a long time. Thank goodness for this forum and, of course, for levo. I am at last seeing the light at the end of the tunnel!
You’re very generous giving up your time to helping on this site when you don’t actually have thyroid issues yourself! Obviously you would want to support your husband and have become very knowledgeable as a result. Those of us with hypo are certainly benefitting. Thank you.
Over the last 10 years or so I have been investigated for quite a few things but thyroid disease was never mentioned. A & E with chest and rib pains, MRI for tremor and taste/ smell disorders, DEXA scan for bone pain. Feelings of dread, anxiety. Never a diagnosis! Began to feel that the GPs had TIME WASTER written across my records. Now at last I can see that all those were symptoms of hypothyroidism and although they have not all gone, they have all improved, especially chest and rib pain which were the most frightening.
Am pleased your husband is doing so well on NDT. He’s lucky to have an expert on hand!!
Thanks again for taking the trouble to help and advise me.
Coincidentally I have just this year thrown out all Teflon- coated and aluminium cookware and replaced with stainless steel. A bit late perhaps but, as they say, better late than never! Foil has never really been an issue for me personally as I am a veggie and live mainly on salads, jacket potatoes and pasta but am still having to persuade the rest of the family that foil is not a good thing!
I do use a microwave oven though. I wonder about the wisdom of that!
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