Not exactly, no. But, you have Hashi's, and Hashi's often starts with a false 'hyper' phase.
Hashi's is an autoimmune disease where the immune system attacks and slowly destroys the thyroid, mistaking it for the enemy.
During an attack, the dying cells leaks their stock of thyroid hormone - T3 and T4 - into the blood stream, causing levels of FT4 and FT3 to rise sharply, and the TSH therefore to drop, making it look very much like hyperthyroidism.
But it's only transient. The excess hormone is eventually used up/excreted, and you become hypo.
Unfortunately, doctors do not tend to know this - I cannot imagine why! And often diagnose Graves' instead of Hashi's.
To be honest I am not 100% certain but she did say today that I was Hyper initially and became Hypo.
It may be that she understands completely and used this phrasing to explain my results but on the other maybe she didn't 🤷♂️
But she was adamant I was in the perfect range /sweet spot and that increasing my dosage would do me more harm than good.
I did ask so what is causing my mood fluctuations.. and got no answer.
However she added thyroid to my blood labs and I mentioned that that I hadn't fasted or delayed my Levo.. this apparently doesn't make any difference. But I know different from this group chat.
Only you can know if you've reached your sweet-spot. It's not up to her to tell you! And, if you still have symptoms, you're not there yet. Doubt she knows much about thyroid - not enough to think it through intelligently, in any case.
gg explains it well regards to common “hyper” phases in early Hashis.
I just looked back at your posts and maybe I missed it but I don’t see anything that even reflects an initial hyper phase for your hashis.
Out of curiosity, do you have the test results that your GP was referring to when saying you were hyper?
Sometimes there might be difficulty for some out of the ordinary cases where hashi/graves hypo/hyper is harder to discern… but in my layman’s opinion I don’t think I see that in your history at all. Even you GP gave you 75-100 Levo as treatment which wouldn’t happen if they thought you were hyper?!
I haven’t read all your posts carefully so might be missing something, but just curious so thought I’d reply.
That just had me crying.. but only because it makes me realise it's real and a possible reason. For years prior to a diagnosis and not for the want of asking for a thyroid test. They were trying me on several different anti depressants which made me feel like hell.
I'm sorry to hear that but it does seem to be a thing with them to ignore the basics of good vit and min levels and hand over the drugs 😕... I too didn't have a clue until I found this forum
I find that I need 4000iu summer and 5000iu winter and that is to maintain a good level around 125... you have good levels of magnesium which helps vit D uptake, you could double your dose and see if that helps? What did the Grassroots calculator suggest for a loading dose?
This is what it calculated for me. However I was advised to try 3000iu for a while then get tested again.Would you consider going higher just to load and see if I feel better asap?
According to What my docs have told me recently.. While I'm Congenital Hypothyroid (as in born w/out a thyroid gland), it is possible to be over medicated, "making you hyperthyroid".. Do I believe it, Not sure anymore, the medical profession here in the states is lazy at best.. Absolutely Dismissive at worst.. I know doc's seem to have a hard on for goin by the numbers, but WE are more than just lab results.. Everyone is different.. for me, I was at my optimal and prime at .150 mcg.. However, over the last 8 years my docs have lowered me as far as to .75mcg.. I feel sluggish, my hair is brittle nails are brittle.. head aches, IBS.. though my mood is oddly ok.. not overly sad or happy, just kinda Meh.. but semi motivated, so it's an odd conundrum! They call it "Practicing Medicine" for a reason.. I'm sorry If I seem flippant, I'm not, I'm just seriously disgusted on the total lack of doctor's attention to someone, who's lived with this condition for 63 years, and know Way more about my body than ANY doc. . Endo or otherwise.. So it's frustrating, But as I said, as it pertains to being hypothyroid/hyperthyroid, most docs will tell you you are hypo, but over medicated enough to say hyper.. I hope that makes sense.. Also, for the record, in my opinion, doctors tend to err on the side of Low dose, as too much say, levothyroxine, can produce Osteoporosis.. which we all would like to avoid.
At least here.. If I feel like being labelled a "combative/non-compliant" patient, I could tell them that I am payin the freight (bill) Including imaging labs etc.. so they should really be listening to me.. but.... Hmmmm....
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