Hello Chouchou, I’m sorry to hear that you are so upset. The Royal Osteoporosis Society have a free helpline that you could phone but unfortunately it isn’t open over the weekend. The Helpline is open Monday to Friday between 9am-12.30pm and 1.30pm-5.00pm.
Perhaps you could speak to someone before you have to speak to your consultant.
This ROS leaflet explains the test you have had done
I know it is ridiculous to say it (I could get an Olympic Good medal for worrying) but try not to worry too much, you will only be in an awful state by the time you meet your consultant.
Before you go, think about what you want to ask him, make a list with a few ‘bullet points’ not too many though or you will lose him.
If you have anyone you could take with you for support it might be helpful for you, if he seems rude then he is less likely to be if you are not alone.
Remember you don’t have to do anything you really don’t want to do, you also don’t have to start any treatment you aren’t ready to start or stop . Even if the doctor is grumpy about it. Take your time before you make a decision. Could you speak to the endo who put you on T3 for advice?
Have you posted anything on the Thyroid U.K. part of Healthunlocked? You might be able to get more help on there.
In the meantime - try not to worry and try to speak to someone on the Helpline before you meet your consultant.
My last blood tests don’t show hyperactive thyroid - but having the PN1P is showing high turnover.
The problem is the endo is very dismissive and last time we had an argument as he didn’t want to raise my t3 when my level was only 4. 4.1 to 6.8
My liver markers were excellent last 2 times and when I saw the bone specialist she was not alarmed by anything. I have researched the upper level is 69 and I’m 109 .
Thank you again for the kind words and suppport.
I’m petrified they will take away the t3 medication and I’ll be back to being a vegetable in bed and in despair.
It’s only the past 2 months I’ve started to deal with the years and years of trauma. By being told I was a waste of space and disgusting as I was so tired and in pain and couldn’t eat when my t3 was 2.1 .
I can imagine how desperate you feel about even the remotest thought of losing your T3.
T3 is a lifeline for so many thyroid patients and yet it seems to be dismissed. In all the time I was being treated for Graves’ disease years ago I never ever had my T3 tested. In the end I started doing my own home blood tests because of that.
The HRT ought to help your bones so that’s good.
Is there anyone you can take with you to the consultation for support?
Good luck, I’ll think of you and send really good vibes to you on Monday 😉
We just wanted to drop by as it sounded like it was a really stressful time receiving the results you mentioned. As others have already noted, please don’t hesitate to look at our information on our website theros.org.uk/information-a... or call our helpline if you want further support.
We really hope that you find the support you’re looking for and wish you all the best,
Please reach out to our friendly specialist nurses on 0808 800 0035, they will be able to talk it through with you. We are unable to give to give clinical advice on our forums, so the best place to contact is our helpline as it's important you feel supported in your situation.
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