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  • marza
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    Post count: 3

    Hi, Hope you are feeling much better by now?

    I am just replying as a newbie here and fellow Brit <img decoding=” title=”Smile” /> and would be grateful for any advice you may have. This site is great but information on treatment is generally on what is available in the US.

    I am 18 months in from diagnosis with initially very few symptoms apart from right eye involvement. I was euthyroid after 6 months on Carbimazole and gradually weaned down to a minute dose twice a week but never stopped completely. Its all kicked off big time now over the last couple of months, I became very symptomatic, especially with dizzyness and insomnia and my bloods were off the wall. I am back on 5mgs Carbimazole as well as 40mgs propanolol a day for high blood pressure and anxiety. The beta blocker has helped but I am absolutely devoid of energy.

    I am due to see my endocrinologist again in a couple of weeks and I will ask again about RAI, I was originally told that it is not appropriate treatment if you have eye involvement. Also sounds like it makes things a lot worse before it gets better? I would really appreciate any comments you might have.

    marza
    Participant
    Post count: 3

    Thank you for your prompt and encouraging response. I think I was lulled into a sense of false security with being initially diagnosed when reasonably symptom free. As you say, it is a permanent condition and I have just been lucky to have gotten on with it so easily up until now. Hopefully I soon will again. <img decoding=” title=”Smile” />

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