First diagnosed in 2011 have had 3 years of remission and it is back so just started carbimazole again and appt with Endo next week hopefully I know what to elect this time so don't feel so much in the dark just wanted it to stay away for ever
It's back: First diagnosed in 2011 have had... - Thyroid UK
It's back
((((Hugs)))) I'm really sorry to hear you have relapsed. I know the feeling when you say you wanted it to stay away for ever, that's how I feel right now.
Hope things are easier for you this time round as you say you are more knowledgeable this time round.
Sorry to hear that, Carefulkate. Don't let your endo bounce you into surgery or RAI if you are comfortable on Carbimazole. Research carefully before agreeing to your thyroid being destroyed.
I am just so bored by sitting still but my pulse races if I do the slightest thing and my muscles all shake Hopefully seeing Endo early next week just to discuss things hopefully I won't react so badly to carbimazole this time as I will keep the dose as low as possible Due to retire so hopefully that will help
thanks for the support x
Don't forget that there is an alternative to Carbimazole if you suffer side effects: propylthiouracil. It's usually known by its acronym (which I can't recall, now I need it! sorry). PPH? PPC? And although hanging on to your thyroid is, obviously, desirable - if you react badly with hyperthyroid meds there ARE alternatives. But you certainly don't have to go back on Carbimazole (which sounds as if it didn't suit you?).
PTU, Humphrey
I am not sure whether it was the carbimazole or just the hyper symptoms I lose muscle bulk and last time it was only my legs but ended up only able to crawl up the stairs and it was after I started the drugs this time started to lose before I took the drugs so it might be the hyper this time my hands are affected too which is miserable can't do much Still onwards and upwards the recovery was a could of months last time hopefully this time I will be as lucky x