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Thank you very much for your help , yea sure could be something else getting old and grey here.
Hello new here, seem to be having relaspe.I took the radioactive iodine 15 years ago. I was going to a thyroid doctor and my md said he could take care of me about two years after i had the treatment now i feel he has not been correctly checking me. I have been begun to get the shakes again , muscle weakness, short tempered, and i feel weak allthe time. The doc keep saying my levels are correct, but i think not.I also since august have had pnemonia twice. I am wondering if my graves has something to do with this? I am headed to a new doctor in a couple weeks , she is a specialist yea dummy me listening to my md and quit going to a spec. I was wondering if anyone else has run in to a relaspe? I also was reading a post from Stu said he was having shakes and muscle weakness. I can tel you how mine came on, had the hand shakes for two years, doctors kept telling me i was depressed. They gave me a beta blocker, still ha dthe shakes and kept getting worse .I was going to get up out of bed and arms and legs would not work, rolled out of bed and could not get up.I finally got my wife and daughter to help me up went to hospital lol, they said i had gilbrees disease. They told my wife i was going to die , she started screaming. They kept pokin me for three days before thye found out i had graves.They said if i had not been on the beta blocker would have had a massive heart failure.. They tried the meds for graves didnt work, ended up taking the rad treatment , so Stu dont keep messing with your doc go to another one.
Hi, vrider, and welcome to our board. I’m sorry you are feeling so terrible.
The problem, from my point of view, isn’t that your doctor seems to be going only by the numbers. It’s that the doctor appears to have stopped thinking about what is causing your symptoms. You don’t mention that your doctor has looked for anything else. Perhaps he/she has and you didn’t mention it. It is, unfortunately, possible for those of us with Graves to turn up with another disease, later on in life. And the symptoms of a lot of diseases are shared. It’s one of the reasons many of us — me, as well as you — endured Graves a lot longer than necessary before the diagnosis. Those of us with Graves see those symptoms as "GRAVES!!," but sometimes it is indeed something else. So, what we need in a doctor is not someone who simply says, "It’s not your thyroid." The doctor can say that, but then needs to say, "But let’s see what it might be." And if the doctor doesn’t say that extra bit, WE need to say it to them to get their thinking jump-started. Anyway, I hope your new doctor is more help to you to figure out what IS going on. And, fingers crossed here that it is simply a function of taking slightly too much replacement hormone. Some of us (hand raised here again) have "some" thyroid tissue left after RAI. It’s not enough all by itself to make us hyper again, but with the addition of the replacement hormone, occasional dose changes need to be made.
Anyway, I hope you get your problem fixed and are feeling well again, soon.
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