Thankyou for the information. I had not heard of myxedema. I will research this to see what all is involved….My eyes are not bulging as of right now-just had all the other symptoms and they have been coming and going. But I have since developed an old symptom: hands trembling and a new symptom that may or may not been related-severe memory loss. Don't remember if this is a Graves Disease symptom or not. I will have to look back at all the symptoms and see.
Hope to see my Endo docter real soon and get my blood levels and eyes checked.
Thanks again..everyone has been so helpful.
lkmanley

Hello. I'm still learning all about GD but I have read that smoking can increase TED symptoms.

Hope you feel better soon.

Thanks, I've heard that too, luckily I don't smoke But I know once you've been in remission, if Graves returns it can attack anything else-such as your eyes, skin, and muscles…I'm focusing a lot on my memory because I have forgotten very simple things that should not be occurring. I'm at the point I'm writing everything down and carrying a notebook with me everywhere I go.
Eyes have been fine for several days, hands still trembling.
Hoping for answers really soon.
Good luck to you as well….
Lkmanley

lkmanley
Thankyou for the information. I had not heard of myxedema. I will research this to see what all is involved….My eyes are not bulging as of right now-just had all the other symptoms and they have been coming and going. But I have since developed an old symptom: hands trembling and a new symptom that may or may not been related-severe memory loss. Don't remember if this is a Graves Disease symptom or not. I will have to look back at all the symptoms and see.
Hope to see my Endo docter real soon and get my blood levels and eyes checked.
Thanks again..everyone has been so helpful.
lkmanley

Yes, trembling hands & brain fog (memory loss, slowness) are some of the symptoms of GD, it is definately a good idea to get tested ASAP, the sooner you catch it the quicker you will be able to stabilise it. Even if you hadn't mentioned the other symptoms, the suspected TED would be enough for a former GD patient to get tested.
Make sure you also get tested for Thyroid Receptor Antibodies as well as the FT3, FT4 & TSH.
Not sure what your previous history has been, but often individuals will relapse if their initial treatment was very short and their levels stabilised quickly, it sometimes happens that FT3, FT4 & TSH all come good quite quickly, but the underlying antibodies are still present in higher levels and this often then results in a flare up down the track.
It is important to get antibody levels well within range before weaning off med's and to have routine testing every 3 months for the first year or two if possible to ensure any fluctuations are picked up early, there are not many doctors who will accomodate this level of care unfortunately though.

But I know once you've been in remission, if Graves returns it can attack anything else-such as your eyes, skin, and muscles…

You don't need to relapse in order for Graves to affect your eyes, skin, muscles, etc. I was somewhat stable on PTU for a year, then had RAI and six months later, developed TED. There was never a remission or relapse period.