Graves' Disease Support Group

Sure...let us know about how much replacement med you are on too. Are your eyes more bothered too...?

{{{big hugs}} :-)

We will gladly help you.....the "regulars" on here long ago realized how VITAL it is to be properly medicated if we are going to feel well while having Graves' disease.

I am on a bit of a quest to help people from suffering the fates we have suffered from not being properly medicated.

Please, when you post your labs, list the ranges (they are often different from lab to lab, geographical region, etc) , date of the labs, meds dose you were taking at the time of the labs and corresponding symptoms.

This will provide a complete picture for us so we can adequately comment.

If you want to feel your absolute best, you'll want to maintain these types of records as you move forward - you will see a pattern and will be able to work with your doctor to "fine tune" your meds and feel great most of the time.

All the best,

Carol

I am on 125mcg at present time. My eyes are really no worse now, but no better either regarding the swelling and redness. I did get good news from eye dr 2 weeks ago. No optic nerve damage and she said my eyes are going back into place by their own, thank god for that. pressure is good. It feels good to get good news. thanks for your reply hugs

I also want to thank you mmz and cd for your help and will post labs when I get them

Fantastic news about your eyes...!

{{{hugs}}} :-)

hugs to you mmz thanks for all your help I am posting my new labs today please help me with them.