I was diagnosed with Graves’ disease back in January. I was started on Methimazole and propranolol because of the overactive thyroid (tsh 0.024) and an extremely high heart rate (over 140). I finally got to see an endocrinologist and found out I was on too much Methimazole and it caused my thyroid to go under active (tsh is now 80.66). Now I am experiencing extreme exhaustion, swelling in hands face and feet, tenderness and trouble swallowing around my thyroid, depression, memory problems, and many other symptoms. My dose of Methimazole was adjusted a month ago now but I don’t feel any better! Has anyone else experienced this? I don’t get more labs done until May 8th but I feel like everything is falling apart around me how do I cope with all this?