I know everyone here feels the same but I just have to say how many times I have gone to the website and felt enormously better after reading some of your posts. When I was first diagnosed, my TSH was 36. I felt ill for a long time, but the same as everyone else, it took forever to get diagnosed. Now I am on 125 mg of Levothyroxine and am feeling better. But I still worry about every little thing. Sometimes my insides shake so much I feel like I am going to explode. I have red dots on my torso that I never had, dry skin that I never had, my eyes are always so red that I look like I've been drinking (maybe I should). My legs ache, my fingers tingle and I cry at the drop of a hat - which I hate, hate, hate. I have trouble breathing and trouble remembering things. I was always so in control and this is killing me. But every time I get a new symptom, I look to this website to see if it is common to the disease (hypo with hashi's). At least if I see it here I know it is indicative of the disease. But I really feel thankful for this website which helps me to sleep at night. It let's me know that there are many others out there who are dealing with the same or even worse symptoms. Thanks to all who write here to help ease the minds of people like me.