When I Was Told That I Have Graves Disease

Last Updated on March 16, 2022 by Anna Baumann

When I Was Told That I Have Graves Disease

I didn’t know what an autoimmune disease was until I was told that I have Graves Disease.  I didn’t know a body could get so confused that it would start attacking perfectly good organs.

A few years ago I was feeling really crummy. I was sweating a lot. A LOT. My heart raced for no reason. My hands trembled, I couldn’t sleep and I felt anxious all the time. I had almost constant feelings of hunger and heartburn, along with other uncomfortable stomach issues. I was jittery and wanted to crawl right out of my own skin. It was so exhausting that getting through the day was like swimming through a deep pool of mud. At first I thought I was just getting old and hormonal so I tried to ignore it. But the longer it went on, the more I knew that something was horribly wrong with me. After a lot of doctor appointments and blood draws, I was told that I have Graves Disease.  My body was attacking my thyroid.

They put me on a drug called Methimazole. This was to calm my thyroid down and hopefully send me into remission. I started to feel a bit better. Some of my symptoms subsided. But then other ones took their place. And I never went into remission.

A close friend of Graves Disease is Thyroid Eye Disease. I found this out when my body started attacking my eye muscles. This caused my eyes to bug out of my head. Now I hate looking into mirrors because I look like a frightened frog. My eyes are always dry and burning, sunshine and headlights are painful, and it’s starting to affect my vision.

This is Thyroid Eye Disease

This Summer (2017) I had my thyroid removed and soon I’ll have surgery on my eyes. There’s no cure for Graves so I guess there’ll always be something I’ll have to do or fix because of it.

I’m an annoyingly upbeat person but it gets to me sometimes. I feel like somewhere along the way I’ve lost the person that I was before all this started. Like I see myself as two people now; Anna BG (before Graves) and Anna AG (after Graves).  Anna BG had lots of energy.  Everyone told her she had beautiful eyes and she hardly ever got sick.  Anna AG is struggling to get her energy back.  She looks freaky and she never feels quite right.

I’m very grateful that Graves is treatable. I might never feel 100% well, but I do feel better than I did. And who knows, maybe Anna BG will show up again one day. I catch a glimpse of her now and then so maybe she isn’t really gone for good…

To learn more about Graves Disease please visit, https://www.thyroid.org/graves-disease/

Annoyingly cheerful Graves Disease Warrior and Dental Office Lifer. Eager to share, help and connect. Big fan of kindness, food, ocean cruises, and reading books while drinking tea.

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