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Rosie Thomas: How I Overcame Crippling, Hyperthyroid-Induced Anxiety
- Posted on Feb 14th 2012 5:00PM by Rosie Thomas
April Brimer
Five years ago, I didn't even know I had a thyroid. And if I heard the word, I may have related it to something that existed in outer space, not in my own body. I also didn't know how important it was to have one that was functioning well -- because when it's not, it will play games with your mind, for reals.
The thyroid is like the body's thermostat. If it's overworking it can make you feel crazy, anxious. If it's underworking, it can make you feel sluggish, depressed and super sad. Mine was overworking and, frankly, it made me feel mental. I thought I needed to move home and live with my mother. I had to cancel shows for the first time and though I didn't go and live with my mother permanently, I went and stayed with her on my grandfather's farm, to take a break from life for a while.
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I felt small and insignificant and embarrassed. "I was so brave once," I thought, and now I was so afraid. It's hard to describe to someone what anxiety feels like: I felt like I was invisible and the world around me looked so normal and I just couldn't find my place in it anymore. Nothing made me feel better -- escaping my body would have been my only relief -- so all I could do was endure it.
There are times in life when we can't get around what we are going through, when there aren't any side roads or backdoor exits or short cuts, and all we can do is get through it. I think of fishermen on a boat when the storm is coming -- it's too late to turn back, so all they can do is hope for the best, tie everything down and pray that they endure.
My anxiety was with me all day long. I would wake up with fear and panic in the early morning and it just never went away. I even started putting blankets on my windows to block out the sun -- that made me so sad. This went on and off for almost two years, and somehow I made a documentary, even got to be in a movie with Steve Zahn (so cool). I got engaged during that time, and planned a big wedding on my grandpa's farm with my darling loving mother, and married the greatest person I had ever known.
It is amazing what we are capable of. That's what I think about often -- how resilient we are. I learned some really valuable things during that time. I learned that I was lovable after all, even when I felt wholeheartedly that I had nothing to offer: No jokes, no songs, no laughter, no wit. "What was there to love?" I thought. Well, there was still me. Me, without my guitar and pretty voice and one heck of a wit, sure, but I still had value and I began to believe it. Rosie, without all that I thought I had to prove, was still valuable and still had something to offer, and that was so important for me to understand. I couldn't have understood that without my loving family and friends and my brand new husband reminding me daily that I would overcome this time and see beauty again and fit back into the world that I felt was passing me by and leaving me behind. My husband left "hopeful" notes for me all around the house, my brother would build me up every day, my father, Papa Tom, would constantly reassure me, "Your perspective is off, sweetie. Everything is the same, you just can't see it right now, but you will again." And one morning, I did.
For the first time, I lived my life simply. Fresh flowers in the house, a stroll down the street in the rain, watching movies that I never sat down to enjoy, having friends over for tea, writing songs in our living room window without the pressure if they were record-worthy, but with the pleasure that I could sing and make music, even if no one ever heard them. "Maybe they were just for me," I thought. I learned about joy. I learned that the small things are big -- I had just been too blind and too self-focused to notice them. I learned how to be a better friend and how to have deeper friendships. It was as if God himself allowed me to pause for a while and learn about all that I was missing out on. My life was passing me by because I was so career-driven, so passionate, so obsessed with how I was going to make a difference and impact others, that I wasn't allowing myself the everyday pleasures to sustain true happiness. Now I was getting it!
Here's what I know: Our bodies are imperfect. Things can break. It is how we handle it that makes all the difference in the world. Perspective is key. I went through my own bit of self-pity during that time -- and still do -- but the minute I do, I overlook that there is great purpose in the suffering. I don't think what happens to us is by accident, I think every event is purposeful: The good, the not-so-good and even the really bad ones. It changes us, doesn't it? It sharpens us, it grounds us and reminds us that we are just, in fact, like everybody else.
I am a person who wants to comfort people and because of the suffering I went through, I have even more compassion for people than ever before. I can promise you this -- some hardships seem as if they are here to stay, like they brought suitcases and a toothbrush along when they showed up, and we panic, but they do leave and the sun does shine down again and life continues, with a better you in it. Be hopeful and take comfort in that. It's true. Now when I sing, it comes from a much deeper place. My heart has more to shout about. I think it's saying, "Thank you," sometimes. Just, "thank you," because now it has even more reason to sing. It is with a humble heart that I share that gift with the world, and I hope most of all, it helps others feel less alone.
Thank you for letting me.
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I have had graves since I was 19, am now 30. I am taking medicine daily for it as I have opted out of surgery or RAI. I have dealt with the anxiety for years.... I have forgotten who I am anymore.... Hoping to one day regain that.
April 25 2013 at 7:26 PM Report abuse Permalink rate up rate down ReplyThank you Rosie for sharing this in so much detail . I am glad you have recovered. When you go through this like I am now you even with the people you love around you because all the thoughts and physical symptoms arefeel so very alone in the world going on inside your head. Like you I wake in fear and panic and never wears off. Well done for getting back your life and good luck xxxxxxxxxx
September 21 2012 at 11:25 AM Report abuse Permalink rate up rate down ReplyI had Grave's disease and didn't know it for about 5 years. I thought everyone else around me was the crazy one. It stated off sooooo gradual, change in skin, just crazy dry and itchy! Hair loss to the point of having to wear a wig! BOILING literally from the inside out, I stayed hot and unbelievably sweaty!! Uncontrollable body shaking, memory loss of basic things, having a conversation with someone and 5 minutes later not being able to tell you almost anything that we talked about. I should have lost tremendous weight but I stayed so depressed that sweets became my refuge. I didn't gain weight but I would have loved the weightloss I should have had:) I was finally diagnosed in 2007 but it took until I almost died June 8 2010 in the ER that it was actually addressed. I attribute the disease to stress and traced it back to about 2003 when my brother died. I took over raising his small son and my 2 small boys along with an his ingnorant maternal grandmother, losing my job, car repossed and losing my house to bringing it on.
If it wasn't for family, friends and my boys I wouldn't be here.....life SUCKED! Luckily
my Mom found a cardiologist to help me, I ended up doing radiation, thyroid medicine and heart medication at the age of 41! My levels weren't even chartable it was so bad! Bless that doctor, he did everything he could for but I finally got a job so I had insurance and was able to go to a endocrinologist. I did a really large dose of radiation that actually worked but now I in the opposite direction, which at first was WORSE than the Grave's disease!
I gained s ton of weight, memory loss, the skin again, depression again, not as much hair loss until my levels got better. At least now my levels are chartable! I am now on a great medicine but battling the weight. I still have moments of sadness when I reflect back, I'm soooo much better now but people don't understand how much this changes your quality of life. It's such a small organ but it controls sooooo much. When I told my friends about it at first they were all like Oh, no biggie I had it when I was pregnant but I'm like no you REALLY don't understand!! It wasn't until I had radiation the first time that they really got it that I was having tremendous issues.
I hate taking medication but I'm doing it....just sucks that it's for the rest of my life but I'll do it because to return to where I came from is SOOO not an option. God bless all those that are dealing with it as I am!!
hi rosie im not into her kind of music as i am a metal man but im so glad this gal is getting better. believe in god i say im living proof from my surgery ordeal!!
February 19 2012 at 1:52 PM Report abuse Permalink rate up rate down ReplyWhat an excellent article, Rosie. You said it so articulately, so graphically that it made everything you went through and all that you learned so much easier to understand for those of us who've never experienced this kind of thing. Thank you. I agree, I think everything we experience serves a purpose, to learn lessons about life and others.
February 19 2012 at 1:12 PM Report abuse Permalink rate up rate down Reply"-- some hardships seem as if they are here to stay, like they brought suitcases and a toothbrush along when they showed up, and we panic, but they do leave and the sun does shine down again and life continues, with a better you in it. Be hopeful and take comfort in that. It's true"
This meant so much to me today--Thank you.
didn't have to suffer so long. the right diagnosis and treatment asap is the answer
February 19 2012 at 12:19 PM Report abuse Permalink rate up rate down ReplyYes, but it can be difficult to find someone in the medical field who is knowledgeable or knows what tests to do or how to refer you. Years ago, I was diagnosed with sarcoidosis; thankfully, it's no longer active tho I still have the damage it left behind. I had visited the doctor several times about the symptoms and he always attributed it to something else. Thank God that I went out of town and became deathly ill, because I ended up at the emergency room of a large hospital in a larger city. Within 30 mts, I had 3 doctors in my room who specialized in treating the disease. When I returned home to follow up with my doctor, he knew nothing about this disease, and I ended up at Duke.
I'm very happy this lady received the proper diagnosis and treatment so she could get her life back. And I appreciate her sharing her experience with others who need that encouragement and hope.
Great story Rosie! Please let everyone know that hyperthyroidism (Graves' disease) is treatable with drugs, radioactive iodine or thyroidectomy and which treatment you chose.
February 19 2012 at 11:14 AM Report abuse Permalink rate up rate down ReplyGood on you for battling through. Welcome back, Rosie, we missed you.
February 16 2012 at 12:44 PM Report abuse Permalink rate up rate down ReplyGood on you for battling through. Welcome back, Rosie, we missed you.
February 16 2012 at 12:44 PM Report abuse Permalink rate up rate down Reply











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