6 Ways to Love Your Body on Bad Days with a Chronic Illness
Here are some of the practices I’ve found that help me cultivate self-compassion, even on the hardest and most painful days.
Health and wellness touch each of us differently. This is one person’s story.
Upon entering the store, I did the usual scan with my eyes: How many sets of stairs are there? How many chairs? Where’s the door if I need to step out?
In the time it took me to calculate, my friends had disappeared into the colorful basement, their hands trailing on the racks of odd dresses and jackets as they went.
I took a deep breath, swallowed my misplaced anger, and took a seat near the door. It wasn’t their fault, I reminded myself. Our culture is not set up for understanding bodies that function differently. How could they know what it’s like to be shaking as I walked?
Here are some of the practices I’ve found that help me cultivate self-compassion, even on the hardest and most painful days.
Health and wellness touch each of us differently. This is one person’s...
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A 100 Percent Difference: Treatment for Graves’ Disease Helps Emily Enjoy College
For Emily Stein, the gift of an Apple Watch led to an unexpected diagnosis. Along with telling the time, delivering texts, and playing music, the gadget tracked her heart rate — and confirmed what the teenager already suspected. “I felt like my heart was always racing,” she remembers. “That was the first sign that something was wrong.”
When Emily started losing weight, had trouble sleeping, and was “more hyper than usual,” her mother knew it was time for her to see a doctor. During a visit with her local cardiologist, she learned that the problem was likely not with her heart at all. “They took one look at me and said I probably had Graves’ disease,”
For Emily Stein, the gift of an Apple Watch led to an unexpected diagnosis. Along with telling the time, delivering texts, and playing music, the gadget tracked her heart rate — and confirmed what...
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Back on Track: 3 Time Olympic Gold Medalist Gail Devers’ Story
Blink and you just might miss the fastest woman in the world. But you’ll never forget her champion’s smile, and her signature fingernails.
Gail Devers became a household name during the Barcelona Olympics of 1992. The young American sprinter raced into our hearts with one of the greatest finishes in Olympic history—a photo finish in the 100-meter sprint finals. Five women finished within 0.06 seconds of each other. Gail won the gold medal and the title “Fastest Woman in the World.”
People around the world instantly recognized her for her huge smile and her even bigger fingernails. But just two years before that race, it seemed like Gail’s racing days were over.
Blink and you just might miss the fastest woman in the world. But you’ll never forget her champion’s smile, and her signature fingernails.
Gail Devers became a household name during the Barcelona...
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Barbara Bush Lived a Full Life With Graves’ Disease
In the days leading up to First Lady Barbara Bush’s death, at the age of 92, news reports about her condition often mentioned that she had Graves’ disease. Those unfamiliar with this thyroid disorder could have been left with the impression that the disorder might have contributed to her death. That is simply not the case. When diagnosed and treated properly, Graves’ disease is not a fatal condition.
“Barbara Bush died with her Graves’ disease, not because of it,” Robert Courgi, MD, an endocrinologist at Northwell Health’s Southside Hospital in Bay Shore, NY, who has not treated Mrs. Bush tells EndocrineWeb, “If you recognize and treat Graves’ disease, patients should do very well.”
In the days leading up to First Lady Barbara Bush’s death, at the age of 92, news reports about her condition often mentioned that she had Graves’ disease. Those unfamiliar with this thyroid disor...
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Being Thin Isn’t All it’s Cracked Up to Be, Teen Says
Every girl I know wants to be skinny, but even at 98 pounds no one wants to trade places with me. It’s not that I’m anorexic or super short, but I have Graves’ disease, an overactive thyroid issue that causes unexpected weight loss, mood swings, irregular menstruation, hair loss, irregular heartbeat, hyperactive behavior, hunger, fatigue, etc. The list is crazy long but long story short, it’s a pain to have.
I was first diagnosed with hyperthyroidism in fourth grade, before I could seek refuge in social media’s female-friendly “accept yourself” ethos. If I could have found happiness in hashtags, I would have, but instead I had to see one of my best friends being called ‘fat’ for wearing a crop top and shorts when she was a little chubby.
Every girl I know wants to be skinny, but even at 98 pounds no one wants to trade places with me. It’s not that I’m anorexic or super short, but I have Graves’ disease, an overactive thyroid iss...
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Boston Marathon: Graves’ Disease Won’t Deter Sarah Cormier From Dreams
At least 90 percent of the time, we’re wise to follow our doctor’s advice, right?
Yet as we all know, the medical profession isn’t perfect. Just ask Sarah Cormier, who four years ago was diagnosed with Graves’ disease, a chronic autoimmune condition for which there is no cure.
“I was achy all the time and really tired, and I had been complaining about it to my doctor, who told me I should just get used to it,” Cormier said, “and that there’s not a cure, so I’ll get used to being tired and achy all the time. And I wasn’t a runner, so she said, ‘It’s not as if you’ll run a marathon or anything, but you’ll get used to it.’ ”
Today, Cormier has a different doctor. And on Monday, she’ll take on her first Boston Marathon, following her first experience at 26.2 miles at last fall’s Cape Cod Marathon.
At least 90 percent of the time, we’re wise to follow our doctor’s advice, right?
Yet as we all know, the medical profession isn’t perfect. Just ask Sarah Cormier, who four years ago was diagno...
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Diagnosed With Graves’ Disease Then Thyroid Cancer – Lorrie
A patient’s thyroid cancer story about diagnosis and surgery.
In this episode we hear Lorrie describe the following:
• Papillary thyroid cancer
• Long delayed pathology results
• Graves’ disease
• Balancing Graves’ disease and a thyroid cancer diagnosis
• Emotional roller coaster of feeling optimistic and other days of sadness.
• The feelings and emotions of related to a cancer diagnosis
• Being careful about the information shared on the internet and potential negativity
• Support network and family
• Nodule size was 1.1 cm, but with history of Graves’ disease, she decided to forego active surveillance
• The day of surgery and overnight in hospital
• The radioactive iodine decision
• Lymph node removal
• Traveling 4 hours to surgery center
• T4 dosage
• Change in life perspective
• Slowing down while making decisions post-diagnosis
• Acupuncture
• Multiple opinions pre-surgery
A patient’s thyroid cancer story about diagnosis and surgery.
In this episode we hear Lorrie describe the following:
• Papillary thyroid cancer
• Long delayed pathology results
• Graves’...
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Disability Story – Graves’ Disease
All throughout my teenage years I suffered from mood swings, irrational behaviour, panic/anxiety attacks, intense compulsive behaviours and bouts of depression. When I finally had the courage to speak to a medical professional about how I was feeling, the issues were disregarded and seen as a part of my teenage development.
When I entered my 20’s the symptoms that were once explained away with teenage development grew worse.
I had a hard time being active, I was lethargic, I was underweight, I couldn’t handle intense light, I shook constantly, and I was extremely sensitive to any kind of stimulation.
I was run completely by my emotions, would go into rages over nothing and would have panic attacks at any show of confrontation.
All throughout my teenage years I suffered from mood swings, irrational behaviour, panic/anxiety attacks, intense compulsive behaviours and bouts of depression. When I finally had the courage to speak...
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Graves’ Disease & Thyroid Foundation: Patient Stories
November 2015, I was diagnosed with Graves’ disease. Before that, I never put that much thought into the enlarged gland in my neck, which I thought was a result from my high metabolism and my vigorous physical activities. I kept telling myself, “I’ve been playing sports since I was 4 years old. I’m fine”. Last year when I noticed a visibly large lump and that my energy levels were low while doing my offseason football training in Atlanta, I made a quick phone call to my mother.
She lovingly demanded all the way from the DMV area [DC/Maryland/Virginia] to stop what I was doing and to go get a full physical. Thank goodness for urgent care facilities.
November 2015, I was diagnosed with Graves’ disease. Before that, I never put that much thought into the enlarged gland in my neck, which I thought was a result from my high metabolism and my vigoro...
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Graves’ Disease in Teens: Overlooked too Often
Plummeting grades, weight change, trouble focusing, it might be easy to blame your teen's behavior on the changes in adolescence. Your family doctor might suspect attention deficit disorder. But Graves' disease, a condition where the thyroid works overtime, can easily be overlooked in kids and teens.
Alissa Espinal loved performing on stage until she hit middle school. "I gained so much weight and I was so self-conscious about it," Alissa told ABC30. Alissa's parents also noticed their daughter had a hard time staying on task.
Plummeting grades, weight change, trouble focusing, it might be easy to blame your teen's behavior on the changes in adolescence. Your family doctor might suspect attention deficit disorder. But Grave...
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Graves’ Disease: Feeling Out of Control in My Body
I became aware that something was wrong with my thyroid as I was trying to fall asleep one night. Why did my heart feel like it was rapidly pounding out of my chest? Yes, I had a stressful moment that evening, but I was mostly calm when I got into bed. No amount of breathing exercises helped, and I called my doctor the next morning.
It took several months for me to transition off of a medication I was taking, get an EKG, find a different, kinder endocrinologist for a second opinion, receive my official Graves’ disease diagnosis, obtain the correct medication, and finally start navigating treatment.
I became aware that something was wrong with my thyroid as I was trying to fall asleep one night. Why did my heart feel like it was rapidly pounding out of my chest? Yes, I had a stressful moment that...
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Have Faith: Actress Faith Ford’s Struggle With Graves’ Disease
It’s Christmas time. A childhood dream is coming true for the girl from Pineville, Louisiana. As she gets ready to tape an episode of a hit new television comedy, she starts to feel hot and jittery. “Just nerves” is what people tell her. But then she realizes she is having trouble remembering her lines. It gets so bad that someone calls the paramedics.
“An anxiety attack,” they say. The young actress is given a glass of milk and a peanut butter sandwich. She knows that something isn’t right. Somehow, she pulls everything together to give her performance. But once the taping is over, the star of the show, Candice Bergen, gives her simple, and ultimately life-saving advice.
It’s Christmas time. A childhood dream is coming true for the girl from Pineville, Louisiana. As she gets ready to tape an episode of a hit new television comedy, she starts to feel hot and jittery....
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Her Unexplained Jitteriness and Weight Loss Were Telling Clues
For nearly a decade, Sherrill Franklin battled an elusive foe. She lost 22 pounds without trying. Her face was flushed, her neck felt sweaty and clammy, and she felt inexplicably jittery. At times Franklin, who lives in a rural community an hour west of Philadelphia, endured bouts of dizziness.
The result was definitive and so was the diagnosis: Franklin’s TSI level was sky high. Such an elevation is a hallmark of Graves’ disease, the most common cause of an overactive thyroid.
Graves’ disease occurs when the immune system attacks the thyroid, causing it to produce too much thyroid hormone. This hormone controls the body’s use of energy and affects virtually every organ.
For nearly a decade, Sherrill Franklin battled an elusive foe. She lost 22 pounds without trying. Her face was flushed, her neck felt sweaty and clammy, and she felt inexplicably jittery. At times Fra...
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How I Managed the Stress of Graves’ Disease During Pregnancy
So much of pregnancy is focused on the health of the growing baby, it can be easy to lose sight of the fact that the health of the person carrying them is just as important. The two are inextricably linked. This becomes even more apparent if, like me, the mother is dealing with a chronic illness. Throughout my pregnancy, I had the delicate task of treating my thyroid disease while keeping the wellbeing of my baby in mind.
So much of pregnancy is focused on the health of the growing baby, it can be easy to lose sight of the fact that the health of the person carrying them is just as important. The two are inextricably l...
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How Vanessa Vanderstraaten Copes With the Disease, Hyperthyroidism
On the surface, everything appears to be going well for 27-year-old actress-host Vanessa Vanderstraaten. She’s got the looks, a good career, and a sweet relationship with fellow Fly Entertainment artiste Andrew Lua to boot. Watching her radiate such energy and positivity on set and off, it’s hard to imagine Vanessa has been battling the disease, hyperthyroidism, since last April.
When did Vanessa Vanderstraaten first notice the signs of the disease?
It all began when Vanessa started losing weight without changing her lifestyle. Despite eating more than usual, the numbers on the scale kept dropping. “Back in April, I was really eating like a pig,” she says with a laugh. “I was hungry every two hours, and my typical daily meal plan went like this: breakfast, snack, lunch, snack, tea, dinner, snack, snack, supper!” Despite her voracious appetite, she lost 4kg within a month.
On the surface, everything appears to be going well for 27-year-old actress-host Vanessa Vanderstraaten. She’s got the looks, a good career, and a sweet relationship with fellow Fly Entertainment ar...
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I Have Graves’ Disease. Thanks to Running, I Got a Diagnosis Quickly
The endocrinologist says with some patients, the moment she walks into the exam room, she can tell they have Graves’. But that’s not me. My eyes aren’t protruding, thankfully, and I don’t have a visible tremor. My thyroid isn’t enlarged. But the blood work—measuring various levels of hormones—painted a clear picture."
It started when I was chopping onions. My heart suddenly sped up for a moment—three seconds at most—before returning to its normal rhythm. Like when you’re driving and press the accelerator, only to realize the car is still in park.
A few minutes later, I was standing at the kitchen sink, and it happened again. The pattern continued for a couple of weeks. My ticker would rev briefly, several times throughout the day.
The endocrinologist says with some patients, the moment she walks into the exam room, she can tell they have Graves’. But that’s not me. My eyes aren’t protruding, thankfully, and I don’t have...
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I Knew Something Was Wrong: Wanda Durant on Her Graves’ Disease Diagnosis, TED And Being Son Kevin’s Biggest Fan
Usually, when you see Wanda Durant, she’s all about the game of basketball. She can often be seen sitting courtside at NBA games, rooting emphatically for her son, Kevin Durant. She roots for him off the court too, uplifting him in all he does as an athlete who deals with a lot of unwanted commentary and criticism.
“I’m Kevin’s biggest fan,” she tells ESSENCE. “He’s always going to be Kevin and that’s it. I understand the arena in which he’s in and being a professional athlete, you are going to have some who love him, but some don’t. I’m still his mom so it doesn’t matter. It doesn’t matter what other people say. I enjoy him.”
Ms. Wanda is hoping to uplift others when it comes to a topic very important to her: Graves’ disease and thyroid eye disease. The mother, grandmother, entrepreneur, and philanthropist is someone thriving with Graves. She was diagnosed 17 years ago after suffering for years with alarming ailments.
Usually, when you see Wanda Durant, she’s all about the game of basketball. She can often be seen sitting courtside at NBA games, rooting emphatically for her son, Kevin Durant. She roots for him of...
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I Was Strong When My Body Was Weak – Christina Rouse
I remember competing in a soccer game when I was seventeen. After running one length of the field, I knew something was wrong. “Right leg, left leg, right leg, left leg,” I thought to myself, trying to will one foot in front of the other, but my legs were like dead weights attached to my body, as if the strings connecting my muscles to my brain had lost their elasticity.
Soon after, I was diagnosed with Graves disease. For seven years, I lived with the side effects of the condition, and there were many. My short term memory was faulty. I can vividly recall a trip to the grocery store with my mother.
I remember competing in a soccer game when I was seventeen. After running one length of the field, I knew something was wrong. “Right leg, left leg, right leg, left leg,” I thought to myself, tryi...
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I Was Weak, Despairing, Confused’: Did Writing a Novel Make Me Ill? – Sarah Perry
On Christmas Eve 2013, with hail falling on Norwich, I set out to jog three miles through the storm on the path beside the river. The spire of the cathedral was obscured by pearly cloud; snowdrops speckled the riverbank; it was pleasant to feel the little cut of ice on cheek. All this I recall with wonder, for that moment has crystallised in my memory as youth’s last day before, at the age of 34, old age struck me like a brick in a sock.
I cannot say when I first began to realise I was ill, for it came on me surreptitiously, with each new symptom readily explained. I was tired, probably; I was anxious, that was it: cared too deeply about the fate of my debut novel, of the work in progress. Yet by the following Christmas I felt as though I were a badly stitched garment coming apart at the seams.
On Christmas Eve 2013, with hail falling on Norwich, I set out to jog three miles through the storm on the path beside the river. The spire of the cathedral was obscured by pearly cloud; snowdrops spe...
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Jake: Graves’ Disease and Agent Orange
The Graves' Disease & Thyroid Foundation recently received an update from community member Jake George and is sharing his story with permission:
I received notification from the VA yesterday that my thyroid eye disease was approved secondary to my thyroid disease as a service related disability due to agent Orange exposure. I received a rating of 30% disability. What this means is the VA determined my thyroid disease was caused by my exposure to agent orange and my TED was caused by my thyroid disease so both are covered by the VA. If you are a veteran who was exposed to agent orange visit the VA www.va.gov to review the PACT act to see if you qualify.
The Graves' Disease & Thyroid Foundation recently received an update from community member Jake George and is sharing his story with permission:
I received notification from the VA yesterday that...
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Julia: Hindsight and knowledge are wonderful things
I am waking up from a nightmare and the sun is gingerly peeping through the clouds. This is how I feel as I hopefully enter the final stages of my thyroid eye disease (TED). It has been a long and arduous journey.
It took 15 years for me to get a Graves’ disease diagnosis by which point my TED was very prevalent and it was this that finally prompted the GP to test for Graves. Over that 15-20 years I had every single symptom of Graves’ and then some, in every one of them, the symptom was treated not the cause. I could list them all but I’m sure you are all fully aware of them.
I am waking up from a nightmare and the sun is gingerly peeping through the clouds. This is how I feel as I hopefully enter the final stages of my thyroid eye disease (TED). It has been a long and a...
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Life or Death: The Power of Health Advocacy | Emily Ross | TEDxYouth@AnnArbor
I assumed that constantly feeling bad was normal" - Graves' patient shares her challenges in getting a diagnosis and coping with chronic illness. (Note: the use of the word "chemotherapy" in this talk actually refers to Radioactive Iodine, which is administered in a single dose in liquid or capsule form).
I assumed that constantly feeling bad was normal" - Graves' patient shares her challenges in getting a diagnosis and coping with chronic illness. (Note: the use of the word "chemotherapy" in this talk...
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My Struggle and Success to Stay Positive While Struggling with TED
I admit that Graves' disease and thyroid eye disease (TED) challenged my natural positive attitude. The symptoms are relentless and unforgiving. Graves' wore me out with the struggle to regulate my thyroid levels with medication. Daily medication had never been a constant for me. I followed the doctor's orders but my body didn't cooperate...a strike against myself. Once diagnosed with TED after an exhausting two-year search, I was desperate to get my eye symptoms under control. Again, I did everything my TED advised but TED was stronger and more stubborn than me.
I admit that Graves' disease and thyroid eye disease (TED) challenged my natural positive attitude. The symptoms are relentless and unforgiving. Graves' wore me out with the struggle to regulate my th...
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Natasha’s Story – Hyperthyroidism
Natasha completed the London Marathon in 2019 after undergoing total thyroidectomy (removal of the thyroid gland) 18 months earlier to treat her Graves’ disease. In her candid blog, Natasha recounts the highs and lows of her journey with what she refers to as her ‘now non-existent thyroid.’
As I awoke to the noise of my alarm, I pushed snooze as fast as I could to get back to that all-important sleep as if it were just another normal day. Although this was not another normal day this was Marathon day.
Months of training, running in all weathers rain or shine. Trying out new classes to make sure that every muscle had a workout. Making sure that not only I could run but I was strong enough to do the distance. As the distances increased, the new aches and pains, and worry if they would last, or if in fact I had done some damage and would not be able to get to the start, also increased.
Natasha completed the London Marathon in 2019 after undergoing total thyroidectomy (removal of the thyroid gland) 18 months earlier to treat her Graves’ disease. In her candid blog, Natasha recounts...
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New UTC Coach Rusty Wright Thrilled to See Daughter Play Division I Basketball
After a crazy couple of weeks, Rusty Wright has had a few opportunities to be just a dad.
The new University of Tennessee at Chattanooga head football coach turned his phone off for four days during the Christmas holiday, focusing his time on his wife, Kelly, and daughter Maddie, a junior forward on the Belmont women's basketball team.
Since being announced as UTC's new football leader on Dec. 21, Wright has fielded texts or phone calls from former Liberty coach Turner Gill, former Louisville head coach Bobby Petrino and even Alabama coach Nick Saban, among many others. There have been numerous calls from career-long assistants, like Wright, who are happy to see one of their own get a chance to lead his own program.
After a crazy couple of weeks, Rusty Wright has had a few opportunities to be just a dad.
The new University of Tennessee at Chattanooga head football coach turned his phone off for four days during ...
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Olympic Track Star Gail Devers Opens up About Living With Graves’ Disease And Thyroid Eye Disease
Gail Devers was at the peak of her collegiate running career at UCLA when her health started to fail.
"My hands were constantly shaking, I had extreme fatigue and my eyes started bothering me," the Olympic gold medalist tells PEOPLE. "I lost so much weight that I looked emaciated, and I had sores on my face and my skin was peeling off."
Despite the strange symptoms and feeling unusually weak, she made it to the 1988 Olympics in Seoul. But at her hurdling and sprinting events, her body would not perform. "Something was definitely wrong," says Devers, 55. "I got there, and the bottom fell out — I ran slower than the first time I'd ever stepped on the track."
She came back from the Games and embarked on a three-year search for answers involving countless doctor visits. The 5'3"-inch athlete remembers her hair falling out in clumps and her weight dropping from 125 lbs. to 79 lbs. Friends, family members and teammates would ask if she was okay, but, she says, "I got tired of having to answer those questions — and of having no answers for myself."
Gail Devers was at the peak of her collegiate running career at UCLA when her health started to fail.
"My hands were constantly shaking, I had extreme fatigue and my eyes started bothering me," the O...
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Patient Story – Kimberly Dorris – A Comprehensive Analysis of Graves’ Disease
This episode is a thorough presentation of Graves’ disease from Kimberly Dorris, an educator and expert, and also a patient. In this episode, listeners will gain a thorough understanding of a disease that is often confused with other diagnoses.
Kimberly Dorris is the Executive Director and CEO of the Graves’ Disease and Thyroid Foundation, a small non-profit organization based in Rancho Santa Fe, California.
She began working with the GDATF as a volunteer in 2010, and took over day-to-day management of the Foundation in 2011. Ms. Dorris has a unique perspective on thyroid dysfunction, having lived with both hyperthyroidism and hypothyroidism. She was diagnosed with Graves’ disease in 2007 and took methimazole for seven years.
This episode is a thorough presentation of Graves’ disease from Kimberly Dorris, an educator and expert, and also a patient. In this episode, listeners will gain a thorough understanding of a diseas...
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Paula’s Story With Thyroid Eye Disease
Paula had a long journey with thyroid eye disease. Now she is using her experience to help at TEDct and support others whose lives are affected by the disease.
My name is Paula and I live in North Weald in Epping Essex. I am 45 years old, married with a daughter
Having suffered with Graves’ disease and thyroid eye disease myself I felt I could support fellow sufferers as I really understood what people were going through. It is a lonely disease that is both mentally and physically damaging.
It took a long time before I was diagnosed with Graves’ disease; my eyes were protruding, the right eye being worse; I was blacking out in hot rooms and felt generally unwell. After three years I had 95% of my thyroid removed followed by orbital decompression on both eyes 4 years later, thanks to Moorfields Eye Hospital.
Paula had a long journey with thyroid eye disease. Now she is using her experience to help at TEDct and support others whose lives are affected by the disease.
My name is Paula and I live in North We...
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Protect Your Eyes: A Baseball Player’s Story
Thyroid eye disease, also known as Graves' eye disease, sometimes occurs in those with Graves' hyperthyroidism. In patients with thyroid disease, the thyroid gland enlarges and produces excess hormones, which can cause an abnormal reaction in the muscles and fatty tissue around the eyes. Eye muscles and connective tissue in the eye sockets are particularly vulnerable to excess hormones, perhaps because the tissue contains proteins that the immune system recognizes as belonging to the thyroid gland.
Symptoms may include dry or watery eyes, a feeling of pressure in the eye socket, bulging eyes, sensitivity to light, double vision, or other vision issues. Swelling may cause the eyes to look puffy, and in some cases muscles may tighten and pull back from the eyes, causing a perpetually startled look.
Roughly one million Americans are diagnosed with thyroid eye disease each year, and women are more than five times more likely to get the disease than men.
Thyroid eye disease, also known as Graves' eye disease, sometimes occurs in those with Graves' hyperthyroidism. In patients with thyroid disease, the thyroid gland enlarges and produces excess hormone...
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UW’s Shawn Kemp Jr. Intends to Drive Past Graves’ Disease
Call it mother’s intuition, but Genay Doyal could sense something was wrong with her son, Shawn Kemp Jr.
Last summer, the junior forward on the Washington men’s basketball team began feeling lethargic, out of sorts, and he couldn’t keep food in his stomach.
“What really worried me and Pat (UW trainer Pat Jenkins) the most, he went from 255 pounds to 232 pounds and that was within two weeks,” Doyal said. “We were like, what is going on?”
Call it mother’s intuition, but Genay Doyal could sense something was wrong with her son, Shawn Kemp Jr.
Last summer, the junior forward on the Washington men’s basketball team began feeling leth...
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Trusted Resources: Community Center
Online groups, photo galleries, and blogs
Angels Announcer Victor Rojas Stays Strong for His Wife in Her Health Battle
6 Ways to Love Your Body on Bad Days with a Chronic Illness
A 100 Percent Difference: Treatment for Graves’ Disease Helps Emily Enjoy College
Back on Track: 3 Time Olympic Gold Medalist Gail Devers’ Story
Barbara Bush Lived a Full Life With Graves’ Disease
Being Thin Isn’t All it’s Cracked Up to Be, Teen Says
Boston Marathon: Graves’ Disease Won’t Deter Sarah Cormier From Dreams
Diagnosed With Graves’ Disease Then Thyroid Cancer – Lorrie
Disability Story – Graves’ Disease
Graves’ Disease & Thyroid Foundation: Patient Stories
Graves’ Disease in Teens: Overlooked too Often
Graves’ Disease: Feeling Out of Control in My Body
Have Faith: Actress Faith Ford’s Struggle With Graves’ Disease
Her Unexplained Jitteriness and Weight Loss Were Telling Clues
How I Managed the Stress of Graves’ Disease During Pregnancy
How Vanessa Vanderstraaten Copes With the Disease, Hyperthyroidism
I Have Graves’ Disease. Thanks to Running, I Got a Diagnosis Quickly
I Knew Something Was Wrong: Wanda Durant on Her Graves’ Disease Diagnosis, TED And Being Son Kevin’s Biggest Fan
I Was Strong When My Body Was Weak – Christina Rouse
I Was Weak, Despairing, Confused’: Did Writing a Novel Make Me Ill? – Sarah Perry
Jake: Graves’ Disease and Agent Orange
Julia: Hindsight and knowledge are wonderful things
Life or Death: The Power of Health Advocacy | Emily Ross | TEDxYouth@AnnArbor
My Struggle and Success to Stay Positive While Struggling with TED
Natasha’s Story – Hyperthyroidism
New UTC Coach Rusty Wright Thrilled to See Daughter Play Division I Basketball
Olympic Track Star Gail Devers Opens up About Living With Graves’ Disease And Thyroid Eye Disease
Patient Story – Kimberly Dorris – A Comprehensive Analysis of Graves’ Disease
Paula’s Story With Thyroid Eye Disease
Protect Your Eyes: A Baseball Player’s Story
UW’s Shawn Kemp Jr. Intends to Drive Past Graves’ Disease
10 Questions About Thyroid Eye Disease (TED) – Andrew Carey and Edward Kuwera
A Conversation With Dr. Raymond Douglas, La Peer Health Systems
Battling Graves’ Disease: When Everything Changed Podcast
Diagnosis and Management of Graves Disease – David Cooper, MD
Endocrine Autoimmunity Expert Recognized for International Impact
Listen to Your Eyes: Conversations on Thyroid Eye Disease
Management of Thyroid Eye Disease – Dr. Don Kikkawa
Talk Show Host’s Diagnosis Introduces Graves’ Disease to the Public
The History of Levothyroxine – The Most Prescribed Drug in the United States With Dr. James V. Hennessey from Harvard University
Thyroid and Pregnancy – Why It Matters, With Dr. Elizabeth Pearce From Boston University
Thyroid Immune Testing – Guidelines, Testing Platforms, and Clinical Impact on Women’s Health: An Expert Panel Discussion
What is Graves’ Disease? What is Hyperthyroidism? With Doctor David Schneider from University of Wisconsin
American Association of Clinical Endocrinologists – Facebook
American Association of Endocrine Surgeons – Facebook
American Society of Ophthalmic Plastic & Reconstructive Surgery – Facebook
American Thyroid Association – Facebook
Australian Thyroid Foundation – Facebook
Autoimmune Association – Facebook
British Thyroid Foundation – Facebook
Endocrine Society – Facebook
Graves’ Disease and Thyroid Foundation – Facebook
Graves’ Disease and Thyroid Foundation Moderated Group
Rare Disease Legislative Advocates – Facebook
TEDct: Thyroid Eye Disease Charitable Trust – Facebook
Thyroid Eye Disease Awareness & Education – Raymond Douglas, MD, PhD
Thyroid Federation International – Facebook
Thyroid Foundation of Canada – Facebook
@amthyroidassn
@autoimmune_diseases
@britishthyroidfoundation
@theendocrinesociety
American Association of Clinical Endocrinologists – LinkedIn
American Thyroid Association – LinkedIn
Autoimmune Association – LinkedIn
Endocrine Society – LinkedIn
Graves’ Disease & Thyroid Foundation – LinkedIn
@AmThyroidAssn
@austhyroidfdn
@AutoimmuneAssoc
@britishthyroid
@clinicalthyroid
@GDATF
@TheAACE
@TheAAES
@TheEndoSociety
@ThyroidEye
@ThyroidFed
@thyroidfriends
#WorldSightDay
Greater Than Graves’ Tumblr
How My Life Was Hijacked by Graves’ Disease and Thyroid Eye Disease
If You Put Your Stethoscope Over This, What Will You Hear?
Learning to ‘Rise and Fall’ With Cerebral Palsy and Graves’ Disease
My Treatment, My Choice: What Do I Need to Know?
One Step at a Time
Paciente con trastorno autoinmunitario de la glándula tiroides presenta inusual infarto al miocardio
The Autoimmune Association Blog
The Detective Work of Autoimmune Disease
The Truth About Chronic Illness in College
This Is What It’s Like to Have an Illness You Can’t Beat
When the Question ‘How Are You?’ Is a Painful Reminder
When the Summer Sun Means Finding Shade Because of Graves’ Disease
A Survey Study of Neuropsychiatric Complaints in Patients With Graves’ Disease: A Reassessment of Self-Reported Symptoms and Current Practice 20 Years Later: Graves’ Disease And Thyroid Foundation
Graves’ Disease in Our Own Words
Rare Is Everywhere
The Autoimmune Connection: Essential Information for Women on Diagnosis, Treatment and Getting on With Your Life
Find a Support Group
Helpful GDATF Links (Facebook, Physician Registry, etc.)
Hyperthyroidism Treatment Options – Updated August 2016
iPad and iPhone Apps for Low Vision
Looking for a Doctor?
Suicide Prevention Resources
#RAREis Scholarship Fund
AAHD Frederick J. Krause Scholarship on Health and Disability
Hannah Ostrea Memorial College Scholarship
Undergraduate Scholarship for Survivors
Co-Pay Relief Brochure