All posts byArthritis Foundation

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JA Mom: “I Know Just Enough to Know I Don’t Know Enough.”

Among patient partners who reviewedArthritis by the Numbers– a collection of verified arthritis facts and figures – was the Soler family of Georgia. Robin Soler has been active with the Arthritis Foundation ever since her younger daughter, Isabela, was diagnosed withjuvenile idiopathic arthritis (JIA). At the time she was one of the youngest children in the state to be diagnosed with JIA at just 12 months old.

Over the past 15 years, mother and daughter have seen about 50 different doctors and scores of other medical experts. Isabela has taken at least 20 different types of prescription drugs – consuming more than 15,000 pills in her lifetime, not including antibiotics and other normal childhood drugs. She has missed countless parties and playdates, and one recent semester had to skip 7thperiod 21 times for doctor’s appointments.

Isabela’s mother, Robin, is a developmental psychologist and senior scientist at the Centers for Disease Control and Prevention in Atlanta. Robin has had her own personal experience with arthritis, diagnosed withfibromyalgiawhen she was 26, though herchronic paingoes back to her mid-teens.

After reviewing arthritis statistics we’ve collected, Robin’s main takeaway: “I am happy to know there is information out there, but I’m concerned about the pictures the numbers paint for parents. We and our children need to be hopeful.”

Continue readingJA Mom: “I Know Just Enough to Know I Don’t Know Enough.”

kathy geller patient story

Rethinking Life With Severe Osteoarthritis

As part of our vetting process forArthritis by the Numbers– a collection of verified arthritis facts and figures – we invited patients to comment on the disease section that most affected their lives. After all, they are the experts on how the disease changes and challenges everyday living.

Meet Kathy Geller, who touched many lives during the years she spent as an Arthritis Foundation exercise trainer and education program presenter – a role model for successful self-management. Following, in her own words, is Kathy’s story about living with severe degenerativeosteoarthritis (OA)and how the statistics she reviewed in Arthritis by the Numbers relate to her personally.

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liz morasso patient story

Liz Morasso: Support Networks Helped Her Adjust to a New Life

As part of our vetting process forArthritis by the Numbers– a collection of verified arthritis facts and figures – we invited patients to comment on the disease section that most affected their lives. After all, they are the experts on how the disease changes and challenges everyday living.

Meet Liz Morasso, a licensed clinical social worker at UCLA’s department of radiation oncology who hasvolunteered for the Arthritis Foundationsince 2002. That’s when, at age 16, she was diagnosed withsystemic lupus erythematosus (SLE)andrheumatoid arthritis (RA). Over the years, she has immersed herself in leadership roles with the Foundation and speaks nationwide to inspire patients living with chronic illness.

Following, in her own words, is Liz’s story about living with these conditions and how the statistics she reviewed in Arthritis by the Numbers relate to her personally.Continue readingLiz Morasso: Support Networks Helped Her Adjust to a New Life

eileen schneider patient story

Patient Partner’s Words of Wisdom About Living With RA

As part of our vetting process forArthritis by the Numbers– a collection of verified arthritis facts and figures – we invited patients to comment on the disease section that most affected their lives. After all, they are the experts on how the disease changes and challenges everyday living.

来认识一下艾琳·施耐德,她是一名注册护士,热衷于为病人辩护。接下来,用她自己的话说,是她和别人一起生活的故事rheumatoid arthritis (RA)and how the statistics she reviewed in Arthritis by the Numbers relate to her personally.

Continue readingPatient Partner’s Words of Wisdom About Living With RA

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Voices: Have You Ever Hidden Your Arthritis?

Three influencers explain why they are outspoken about theirrheumatoid arthritis (RA).

Thérèse HumphreyThérèse Humphrey

@TerezHumphrey; TerezFreemanHumphrey

Diagnosed in 1986, I kept my RA to myself because no one understood. There weren’t any treatments to stop the progression, and my doctor told me I could end up in a wheelchair. I was scared, and I wasn’t sure myself what was going on, so why burden others? Maybe if I didn’t talk about it, it would just go away.

Keeping it to myself only made me feel more isolated. In 2011, I started using social media to find others with RA. It is there I found my voice. By talking about the reality of living with RA, I finally felt validated, and more importantly, I was giving others – especially the newly diagnosed – encouragement and hope. It took me a long time to realize that being open to others is vital to teaching them the reality and impact of RA. Today, I am a passionate patient advocate and want to educate everyone who’s willing to care and listen about RA.

Continue readingVoices: Have You Ever Hidden Your Arthritis?

sharae mansfield

Benched by RA, Pro Hoops Player ShaRae Mansfield Still Shoots to Win

ShaRae Mansfield vividly remembers getting the call 17 years ago saying the Houston Comets had drafted her to play in the Women’s National Basketball Association (WNBA). For the Western Kentucky University (WKU) student, the chance to play professional basketball was a dream come true.

But her WNBA career was short-lived. While she had mad skills on the court, excelling at both points and rebounds, she also had frequent pain in her shoulders, hips and especially her left knee, made worse by a torn anterior cruciate ligament (ACL). ShaRae had undergone six surgeries on it, but her continued knee problems led the Comets to release her before she completed even her first season.

Continue readingBenched by RA, Pro Hoops Player ShaRae Mansfield Still Shoots to Win

rheumatoid arthritis patient stories

Life Doesn’t Stop with RA: How Three People Keep Doing What They Love

Mark Rucker: “Adopt a healthier lifestyle”

mark ruckerWhen Mark Rucker was diagnosed in 2015 withrheumatoid arthritis (RA)at 44, he had mixed emotions. He was glad to know what had been causing the often unbearable pain in his hands, feet, jaw and toes for the past year. But, he recalls, “I always thought RA was a disease that only affected elderly women, not someone who was in the midst of training for their second Ironman competition.”

A real estate attorney in Lexington, Kentucky, Mark in the past had been a self-described “385-pound couch potato.” Being told in 2011 that he was too big to ride on the rollercoaster with his kids spurred him to change his lifestyle. He traded in sugary sodas for water, cut processed sugar and addedfruitsandvegetablesto his diet, and began to walk a mile each day during his lunch hour. He lost 135 pounds, and those lifestyle changes led him in 2013 to complete his first Ironman – a 2.4-mile swim, 112-mile bike ride and a 26.2-mile marathon.

Continue readingLife Doesn’t Stop with RA: How Three People Keep Doing What They Love

meg maley dating arthritis

Dating with Arthritis: Reality Couple Get ‘Real’ About What Works

Reality-star couple and Arthritis Foundation fundraisers Meg Maley, CBS’ “Big Brother” Season 17 houseguest and person withpsoriatic arthritis (PsA), and Mike Holloway, winner of CBS’ “Survivor” Season 30, share the real deal of their experience dating with arthritis as the third wheel.

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charcandrick west jia

Every Catch Deserves a Touchdown Dance

Charcandrick West, professional football player with Louisiana roots, gets real about what keeps him going, how no hurdle is too high and why he likes to win on and off the field.

Q1: When did you realize you wanted to play football professionally?

我不记得我第一次接触足球是在什么时候,但当我第二次接触足球时,大概是在6岁左右,我就迷上了它。我还记得当我还是个孩子的时候,从球场上抬头看到我的爸爸妈妈在为我加油。我为比赛付出了所有,让看台上的人感到高兴,这是一种兴奋。

I knew that I had the “it” factor – and my parents believed in me, too, which made all the difference in the world. My goal was to leave my legacy in my hometown of Cullen, Louisiana, and graduate to the “bigs.”

Continue readingEvery Catch Deserves a Touchdown Dance

Double Take: Twins with RA Fight It Together

Identical twins Annamarie and Ginamarie Russo share many qualities: They look and sound alike, they love acting and traveling – and both haverheumatoid arthritis (RA).

在将近20年的时间里,这对34岁的双胞胎姐妹都不享有风湿性关节炎。Ginamarie was diagnosed with juvenile RA (now calledjuvenile idiopathic arthritis) when she was 12; Annamarie was diagnosed 18 years later, at age 30.

Continue readingDouble Take: Twins with RA Fight It Together