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Chronicling the good, the bad, and the ugly of rheumatoid arthritis.

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I AM INVISIBLE NO MORE

My three-part documentary-style film series for those living with invisible disabilities and illnesses is NOW LIVE on youtube!

 

Click here to watch

Please share these videos to help raise awareness

 

#MySymptoms Poem

This week many of us arthritis warriors raised awareness for World Arthritis Day on October 12th by either sharing our stories, statistics, or wearing arthritis gear. I recently shared a poem on The Mighty giving a glimpse into the symptoms I experience while living with rheumatoid arthritis. I am inviting you all to join in on sharing a poem about your symptoms through the #MySymptoms Poetry Link Up.

Making a Difference with Diversity, Equity, and Inclusion in Books

To help amplify the voices of diverse authors, I have curated a list of children’s books from the author community.

TheRAconnection.com- Join today, it’s free!

This year I began working with theRAconnection, as a moderator and blogger. If you are living with RA, PsA, OA, Lupus, AS or are a loved one, caretaker, spouse, friend etcetera, of someone you know living with these conditions, then you are in the right place! I have...

The Good, the Bad and the Ugly of a Total Knee Replacement

Growing up I remember doing class assignments that asked us where we envisioned our lives to be in five, ten, twenty years. Being diagnosed with rheumatoid arthritis at eighteen and having a total knee replacement at twenty-nine years old, was not on my radar.

Seven Go-To Shoes Those Living With Rheumatoid Arthritis Must Know About

I have been reviewing and recommending comfortable, stylish footwear for almost 11 years and I’m excited to share eight of my favorite go-to shoes I’ve owned over the years. You can read more about my journey with rheumatoid arthritis and how I started, BarkingDogShoes.com

15 Life-Changing Habits People with Chronic Illnesses Can Do All Year

I realized that as we get older, our priorities change. Those of us with chronic illness, autoimmune illness and various disabilities, usually have the same priorities as our peers, but the one thing that will always have to be the biggest priority is: our health.

Chronic Readers Club Q & A Interview

Chronic Readers Club was inspired by a combination of things. Since becoming chronically ill, I’ve felt a need to connect with other people who truly understand what my life is like. The idea to send books was inspired by my love of reading, which was instilled in me by my mom. She’s actually a librarian!

Breaking Free from Chronic Illness

Ways to break free from and cope with the constraints of chronic illness, in order to live your best life.

Arthritis Warrior Wednesday

Hi! My name is Erika. I’m 31 years old and I was diagnosed with rheumatoid arthritis at the age of 28.

Who Are Your Arthritis Anchors?

Now you may be thinking to yourself, well what is an arthritis anchor? Those who truly care and support us shine their light and help us navigate the ups and downs life can bring, by walking right beside us. These people are our anchors.

Why the Coronavirus Scare Resembles What It’s Like to Live with a Chronic Illness

As individuals, we all face unknown aspects of our lives at one point or another. Now as a collective, we are all in a state of unknown together regarding the COVID-19, better known as the Coronavirus. Mass fear and hysteria of the dangers of this virus have people in a fight or flight survival mode. It’s in our human nature to run from a threat and to protect oneself and loved ones. Though interestingly enough, many people who live with a chronic illness have experienced this survival mode on an ongoing basis.

Arthritis Warrior Wednesday

I was diagnosed with RA in 2012 after childbirth. I’m a full-time working mom in Los Angeles.

When I Was Questioned for Using a Disabled Parking Placard

Almost ten years ago, my integrity was questioned regarding my chronic illness and disability for the first time. I was about four years into my diagnosis with rheumatoid arthritis, and despite the dark cloud that loomed over my head on a daily basis, I felt on top of the world.

I’m a Nominee for the 2018 WEGO Health Awards- Here is how you can help!

I am excited to announce that I have been nominated for the WEGO Health Best in Show Blog Award in the 2018 WEGO Health Awards.

Soothing Winter Cauliflower Soup and Flatbread [Vegan and Gluten-Free]

Savory vegan cauliflower soup with gluten-free and vegan flatbread.

Two-Way Veggie Pizza [Gluten-free, Vegan]

A two-way veggie gluten-free vegan pizza that can be made with an assortment of vegetables with or without sliced tomatoes.

Arthritis Warrior Wednesday

I was diagnosed in 2012 while I was going for my masters in my mid 40’s. It was very aggressive and my father also had a very aggressive form of Rheumatoid Arthritis.

Connect2Health Conference and WEGO Health Awards Recap

If you weren’t able to tune into the WEGO Health Award ceremony on the main stage at Connect2Health via Facebook live in Boston last week, you can view some of the award speeches and more here.

Rheumatoid Arthritis vs. Social Life: How to Cope and Thrive

One thing that we aren’t sent home with though, is a prescription on how to navigate our social life- which is a big part of our mental and emotional health, that can be impacted greatly by illness.

Arthritis Warrior Wednesday

Hi everyone, I’m RA Guy! I’ve been living with rheumatoid arthritis for almost two decades now, since the age of 29.

Why the Coronavirus Scare Resembles What It’s Like to Live with a Chronic Illness

Why the Coronavirus Scare Resembles What It’s Like to Live with a Chronic Illness

As individuals, we all face unknown aspects of our lives at one point or another. Now as a collective, we are all in a state of unknown together regarding the COVID-19, better known as the Coronavirus. Mass fear and hysteria of the dangers of this virus have people in a fight or flight survival mode. It’s in our human nature to run from a threat and to protect oneself and loved ones. Though interestingly enough, many people who live with a chronic illness have experienced this survival mode on an ongoing basis.

read more
Rheuma Tips! Did you know? #17

Rheuma Tips! Did you know? #17

My tip for this month is to find a quiet place and take a moment to write down a list of everything you are grateful for. A friend of mine recently posted that you, “Can’t spell RA without Gratitude.”

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Arthritis Thought of the Month: Question #17

Arthritis Thought of the Month: Question #17

Are you grateful that you got sick? This question may seem a bit odd to some. Why on earth would you feel grateful for something like a diagnosis, that turned your life upside down? Those feelings and thoughts are valid. Then there is the other side of the coin, where people have been able to see the blessing and silver lining. It’s normal to one day feel positive and another negative about getting sick. How would you answer this question right now at this point in your life? Let me know in the survey below!

read more

Keeping it Real With Arthritis Stories

Whether you are living with rheumatoid arthritis or another type of arthritis, we all have a unique story that deserves to be voiced, heard and shared. Equally of importance, is showing an accurate depiction of those living with the disease and providing a real-life glance of who the person istheir interests, passions, hobbies, goals, career, likes, dislikes and so on, behind the veil of arthritis.

Not only can sharing our stories raise awareness but also illuminate our paths for us to see that we are not alone on this journey and have  common experiences with one another.

Rheuma tips! Did you know?

Arthritis Thought of the Month

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“On my journey with rheumatoid arthritis, I have realized that it’s not only about fighting the condition. Living with it one day at a time- is what it’s all about. Every day I chose to keep going, rise above, and embrace all the good, the bad, and the ugly of RA.” -Effie

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