Hey Chronic warrior,

You Belong Here

With Us!

Come join us if you are living with chronic illness, rare disease, long COVID, or are still undiagnosed. You are NOT alone!

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Meet Our Ambassadors

Audrey Q.

USA

Chlöe G.

United Kingdom

dawn veselka

Dani K.

Australia

diana boyesen

Jessica B.

Canada

Nicole W.

USA

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Meet Our NonProfit

PARTNER

Chronic Warriors Org, inc. is our non-profit arm that handles all the fundraising in order to keep our programs free for all of our amazing illness warriors!  They fundraise, apply for grants, partner with companies and organizations and work hard to keep our Collective growing! Check them out and shout out some love and gratitude. We couldn’t operate these programs without them!

Warrior Stories

EDS

EDS

Growing up, my stomach was my biggest problem. I got pneumonia when I was 10 years old, which led my stomach to reject anything I tried to eat after multiple rounds of antibiotics and steroids. After that, I was in and out of hospitals and dependent on an NG tube for...

Fighting 2 Rare Diseases

Fighting 2 Rare Diseases

I was diagnosed at age 8 with the rare, genetic disease Familial Adenomatous Polyposis (FAP), which I inherited from my mother. FAP is caused by a mutation to the APC gene and causes 100s to 1000s of precancerous polyps to develop in the cancer. These polyps will turn...

My Epilepsy Adventures

My Epilepsy Adventures

Every four minutes someone somewhere in the United States is diagnosed with epilepsy, and this is the story of how I became 1 in 26. My name is Robyn, and I’m an epilepsy patient from Maryland, and this is my story. My story begins on the evening of December 30th,...

Latest from the Blog

Doing well?!

Doing well?!

For the past couple weeks, I have still been getting used to my new job. It’s slowly becoming a routine for me now.  I personally cannot believe that overall, I have only had two days where I felt pretty badly since beginning this job. I  had no idea just how much the...

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