iamvisable – “Can you see me now?”

Supporting and empowering individuals living with an invisible, chronic illness.

iamvisABLE is a 501(c)(3) Nonprofit Organization that aims to utilize storytelling as a tool to connect, support, and empower individuals living with an invisible, chronic illness.

WHO WE ARE

Building community through storytelling.

Through shared narratives, we aim to amplify voices and foster a more inclusive and informed society, where every individual’s story is valued and heard.

STORIES SHARED
COUNTRIES
DONATIONS

Our stories connect us.

Join us in our mission of supporting and empowering individuals living with a chronic disease.

TAKE ACTION

Our Campaigns

  1. I Am – Relaunch Campaign

    The I Am – Relaunch Campaign aims to raise funds to reduce feelings of isolation for those living with an invisible, chronic illness and increase awareness efforts through storytelling and community events.
OUR MISSION

Our mission is to utilize storytelling as a tool to connect, support, and empower individuals living with an invisible, chronic illness.

Come JOIN US

Community Connect

A virtual group event aimed to foster connection, support, and empowerment around navigating life with an invisible, chronic illness. Join us in welcoming you and others into the iamvisABLE community. We’d love to meet you!

  • Virtual
  • February 27, 2025 @ 05:00 PM PST

Recently Published

Ellie

Ellie

manage you do chronic is the word they give you when you’ve run out of options“learn to live with it” they say, no cure – just pain managementso manage you do you push down the fear of what the future holds,the grief of what you’ve lost in the past you’ve had to grow up too fast  the…

Tiffany

Tiffany

“When people hear the word ‘epilepsy,’ they often think of dramatic convulsions or flashing lights. But what they don’t see—the part that lives in silence and shadow—is the reality of living with an invisible illness. For the last 15 years, I’ve lived with epilepsy. On the outside, I may look like I’m doing just fine….

They Just Don’t Know

They Just Don’t Know

They Just Don’t Know A Caregivers PerspectiveBlog written by Ray I can remember early on in my marriage witnessing acts of kindness by different men caring for their disabled wives while out in public. I thought very highly of those men. I would challenge myself, saying in my head, “Do you love Marisa enough to care…

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