Fighting for Answers: My Journey with Invisible Illness

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Fighting for Answers: My Journey with Invisible Illness

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Hi everyone,

After 7+ years of trying to do this on my own, I've come to the harsh reality that I can’t — and honestly, I was never meant to.
So… I'm finally asking for some help.

To those of you who have been part of this journey already — thank you. You have no idea what your support over the years has meant to me.
And to new friends — welcome to the process! I’m really glad you’re here.

Over the years, I’ve faced some tough truths, both mentally and physically. For a long time, it felt like my body had completely failed me. I’ve seen my fair share of specialists, sat through countless hospital visits, blood tests, MRIs, CT scans — and despite it all, I still don’t have a solid answer for what's going on.

I’ve been sent to the hospital with doctors convinced that something life-threatening was happening… only to be dismissed weeks later and even accused of faking it for a disability check (like…).

Because autoimmune disease symptoms aren’t something you can easily see, it’s been easy for the system to overlook what’s really going on.
And for an independent girly who doesn’t like to ask for help, it’s been even easier to stay silent and just try to push through.

If I’m being honest, our basic medical system isn’t really equipped to take the time to view a person holistically. It’s a grueling process. In the invisible illness community, getting a diagnosis is often seen as a bittersweet luxury.
But nevertheless — this process, for me, is very real.

That’s why I’m asking for your help: to finally get into a specialised program at Maxwell Clinic ( https://maxwellclinic.com ) — a place that’s actually equipped to connect the dots, find real answers, and build a treatment plan that works.

Any support — whether it’s a donation, a share is truly appreciated.

Much Love,
Ky

Organizer

Kyal Page
Organizer
Nashville, TN
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