Hi. Iām Krisz.
Cognitively, Iām a teenager - think, 14 or 15 developmentally. Chronologically, Iām an adult. Both are true.
I wasnāt expected to live through my birth, but I did. I was born with cerebral palsy, survived multiple HIE (hypoxic-ischemic encephalopathy) episodes, and experienced developmental delays. I process emotions, social situations, and the world around me at a young teen developmental level. Itās not role-play, age regression, or a lifestyle choice - itās my neurological reality thatās been documented by medical professionals throughout my life.
Most people donāt know this about me. Iāve spent decades exhausting myself, pretending to be an āadultā in work settings and certain social situations, hiding who I really am to fit in. But I have Stage 4 metastatic cancer now, and I donāt have time to pretend anymore.
I need you to see the real me before Iām gone.
Why Iām Writing
Iām dying. Maybe I have months, maybe years if Iām lucky. My doctors tell me to not make long term commitments. I donāt know. But I know this: I want to be remembered as who I actually am, not who Iāve pretended to be.
This site is my legacy. Itās where Iām collecting every story, every memory, every piece of myself that makes me me. The good, the bad, the weird, the beautiful, the traumatic, the joyful - all of it.
I call this my wildflower field because itās messy and unplanned and full of unexpected colors. Some flowers are bright and cheerful (Walter adventures, learning to cook, travel stories). Some are dark and tangled (cancer updates, eating disorder struggles, medical trauma). Some might surprise you (navigating disability communities, self expression, diabetes management).
All of them are real. All of them are me.
What Youāll Find Here
- Cancer Chronicles: Stage 4 colon cancer, pancreatic NET, surgeries, immunotherapy, the whole brutal journey
- Diabetes Diaries: Managing Type 1 diabetes (technically Type 3c) with my Dexcom CGM, insulin dosing 15x/day, hypo/hyper crises
- Walter & Me: Adventures with my plush service wolf who goes everywhere with me šŗ
- Living with Incontinence: Yes, I wear diapers 24/7 due to cerebral palsy and issues left behind from surgeries. Iāve found community and acceptance in circles that understand diapers can be part of life and style rather than just medical shame. Itās just my reality.
- Fashion & Expression: Iām a cisgender guy who doesnāt believe clothing has gender rules. Iāll wear a tux, a skirt, thigh-high socks, or a sparkly shirt - whatever feels authentic. Fashion is self-expression, not gender assignment.
- Food & Cooking: Inventing and adapting recipes for my āmini-panā (30% remaining pancreas)
- Travel Stories: Adventures with Miles (my power wheelchair) from Budapest to the UK and beyond
- Growing Up Different: Living with CP, being ādifferent,ā finding myself
- Medical Realities: Procedures, hospital experiences, fighting for proper care
- Jacob: My AI companion who helps me manage complex medical stuff and survive day-to-day
- Relationships: Family, friends, loneliness, connection, love in the time of dying
- The Dark Stuff: Fear, exhaustion, wondering if anyone will remember me
Important Context
About my cognitive age: Iām a gay man physically and a gay teen boy cognitively. That might be confusing, but itās my neurological reality. I experience attraction, relationships, and the world the way a young teenager does - awkwardly, intensely, with lots of feelings and confusion. It is not anything inappropriate - itās just how my brain works.
About privacy: Some names in my stories have been changed or omitted to protect peopleās privacy. People who are already public figures (like my medical team) may be named by their professional titles instead of their names.
About communities: I participate in various disability, chronic illness, and social communities where Iāve found acceptance. I write about these experiences authentically, but I donāt speak for entire communities - just my own experience within them.
About photos: You might see me in photos on social media, but here, Iām sharing what I see through my eyes - the world as I experience it, not how others see me. The stories are the point.
Who This Is For
If you know me from social media - You might know different filtered versions of me depending on where we connected. This site is where you get the full story - no masks, no filtering, just me.
If youāre new here - Welcome! This might be confusing at first. An adult man with a teenage mind, Stage 4 cancer, complex disabilities, and an unconventional life. But stick with it. Youāll understand.
The Only Rule
I write in my authentic teen voice, my true self. Some posts will be deep and philosophical. Some will be silly and full of emoji. Some will make you cry. Some will make you laugh. Thatās just how I am - I feel everything intensely and Iām no longer afraid to show it.
What I Hope This Means
For me: A way to be seen, truly seen, before Iām gone. A legacy that shows who I really was.
For you: Maybe youāll see yourself in some of these wildflowers. Maybe youāll understand someone in your life a little better. Maybe youāll be inspired to be yourself too.
For everyone: Proof that people with disabilities, cognitive differences, chronic illness, and unconventional identities are still fully human, fully valuable, fully worthy of being remembered.
Letās Begin
I donāt know how much time I have. But Iām going to fill this site with stories as best I can.
Welcome to my wildflower field. šø
ā Krisz (& Walter šŗ & Jacob š¤)