• About
    • About Awareness Day
    • 2026 Awareness Day
    • Logo
    • Ribbon
    • Gallery
    • Committee
    • Latest news
  • Get involved
  • Patient stories
  • Mast cell info
    • About mast cell diseases
    • Mast cell diseases fact sheets
    • Expert interviews
  • Support
  • Contact
  • About
    • About Awareness Day
    • 2026 Awareness Day
    • Logo
    • Ribbon
    • Gallery
    • Committee
    • Latest news
  • Get involved
  • Patient stories
  • Mast cell info
    • About mast cell diseases
    • Mast cell diseases fact sheets
    • Expert interviews
  • Support
  • Contact
Contact
  • About
    • About Awareness Day
    • 2026 Awareness Day
    • Logo
    • Ribbon
    • Gallery
    • Committee
    • Latest news
  • Get involved
  • Patient stories
  • Mast cell info
    • About mast cell diseases
    • Mast cell diseases fact sheets
    • Expert interviews
  • Support
  • Contact
  • About
    • About Awareness Day
    • 2026 Awareness Day
    • Logo
    • Ribbon
    • Gallery
    • Committee
    • Latest news
  • Get involved
  • Patient stories
  • Mast cell info
    • About mast cell diseases
    • Mast cell diseases fact sheets
    • Expert interviews
  • Support
  • Contact

Luka

  • America

“I’m unnoticed and I’m unmistakable.”

Unnoticeable. Unmistakable.

Living with masto since 3 weeks of age

Luca is 13 years old and loves football, lacrosse and spending time with his friends. But he has been living with mastocytosis since he was just three weeks old.

His symptoms have included hives, dizziness, a drop in heart rate and severe reactions requiring emergency treatment. During one episode at summer camp, Luca needed three doses of epinephrine before being rushed to hospital.

Today, Luca can attend school, play sports and enjoy activities that once triggered reactions. But managing his condition still means daily medication, weekly infusions and the challenges of living with an illness that others can’t always see.

For Luca, it’s also about the embarrassment of being pulled out of class for testing or needing to visit the school nurse.

Every story matters. Share yours.

Like Luka, many people living with mastocytosis, MCAS and other mast cell diseases face challenges that others may not see or understand.

By sharing your experience, you can help raise awareness, build understanding and remind others that they are not alone.

Your story deserves to be heard.

Share Your Story

Other stories

Charlotte

Charlotte & Oliva

  • UK
“Some days we're absolutely fine... and then it can go polar opposite.”
Read story

Silvia

  • Argentina
"I was diagnosed with mastocytosis when I was 10 years old."
Read story

Luka

  • America
"I'm unnoticed and I'm unmistakable."
Read story

Sign up for our newsletter

Get updates from the International Mastocytosis and Mast Cell Diseases Awareness Day committee.

Subscribe
  • About
    • About Awareness Day
    • 2026 Awareness Day
    • Logo
    • Ribbon
    • Gallery
    • Committee
    • Latest news
  • Get involved
  • Patient stories
  • Mast cell info
    • About mast cell diseases
    • Mast cell diseases fact sheets
    • Expert interviews
  • Support
  • Contact
  • About
    • About Awareness Day
    • 2026 Awareness Day
    • Logo
    • Ribbon
    • Gallery
    • Committee
    • Latest news
  • Get involved
  • Patient stories
  • Mast cell info
    • About mast cell diseases
    • Mast cell diseases fact sheets
    • Expert interviews
  • Support
  • Contact
Facebook Instagram Linkedin X-twitter Youtube
  • Terms of use
  • Contact us
  • Terms of use
  • Contact us

© 2026 Mastocytosis & Mast Cell Diseases Awareness Day

© 2026 Mastocytosis & Mast Cell Diseases Awareness Day

Inactive

  • Causes
  • Events
  • Stories
  • Membership & Giving
  • Gifts in Kind
  • Causes
  • Events
  • Stories
  • Membership & Giving
  • Gifts in Kind
Donate
Facebook Twitter Instagram
  • Terms of use
  • Contact us
  • Terms of use
  • Contact us