Dear Friends,
My name is Konrad, and I am the father of an extraordinary 4-year-old named Zion. Zion is full of life, laughter, and dreams, just like any child his age. But Zion is also battling LMNA muscular dystrophy, a rare and relentless condition that weakens his muscles over time, affecting his ability to walk, move, and one day, even breathe.
When we first heard the diagnosis, we were devastated. The future we envisioned for Zion seemed to collapse before our eyes. However, as parents, giving up is not an option. Every day, we are driven by a single hope: that a cure is possible. And with your help, we can turn that hope into reality.
The journey for families like ours is incredibly challenging. LMNA muscular dystrophy is rare, which means that research funding is limited, and support systems are scarce. That's why organizations like Cure CMD are our lifeline. They provide resources and community support and are at the forefront of funding groundbreaking research that could lead to a cure.
Your generosity can make a world of difference. Every dollar you give will:
- Support families struggling with the daily realities of this condition.
- Fund critical research aimed at finding treatments and, ultimately, a cure.
Zion deserves a future where he can play freely, chase his dreams, and live a full life without limits. Every child affected by LMNA muscular dystrophy deserves that chance. With your help, we can make it happen.
Here's how you can help:
- Donate: Contribute whatever you can. No amount is too small!
- Spread the Word: Share my fundraising page with your friends, family, and social networks. Let’s spread awareness so we can raise more!
Together, we can be the difference. Thank you for standing with us.
Your support means the world to me!
With gratitude,
Konrad