My name is Valeria Martinez, and I am writing to you today to share my story and ask for your support in my fundraising efforts for Cystic Fibrosis research, advocacy, and support programs.
I am a 9 year old girl who loves spending time outdoors playing softball with my friends and family. However, my life is not like most kids my age. I have Cystic Fibrosis, a disease that affects my lungs and digestive system. It means that I have to do breathing treatments, take lots of medicine, and sometimes have to stay in the hospital.
Despite the challenges I face, I am determined to make a difference in the lives of others living with Cystic Fibrosis. That's why I am committed to raising awareness and funds for research, advocacy, and support programs that help people with this disease.
Thank you for your time and consideration, and I look forward to hearing from you soon.
Please support me!
We are at a pivotal moment in the history of cystic fibrosis and your support matters. With your help, we can invest our resources in research today, while raising funds for tomorrow, to ensure we have what it takes to reach the finish line. Together, we can make CF stand for Cure Found. Please help me reach my fundraising goal!
Hay aproximadamente 30.000 estadounidenses que viven con fibrosis quística. Son mamás, papás, hermanas, hermanos, hijas, hijos y amigos que luchan todos los días solo por respirar. Camino por ellos. ¿Te unirás a mí y apoyarás mi objetivo de recaudación de fondos?
IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated July 5th, 2023
The CF Foundation is committed to ensuring the health and wellbeing of individuals attending Foundation events. Individuals attending CF Foundation events must abide by the Foundation's Event Attendance Policy www.cff.org/attendancepolicy, which includes guidance for event attendees living with cystic fibrosis.