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Welcome to Nikki Meador's Page

Nikki Meador

Nikki Meador

I am excited to share that on June 9th I will be honored by the Cystic Fibrosis Foundation at the annual Brewers Ball recognizing outstanding young professionals in Richmond.  I have committed to raise $3,000 to help the Foundation realize its mission of controlling and curing cystic fibrosis (CF).

About me:
I work for VCU Health in administration and am passionate about a career in which I help people daily to meet their healthcare needs.  I was drawn to VCU Health because of the mission for research and education where we are continuously advancing medicine.  The nomination to serve as a Richmond’s Finest Honoree merges my passion for healthcare and my passion for philanthropy into one! I am so honored to get to take a personal role in raising money and awareness for Cystic Fibrosis and am grateful for anyone that helps me by donating towards this effort!

You can help me meet my fundraising goal two different ways:
  1.   Make a direct donation
  2.   Purchase a $75 ticket to attend the Brewers Ball, one of the best events of the year in Richmond.  The event will take place June 9th at 7:00pm at the Science Museum of Richmond.  This includes all you can eat & drink, and a branded pint glass. 

Your generous gift will directly help support vital CF research, medical and education programs. Donating is easy and secure! Just click the Donate button on this page to make a donation that will be credited to my fundraising efforts. Any amount you can donate will be greatly appreciated!  If you prefer a cash or check method of donating please let me know. 

What is Cystic fibrosis and why should you donate:
Cystic fibrosis is a devastating genetic disease that affects the lungs and digestive system. More than ten million Americans are symptomless carriers of the defective CF gene. Advances continue to be made in finding a cure, but your help is needed now -- more than ever -- to help keep up the momentum of this life-saving research.

Sixty years ago, children with CF usually did not live long enough to attend elementary school. Today, because of Foundation-supported research and care, the median survival age of people with CF is about 40. This is remarkable progress, but not good enough. We continue to lose precious lives to CF every day. To learn more about CF and the CF Foundation, visit www.cff.org. Together, we can make a difference in the lives of those with cystic fibrosis.

Thank you for supporting the mission of the CF Foundation!

- Nikki Meador


raised of $6,000 goal

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