Victoria the PWS Warriors's Walk-a-Mile in their "Genes" Campaign!
Victoria never ceases to amaze us. Despite the countless obstacles she faces, a multitude of diagnoses, and a life filled with medical appointments and procedures, Victoria is so full of joy and infectious smiles. Over the years, we have raised money for various other PWS organizations and this time we are raising money for PWSA to further support the Advocacy work that we've been doing for Victoria's future! Would you consider making a donation on her behalf?
PWS families are inspired by our loved ones with PWS, and PWSA | USA is taking action to ensure that all members of our PWS community have the benefit of passionate advocacy, exceptional family support, and life-changing research. Rare disease effects an estimated 30 million Americans, and PWSA | USA continues to work to meet the needs of our PWS rare disease community.
To celebrate Rare Disease Day 2023, PWSA | USA is introducing it's Walk A Mile in Their Genes campaign. So much of the PWS journey is beyond our control, but we can continue to make our voices and our stories heard through advocacy and community outreach. By joining our "Walk a Mile" advocacy campaign, participants will not only raise awareness about PWS, but they will raise much needed funds that enable PWSA to continue to provide the services our community needs. This virtual/in-person fitness challenge is open to all ages and fitness levels to promote health and wellness while supporting the Prader-Willi community. (But really, I don't care if you actually walk a mile or not. )
All funds raised will help to support PWSA | USA's work in Family Support, Advocacy, and Research! The best gift you could give to Victoria is a donation (in any amount) to support the important work of Prader-Willi Syndrome Association USA! Thank you!
Achievements
PWSA $1k Club
I've raised my first $1000 help me reach my goal!
Personal Progress:
of Goal
$1,745
Raised
$3,000.00
Fundraising Honor Roll
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