Walk a Mile in Daschel's Genes
Thank you for visiting our page! If you’re here, you most likely have heard of Prader-Willi Syndrome. This makes you rare, because PWS is a rare disease! It affects approximately 1:15,000 people. This means that people who have PWS, most often, do not have the benefit of research-based interventions or the support of knowledgeable professionals.
That's why PWSA | USA is introducing its Walk A Mile in Their Genes campaign to raise awareness for PWS and celebrate Rare Disease Day 2023! Where so much of our PWS journey is beyond our control, we can continue to make our voices and our stories heard through advocacy and community outreach. By joining our "Walk a Mile" advocacy campaign, you can raise awareness about PWS, but also raise much needed funds that enable PWSA to continue to provide the services our community needs.
All funds raised will help to support PWSA | USA's work in Family Support, Advocacy, and Research! The best gift you could give Daschel to me 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 Gift
I'm leading by example / I donated- will you JOIN me?
Personal Progress:
of Goal
$1,340
Raised
$1,000.00
Fundraising Honor Roll
Carolyn Schweizer
$100
Facebook Fundraiser
$100
Facebook Fundraiser
$100
The Mattioni Family
$100
The Blount Family
$100
Cindy Szapacs
Evelyn Whiteside
Ed and Linda Szapacs
$100
Facebook Fundraiser
$60
Facebook Fundraiser
$55
Shayla Gahagan
$50
Facebook Fundraiser
$50
Facebook Fundraiser
$50
Facebook Fundraiser
$50
Facebook Fundraiser
$50
Facebook Fundraiser
$35
Wooldridge family
$25
Pat and Mike Leahy
$25
Facebook Fundraiser
$25
Facebook Fundraiser
$25
