I'm participating in the Hemophilia Walk on April 30th - a fundraising event to support my husband Jason, my son Jaizer and my daughter Presley who are affected by VWD- Von Willebrand Disease. This will be our second Walk, last years 6th Annual walk was our first year and we made it to 5th place. This bleeding disorder fundraising event will support the National Hemophilia Foundation. Inherited bleeding disorders are a life-long condition. Currently there is no cure, but scientists are actively engaged in finding cures and improving treatments.
That’s why I’m raising money and I hope that I can count on your support of this exciting event! Thousands of families in our community, and across the country will benefit from your support and the success of the Walk.
Select the link in red - Team JAIZER the "Spartans" -(make sure to select "Team JAIZER the Spartans" this way you will be registered under the correct Team)
If you like to participate in the walk Select "Join our Team"
If you like to donate Select "Support our Team"
You can also support my fundraising efforts by forwarding this email to as many people as you can to inspire them to donate as well! Every step does make a difference in the lives of people affected by bleeding disorders.
Thank you in advance for your support and together, we will make a difference.
The National Hemophilia Foundation is dedicated to finding better treatments and cures for inheritable bleeding disorders and to preventing the complications of these disorders through education, advocacy and research. "Coming together is a beginning. Keeping together is progress. Working together is success."