We cannot forget the heart and soul behind this cause. We are parents to a child who had Niemann Pick A (now known as ASMD), Wylder James. We have experienced extreme pain through the greatest gift of our life. We would have walk through fire if it would have saved our son. We are parents who can roar all I want about the unfairness of a disease, but instead we recognize that we are not alone. We are among other incredible parents who have and will warrior this fight. Parents who recognize there children have an incurable disorder and will love them all the way through it. Parents who will do all they can to protect their children from as much pain as possible, and then finally do the hardest thing of all, just as we did, parents who will love them until the end of their life, until they will be reunited in Heaven. We have learned that fighting for treatment options for this disease is a fight worth fighting for everyday. For the parents, warriors and families to come, we will keep up the fight. We have made remarkable headway in 6 years since starting Wylder Nation Foundation, but there is much more to do.
2020 has been full of hardships across the globe. For this reason we have chosen not to have a 2020 Living Like A Warrior Gala this year. That does not mean that the fight for this disease is wavering. It requires steadfast perseverance and a great deal of funding. We hope that you will join us, via the gift of the web, and see the value in fighting beside us and donate today. Treatment is closer than it has ever been. Thank you for considering a donation for the WARRIORS past, present and future. For Wylder.
LIVE LIKE A WARRIOR
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