Ron Perryman, like most young dads, looked forward to seeing his two beautiful little girls when he came home from a long day at work. He lifted them in his arms, exchanged butterfly kisses, and bright, gummy smiles. Livy age five and LaLa age three are the pride and joy of their father’s doting heart. So, you can imagine the devastation Ron and his wife Amy felt in the Autumn of 2006 when he was diagnosed with the terminal illness A.L.S. (Amyotrophic Lateral Sclerosis). A.L.S, also known as Lou Gehrig’s Disease, is a brutal, unrelenting illness of the neurological system that strikes people between the ages of 40 to 70.  

The costs associated with the care and eventual loss of a parent stricken with this rare disease can be overwhelming. Social security and welfare are not the answer as they cannot even come close to covering all expenses. Each year corporations, businesses, and people like you seek charitable organizations to donate revenue. You are the answer. You can help two children who are about to lose the most influential person in  their lives—a parent. While there is no way to replace time, and there is no amount of money that can fulfill the place of a hug or a listening ear; there are opportunities for a college education, dance classes, good meals, trips to the park—all of which can be provided for with your donation

Ron Perryman, the son of Robert and Carolyn Perryman ( residents of Atlanta Ga,) and brother to Robert Perryman Jr. (former New England Patriot), Rorery Perryman, and three sisters Kim, Kelly & Kirsten was left

with only two choices after news of his diagnosis-- surrender to it or "Get in the game!"  Together with the help of his wife Amy Perryman daughter to  Bob and Geraldine Farrrow (residents Woonsocket RI) sisters Robin Sevigny, Barbie Sheehan & Chelsea Farrow started the Ron Perryman Trust. The money donated helped  establish a yearly golf tournament run each Columbus Day weekend