@DiscoBiscuitsRT#Brownie helping spread awareness for the rare genetic mutation my son is battling (CACNA1A) with little help from insurance companies. Thank you!
@BillyStrings Please follow Mick Foley, Mankind, Cactus Jack, Dude Love's Lead and spread awareness for the rare genetic mutation my sin Trey is battline Fundraiser by Kristi Levine : Support Trey’s Therapy, Equipment, & Medical Fund
@SenWarren can u please read and share my 3yo son Trey’s battle through a rare genetic mutation #CACNA1A. Not $1 is spent on research until 3 people w/ same variant are found. Trey is the only one with his https://t.co/rqx3DDjcyF
@BarackObama Can you please repost my son’s GoFundMe. Only a few hundred people in the world have #CACNA1A but my son Trey is the only person on earth that has what he has. U can imagine insurance is denying everything. https://t.co/rqx3DDjcyF
@JamBase@RelixMag@PeterShapiro@LiveNation@treyanastasio Please help me spread the word about my son Trey, who is battling a rare genetic mutation #CACNA1A. He can’t stand, walk or talk and insurance companies consider his equipment as “cosmetic” GFM: https://t.co/rqx3DDjcyF
@TomMarshall111 please follow Brian Moss’s (Spafford) lead and help raise awareness for my son who is battling a rare genetic mutation. https://t.co/rqx3DDjcyF