Please join us to raise funds for the Transverse Myelitis Association! Every penny counts. When our daughter was diagnosed at 13 months old we had no idea what TM was or what we could do to help our daughter. We were scared, alone and afraid for our child's future. Through the TMA we have been connected to other families and caregivers affected by TM, we have been given the opportunity to attend Camp each year, where our children get be kids and don't have worry about therapies and appointments. We have received educational sessions with leading doctors in neuroimmunological diseases. We no longer feel alone and scared because of the TMA! Please consider making a donation in honor of Alyssa. No one should be left in the dark and with your help the TMA can reach more hospitals and doctors to educate, advocate and raise awareness.