Mom with ALS Seeking Support for Treatments

My name is Melissa. I have an amazing 3-year-old daughter. Just three weeks after her first birthday, I received a devastating diagnosis of ALS (Amyotrophic Lateral Sclerosis). ALS is an aggressive, terminal condition that attacks the motor neurons leading to progressive paralysis. There is currently no cure for ALS and treatment options are limited and only extend life by a few months.

My disease has progressed to the point that I am now wheelchair bound, have limited limb function, require respiratory support and will soon be getting a feeding tube.

Our family needs support to pay for medical expenses, supplements, treatments, travel costs to see specialists and eventually costs to ensure our home is accessible and that my and our daughter's care needs are met. Caregiver costs are approximately $60,000 per year.

We appreciate all donations and thank you for your support. Please also consider donating to Project ALS, The Les Turner Foundation and the Healey Center at Mass General for the advancement of important ALS research.

Watch this video to learn more about my journey: Melissa's Story