I am Mark Cardilli
living with ALS
Maine
People DON'T understand that we don't have time on our side and we need solutions ASAP.
I’ve been fighting this disease since July 2019. We need more people in the political sector fighting for us alongside the FDA. People DON’T understand that we don’t have time on our side and we need solutions ASAP. … It is so difficult to get into clinical trials and get drugs approved quickly. When you have ALS, you’re willing to take chances as you’re going to die otherwise. The people making the decisions need to put themselves in our shoes and really make decisions as if they had ALS too. We’re all ALS and deserve hope and better chances.
