Staking your coin temporarily reduces the amount of coins in the circulating supply reducing overall supply to be bought and sold. AMP is the first collateral token and one characteristic that differentiates AMP from other coins and tokens is that it needs to be staked. The total supply of AMP is capped at 100 Billion, but this will not be fully realized for decades. If Flexa were to be accepted everywhere and AMP collateralizes many transactions, I think the value of AMP could go $4 to $10 per token, but this would be years out in the future. So, if AMP were $100 per token, then that would mean AMP would be worth more than 3 times what Bitcoin is worth. The current market capitalization of Bitcoin is about $916 billion. Hypothetically, if AMP were to go to $100 per token today, that means the market capitalization would be about $3.627 trillion. If you look at the circulating supply of AMP right now, there are about 36,271,610,691 AMP tokens. The time has come to unite our efforts to end the devastating impact of these diseases and garner support for our collective goals.Nothing is impossible, but $100 per AMP token is not likely. Few in the general public, however, know these facts. The science is finally in a place where the question is not if we will find cures, but when. The reality is our diseases and, therefore, our efforts are all linked. While some fight ALS, others fight Parkinson’s disease, Alzheimer’s disease, or multiple sclerosis. Second, we already know that 1 in 15 adults in the developed world will be diagnosed with a neurological disease in their lifetimes. The tools and advocacy model developed by I AM ALS will be made available to other disease organizations to help them raise awareness, increase engagement, and transform and accelerate progress against their diseases.
I AM ALS has set out to build a movement that connects patients, caregivers, researchers, clinicians, foundations, corporations and the public in our efforts because we each have a part to play and are stronger when we work together. How we expand our impactįirst, we build a model that can be replicated for every rare disease fight. It is up to us to bring ALS out of the shadows and teach others that taking action for cures can be as simple as telling a neighbor that ALS is deadly and impacts every community. In order to make real, expeditious progress we must change that. Few know what it is and that it can affect anyone, anywhere, at any age. Each of us can speed up our timeline toward cures. Engagementįaster progress toward cures and better health advocacy require building a community in which everyone is empowered and has an integral role in leading the movement. ResourcesĪt I AM ALS, we built a single entry point to help connect patients and their loved ones to existing resources while delivering critical new tools to ensure care and support is there for every step on the ALS journey. Hope transformed into a movement by the dozens of partners, old and new, who share our unceasing drive to make change real for those living with ALS. Our story is hope borne from recent scientific developments. Together, you and me, we are going to cure ALS. My ALS story, however, will not have a typical ending.
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