ALS Research

'Right To Try' Congressional Bill for ALS Patients

 'Right To Try' Congressional Bill for ALS Patients
By Matt Bellina on Jul 14, 2016 at 06:28 PM in ALS Research

Without any intended insult, Matt Bellina does not believe it is the role of interest groups or bioethicists who have never met him to dictate how he should find value in his remaining days. If some believe that living without hope is superior to living with the risk of side effects that is their personal business.

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Familial ALS Solution - NOW!

Familial ALS Solution - NOW!
By Steven Perrin on May 07, 2015 at 03:20 PM in ALS Research

The health care system can start to eradicate familial ALS today. The technology exists. But is the world ready to accept the technology and utilize it to rid families of this devastating disease?

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