Lou Gehrig’s Disease

ALS is a catastrophic terminal disease that, within a few years of diagnosis (the physicist Stephen Hawking was an exception), eventually causes total paralysis. It is also a tragic condition that euthanasia/assisted suicide activists zealously wield to justify killing as an acceptable answer to suffering.

Now, the understandable fear of ALS is being deployed by academic advocates as a means of breaking the (U.S.) requirement for a six-month terminal diagnosis and self-administration in assisted suicide.

In jurisdictions where MAiD [the euphemism for assisted suicide that seeks to turn life-ending it into a medical “treatment”]is legally available, such laws are intended to support patient autonomy and alleviate suffering. However, for patients with ALS, the clinical reality of progressive paralysis combined with legal requirements for self-administration of lethal medication creates a cruel dilemma. Approximately one-third of affected individuals express interest in MAiD if their suffering becomes intolerable [12], yet current laws require that it be initiated while patients retain the physical ability to self-administer the prescribed medication.

However, patients are not legally eligible to access MAiD until it is determined they have a life expectancy of six months or less. This creates a narrow and clinically unrealistic window where waiting until they meet legal eligibility may mean they are no longer physically capable of completing the required act, regardless of prognosis, suffering, or intent.