20 Mar 2020 Official House of Commons Petition for Spinal Muscular Atrophy Medication
Well, we don’t just want to oppose Ms. Lamb’s efforts and the government’s bills. We also want to propose and support efforts to eliminate the perceived “need” for assisted suicide. To that end, we want to share an e-petition worthy of your support, and ask you to consider signing it and encouraging others to do so as well. This petition urges the Health Minister to review a new, but prohibitively expensive, drug that can be given to an infant with SMA that may partially cure SMA. We asked James Schutten if he thought this petition was worthy of support. He responded:
We do think it is a good petition to support for two reasons:
First, if infants get this drug they could potentially avoid being wheelchair-bound and, as in my case, avoid getting a tracheotomy and a feeding tube.
Second, by being able to avoid these conditions it would save the government money on hospital stays, home care, and other programs that the government has in place to support families with a child with this disability.
So will you join us in signing this petition today and asking others to support it as well? The last day to sign is Wednesday, March 25th, by 3:40 p.m. (EDT).
(NOTE: there are lots of political e-petitions out there, most of them unhelpful or useless because they are not recognized by the House of Commons as official petitions. When signing e-Petitions, ensure they are official House of Commons petitions hosted on the House of Commons website. These are the only type recognized by Parliament.)
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