À propos
ALS (also known as Lou Gehrig's disease) is a terminal disease with no survivors. ALS is a nervous system disease that weakens muscles and impacts function. Ultimately, ALS patients will lose the ability to walk, talk, and eventually breathe.
My brother Bill was diagnosed in 2018 and passed away in 2020 just a few weeks shy of his 43rd birthday.
There are promising treatments in clinical trials that have shown to reverse some of symptoms of ALS and prolong the lives of those diagnosed. Unfortunately, ALS is the forgotten or ignored disease and the FDA will not fast track these treatments.
100% of revenue made from my sales will go to those who are making a difference in the lives of those living with ALS. The ALS Association will not receive a dime because they have proven themselves to not fund treatments that work but to only fund treatments that will put money back into their accounts.
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Derniers produits créés
Voir tous les produitsVeste À Capuche SWEATSHIRT de sensibilisation à la SLA
Prix de vente 88,79 $CA. Prix Initial 104,45 $CA.
sac de sensibilisation à la SLA
Prix39,20 $CA
Veste À Capuche SWEATSHIRT de sensibilisation à la SLA
Prix de vente 90,78 $CA. Prix Initial 106,80 $CA.
T-shirt de sensibilisation à la SLA
Prix de vente 41,87 $CA. Prix Initial 49,25 $CA.
T-shirt Sensibilisation à la SLA
Prix de vente 40,25 $CA. Prix Initial 47,35 $CA.
Derniers produits vendus
Voir tous les produitsT-shirt de sensibilisation à la SLA
Prix de vente 41,87 $CA. Prix Initial 49,25 $CA.
sac de sensibilisation à la SLA
Prix39,20 $CA
Veste À Capuche SWEATSHIRT de sensibilisation à la SLA
Prix de vente 90,78 $CA. Prix Initial 106,80 $CA.
T-shirt Sensibilisation à la SLA
Prix de vente 40,25 $CA. Prix Initial 47,35 $CA.
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