A Toronto family is asking for their community to help raise funds for their daughter Eva Batista, who was diagnosed with Spinal Muscular Atrophy (SMA) Type 1. The family is raising money to get accessed to receive Zolgensma, a life saving drug that will replace the missing SMA 1 protein and has been research as the most effective treatment for SMA 1 patients to live a long and healthy life. The cost of medication is 2.1 Million Dollars USD. Eva is only 8 weeks old. This story is beyond heartbreaking, lets do all we can to help this family as there is always hope!
For more information please check out there fundraiser and share on your social media: https://www.gofundme.com/f/foreva-strong
Official Instagram: https://www.instagram.com/forevastrong.sma/
Please Please donate if you can or share the fundraiser on social media.
Lets get this medication for Eva!