Donations For Baby Eva

Not too long ago, Diya Jeethan, one of our Grade 1 students, happened to see a news clip about a 1 and a half year old child called Baby Eva who has a rare disease muscular disease called Spinal Muscular Atrophy or SMA. The treatment for this disease is a whopping 2 million dollars!

Baby Eva’s parents are unable to afford this medicine and have appealed to people to donate what they can so they can see their child celebrate her second birthday. Diya is hoping that everyone at Fern will donate at least a loonie or a toonie so they can help baby Eva get this life-saving drug. She has been going from class to class speaking about Baby Eva and to support her cause, some students have made posters to spread the word.

Thanks to the empathy and initiative of Diya and so many kind students at Fern, the collection box for Baby Eva has already begun jingling! If you’d like more information on this story, please feel free to click on: https://toronto.ctvnews.ca/why-a-life-saving-drug-for-babies-with-a-rare-muscular-disease-costs-2-8m-for-families-1.4654033

Thank you.

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