Hi all, I just wanted to let you know we are close from reaching 3,300 signatures on our petition for Spinal Muscular Atrophy (SMA). Thank you SO MUCH for your support!! Will you help me to get more support by sharing this petition with others on social media (Facebook, Instagram, Twitter, etc.)?? If enough of us sign, we can't be ignored! Here's a link to share:
The Korolenko's family started their crowdfunding effort of collecting $2.1 million for their daughter, Eva, back in July of 2020. Yes!! So many months elapsed leaving little Eva without an adequate treatment!! Eva was diagnosed with Type 1 SMA before July of 2020, and now she is nearly 16 months old. While her family is still far away from reaching that amount, they fight bravely for Eva's life in hopes that their only wish will come true soon eventually. Type 1 SMA progresses rapidly in newborns and toddlers and Zolgensma doesn't reverse any damages already done to babies. So, there is a lot at stake to fight for, fight for little human lives!!
Thank you!