Nasisa fight against sma

We are the parents of Nafisa, a beautiful 7-month-old baby girl who has been diagnosed with Spinal Muscular Atrophy (SMA) Type 1. It's a rare genetic disorder that affects her muscle tone and movement. It was a shock for us to learn that our little angel has a serious illness that could impact her ability to walk, breathe, and eat. As parents, our world came crashing down when we heard the news. We couldn't believe that such a tiny and innocent being would have to go through this. But, as we gathered our strength to face this challenge, we knew we had to do everything in our power to give Nafisa the best chance at life. We have consulted with multiple doctors and specialists, and they have all recommended a costly drug called ZOLGENSMA, which is not available in our country. We have been informed that this treatment will cost 1.8 million dollars, an amount that we simply cannot afford. We have started a fundraising campaign to help us reach our goal, and we are asking for your support. Every dollar counts, and we know that with your help, we can make a difference in Nafisa's life. We want her to have the same opportunities as any other child, and we want her to grow up healthy and happy. Our daughter is counting on us, and we cannot let her down. We are forever grateful for any support you can provide, and we thank you from the bottom of our hearts.