This little princess is 6 months old now and she is the daughter of a very 💕special friend 💕My friend and her family are in need for any kind of help or advice. Let's spread the word so little Maya and many other children in the same or similar condition can have some hope for a brighter future 👶🏻❤️. I have created this account with the intention to help as I truly believe in human compassion. They are also looking into governamental help but all this takes time and unfortunately little Maya doesn't have time to wait. Any kind of help would be very much appreciated 🙏🏻💕
Little Maya, 6 months and was born with a serious generative disease. SMA Type 1. This is a Spinal Muscular Atrophy that makes the muscles weaker and cause problems with movements and breathing. It's a serious condition that gets worse over time. If it's not treated the life expectancy is 2 years. The treatment cost around £600K per year (that's why any penny would be very much appreciated). This medicament can only be found in America.
From the bottom of my heart I thank you all 🙏🏻💕