Hello dear people!

My name is Valeria and I am a mother of Michaela Georgieva who is now 6 years old with Spinal Muscular Atrophy type 1.

When she was a baby we found out about the severe disease, since then we have been lying in hospitals for months, fighting for medicine and for life. He was having crises, pneumonia, in intensive care. We fought for life-sustaining medicine, which he now takes every day.

Michaela is a very sweet and sunny child, stricken with this severe disease, she is on ventilator for 24 hours, lying down, has slight head and arm movements but is generally immobile. She cannot breathe on her own and is fed on a probe. Every day is a struggle but she has been through a lot and survived. We believe that good is ahead, that a miracle can happen.

Now we need your support as we need to purchase machines and supplies. We constantly need things related to her needs and the only help we get is her TELC which is not enough. Supplies are expensive, they are used every day and she cannot be without them. She also takes a lot of medication, probiotics and a lot of other things to keep her healthy and not sick.

Thank you from the bottom of our hearts for every gesture and support! Thank you!!!