Description
A baby girl lit up our life name Eve and was illuminating her parents with unspeakable happiness until discovered at the age of 6 months Rare genetic disease atrophy spinal muscular atrophy 4 months after the discovery of the disease, who diagnosed doctors without tests because of delayed conversion until now 4 months Beautiful, which comes out of the hospital only a few days and come back to the pain and difficulty to find the vein and shortness of breath and we do not feel the need of oxygen and need 24 hours of oxygen is only need your prayers. pray for them please
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