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Emmita is a baby from Argentina, more precisely Chaco, with spinal muscular atrophy (SMA), a very rare degenerative neuromuscular genetic disease that does not allow her to move or breathe easily. She needs a specific drug that canât be found in ARG
Emmita is a baby from Argentina, more precisely Chaco, with spinal muscular atrophy (SMA), a very rare degenerative neuromuscular genetic disease that does not allow her to move or breathe easily. She needs a specific drug that canât be found in ARG
That vaccine costs TWO MILLION DOLLARS. WE NEED YOU TO DONATE. The family gave various methods to donate from foreigner countries which I will be showing later on the thread. DONATE WHATEVER YOU CAN. Every dollar counts.
A PETITION TO SIGN https://www.change.org/p/laboratorio-novartis-emmita-es-una-beba-que-necesita-el-medicamento-m%C3%A1s-caro-del-mundo-para-vivir?utm_source=share_petition&utm_medium=custom_url&recruited_by_id=3cdde945-c494-4bc5-a432-0879b34f1069">https://www.change.org/p/laborat...
GOFUNDME https://gofund.me/46542be0 ">https://gofund.me/46542be0&...
PAYPAL
natali.torterola@outlook.com
natali.torterola@outlook.com
Iâm posting this in english so we can reach more people, however english is not my first language!! be aware there could be some mistakes in my translations
