Jasmina's diagnosis is "congenital bilateral cleft upper lip" or "cleft hare's lip" in common parlance. In addition to the cosmetic defect, these children have difficulty swallowing and sucking food and pronouncing their first syllables clearly. If the defect is not corrected, there is a high risk of speech and bite problems, which can lead to withdrawal and inhibitions.
Jasmina's parents love their daughter and want the best for her. They found a clinic that was willing to operate on her in two stages, whereas others were willing to operate on at least five. For the parents, the number of surgeries was the key to their decision.
The surgery has already been scheduled for October 5. As the clinic is private, the costs will be proportionate. The family cannot cope alone, but they are hoping for help from concerned people. You can support the collection of funds for little Jasmina by donating any amount.
Experienced surgeons are planning to perform a stage by stage cheilorinoplasty, which is an operation to remove soft and hard palate defects by suturing the cleft. After the surgery, there is a long road to recovery, working with specialists, but the first and most important step will be done, if the Almighty wills it.
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