Romela is only 11 years old, yet she is already going through a difficult health journey.

She is currently under the care of the neurology department at Wigmore Hospital, and in order to continue her treatment, she now needs to undergo whole genome sequencing (WGS).

This test is critically important because it may help confirm or rule out the syndrome mentioned in her medical report. In Romela’s case, an accurate diagnosis is essential for planning the next steps of treatment properly and finding the medical approach that best fits her condition.

Let us help Romela receive the genetic testing she needs. Your support could make a decisive difference in her treatment journey.

We conduct our charitable fundraising campaign in collaboration with the IMAST app. https://m.imast.am/PfkZ/HFG