Little Elmira from the Omsk region is just beginning to explore the world. But her family lives in constant anxiety. The girl's older brother has primary immunodeficiency — a rare and dangerous genetic disease of the immune system. To protect Elmira, it is urgently necessary to find out if she has inherited the genetic mutation.
An expensive genetic test is the only way to learn the truth. It is essential not only for Elmira but also for her parents. The research will show who is a carrier of the mutation and how it was passed on to the children. This will give doctors a precise plan of action: either to gain certainty that the girl is healthy, or to start the necessary treatment immediately, without losing precious time.
The same urgent help is needed for our other beneficiaries who are waiting for their chance at an accurate diagnosis. Every test is an opportunity to determine the cause of the illness and to find an effective treatment. Let's join forces to give Elmira and the Foundation's other beneficiaries a chance at a safe future.
Verified by Tooba
Verified by Tooba
