About us
LAMA2 Bulgaria Foundation
Supporting children with muscular dystrophy and their families
We are Genadi Samokovarov and Teodora Gerganska, parents of Bozhana and Marko.
Bozhana, our first child – she is healthy, active, and full of life. Marko, our second child, was born with the rare genetic disorder known as LAMA2 muscular dystrophy.
Despite the difficult diagnosis, Marko is a smiling, bright, and cheerful child. We created LAMA2 Bulgaria to support children affected by LAMA2 in Bulgaria and to fund the scientific research needed to develop a treatment.
Our mission
Hope for the future
Connecting families
Helping families find each other and share experience
Following the science
Following research progress and sharing it with our families
Finding the unfound
Many families don't know about us. Help us reach them
Contact us
Contact
Have questions or want to help? Get in touch!
You can contact us using the form below, by email contact@lama2.bg or on facebook
For a stronger tomorrow
Your donation supports families and scientific research toward a therapy.
Thank you from the heart!