Thanks to your help, tickets to and from the place of treatment were purchased for Lisa!

Lisa was born with a rare genetic condition called "spondylometaphyseal dysplasia". This is a disease characterized by damage to the vertebral bodies and bones. As a result, children with this diagnosis have disproportionately short stature, shortening of the trunk and limbs, and the development of degenerative joint diseases. Now at the age of 15, Elizabeth's height is only 122 centimeters. In 2014, Liza underwent surgery on her hips, which were rotated into position and fixed with metal structures. After this surgery, Elizaveta's gait improved, her lumbar lordosis decreased and she added 9 cm to her height. However, despite the positive results, Elizaveta also developed a significant worsening of her spine and thoracic deformity, as well as stenosis of the cervical spine. The doctors referred the girl to a prosthetic and orthopedic center where she was treated with a Chenault-type corset. Corsetting is the only way to stop the progression of Elizabeth's spinal deformity. Now the girl has been sent to the prosthetic and orthopedic center for treatment of the spine with a Chenault type corset. But this center is located in another city, and the price of air tickets for the family is very high. With your help we can help Lisa to get to the necessary treatment in time!