N. Rajmond Brendon, or Rajmi as he is known to his family and friends, was born in 2013 as the third child in the family. For a long time, there was no sign of anything wrong with his health - he was just as happy and energetic a child as any other.

But when he was 4.5 years old, his parents were confronted with a shocking diagnosis: Rajmi suffers from Duchenne muscular dystrophy (G7100) - a rare, progressive muscle disease that gradually weakens muscles, leaving him with limited mobility and eventually requiring full nursing care.

Since his diagnosis, the family has done everything possible to ensure that Rajmi has the best possible quality of life. They travel to Budapest three times a year for development and physiotherapy. These treatments play an important role in keeping Rajmi's muscles functioning as well as possible for as long as possible.

But now Rajmi's condition has reached a stage where he needs more support. Weekly physiotherapy would be essential to strengthen his muscles and slow his deterioration. This would be available in Pécs, where he would be treated once a week by an expert physiotherapist.

The family does what they can, but the cost of travel and treatment is a constant financial burden. They need external support to help Rajmi continue to develop and remain mobile.
Together, let's help Rajmi continue to attend physiotherapy and get the improvements he needs.