My name is Mark Hideghéty, I’m three years old and was born with a rare genetic disease, called mucopolysaccharidosis (type II/III, Hunter/Sanfilippo syndrome). This disease has been slowing my development. I cannot walk, although my parents are doing everything possible to put me on my feet!
We could express our gratitude in many ways,
but this word has it all:
THANK YOU ❤️
Thank you for your generous support. It gives us great pleasure that you thought of our son Mark.
Thank you for easing our way in Mark’s development, who has come a long way since then. We are grateful because with the amount you raised, we were able to have many therapies that helped Mark a lot. Every step is a huge effort for him, but he is a great fighter, faithfully and with a smile he endures every day. We also go for special movement development exercises, speech development, mental development with special tutors, massage and hippotherapy…
None of this is funded by the government, therefore is your support significant for us.
we’ve gotten to the point where
he can walk nicely with the aids, albeit backwards,
he can walk nicely with the aids, albeit backwards,