When Daniyar was just 3.5 months old, doctors diagnosed him with spinal muscular atrophy type 1 (SMA). At 6 months old, he received life-saving treatment with a gene therapy drug, and since then his parents have been doing everything they can to help him develop.
Daniyar is now 3 years old. Thanks to regular lessons, he has learnt to sit up independently, can hold his head up confidently, has good use of his hands and is even trying to stand on his own. But for further progress he needs specialised rehabilitation at the medical centre, where he will be able to work on the Galileo vibration machine, an important tool for strengthening his retained muscles.
‘When we hear from doctors that our son has a chance of success, it is a great happiness for us parents,’ says Daniyar's mum.
Rehabilitation is as important for children with SMA as treatment. It helps to maintain and develop existing skills, prevents loss of strength and prepares the body for new opportunities. By supporting Daniyar, you will give him a chance to keep moving forward!
❤❤❤❤🙏🙏🙏🙏
Здоровья тебе малыш 🙏🙏
Амин
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