6000 euros for surgery – rare genetic defect: sick girl needs help

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6000 euros – a lot of money. But ridiculously little compared to the difference the sum makes to a child. “The Crown helps – Styria” is eager to help the little one. Do you support us?

It’s easy to see how much the parents love their little Mia, how much the heart of the family is the sunshine. And that the couple would do anything to help the child.

Mia is now four. But she can’t talk, so far she can only walk with orthotics. It’s a genetic defect that causes her muscles to contract, forcing individual limbs to spasm. The little girl has been in therapy since birth. Sometimes she is cheerful, often enough apathetic.

Specialist has already helped many children
Only 21 children in Europe have this developmental disorder, the mother says, a genetic defect that causes muscles to shrink and causes pain and cramping. Before an operation with a doctor in Spain, a specialist recognized throughout Europe (he has already helped one of our “Die Krone hilft – Steiermark” protégés a lot!), the mother, who earns her own money, has fallen heavily into debt .

The procedure cost 6,000 euros, and it’s 8,000 in total with everything else that comes up during the trip. With such a syndrome you cannot go abroad as with a healthy child.

Making ends meet somehow
As I said, no one is complaining here, the three of them (the father takes care of the child during the day) somehow managed to make ends meet with everyday life and the extra expenses. But the mother just cannot raise such an amount, it is beyond all dimensions. And yet the amount is so ridiculously small compared to how Mia will benefit from it.

Can we help? That would be great! “The Crown Helps – Styria”, KW Mia, AT072081502500718404.

Source: Krone

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