The Save a Heart Association paid today the amount of 675 EURO representing medical recovery according to the attached payment order.
Our fight continues!
Thank!

The Save a Heart Association paid today the amount of 10000 RON representing medical recovery according to the attached payment order.
Our fight continues!
Thank!

The Save a Heart Association paid today the amount of 975 EURO representing medical recovery according to the attached payment order.
Our fight continues!
Thank!

Since Teodor was diagnosed with Duchenne Muscular Dystrophy, our life has turned into a constant battle between hospitals, recovery centers and numerous investigations. We feel overwhelmed, because, in Romania, there is no treatment for this devastating syndrome. But a ray of hope appeared from Spain, more precisely from Barcelona.

In November 2023, I arrived here, and since then Teo has done all the necessary investigations. With great efforts, we managed to enter the public health system, where he was given more detailed checks. The final verdict was clear: Teo must stay here in Barcelona to benefit from a revolutionary vaccine that can stop the progression of the disease and help him keep his muscles functional. Until he receives this life-saving vaccine, he has been recommended intensive care to keep him in the best possible shape and to protect him from pain.

Unfortunately, for us, the costs are huge: the therapies reach 1500€ per month, and the rent to about 2000€. We have exhausted all our savings, as parents, doing everything in our power to help Teo. But now, we are facing a desperate situation. In order for Teo's condition not to suddenly worsen, we must stay here, in Barcelona, and continue these vital therapies.

Please help us keep our hope alive and continue the treatments that give Teo a chance at a life without suffering! Any support matters enormously in our fight for our son's health.

So far, ultrasounds of the lungs and heart are good. The X-ray on the column is also good.

I started physical therapy - two days a week. Tomorrow we will meet with the doctor who has taken measures for us for orthotics, we see what he will tell us. The important thing is that we are in a database and as soon as a treatment appears we are notified. It's already an exepriment that can be applied in America, in Europe still not. We pray to the good God to approve it here as soon as possible. From what we have learned, the Hospital "Sant Juan de Deu" will be the first in Europe to use it. We'll be back with information.

We still don't know the schedule for next week.

(Iulia Radu, Teodor's mother)

From today, Teo has begun physical therapy sessions . He's a champion, he works very well  thanks to you, dear people. Thank you from the bottom of our hearts!"

(Iulia Radu, Teodor's mother)

Since yesterday I started my first visits with Teo. He was very excited to experience every part of the hospital, from today we continue...

Thank you to everyone who supported Teo! Unfortunately, the disease evolves very rapidly. 3 months ago it was still going quite well, but already difficulties are observed in walking. There is no cure anywhere in the world for Duchenne muscular dystrophy, at the "Sant Juan de Déu" Hospital in Barcelona, a treatment is being experimented upon after it has been shown in the US that it can slow down the course of the disease. These children remain in a database and when Spain also recognises the treatment, they will be able to benefit from it in the future.

I want to believe that we can avoid getting into the wheelchair, to how the disease evolves would be the next step. Teo will still need financial help for orthotics, which are not included in the original bill.

Please continue to be with him. Eternally grateful, I hug you with love! 🙏❤️

(Iulia Radu, Teodor's mother)

My dear ,Teo arrived in Barcelona !!! Thank you from the bottom of my heart ,thanks to you it was possible to help him and him . Since Monday begin investigations ,we keep you informed . Eternally grateful