The special researcher did an outstanding job and explained to us about the entire study and its results. We asked questions and received all the answers in just 10 days!
A few months ago, we received the bad news that our Uri has a rare and severe disease – Hunter’s syndrome. We received training on the disease, how it develops, what is the relevant treatment, what are the reactions to the treatment, and above all, that the treatment only slows down the disease.

We were embarrassed and confused with lots of questions, many of which had no answers. The disease is rare, there is no one experience – but there are some experimental treatments. In short, there is more to it than meets the Eye.

A good and close friend referred us to you – Medint. The special researcher, Dr. Idan, did an outstanding job. First, he inquired the doctors about what Uri’s specific condition was, and immediately began his unique and dedicated work – searching and finding every place where there was knowledge on the subject – all the latest research, all the available treatment methods, all the medical centers in the world that specialize in the matter. The major doctors in the field, from all over the world, were inquired by him and he expressed their opinion on the case specifically. He then composed everything in an incredibly organized and concise manner. In addition, he had a conversation with us and explained about the entire study and its results. We asked all the questions and got answers – all this in only ten days!

Today we are facing a bone marrow transplant – a proposed treatment, that was researched by Medint. The doctors used the information and consulted with the relevant authorities and now we feel confident to go with the treatment – which, with God’s help, will stop the disease and bring complete healing to Uri for many good days and years. We will always know and remember that Medint were the faithful messengers for all the good of our child!

Cherished and appreciated, the family.