Hello, good people!

Please read the difficult story of my son Michael, who will soon be 10 years old.

My child was born in 2015 without any signs of intellectual disability. He was even passing the development of his peers. At 4 months and 2 weeks he started repeating "Come on!". At one year and three months, I'll never forget, he said to me.

My maternal sense kept telling me not to give the vaccines or to delay them. Until one day, I made that mistake and he became another child. Everything he could seemingly erased from his memory. Everything that could seemed to be erased from his memory. It was as if he'd had a stroke and had to learn all over again. Eye contact was almost lost. He stopped addressing his name. It took years to learn normal things that other kids could do in weeks and months. Fortunately he kept himself physically, except he had digestive issues.

All of the doctors and specialists we have been to in Bulgaria have told us that the child is autistic and nothing can be done. There is no cure!!! I had started to come to terms with this until a friend of my mother's, put us in touch with the clinic of Dr. Burak Tatl-a pediatric neurologist. And lo and behold my mother's intransigence drove us to him in Istanbul. Michael was 6 and a half years old. There we did all the tests, and after the examination by Dr. Tatl's team, the doctor started talking to us about genetic tests!!! We decided to do them and it turned out that the child had a rare genetic mutation and the vaccine had "crushed" him!!! And that's how Michael's treatment started in the clinic of Dr. Burak Tatl, Istanbul.

It was spring, when he started repeating everything, as if he had woken up from some nightmare... We started to see the huge steps he was taking every day and we were convinced that it had nothing to do with autism. We've been in Dr. Tuttle's clinic for over 3 years now and my son has STARTED talking, understanding, increasing his mental skills, and even physically improving.

At his last visit to the doctor, he began to diligently persuade her to do exosome therapy, which Michael has a high probability of starting to talk like all children and all that he is experiencing will go away. Believe me my child does, unbelievable nervous crises and cries out loud, inconsolably when he is not understood. YES wanting to drink water and not being able to tell in any way... Regarding the exosome therapies, this of course is not watered down with one treatment, it takes at least 5 treatments a session and they are done every month. A sum of 15,000 euros is needed for all of them, just the treatments, without the other costs, such as a doctor's examination, etc. ... Sums that are unaffordable for a single mother like me, working as a personal assistant to the child. The child sees a speech therapist and a psychologist who are also tied to personal finances. And as a single parent, everything falls on my shoulders and my mother's shoulders related to Michael's overall upbringing and struggle to get well...

Please, dear friends, help so that Michael can be like all children... Let Michael live his childhood in games and lessons like his peers!

Thank you!

Sincerely, Veronica - Mikhail's mother