My name is Karin Binjamin, a 32-year-old mother to 4 beautiful kids who is trying to provide the best life possible for them. 3.5 years ago, our lives changed forever when we found out that our perfect little baby girl, Yuli, has a rare genetic mutation called Grin2b. Her specific mutation is the first and only one of its kind, making her extra rare. We do not know what she sees; she has really bad epilepsy, she is non-verbal, and quadriplegic. Because her mutation is so rare, we have no idea what the future holds for her. As her mom, I have made it my personal mission to help my daughter reach her full potential. I want her to enjoy life and not to suffer.

Asking for help, let alone money, is one of the hardest things that I have had to learn how to do. But with special needs children, it really does take a village.

A few months ago, Yuli had a series of seizures lasting over 30 minutes each. This caused a huge regression, and it is as if she forgot everything she was taught all these years. I was so traumatized by these long episodes that I began to research alternative medicines and procedures. I knew that in 2025 there has to be a better option for life for her. That is when I found Neurocytonix.

Neurocytonix is trying to do the impossible and help repair damage to the brain that was once permanent. Studies show that they are extremely successful, and the outcomes speak for themselves.

What made them a point of interest for me is the fact that there is little to no risk involved that can harm her life.

The cost of this new technology is $50,000

For the treatment, flights, and stay. The treatment is 32 days long, and Yuli will need to go into a machine called a cytotron daily for a month. This could really change our lives forever, and every dollar counts!

I will be more than happy to answer any questions that you have regarding Yuli's condition, her treatments and care just let me know!

Please help me help my daughter.