Over the last few months I've been researching a therapeutic intervention that was recently brought to my attention. The further I delved into this new treatment the more excited I became. I have waited the lifetime of my son for this remarkable breakthrough in science. Gratefully, the Pastors of Claremont United Church of Christ also saw the value that I saw in this scientific breakthough and set up a Go-Fund-Me account that provides more information and a place where those who are able, can help support us through the month long treatment at the NeuroCytonix Center. Below is more detailed information that has been posted on the Go-Fund-Me account. The URL is also pasted below for those interested in donating. With much thanks from the bottom of my heart! You can follow along here for updates on Julius' progress and this very hopeful journey.
Julius surprised the medical staff when he survived his birth after suffocating for 22 minutes. He is now a young adult living with severe cerebral palsy who continues to endure multiple obstacles. Among them is being grossly underestimated in his intelligence and awareness due to his physical appearance. Julius lives in a body that is outside the fluent connections from his brain, a system of neuro-physiology that most of us take for granted. His mother, Alice, is an artist, a researcher and an educator. She has been Julius’ primary caretaker throughout his life, giving up her own career as a professor in higher education to focus on his welfare. Julius’ little sister is in elementary school and came into the family when Julius was 15-years-old. She is creative in her thinking and talented in dance and song. Already, she has become an advocate for her brother and loves curling up with him in front of a movie. People often mistake Alice as medical staff, due to her in-depth knowledge for Julius’ complicated care. She reminds them, her medical training comes through her loving relationship with her son, not through medical school. Yet, it is not unusual for Alice to correct or guide medical personnel about her son’s care and is often treated as a partner in his treatments by doctors who admire her dedication and non-wavering belief in Julius. This year, Alice’s hope, was lifted when she learned about a breakthrough in tissue engineering technology that could improve Julius’ quality of life. “Is this legit?” she thought. So, she searched further. It’s called CYTOTRON/RFQMR a medical device utilising Rotational Field Quantum Magnetic Resonance (RFQMR) technology. In simple terms it is a brain magnetic stimulator (similar to an MRI) to promote cell regeneration through fast frequency radio bursts that break down old-dead cells, clearing out scar tissue and allowing room for new cells to grow. Alice’s eyes teared up. The time she invested in research, letter-writing, laboratory visits and seminars gave her an understanding that even with the best advancements of stem cell therapies, scar tissue interferes with cell regeneration. This treatment addresses that very specific problem. Next, she needed to know- Is it safe? Truth be told- YES! The CYTOTRON/RFQMR is in use in the United States for neoplastic disorders of cancer and diabetes. It is also being used to treat Cerebral Palsy and other neuronal disorders, that the technology was intentionally developed for by its inventor Dr. Kumar, Rajah Vija. In the shadow of a double blind study with 22 participants living with cerebral palsy, the treatment is yet to be approved in the USA for C.P. But this does not mean Julius is disqualified from receiving the treatment. NeuroCytonix is a state-of-the Art Treatment Center located in the Monterey area of Mexico City. The parents of a child who received the treatment in India are responsible for establishing the centre in Mexico. Thanks to their advocacy, NeuroCytonix is only a few hours away via air-travel. The application process requires a medical review and not all candidates are accepted due to their medical baselines. Julius’ relatively stable health and neurophysiology, have given him the baseline required to be an accepted candidate. The family and Julius’ medical specialists here in the U.S. have been working diligently over the past few months to prepare Julius. If you and anyone you know can help offset the costs for this breakthrough in medicine for Julius and his family, please do not hesitate. As Alice ages, it is becoming more difficult for her to lift her son, and yes, she still lifts him every day. The spastic stiffness in Julius’ body is taking a toll on both of them. Reducing spasticity is the most common improvement seen in other patients receiving Cytotron Therapy and there are several other benefits that are possible when blockages are removed so that cells can proliferate in the brain, a natural occurrence known as plasticity. Alice will keep supporters informed of Julius’ progress through a blog with information shared to those who are interested in following along. https://www.gofundme.com/f/help-julius-access-lifechanging-treatment?attribution_id=sl:74857c97-d01c-4909-8d53-2fff98c7d03d&lang=en_US&ts=1750439530&utm_campaign=fp_sharesheet&utm_content=amp13_t1-amp14_t2-amp15_t3&utm_medium=customer&utm_source=copy_link&v=amp14_t2
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