Open Daily: 10am - 10pm | Alley door pickup 10am - 7pm 3038 Hennepin Ave Minneapolis, MN
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  • Open Daily: 10am - 10pm
    Alley-side Pickup: 10am - 7pm

    3038 Hennepin Ave Minneapolis, MN
    612-822-4611

Open Daily: 10am - 10pm | Alley-side Pickup: 10am - 7pm
3038 Hennepin Ave Minneapolis, MN
612-822-4611
DNA is not Destiny: A Continuing Story of Hope of a Parkinson's Patient

DNA is not Destiny: A Continuing Story of Hope of a Parkinson's Patient

Bantilan, Feliciano

Paperback

Biographies GeneralHealth General

ISBN10: 1499119062
ISBN13: 9781499119060
Publisher: Createspace
Published: Jan 1 2015
Pages: 100
Weight: 0.32
Height: 0.21 Width: 5.98 Depth: 9.02
Language: English
The book tells the story of my struggle with Parkinson's disease. At 56, I received advice that I had early stage Parkinson's disease. At that time, I had no idea what the disease meant. My ignorance led me to take the diagnosis lightly - until I had great difficulty moving. My mobility was so impaired that I could not raise myself up on bed. I slept on a mattress spread on the floor. From then on, I was relentless in my resolve to fight the illness. I persisted in my search for a treatment that addressed the molecular mechanisms generating the disease - conventional wisdom notwithstanding. My persistence paid off - I chanced upon the website of Dr Amy Yasko. As far as I know, her protocol is the only one that addresses the molecular mechanisms. How does Parkinson's disease arise? The confluence of three factors - genetic predisposition, microbial load, and toxin load - generates neurological diseases in general - and Parkinson's disease in particular. The factors are jointly necessary but not sufficient separately to express the disease. My illness arose from my specific DNA mutations. My mutations blocked some processes, creating imbalances in intermediates and end-products, thus messing up the machinery in my cells. Toxins - like heavy metals such as mercury, aluminium - blocked some additional processes in my cells, even in the absence of a mutation. Microbes sequestered heavy metals making it difficult for my body to find them in order to eject them. The key mutation of my CBS gene (cystathionine-beta-synthase) started my Parkinson's illness. The mutation is an up-regulation, meaning an increase in the enzyme activity, resulting in ammonia production higher than normal. Because of the mutations in my three other genes, not enough BH4 molecules were available to transform ammonia to harmless urea. Consequently, instead of urea, my body produced peroxynitrites and superoxides - very nasty molecules that lit a firestorm in my brain, leading to neuro-degeneration or death to my dopamine-producing neurons. When I was young, my body repair mechanism was efficient and effective in restoring or replacing degenerated or dead neurons in my brain. As I grew older, my repair mechanism began to falter. Meanwhile, the microbial load was increasing - more and more heavy metals escaped detection, while toxins grew in concentration, blocking more and more reaction processes. In the end, my body succumbed to the combined assault from the three forces - genes, microbes, and toxins - resulting in my Parkinson's illness. How does the Yasko protocol work? The protocol bypasses the mutations by using RNAs, as well as other supplements, i.e. putting in by hand the requisite intermediates thus enabling the reaction machinery in our cells to get going again. After a year and three months into the protocol, I began to recover some of my mobility, as well as some of my brain. And something more - all of a sudden, I began to think in verse. At age 65, I began writing poetry at the start of my partial recovery. I used my new ability to explain Einstein's insight into reality via the rhymes and rhythms of verse. I published my first book in 2013, entitled Einstein in Verse: Introduction to Special and General Relativity. In 2014, I wrote and published five books - a book on life in poetry, three books on stock investing, and this book. Four years into the protocol, my body improved significantly. My thinking brain has fully recovered, attested by six books, one in 2013 and five in 2014 - enhanced by a new ability - the ability to think in verse. I feel I added 4o% dopaminergic neurons in my brain, starting at 15%, totalling 55%. Indication of this comes from the reduction in levodopa dosage by 40%. Likewise, my overall mobility improved by 40%, starting at 15%, totalling 55%. I have come a long way - when I could not raise myself up on bed. All indications point to the direction of a fuller recovery. DNA is not Des

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