Why I created This Website

Welcome to the Huntington’s Initiative. My name is Antonio Evans Maltese, 26, disabled, and I have something to say: Together, we can do anything. Through the use of genetic modification therapy, stem cells, and CRISPR technology, the sky is the limit. Help us and join the fight. I appreciate and encourage any comments or questions, and can be reached at Bluejenie@gmail.com.

German speakers and listeners may click hier: Hier ist Präsentation

Wenn Sie mehr auf Deutsch hören möchten, können Sie hier finden: https://drive.google.com/drive/folders/1_Xnyt6ggVYMjxspk2XDXTRi_1ofDIVPQ

My new phone number is: 434-326-4110. I can be faxed, as well. Blessed be Jesus Christ.

P.S. Google is weird with their algorithms. You can simply Google search, Huntington’s Initiative WordPress— and bam! My Initiative home base.



There has been news as of May 10th, 2023, and I will be updating my website accordingly. Stay tuned ;O… https://youtu.be/_AWiRS6ud7k

Lea Wenzler, aus Stuttgart, ueber Huntington’s Disease/Krankheit 04/18/2021 Virginia Commonwealth University–Deutsch 425 Capstone Projekt.

I have been diagnosed with many diseases, most notably a CAG of 43 testing positive for terminal Huntington’s Disease, Multi-Focal Avascular Necrosis, Antiphospholipid Antibody Syndrome, and most recently infertile, being diagnosed with Hypogonadism. Remember Henrietta Lacks at John Hopkins? This is new. I will be providing a Google Drive Link of my Variantyx 30x Whole Genome Sequencing RAW BAM Data here: https://drive.google.com/drive/folders/1k1dXzOgKQPA7kWt42cKCyZliDT6FmcjN?usp=share_link (2:43 PM, May 18, 2023)

PLEASE HELP: https://www.paypal.com/pools/c/120615781328258450

For anyone interested in purchasing my Whole Genome Sequences, you may pay $250 here, or via email at “Bluejenie@gmail.com”. This was a very expensive medical test and private test. Thank You and God Bless.

Nebula Genomics by George Church 100x Whole Genome Sequencing: https://drive.google.com/drive/folders/12VcrNgObM6P8-Puo_SzR6tIbINo7xD3y

If you’re willing, I want you to be a part of it. I’m a fighter. I’m stubborn, and I’m going to fight for a cure or die trying.

I created this website to bring awareness to Huntington’s Disease, not just for me, but for people like my dad, my grandma, and so many others—those who still hope and those who have lost all hope. Since so few people (30,000 Americans and 200,000 at risk) are affected by Huntington’s Disease, the cure seems out of reach. Pharmaceutical companies, however, have never met Antonio Maltese. Mark my words: I’m going to do everything in my power to bring awareness to the first-ever genetically mapped neurodegenerative disease and let everyone know, no matter how big or how small, everyone has a story. Everyone deserves a fighting chance, even the 0.0001%. “Valkyries take flight— WWIII beckons.” Antonio Evans Maltesè

SHOW starts at 4:30. ;0

UAI bad CareAdvantage

Those who have a ‘why’ to live, can bear with almost any ‘how’.” Frankl quoting Nietzsche

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