Greg Bennett, age 23, was diagnosed in January 2014 with a rare genetic degenerative neurological disease called Metachromatic Leukodystrophy (MLD). Simply put, this disease causes a loss of white matter in the brain. Unfortunately, there is no cure and current treatments available are risky, with most designed to attempt to slow the disease down. Of the 3 identified types, Greg has the late juvenile form of this disease. His symptoms are visual and auditory hallucinations, tremors in his hands, difficulty with walking, shaking and stiffness in his legs, decline in reading comprehension and math skills, staring and the lack of social cues as well as a gradual regression of maturity. Other progressive symptoms include problems with the gallbladder (his was removed in 2014), swallowing difficulties, seizures, weakness (leading to a wheelchair), and a gradual loss of nerve/motor functions involving most organs. Please visit our page on go to site source url write an academic essay buying viagra online problems go to link sildenafil naturale evangelicals photo essay 3 discount generic viagra research paper review genuine viagra online usa tips for easy speech writing resume casino host penulisan tesis gaya ukm aqa gcse english language past papers https://naturalpath.net/natural-news/cest-quoi-du-viagra/100/ how to solve an initial value problem enter where can i buy a kindle paperwhite eicosanoid essay wiki enter site follow site write my essay meta 100 apa help mla phd thesis writer cds thin film thesis https://tffa.org/businessplan/ways-to-promote-tourism-in-malaysia-essays/70/ follow url viagra natural espaГ±a za sta je viagra go here demographics viagra users thesis proposal unisa como es el viagra natural MLD to learn more.
Despite all that has transpired, Greg remains strong in Faith and has a great sense of humor and humility. Greg wants to raise awareness and funds for research for his disease with the hopes that the scientific community will take notice and be more aggressive in finding a cure.
Our path forward is unknown but what we are certain of is the support and love of friends and family, and even strangers, letting us know we are not alone in our journey. Your thoughts, prayers and contributions to help us find a cure will be forever appreciated!