Table of ContentsSpectrum IdentificationImmersion Plan and LocationAssumptions, Considerations, Learning ExpectationsI will become a member of the Global Foundation for Peroxisomal Disorders organization. Via the Internet, I will contact one of the leaders of the volunteer group within the next month to explore only my possibilities. I will draw at least one of my friends via email to help organize with me by next week. I will spend at least one day a week helping affected children until the end of the year. Say no to plagiarism. Get a tailor-made essay on “Why Violent Video Games Should Not Be Banned”? Get the original essay Identifying the Spectrum I'm going to dive into the amazing Hues for Hope event, which will be held in the city of Tulsa. This show benefits the Global Foundation for Peroxisomal Disorders organization by raising funds to advance treatment alternatives for peroxisomal disorders. This is an event that will fall into the category of those affected by a rare terminal illness on the diversity spectrum due to my dedication to charitable activity. I decided to immerse myself in voluntary organization because I have a special attitude towards people, especially children, with peroxisomal disorders, who need help and support from the World Disorders Foundation peroxisomal, or GFPD. I chose to immerse myself in the discovery capabilities of GFPD as a well-known volunteer community whose goal is to support and help children and their families who have gone through difficult times related to the diagnosis of Peroxisomal Disorder . Currently, the surrounding community of the City of Tulsa faces challenges related to periodic outbreaks of paroxysm attacks. This disorder presents a common and complex neurological disorder that influences individuals of all ages. However, I intentionally chose the Hues for Hope event because it primarily considers children affected by this hideous disease, also known as PBD, and aims to celebrate these little patients. influenced by this rare disease by raising funds for their treatment. Recently, I met sick children, who became my friends; therefore, I realize how difficult it is to constantly experience a sudden frequency or worsening of symptoms, such as seizures and spasms. I am very interested in communicating, supporting and helping patients with the same diagnosis, as Shades of Hope Event designs original art performance by Oklahoma artists and people facing peroxisomal disorders and will include topical art games and live craft auctions, a tour of the Woody Guthrie artifact, dinner and an open bar. The celebration should be incredibly beautiful and joyful and I think such an experience will be meaningful for me as I immerse myself in the inviting atmosphere and culture of the charity, as well as the original art exhibition. Immersion Plan and Location I plan to visit the Hues for Hope Event, benefitting the World Foundation for Peroxisomal Disorders, the organization that focuses on helping, supporting and treating families and children who have overcame a peroxisome biogenesis disorder. I will attend the performance, which will last three hours, on Friday October 5, 2018 at 6 p.m. The event will take place at the Pearl District Building in downtown Tulsa. The address of the Building is 1209 E 3rd St, Tulsa, OK 74120, USA. I discovered this place and its opening hours on the Internet.