IndexSpectrum IdentificationImmersion Plan and LocationAssumptions, Considerations, Learning ExpectationsI will become a member of the Global Foundation for Peroxisomal Disorders organization. Through the Internet I will contact one of the volunteer group leaders within the next month to just explore my options. I will entice at least one of my friends via email to participate in the organization with me within the 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 Shouldn't Be Banned"? Get an Original Essay Spectrum Identification I am going to immerse myself in the unique 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 promote treatment alternatives for peroxisomal disorders. This is an event that will fall into the category of those affected by a rare end-of-the-diversity-spectrum condition due to my attachment to charitable work. I decided to immerse myself in volunteer organizing because I have a particular attitude towards people, especially children, with peroxisomal disorders, who need the help and support of the Global Foundation for Peroxisomal Disorders, 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 experiencing difficult times related to the diagnosis of peroxisomal disorder. Currently, the community surrounding the city of Tulsa periodically faces challenges regarding manifestations of paroxysmal attacks. This disorder presents a common and complicated neurological disorder that affects individuals of all ages. However, I intentionally selected the Hues for Hope event because it primarily considers children affected by this horrible disease, also known as PBD, and aims to celebrate these little patients affected by the rare disease by raising funds for their treatment. I recently met some sick children, who have become my friends; therefore, I realize how difficult it is to consistently 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, considering that Hues for Hope The event will feature an original artistic performance created by Oklahoma artists and people dealing with peroxisomal disorders and will involve topical art games and auctions from alive with handcrafted objects, visit to the Woody Guthrie artifact, dinner and an outdoor bar. The celebration is expected to be incredibly beautiful and cheerful, and I think that such an experience will be meaningful for me to immerse myself in the inviting atmosphere and culture of charity, along with the original art exhibition. Dive plan and location I plan to visit Hues for Event of Hope, benefiting the Global Foundation for Peroxisomal Disorders, the organization that focuses on helping, supporting and treating families and children who have overcome a peroxisomal disorder peroxisome biogenesis. I will attend the show, which will last three hours, on Friday 5 October 2018 at 6.00 pm. The occasion will take place in the Pearl District Building in downtown Tulsa. The building address is 1209 E 3rd St, Tulsa, OK 74120, USA. I discovered this place and its program on the Internet by browsing the official website of the Pearl District Building. I chose this particular location because it is Oklahoma's most exciting wedding location appeal.