Campaigns
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Hi! My name is Jonet! I am a fun loving young lady who just happens to have Down Syndrome. I struggle with anxiety and depression. My family helps me with all of my daily care through their loving support. I love to spend time with my family in the mountains. I would love to take a vacation to the beach. I haven’t seen the ocean in 5 years and we could only stay for a few hours. This trip would be the biggest blessing to me. It would be a true vacation.
- 100.00% Funded
- $2,200.00 Pledged
- Campaign has ended
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Landon has severe autism and is non-verbal. He LOVES all things sensory, especially jumping! Since he was able to sit up as a toddler, before even walking, he has hopped on his knees everywhere. To this day, he is still his parents’ bouncing baby boy! Landon’s dream is to have a bounce house! His family would greatly appreciate any support as they are very expensive and this would be a great outlet for his sensory needs.
- 100.00% Funded
- $2,200.00 Pledged
- Campaign has ended
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Nyasia is a sweet, quiet girl who loves music, animals, fish, and swimming. She has been diagnosed with low-functioning autism and is non-verbal. Nyasia loves to watch videos on Nick Jr., like Dora the Explorer, and she loves to watch YouTube videos of different Florida theme parks. Nyasia gets very excited. watching these videos and dreams of staying in one of the enchanted cottages at Sunshine Foundation’s Dream Village so she can go to these Florida Theme Parks. She is especially excited at the thought of going to Universal Studios and Sea World.
- 100.00% Funded
- $2,200.00 Pledged
- Campaign has ended
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Hello! My name is Timothy. I have been diagnosed with cerebral palsy, autism, ADHD, anxiety disorders, cognitive impairment, and more. I really enjoyed WWE wrestling, and I’ve loved Spider-Man since I was very young. I like to watch WWE wrestling and Spider-Man and other wrestling shows on YouTube. I just recently watched the new Avengers, and I love the movie! I spend a lot of time by myself and with my wrestlers. When I try to make friends, people just don’t understand me. So sometimes for me, I just melt down because people don’t understand what I’m saying or they don’t understand how I feel or I’m not understanding something. I do have two brothers that spend time with me, and I also have a sister, all of whom do understand me. I’m having a very hard time in school. I cannot seem to progress at all due to my impairments. I cannot tie my shoes, and I always wear pull-up clothes because buttons sometimes give me sensory issues. I just can’t button very good yet. It is really hard for me to make friends and keep them just because I feel like if they don’t understand me so I would just rather be by myself sometimes. Sometimes people make fun of me because I have braces. I often ask my mom and my dad why my feet are crooked. I do have to use a wheelchair if I have to go long places because my feet do hurt. At recess I do have one friend, and she reads to me a lot as I do have dyslexia and dysgraphia. I have selected a Disney dream because I just think it would be really awesome! Maybe, just maybe, I could meet Spider-Man and some of the other Marvel Heroes. I’ve always always loved Spider-Man, and I think it would be really great to meet him. I would also like to see Mickey and do some of the water rides. I think I would have a wonderful time during this, and I sure hope that I can get there someday soon. Thank you for reading my story. God bless you all.
- 100.00% Funded
- $2,200.00 Pledged
- Campaign has ended
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My name is Mason. I was born with Down Syndrome. I am anxiously waiting for my dream come true trip. I wish to ride the Hogwarts Express train and go to the Wizarding World of Harry Potter. Please help me get to Hogwarts.
- 100.00% Funded
- $2,200.00 Pledged
- Campaign has ended
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Mariah is six years old with immunodeficiency, autism, cerebral palsy, a feeding tube, and lung disease. But despite everything she has been through, she smiles through it all. Her parents try to keep her life as normal as possible in-between hospitalizations. She can’t sit up or talk or walk, but dad says, “She is the most happiest little girl I know. Just with her smile, she brightens up a room.” Her parents’ Dream for her was to go to Disney because Mariah loves Mickey Mouse, but when Covid hit, they decided going there would not be the best decision for her. So, they have changed her Dream to a shopping spree. Dad says, “What little girl doesn’t like shopping, right? We would love for her to get a shopping spree so she can shop for new clothes, shoes, toys, and stuff for her room.”
- 100.00% Funded
- $1,100.00 Pledged
- Campaign has ended
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It’s hard not to smile when you meet this handsome 11 year old, since Aaron, from Hudson, FL, is always giggling and even asks for a hug as a way of saying “Hello!” Aaron has 11 different diagnoses, yet remains very happy and affectionate through doctors appointments, injections and medications. Being non-verbal with epilepsy and an Immune system deficiency, Aaron’s DREAM is to have a sensory room at home where his OT and ABA therapists can provide his 30-hour a week therapy at home, instead of driving across town to an office. The goal is to provide an indoor swing, bubble tube and a ball pit for sensory play. This dream will benefit him by providing indoor exercise with the swing, having access to occupational therapy equipment and giving him the lights and sounds for sensory output. A quiet corner will give him a place to relax after an epilepsy episode with soothing music. As a pre-teen that craves his own space, this will be the first time Aaron will have a room to call his own that he doesn’t have to share with his autistic, younger brother, Bubba! Can you help Aaron’s dream for a sensory room come true?
- 100.00% Funded
- $2,200.00 Pledged
- Campaign has ended
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Gage has been diagnosed with non-verbal autism. He is also seeing an eye specialist because of something going on with his eyes and focusing. Gage loves to stack and build things, run and climb, and any activity associated with water. His mom thinks he will make a good builder or designer when he grows up. Gage would be excited to receive a sensory room for his dream. He loves the idea of having lots of things to see and touch and his mom thinks this would benefit him greatly. Gage is the happiest and loving little boy.
- 100.00% Funded
- $2,200.00 Pledged
- Campaign has ended
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Tyrese has been diagnosed with cerebral palsy. Playing basketball is one of Tyrese’s favorite things to do. He plays basketball at home on a small court with his dad. Tyrese is hoping to be a basketball player when he grows up. Tyrese and his family feel that although his diagnosis affects his walking, it never stops him from playing, trying every day to get stronger, or having Dreams. Tyrese’s Dream is to go to the Florida theme parks. He chose this Dream because he feels it gives him a chance to enjoy himself, have fun just being a kid, and show that with his abilities, he can still get around rather than having people look at him for his disability. Tyrese also says that having this Dream Come True gives him hope that one day, his dream of walking and becoming a basketball player will come true as well.
- 100.00% Funded
- $5,500.00 Pledged
- Campaign has ended
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Jon was born like everyone else in July of 2002 but suffered from a drunk driving accident when he was an infant. He has been diagnosed with autism, traumatic brain injury, cerebral palsy, epilepsy, dysphagia, and low vision. Jon is kind and gentle. He smiles while working through all of his therapies, even when they hurt. Jon cheers up all of his therapists and teachers with his happy disposition. Jon’s health has been declining over the years and will continue to decline due to the damage caused by the drunk driving accident. Jon’s wants to be a dad when he grows up. His Dream is to travel back to San Diego, California for a vacation one more time because that was where his first vacation was with his forever family. He wants to visit the beach and go to the movie theater.
- 100.15% Funded
- $2,003.00 Pledged
- Campaign has ended