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    How a Father’s Loving Act Went International

    Date Posted: October 15, 2019
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    How a Father’s Loving Act Went International

    To a father, his children are a true gift and treasure. They always wish the best for them and would do anything to see them happy. For Gavin Leonard, he just wanted a way to be closer to his daughter and create memories that would last a life time. About 2 years ago, he began writing children’s books to read with his daughter. He never expected this small fatherly act would connect him with people and organizations across the Globe.

    Gavin’s Inspiration and Motivation

    From the moment Gavin laid eyes on his daughter, he knew he would do anything for her. As she got a little bigger, he started thinking of a way to remember the adventures they had together for when she was older. A friend told him how he began a blog to keep track of all the adventures he had with his kids, Gavin couldn’t help but love the idea. He began doing just that and to his surprise, found people were actually interested in following his posts. At the time, Gavin didn’t know where this would lead but luckily enough, his love for his daughter would open doors he couldn’t imagine. When family and friends came to visit, they would always comment on how beautiful she was and that she could be an actress or model. Gavin knew they meant well, but to him it was a bit strange to think of a new born in this way. Additionally, they would always call her a “princess” but Gavin began replying, “she’s not JUST a princess”, for he knew she would be able to do anything she dreamed of. The reason Gavin felt this way came from the books he read to her. To him, they were always the damsel in distress and in need of being saved. Not his daughter! She would be strong and capable on her own. He often made comments about this to his wife, until one day she said, “if you don’t like the books you read… then write your own!?”. And so, he did!

    The ‘Not Just a Princess Book Series’ is Born

    Gavin made a plan and wanted his princesses to get away from the typical fairy tale and make it more real. So, what better title for the series than “Not Just a Princess”? His initial plan was to have his daughter (the princess), have a job and need to solve a problem that came up. But after a while, he knew she would need help and began creating new princesses. The common theme throughout the previous 6-book series is the princesses’ strengths, smarts, and abilities to work together to help one another overcome their problem. He wanted a story for everyone and made the princesses different in all aspects including being different culturally, appearance, etc. He never expected the books to be published but his daughter loved them so much he figured why not try.

    The Newest Princess and the International Connections she made

    Most recently, he decided to go further and include a second princess with a disability. Gavin wanted to show the world the truth of people differently abled. Instead of talking about a disability, he wanted to spread awareness that people have all different strengths and weaknesses no matter who they are. He thought back to his time living with family in China. While there, he spent a lot of time with his niece Nora, who has down syndrome and learned a lot for himself. When I had the opportunity to speak with him, he told me a story of what truly opened his eyes. “Nora loved water”, he said. Her and her siblings would often swim and play. One day when he was with them, he had been throwing Nora’s siblings into the water for fun, when Nora asked to go next. He hesitated out of care and in fear she may get hurt or scared. But her father set the record straight and what he said to Gavin really stuck with him. He said, “she’s just like her sisters and she can be thrown too.” Gavin went and threw her next and after seeing her joy and excitement, he realized nobody should ever be treated differently like that. In honor of his niece, this story follows Nora, a champion swimmer with down syndrome, and how she helps the others solve a problem. But it doesn’t stop there. For this story he wanted to do more than just spread awareness but instead, use it to give back in a better way. Gavin began looking for local charities and connected with Down Syndrome Ireland and the Special Olympics. After hearing all that Special Olympics does for their athletes across the globe, they decided to begin promoting it worldwide. That led to Gavin connecting with us at the Dreamscape Foundation and other nonprofits as well. He explained he planned to donate all proceeds from the book’s sales to different charities and wanted to connect to as many as possible.

    The Release and Final Details

    Should all go as planned, the book is anticipated to be released in Ireland on October 24th, 2019. But you can purchase anytime through Dreamscape Foundation’s direct link!! The charities involved as of now include the Dreamscape Foundation, Special Olympics: Ireland, UK, Down Syndrome: Ireland, and US, and Brainwave UK. All of these organizations will have their own links available to purchase after the book is released! Those links will be used to directly support that organizations, or by purchasing from Not Just a Princess directly the proceeds will be distributed evenly to all organizations. That is how what started out as a way for Gavin Leonard to share time with his daughter, turned into an international movement to spread awareness and give back to the disabled community. Gavin is an amazing guy and has nothing but love in his heart. On a final note, what he wishes to highlight most is how excited he is to be working with various nonprofit organizations on this project and to have the opportunity to raise funds for their continued good work! To keep up with Gavin and the Not Just a Princess book series you can follow them on Facebook, Instagram, or Twitter. Written by: Nicholas Sibilia
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    Living with Learning Disabilities

    Date Posted: August 16, 2019
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    Living with Learning Disabilities

    We see children struggling to learn within our school systems each and every day. Learning disabilities are extremely common and in fact according to the National Center for Learning Disabilities, one in every five children are affected. These children are more likely to fall behind causing them to repeat a grade, get in trouble at school/with the law, and eventually they could drop out making it difficult to pursue a career as an adult. How this is prevented is simple, but first you must understand what a learning disability truly is.

    The facts

    The Learning Disabilities Association of America defines a learning disability as a neurological disorder that comes in many different forms. The forms include dyscalculia, dysgraphia, and dyslexia. Dyscalculia affects the way the brain processes numbers and math facts. Dysgraphia affects a person’s handwriting and fine motor skills. The most well-known is Dyslexia, and this affects reading and language-based processing skills. Kids can be ashamed and carry this disability with them into adulthood. Some may never disclose their disability with close friends or even their significant other. But, what people don’t realize is these kids are just as smart as their peers! Looking for the early signs and identifying the problem(s) will help significantly with your child’s early development skills and reaching their full potential.

    Looking for the signs

    It can be very challenging to identify if your child truly has a learning disability or not. Pay close attention to the little warning signs when you start introducing them to the first stages of school (informational learning, i.e. memorization). There are different ways to pinpoint if your child has a problem. Preschool/Kindergarten:
    • Difficulty connecting sounds & letters or pronouncing words
    • Problems with counting
    • Difficulties using crayons/paint
    • Trouble being understood by strangers
    • Difficulty with dressing themselves
    Elementary School:
    • Can’t speak in full sentences
    • Continuously forgets newly learned information
    • Trouble holding pencil/writing
    • Problems following directions & routines
    • Can’t play age appropriate games
    Now that you have identified the signs it is time for you to take the next steps for your child or loved one to live up to their full potential!

    Next steps

    The first step after you have a suspicion that your child is struggling it is time to seek professional help and have an evaluation done. There are plenty of resources for you to take action. The easiest would be to see your pediatrician to meet with them and discuss your concerns. You could also contact the school your child is attending and let them know you would like to have your child evaluated or to keep them updated with the evaluation process. Most likely, they will have noticed the signs or will recommend you to someone you should see for the professional evaluation. After they evaluate your child’s basic skills, they will go over their results and tell you if your child should need to receive special education services or additional help. If this is the case they will go over a learning plan based on where the help is most needed. Most schools accommodate to the specific learning plan for any child with a disability or already have a plan set for different types of disabilities. During this process, your child could become very self-conscious or embarrassed. This is normal and happens quite often, that is why as a parent it is important for you to help continuously build up their self-esteem. Some easy ways to do this are by pointing out things your child is good at and praising them for that specific attribute. Also, getting them involved in activities they know they do very well at! This will help develop their self-worth and determination to keep striving to succeed even with the extra difficulties. Living with a learning disability can be difficult for all parties. Remember, this does not make someone less than anyone else and with your help, love, and support your child will strive to be the absolute best at anything they put their mind to!    
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    6 Things You Probably Didn’t Know About Down Syndrome

    Date Posted: February 15, 2019
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    6 Things You Probably Didn’t Know About Down Syndrome

    Education starts with awareness. That’s why we’re taking the time to cover some of the disabilities in today’s society you may have heard of, but know surprisingly little about them. Our blog series starts with Down syndrome. Read along as we cover some basic facts about this disability, it’s features, and risk factors.

    6 Facts About Down Syndrome

    What is Down syndrome, exactly? Get better acquainted with this genetic condition with these 5 helpful facts.

    Down syndrome is causedby extra copies of chromosome 21.

    This extra chromosome may be partial or whole, and can lead to one of three different types of Down syndrome: Trisomy 21, Mosaic Down Syndrome or Translocation Down Syndrome.

    Trisomy 21 is the most common form of this condition.

    Trisomy 21 occurs when three copies of chromosome occur instead of two. It accounts for 95% of cases. Mosaic Down Syndrome and Translocation Down Syndrome are much rarer, accounting for 4% and 1% of all cases.

    Symptoms can vary greatly from one case to another.

    Down syndrome isn’t the same across the board. Cases vary from mild to severe. Symptoms may include some or all of the below:
    • Small Head
    • Flattened Facial Features
    • Eyes with An Upward Slant
    • Ears of Small or Unusual Shape
    • Short Neck
    • Poor Muscle Tone
    • Broad, Short Hands with a Single Palm Crease
    • Small Hands and Feet
    • Short Fingers
    • Extreme Flexibility
    • Short Stature
    • Brushfield’s Spots
    Down syndrome also includes cognitive and physical impairments of varied severity. However, many individuals with Down syndrome may hold their own job, live independently and enjoy everyday activities.

    The life expectancy of individuals with Down syndrome has increased over the years.

    Medical advancements have significantly increased the average lifespan of individuals with Down syndrome. In 1983, the average life expectancy was 25. In today’s society, the average lifespan is 60.

    Approximately one-fourth of U.S. families are impacted by this condition.

    While the cause for Down syndrome is unknown, the risk increases with the mother’s age.

    It is the most common chromosomal condition in the U.S.

    More than 400,000 individuals have Down syndrome in the U.S. with it occurring on average in 1 of every 691 babies born.

    Why Dreamscape Foundation is Talking About It

    Here at Dreamscape Foundation, we work day in and day out to help individuals with disabilities acquire the tools, programs, and resources they need to live a full life. While our focus is primarily on visual impairments, we don’t view ourselves as a singular community. We understand that the demand for special needs stretches beyond are individual cause, and that change happens through education, understanding, and support. That’s why we want to take the extra step in informing our community of other common disabilities in order to help form a bridge of understanding and connection. If you’re currently seeking local Down syndrome resources in Florida, we encourage you to visit the Global Down Syndrome Foundation online. If you’re an individual looking to raise funds to meet specific needs for yourself or a loved one, talk to us. We collaborate with individuals and organizations to help provide essential resources for individuals with disabilities.
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    A Volunteer’s Look at a Night to Shine

    An image of Parker and Sammy together in patriotic clothing and cooking aprons. Sammy advocates alongside Parker for disability awareness and is volunteering for the SWFL Night to Shine event.
    Date Posted: February 1, 2019
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    A Volunteer’s Look at a Night to Shine

    An image of Parker and Sammy together in patriotic clothing and cooking aprons. Sammy advocates alongside Parker for disability awareness and is volunteering for the SWFL Night to Shine event. Sammy Callari is just one of many who will be volunteering to help bring SWFL’s “Night to Shine” alive this February. However, this isn’t his first rodeo. Sammy has volunteered for this event before and has a strong passion for the impact it has on the disabled community.

    Who is Sammy Callari?

    Sammy is a former MMA fighter who became a personal trainer. It was there he met Parker, a 13-year-old boy with Down syndrome who became his client, then his friend. “Our personalities just clicked from day one,” Sammy said. The pair’s near-instant chemistry quickly evolved into a brotherly bond. As an underdog himself, the young trainer connected with his client’s challenge of having to fight for acceptance. Sammy taught Parker how to make strides in his physical health but to Sammy, those lessons paled in comparison to the lessons Parker imparted upon him. “My volunteering work came after my relationship with Parker,” Sammy explained. “I felt overjoyed and extremely happy my first session with him. I will never forget it. We didn’t do anything out of the ordinary but I left the gym feeling very happy. I wondered, ‘What did this thirteen-year-old do to me to make me feel so full of life?’ And a lot of it comes down to Parker and the individual he is.” Thus, participating in an event like Night to Shine was a no-brainer. Like Parker, Sammy wants the world to understand and appreciate the disabled community as a part of their community.

    What is a Night to Shine?

    Night to Shine is an event created by the Tim Tebow Foundation but quickly found momentum across the globe. It’s both an all-expenses-paid prom for members of the disabled community and a free night out for their family and caretakers. The event takes place on February 8 this year from 6 pm to 9 pm EST. Currently, there are 3 locations in the area hosting the event: one in Naples, one in Sanibel Island, and one in Cape Coral. The event has grown every single year, swelling from one location to three. Already, registration is full as all 3 locations expect a packed house ready for an unforgettable experience.

    Sammy’s Take on the Event and Volunteering

    Sammy is volunteering again this year to help make Night to Shine a success. The impact of previous events made him want to be a part of it yet again. “It was unbelievable,” he said. “It’s one of those things you just have to be there to experience. We’re all looking forward to it this year.” Night to Shine focuses on putting their disabled guests in the spotlight for a night. Every single individual will walk down the red carpet and is crowned king or queen of the prom in acknowledgment of their significance. They are part of our community with differences worthy of celebration. Yet the guests aren’t the only ones who feel rewarded at this event. Volunteers give their time but take home with them the priceless gift of reminding these special members of their community they’re loved. “I think giving back is one of the greatest feelings when you do it with the right intentions,” Sammy said. “I don’t do it for the money; I don’t do it for the notoriety; I don’t do it for the publicity. I just do it knowing inside of me that it’s the right thing to do.” “My calling for helping people with disabilities is because a lot of society puts people with disabilities in a corner and say, ‘No, you can’t do this; you can’t do that,’ and that upsets me inside. I believe everyone has abilities inside of them and things they can do and that’s what we should be focused on.” For more information on this year’s Night to Shine, visit https://www.swflnighttoshine.com/.
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