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Ashton

Who We Are

Ashtons brother helping him brush his teeth.

About Us

  

Little Seedz, a non-profit organization, is committed to helping people with developmental disabilities (DD) experience the joy of participating in activities they may not otherwise have access to. This is only possible with the support of compassionate individuals like you. People with DD often miss out on the simple pleasures that many of us take for granted, such as concerts, theatre productions, fine dining, camping, driving a car, festivals, sports & sporting events, and travel. Little Seedz is here to make a difference. We are a beacon of hope for those who wish to live life to the fullest. Our goal is to help our community members lead more satisfying and fulfilling lives, filled with joy and inspiration. 

Our Vision

 To cultivate an environment where every "little seed" flourishes, reaching their full potential and nurturing the "BIG Dreams" that will shape a brighter future.  

Our Mission

  

To champion the full potential of individuals with developmental disabilities, ensuring they have the support and opportunities to explore their dreams, build meaningful relationships, and actively participate in all aspects of life.


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Why We Do It

Our Story

  

Little Ashton came into this world on the first day of a historic year. While the world was battling a devastating pandemic, Ashton was fighting his own battles…

Ashton, a symbol of resilience, was born prematurely at 33 1/2 weeks old, weighing only 4 lbs. 15 oz., on January 1, 2020. He was born addicted to opiates and methamphetamines, 

  

Little Ashton came into this world on the first day of a historic year. While the world was battling a devastating pandemic, Ashton was fighting his own battles…

Ashton, a symbol of resilience, was born prematurely at 33 1/2 weeks old, weighing only 4 lbs. 15 oz., on January 1, 2020. He was born addicted to opiates and methamphetamines, and with a congenital heart defect called “Transposition of the Great Arteries”. Despite these challenges, he fought on. The adoptive parents, after finally being granted permission to start visiting him in the PICU after three weeks, fell instantly in love with him and spent as much time with him as allowed. The nurse told them that only two days before they came into his life, his vitals had begun significantly dropping, and they thought they were going to lose him. They said that there must have been a miracle because he was improving, though not due to any medical explanation.

This improvement was on borrowed time, however. Ashton was in desperate need of open-heart surgery as his condition was one in which the artery that sends oxygen-rich blood to the body and the artery that sends oxygen-poor blood to the lungs were reversed. Being so small made him too fragile to undergo such surgery; therefore, they couldn’t perform it for five weeks after birth. To add insult to injury, the night before he was scheduled, his parents were informed that Ashton would have to wait another week as the heart surgeon became too ill to perform.

Having to wait six weeks to fix his heart took its toll on Ashton. He developed lung disease due to getting too much blood in his lungs. Moreover, he developed an acute kidney injury before surgery, which prevented him from getting the complete surgery he needed the first time. Due to this, six weeks later, he had to have a second open-heart surgery and had to be intubated and on a ventilator.

Ashton was finally discharged from the PICU on April 18, 2020. He was sent home on oxygen and with an NG Tube as he could not eat food on his own. He had to receive blood thinner shots twice per day to prevent additional clotting, as he had encountered while an inpatient. The doctor stated that he could not do “tummy time” for the first six months to allow enough time for his chest to heal from the open-heart surgeries. Eventually, his NG tube was replaced with a G Tube.

Ashton was diagnosed with Provisional Cerebral Palsy early on. This opened services for DDD ALTCS. He was able to receive speech therapy and occupational therapy (OT), as well as in-home nursing, 40 hours per week. Eventually, he was able to receive attendant care, habilitation, and respite. During an OT session, parents were informed that he struggled with his fine motor skills. They stated that not being able to do tummy time contributed to

This, as that position strengthens the web between the thumb and pointer finger in babies, allows them to develop their motor skills.

Ashton’s conditions led to the expansion of The Little Foundation. The owner, Paul Little, was providing services for Ashton one day when a conversation took place, leading Paul and Ashton’s parents to realize they were the perfect combination to go into business together, helping others as The Little Foundation had helped Ashton. The company grew and ultimately branched out into other opportunities, one of which is called “Little Seedz.” Ashton's story, a testament to the power of love and resilience, has inspired the work of The Little Foundation, touching the lives of many.

Today, Ashton is a 5-year-old, happy, healthy, and fun-loving kid who is a beacon of light, whose smile brightens up any room. The struggles he faced coming into this world never showed on his face or in his character. He is a lover of life and people and most certainly destined to be a healer in some capacity. You will often find him looking for a band-aid to make someone feel better, whether they have a physical or emotional “boo boo.” His positive spirit is infectious, uplifting those around him. He loves God and shines His light everywhere he goes. He is kind, thoughtful, funny, loving, and charming. People often tell his parents, “This kid is going to be a future 'heartbreaker.” We like to think of him, however, as a future 'heart-fixer.”

Opportunities and Selection Process

Winners Picked Quarterly

  

Little Seedz raises money through contributions from the community and business owners, as well as various fundraising events. For our first year, we are offering a quarterly “BIG Dream” come true for one lucky individual with Developmental Disabilities within the State of Arizona. We want to provide people with the opportunity to participate in something that they have always dreamed of doing but never thought they could. With the help of The Little Foundation, we aim to “Make the Impossible, Possible”. To be eligible, you must submit information about your “BIG Dream” event, why you should be chosen, and a little bit about yourself. This can be submitted via e-mail to the Little Seedz website. Please do not put any personal and specific information, such as first name only, as the winner or their guardian will have to consent to your picture and your first name being used on our website for publicity purposes. This is an excellent opportunity for agencies throughout the state to help the people they assist create videos, essays, or any other form of expression they choose to communicate their “BIG Dream”. Agencies can assist with the application process, provide resources for creating the submission, and support participants in realizing their dreams. Parents, caregivers, friends, and family get the chance to spend time getting to know you, share personal stories, and have conversations that make others realize that you are not that different from them. We all have the innate desire to be loved, have meaningful connections, and be accepted as equals. 



  

Please keep in mind that the “BIG Dream” is something local, some examples are;

Camping/Glamping

Staycations

Birthday Celebrations

Clubbing

A particular occupation for a day

Best Day Ever- all about YOU

Opera

Theatre Events

Ice Skating

Grand Canyon Tour

Driving a car

Picnic on the lake

Tubing the Salt River

Spending the day on a boat at the lake

Horseback Riding

Play a sport

Play in the snow

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Little Seedz

14831 W Dovestar Dr, Surprise, AZ, USA

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