43e8 Welcome to Sammy’s Friends Foundation. In Madison, NJ, we offer discounts to children in need of developmental therapy.
 
 
 

Please feel free to contact us at anytime if you would like to donate or are willing to learn more about us. We strive to respond to all inquiries.

Sammy’s Friends Foundation

P.O. Box 344
Madison, NJ 07940

                  
 

                  

See our Donors Here!!


 
 

We support families in 3 ways:

• Educate Parents About 
  Development

• Therapy Rebate Coupons

• Online community For Parents

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Special Children have Special Needs:

Although medical doctors and specialists are essential to help these  children achieve medical stability, they typically require intensive,  specialized therapies...

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Welcome to Sammy’s Friends Foundation

Where Therapists and Families comes Together

Baby Sammy in exersaucer

We are a private charity organization based in NJ. We strive to educate, support, and provide monetary assistance to cover developmental therapy costs for families with children of chronic illnesses.

Samuel a.k.a. Sammy

Sammy was a sweet baby boy who loved cuddles, bath time, and the good oldies songs. He was also a child with complex medical diagnosis including Infantile Spasms and Williams Syndrome. In his short journey on earth, Sammy had touched many people’s hearts. In loving memory of him, this foundation is established to carry on his legacy and to help other special children like him.

Sammy’s Friends is founded by Samuel’s parents, Shaun and Yichien. Shaun is a clinical research scientist for a local pharmaceutical company while Yichien is a pediatric speech language pathologist.

In 2011, their precious baby boy, Samuel, was diagnosed with Infantile Spasms at 4 months old. Infantile Spasms is a devastating childhood epilepsy disorder and is notoriously difficult to control. Children with this diagnosis typically face a multitude of developmental delays and challenges. After undergoing trials of various anti-epilepsy drugs, Samuel finally became seizure free with a ketogenic diet at 8 months old.

Samuel’s parents sadly lost Samuel at 16 months in June 2012 due to an acute, viral induced onset of Pancreatitis. During his journey, Samuel’s parents have met various wonderful doctors, nurses, and most important of all, developmental therapists who helped Samuel achieve his full potential. As they recalled their loving memory of Samuel, they decided to extend Samuel’s legacy by helping families to provide the best possible care and therapies for their special children so that they may also live their each day to the fullest.

We encourage you to browse our site for more information regarding our foundation. We would be happy to answer any questions you may have.

Contact us Today to Learn more!

 
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