FAMILY SPONSORSHIP

Your support provides hope

LARGE OR SMALL, YOUR SUPPORT MATTERS

At Sara’s Garden, we ensure that serving families is at the heart of everything we do. We strive to provide independence… freedom from drugs… freedom of mobility… freedom to live life to its fullest! However, despite all of the success we have had in changing lives here at Sara’s Garden, families are still in need of assistance. In the United States, HBOT and CE are not recognized as being therapeutic or covered by insurance for many of the conditions that we have success in treating.

Insurance companies will pay for your drug prescriptions… for you to have an invasive surgery… for your wheelchair… for just about anything that will keep you disabled and further dependent on the system to provide for your well being. Families come to Sara’s Garden because they are tired of hearing that there is no hope for their loved ones. They want more for them than what they have been told is possible.

Below is a list of families that are currently in need of financial support in order to afford treatment for their loved ones. Click on a name to get to know the families that need your help and then donate to the ones that touch your heart.

Support Terren Weidman

Terren was born July 16, 2013 at a full term of 40 weeks. He weighed 7lbs. and 6oz. All 10 toes and 10 fingers were accounted for. He came out with such beautiful grey eyes (since then they have [...]

Support Ashlyn Impton

On December 9, 2008, we had a beautiful little girl and we named her Ashlyn. She was more than my husband and I could ever imagine. She had 10 little fingers, 10 little toes, and the cutest [...]

Support Peyton Goecke

Of all the great things that will happen to us in our lives, having children is leaps and bounds better than anything else. It has given us another heart beat and soul to share our life with. [...]

Support Nico Zayas

On April 25,2018 my world was shattered in a million pieces when my son Nicolas was found unconscious and not breathing after drowning in our bathroom toilet. He was rushed to the hospital while [...]

Support Finley Cunningham

Your support for Finley and our family over the past four years has been both amazing and humbling. We are so grateful for your encouragement from the first ultrasound when it was discovered that [...]

Support Aubrie Hysell

Someone once said, “Sometimes, real superheroes live in the hearts of small children fighting big battles.” This is true about Aubrie Hysell. Aubrie is a six-year-old girl who is very energetic, [...]

Support Tracy Lickly

As many of you are aware, on August 14th, while working at the beauty shop, I began to experience eye pain, mental fogginess and extreme fatigue. I felt like I needed to take a nap in order to [...]

Support Bryce Hammond

Our amazing Bryce was born to us in February of 2006. He was in every way, our perfect little baby boy. He giggled, played, cooed and did everything “typical” for an infant boy in his first few [...]

Support Melanie Dzyak

As many of you are aware, Melanie found out last Christmas that her two-and-a-half years of unexplained “episodes” were actually seizures caused by the presence of a rare epidermoid brain cyst. [...]

Support Melody Pickard

Since birth, Melody has been our strong, sweet baby girl; even referred to as a miracle baby. We had two children prior to Melody’s birth with no complications. We were not expecting anything [...]

Support Kalli Bruner

After having a child in 2016 born with mild-moderate hearing loss, we were apprehensive and nervous about the birth of our second child. On January 4th, 2018, our second daughter Kalli Mae Bruner [...]

Support Caleb Martin

We are the adoptive parents of Leah and Caleb. They are biological siblings and each was placed in our home at the age of 6 weeks. Their biological mother suffers from bipolar disorder and has [...]

Support Jaedyn Knight

My wife and I have a beautiful family of seven. Our five children share a special sibling bond that we are proud of. Jamison, Abrie, Jaedyn, Jolie, and Joey enjoy time together and being each [...]

Support Gabe Lorenz

Tectal Glioma. Strange words that we had never heard before. When our son Gabe was seven, we were spending the winter in Indiana with family. He began experiencing extreme headaches. It was [...]

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Contact Us

<p style="text-align: justify;">If you have any questions or would like to receive any additional information on our Sara’s Garden here at Sara's Garden, please feel free to contact us. We would love to address any questions you may have.</p>

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