Support Katelyn Haberkorn
There are so many things to be grateful for, yet every day feels like an uphill battle. I have been on this journey to find relief from chronic pain for
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 Diane Schroeder
I have always heard how awful the shingles virus was. Unfortunately, I found out just how true that was for myself in April 2025. In my case, the shingles virus
Support John Cope
In 2021, we had the surprise of our lives when John began having frequent headaches and vision loss. This eventually led to issues with recall and memory. After some difficulty
Support Amanda Pirooz
As you know, I once radiated life. I had a career in healthcare, helping others in hospitals, nursing homes, and behavioral units. I was a passionate cook, a lover of
Support Rylee Hannah
In many ways, Rylee is a typical 18-year-old girl. She rolls her eyes, sighs in annoyance, loves fashion, glitter, music, and food. She enjoys people, participating in an adaptive ice
Support Sue MacDonald
Dear family and friends, As you know, I’m a Christian preschool teacher, and I’m really hoping to teach again in the fall. In the fall of 2023, I had COVID.
Support Fetema Wilson
I contracted COVID-19 in late October of 2022, which left me exhausted and dragging for the rest of the year. By January, I needed paramedics to transport me to the
Support Greg Anderson
In August 2018, I was on a motorcycle trip traveling through British Columbia. I started feeling sick so I decided to return home. In Wisconsin, I stopped to visit my
Support Jolie Heberling
I think you all know by now that I have this fun little condition called MS, or Multiple Sclerosis. While it is different for everyone, for me it has been
Support Mary Kraft
As many of you know, Mary was born with a brain malformation called Lissencephaly, which means “smooth brain”. It is a neuronal migration disorder where the brain stopped forming correctly
Support Katelyn Haberkorn
There are so many things to be grateful for, yet every day feels like an uphill battle. I have been on this journey to find…
Support Diane Schroeder
I have always heard how awful the shingles virus was. Unfortunately, I found out just how true that was for myself in April 2025. In…
Support John Cope
In 2021, we had the surprise of our lives when John began having frequent headaches and vision loss. This eventually led to issues with recall…
Support Amanda Pirooz
As you know, I once radiated life. I had a career in healthcare, helping others in hospitals, nursing homes, and behavioral units. I was a…
Support Rylee Hannah
In many ways, Rylee is a typical 18-year-old girl. She rolls her eyes, sighs in annoyance, loves fashion, glitter, music, and food. She enjoys people,…
Support Sue MacDonald
Dear family and friends, As you know, I’m a Christian preschool teacher, and I’m really hoping to teach again in the fall. In the fall…
Support Fetema Wilson
I contracted COVID-19 in late October of 2022, which left me exhausted and dragging for the rest of the year. By January, I needed paramedics…
Support Greg Anderson
In August 2018, I was on a motorcycle trip traveling through British Columbia. I started feeling sick so I decided to return home. In Wisconsin,…
Support Jolie Heberling
I think you all know by now that I have this fun little condition called MS, or Multiple Sclerosis. While it is different for everyone,…
Support Mary Kraft
As many of you know, Mary was born with a brain malformation called Lissencephaly, which means “smooth brain”. It is a neuronal migration disorder where…
Support Katherine Lopez
As most of you know, I am from Fremont, Ohio. I raised three children by myself and worked in a factory in order to finally…
Support Adria Gerig
Our daughter, Adria Gerig, was born with Spina Bifida on November 19, 2013. Her journey has been amazing and truly a testimony to God’s faithfulness…