family stories

Noah M.

July 14 is a day forever etched in our hearts – a day no parent ever hopes to face. Our son Noah was diagnosed with germinoma brain cancer at just 12 years old. The shock and disbelief felt like a nightmare we couldn’t wake from. Three days later, we were discharged and began waiting for a second opinion…

 

Mason L.

Our son Mason is extremely medically complex, with Down Syndrome, Epilepsy, Chronic respiratory failure and autism. We have spent countless days, weeks, and months being hospitalized…

 

Silvi R.

As both a Logan Strong Foundation (LSF) board member and a current LSF family for the last 2.5 year, I have a unique perspective. I know that my fellow board members have my back, but it still always amazes me how quickly the board acts when any family is in need…

 

Reese J.

We cannot begin to express the depth of our gratitude for the incredible support we’ve received from the Logan Strong Foundation. When our child was diagnosed with hepatoblastoma, our entire world was turned upside down. It was a time filled with fear, uncertainty, and overwhelming challenges—emotionally, physically, and financially…

 

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