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Alex's Lemonade Stand Foundation Blog

Welcome to the official blog of Alex's Lemonade Stand Foundation!

September 19, 2019
  • “Never in a million years did I think my kid would have cancer," said Kim, whose son Matteo was diagnosed at 6 months old with kidney cancer.
    “Never in a million years did I think my kid would have cancer," said Kim, whose son Matteo was diagnosed at 6 months old with kidney cancer.
  • “Having a child with cancer changes you. You breathe deeper, love harder, forgive more. Is it hard? Absolutely. By far it’s the hardest thing I have ever faced as a parent,” said Tina, mom to Kensley, who was diagnosed with leukemia in May 2019.
    “Having a child with cancer changes you. You breathe deeper, love harder, forgive more. Is it hard? Absolutely. By far it’s the hardest thing I have ever faced as a parent,” said Tina, mom to Kensley, who was diagnosed with leukemia in May 2019.
  • “I believe research saves lives and I do not want to see any more children die from cancer,” said Angie. Angie’s daughter, Sara, died when she was 18 years old from relapsed germinoma.
    “I believe research saves lives and I do not want to see any more children die from cancer,” said Angie. Angie’s daughter, Sara, died when she was 18 years old from relapsed germinoma.

The night before 6-month old Matteo was diagnosed with a rare pediatric kidney cancer, his mom, Kim stayed up late baking cookies for an upcoming lemonade stand at Power Home Remodeling to support Alex’s Lemonade Stand Foundation.

“Never in a million years did I think my kid would have cancer. We knew about childhood cancer. We were aware. But we did not think it would be us,” said Kim.

Everyday, 43 children are diagnosed with childhood cancer. A childhood cancer diagnosis brings with it... Read More

August 21, 2019
Sixteen years ago, when I did not even know what USC was, or any university for that matter, I was diagnosed with cancer—tumors called astrocytoma were in my spine. I was just 2 years old at diagnosis, so my treatment and recovery plan was naturally placed in the hands of my parents. From that point forward, I lived with and relied on two adults who knew more about my condition than I did.  

For my four long years of high school, I woke up at 5:30 every morning to go to swim practice and then stayed up late nearly every night to finish my chemistry homework. I desperately wanted to get into my dream school, the University of Southern California (USC), nearly 3,000 miles away from my home in Connecticut. And then, I got my acceptance letter—reaching my long-awaited goal. Yet, my struggles were far from over.

I walked into my dorm room for the first time last August and to the outside world, I looked like any other eager, nervous 18-year-old, ready to start her freshman... Read More

July 17, 2019
Today is Glioblastoma Awareness Day. For children battling this rare brain tumor, treatment options are limited and after relapse, the disease tends to spread quickly. 

Today is Glioblastoma Awareness Day. For children battling this rare brain tumor, treatment options are limited and after relapse, the disease tends to spread quickly. 

In 2016, we shared the story of Chloe Cox, a then 12 year old from Texarkana, Texas who had been diagnosed with glioblastoma. Chloe’s family utilized the ALSF Travel For Care program to help cover the costs of hotel rooms 300 miles... Read More

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