2026 Recipients

This page contains stories of recipients this calendar year who have received KARE Funds . Please feel free to read the stories to understand the positive impact donor funds are having on so many families meeting the mission of the Foundation. THANK YOU DONORS!!!

Some families request anonymity and the KARE Foundation honors their wishes.

Meet the Jacob Family

Sometimes our connection to a KARE recipient runs especially deep—and the Jacob family is one of those moments.

Dee and Bob Jacob are deeply rooted in the Guilford, Connecticut community. Dee served as President of the Shoreline Chamber of Commerce and was instrumental in helping establish the KARE Foundation within the Connecticut shoreline community back in 2021. She generously shared her time, guidance, and influence, becoming a strong supporter of the Foundation and a passionate advocate for our mission. On a more personal level, Dee also taught CCD to Paul’s twin daughters during their high school years, and the Jacob and Dostie families remained connected throughout the years. Bob and Dee are parents to five children—one of whom is the same age as Paul’s twins—making this connection feel even more personal.

In January of 2025, life changed abruptly for the Jacob family. Bob began experiencing troubling cognitive symptoms, and Dee immediately knew something wasn’t right. She brought him to the emergency room, where an MRI revealed a brain tumor. After a brain biopsy, they received devastating news: Bob was diagnosed with a highly aggressive Stage 4 small cell Glioblastoma. A Glioblastoma diagnosis alone is overwhelming—but learning it was the rare and even more aggressive mutation made it even more devastating. Bob underwent a resection of the tumor five days later.

Shortly after Bob’s diagnosis, Dee reached out to the KARE Foundation—not for help, but for guidance. She wanted to talk through Bob’s diagnosis, treatment options, and what the road ahead might look like. At that time, Dee was still working and the family was doing everything possible to navigate treatments while hoping for stability.

In September, Dee contacted KARE again with heartbreaking news—Bob had experienced a recurrence of the tumor, requiring a second resection surgery. With the recurrence, Dee made the decision to accelerate her retirement from the Shoreline Chamber of Commerce, so she would be available to be by his side.

Following his second surgery, Bob was unable to return home for over four months. During a transition from acute rehabilitation to skilled rehab, he suffered a fall that resulted in a brain bleed and hygromas. After three weeks and the placement of a brain shunt, he returned again to acute care and then back to skilled rehab. After Christmas, it became clear that Bob was no longer making progress. He showed increasing signs of decline—sleeping more, responding more slowly, his voice growing softer, and experiencing more frequent episodes of delirium.

After consultations with Bob’s Neuro-Oncologist and Geriatric physician, the family was faced with the most heartbreaking decision of all: shifting the focus of care to keeping Bob comfortable and bringing him home.

This stage of the journey is beyond devastating. When KARE received word from Dee that Bob was entering this phase, we immediately understood the emotional toll—and the financial strain families face at this point, when so many necessary expenses are no longer covered by insurance. Without hesitation, the KARE Board unanimously approved support for the Jacob family.

We are honored, humbled, and profoundly grateful to stand beside a family fighting this horrific disease—one with such deep connections to our foundation, our family, and our hometown.

Please keep Dee, Bob, and the entire Jacob family in your thoughts and prayers.

Meet Our January Recipient

Our next KARE Foundation recipient found us the same way so many families do—out of desperation, hope, and an urgent need to help someone they love. The person reached out after discovering KARE through our public Facebook page and visiting our website. She is the sister-in-law to her brother’s wife in Connecticut who was recently diagnosed with Glioblastoma. We are keeping the names out of the story since the family does want anonymity.

The sister was searching endlessly for answers—trying to understand this devastating disease, explore treatment options, and find any possible financial assistance for her brother’s family. Her message immediately brought me back to the early days of Paul’s diagnosis… the fear, the confusion, and the overwhelming anxiety of not fully understanding what Glioblastoma meant—while simultaneously facing an uncertain future that would impact our family physically, emotionally, and financially.

When Paul was diagnosed, our community rallied around us. A medical fundraiser and the incredible generosity of others allowed our family to focus on what truly mattered—Paul and his treatments—especially during the added challenges of COVID. Those memories made this story deeply personal.

After connecting with the sister, I learned just how suddenly life changed for the family. Her sister-in-law, just 50 years old, lost function on the left side of her body in November 2025. Knowing something was terribly wrong, she was rushed to the emergency room—where the family received the devastating diagnosis of Glioblastoma. Even more heartbreaking was learning the tumor is located in an inoperable area of her brain.

She is now undergoing the standard treatment protocol of radiation and chemotherapy in hopes of shrinking the tumor. If these treatments are not effective, there are no additional options available given the tumor’s location and pathology. Despite this unimaginable reality, the family is determined to do everything possible to extend their sister-in-law/wife/mother’s life and cherish every moment they have together.

The family has three children – 27, 23 and 16. The family has also been required to renovate their home to make it handicap accessible. During the renovations, their local fire department stepped in twice a day to help her get safely in and out of the home for treatments—a powerful reminder of both the family’s need and the compassion of their community.

The financial burden, however, is overwhelming. Between home renovations, in-home care not covered by insurance, and loss of income to care for her, the stress on this family is immense.

When the KARE Board reviewed their situation, there was no question—we needed to help. The family deserves the time and space to focus on her and the moments they have together, without the crushing weight of financial worry. We truly believe Paul continues to guide our connections to families in need, and we are so grateful that the sister reached out to us.

Supporting the family is exactly why the KARE Foundation exists—and we are honored to stand beside them during this incredibly difficult journey.

Blessings all!