Living on in our hearts forever

Living on in our hearts forever

We always knew Daniel was one in a million. As it turns out, he was more like one in a billion. To be under 30 and die from CJD is that rare.

Daniel had just turned 18 in the fall of 2012 when he first mentioned blurry vision. Six months later, he could barely walk. Daniel was scared, anxious and depressed. He couldn’t sleep. He struggled to reach for a glass of water and his hands would tremble as he raised the glass. His voice was shaky. His laughter sounded oddly high pitched. He choked on food. His body was failing him and doctors didn’t know why. Every day, a little more of Daniel slipped away.  He would eventually lose the ability to talk and he became completely immobile. Daniel died on Valentine’s Day 2019 at the age of 24. 

Before Daniel became sick, he had this deep and hearty laugh. He had an awesome sense of humor. Daniel had a smile that just beamed from the inside of his soul out. He was always happy and naturally saw the bright side in every situation. In Daniel’s mind, the world was full of joyful opportunity. He was athletic, a skateboarder, a runner, and a diver. But what Daniel loved most was snowboarding. Daniel wasn’t very talkative. He was a much better listener. He knew how to listen deeply and he heard things you didn’t say. He just understood the subtle fears people carry. He was compassionate and empathetic. You could feel his warmth just standing next to him. One of the things we loved most about Daniel, was how inclusive and welcoming he was. Daniel didn’t know a stranger. He embraced everyone. He had a way of making anyone and everyone feel special, loved, like you were his best friend.

In a search for diagnosis and cure, Daniel would have more than 700 blood tests, 12 MRI’s, 4 PET scans, 10 CT scans, 5 Spinal taps, 6 ultrasounds, 2 EMG’s, 5 EEG’s, 3 EKG’s, 2 echocardiograms, 2 Skin biopsies, a muscle biopsy and full genetic testing.  He was seen by top neurologists at Johns Hopkins, Boston Mass, Columbia Presbyterian, Mayo Clinic and NIH Undiagnosed Diseases. We didn’t find out Daniel had CJD until after his death. 6 ½ years living with CJD is one of the longest on record.  Most people only live a few months.

We are sponsoring a Strides for CJD walk in Virginia because we want to educate people about this disease and we need to help find a cure.

About Fundraising

Donations of $250 and above are considered sponsorships.

Sponsorship Levels:

  • Premier: $20,000
  • Diamond: $10,000
  • Platinum: $5,000
  • Gold: $1,000
  • Silver: $500
  • Bronze: $250

Premier, Diamond, and Platinum Sponsors will have their name or logo* displayed on participant T-shirts, the Strides for CJD website, and signage. Gold Sponsors will have their name or logo* displayed on the Strides for CJD website, and will have their name (not their logo) listed on participant T-shirts and signage. Silver and Bronze Sponsors will have their name listed on the Strides for CJD website only.

The deadline for Sponsors' names (individuals) or logos (companies) to appear on participant t-shirts is Sunday, August 9th at 11:59pm Eastern time. Sponsorships made after the sponsorship deadline will have their name or logo* displayed on the Strides for CJD website only. 

Text to Give

To donate to our event text STRIDES2026 to 50155.

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Please note, sponsorships/donations do not include registration; rather, sponsorships/donations and registration are separate transactions. To register*, please click here.

*Registration fees do not count toward the sponsorship and team fundraising deadline or the fundraising competition. They will not appear on the team or individual fundraising thermometers.

Our Team

  • Paul Nugent Paul Nugent
  • Lou Nugent Lou Nugent

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Our Supporters

  • Paul Nugent 2 days ago $500.00
  • Paul Nugent 2 days ago $500.00

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About Strides for CJD

Strides for CJD is an annual walk/run to raise awareness of Creutzfeldt-Jakob Disease (CJD), a rare neurodegenerative disease that has no treatment or cure. Through this event, anyone -- anywhere -- can pay tribute to their loved ones and raise funds for the CJD Foundation, a 501(c)(3) organization.

Funds raised support our programs including:

  • Our 24/7 helpline, support groups, conference, and other family programs throughout the year.
  • Research grants to help scientists make important discoveries and bring us closer to a cure.
  • Medical education to help raise awareness and understanding of prion disease.