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.


Registration Information

  • Register by Wed., Aug. 24th, 11:59pm ET to receive a free Strides for CJD t-shirt with your registration.
  • Registration costs $30 for adults and $20 for children 12 and under thru Thurs., Sept. 15th, 11:59pm ET. After that, costs jump to $35 for adults and $25 for children 12 & under.
  • Online registration ends Thursday, 12:00pm ET the Thursday before your event. After that, you can register on-site the day of your event.

Text to Give

To donate to Daniel Nugent's Team, text Strides2022 Daniel to 50155.

About Fundraising

Donations of $250 and above are considered sponsorships.

Sponsorship Levels:

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

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 listed on participant T-shirts and signage. Silver and Bronze Sponsors will have their name listed on the Strides for CJD website only.





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Our Team

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Our Supporters

  • Anonymous November 2022
  • Strides '22 Fairfax Square-Donations November 2022 $105.00
  • Eva Cardenas For CJD cure! October 2022 $53.00
  • Lori & Mike Rowen In loving memory of Daniel. October 2022 $106.00
  • Susan Timoner October 2022 $53.00
  • Joan Nugent August 2022 $1,200.00
  • margaret Lewis August 2022 $1,060.00
  • Anonymous August 2022 $1,000.00
  • Anonymous Happy birthday Daniel. Miss you so much. September 2022 $500.00
  • Theresa Nugent August 2022 $500.00

Recent Activity

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.