Education, impact stories, and updates from our community. Every post is written to help HD families, raise awareness, and fund the cure.
When Tiffany's husband started showing symptoms of Huntington's Disease, they didn't know where to turn. Then they found the UC Davis HD Center of Excellence — and everything changed.
In 2025 we focused on the 90+ Northern Nevada families already living with HD — funding the UC Davis clinic that is their lifeline. Here is the year-in-review and what it means for 2026.
If one of your parents has HD, you have a 50% chance of carrying the gene. Testing can tell you definitively. But the decision to test — or not — is one of the most personal choices a person can make. Here is what you need to know.
There is no HD clinic in Nevada. But there is specialist care within reach, a community of families who understand, and an organisation fighting to keep those resources funded. Here is everything Northern Nevada HD families need to know.
Holly was diagnosed with Huntington's Disease in October 2023. Her husband Mikey says the UC Davis care team didn't just treat her — they walked into the journey with them.
Sixteen years ago, Leilani Dunmoyer's mother was diagnosed with Huntington's Disease. Today, Leilani is gene-positive, her brother has HD, and her three children are at risk. The UC Davis team has been with them every step.
Peter Jacobsen and Jim Hardy designed it. The Sierra Nevada surrounds it at 6,000 feet. And in 2026 it is the backdrop for Northern Nevada's most purposeful charity golf tournament. Here is why Gray's Crossing is worth the drive.
A $3,500 title sponsorship at NVforHD puts your brand in front of 100+ Reno/Truckee professionals, associates you with a cause people genuinely care about, and funds HD specialist care for Northern Nevada families. Here is exactly what you get.
Zero overhead. One cause per year. Every dollar tracked. Here is exactly what NVforHD has raised, where it went, who it helped, and what your donation or tournament entry pays for in 2026.
If you have HD, your children have a 50% chance of inheriting it. But that coin flip can be eliminated — before the next generation is born. Here is what every HD family needs to understand about genetics, testing, and options.
HD progresses through three stages — each stripping away something else. Knowing what is coming does not make it easier. But it helps families prepare, plan, and fight back with the right support.
Peter Jacobsen designed it. The Sierra Nevada surrounds it. And every dollar you spend there goes to families fighting Huntington's Disease. Here's everything you need to know.
HD combines the cruelty of Parkinson's, ALS, and Alzheimer's into one hereditary disease. If one of your parents has it, flip a coin. That is your chance.
There is no HD specialty clinic in Nevada. For over 90 families in Reno, Sparks, and the Sierra Foothills, UC Davis in Sacramento is the closest lifeline they have.
Brandon and Rylee Puccini are expecting a healthy baby, HD-free. It started with a golf tournament in Truckee and a grant from HelpCureHD. Here is how preimplantation genetic testing is changing the story for HD families.
You do not have to be a golfer or a millionaire to make a real difference. Here are five concrete ways to support HD families in Northern Nevada right now.
Join us at Gray's Crossing in Truckee. Play golf. Donate. Fight HD.