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2nd Annual Teeing Off for Katie

Friday, September 18, 2026
Lonnie Poole Golf Course | Raleigh, NC

Following a successful inaugural event, we look forward to another memorable day on the greens in support of CurePSP!  We are proud to honor Katie Lyons, who is courageously living with PSP, through this special event.

Not Playing? You Can Still Donate

You can still be part of the team! Every donation helps support CurePSP’s mission to improve care, raise awareness and fund research for PSP, CBD and MSA. Donate today and help us make an impact together!
 

Single Player Registration Fee

Join us on the course for a great cause. Your $175 entry supports research, education and care for those affected by PSP, CBD and MSA.
 

Foursome Registration Fee

Bring your team! Register a foursome for $700 and enjoy a day of golf while funding critical research and support programs.
 

Silver Sponsorship

Become a Silver Sponsor for $700 and show your company's commitment to supporting families facing PSP, CBD and MSA.
 

Gold Sponsorship

Elevate your support as a Gold Sponsor. Your $1,200 contribution provides greater visibility and helps expand our mission.
 

Platinum Sponsorship

Stand out as a Platinum Sponsor with a $1,500 gift, our top level of recognition and support for this event.
 

About The Event

Enjoy a fun and meaningful day of golf, complete with a breakfast and lunch buffet.  After the tournament, stick around for a BBQ celebration sponsored by Graybar featuring special guest speakers Rich Spain (CurePSP's Director of Development), Jack Phillips (CurePSP's Board Chair), and Bryan Metoyer (World Marathon Challenge finisher).  Thanks to the generosity of Schneider Electric, all registration fees and donations made by Schneider Electric employees will be matched, doubling the impact of your support!

In September of 2023, Katie was diagnosed with progressive supranuclear palsy (PSP), an adult-onset, neurological disease that impacts movement, thinking, speech and vision.  For Katie and the tens of thousands of other families in the US dealing with this incurable disease, we want to raise awareness and funds for
CurePSP, whose mission is to help all people affected by this through research, access to care, clinical trials and finding a cure.

For questions, email Pete Lyons at pjlyons522@gmail.com.

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