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WPI WPI is dedicated to solving ME/CFS and other complex infection-associated chronic diseases.

A medical research center dedicated to the discovery of the mechanisms of disease, creating diagnostics, and promoting effective treatments for those who suffer from ME/CFS and other chronic post-infectious diseases.

Just a reminder! TODAY: WPI and  will be hosting a Boba Fundraiser to raise funds for The   Network for patients living ...
10/27/2026

Just a reminder! TODAY:
WPI and will be hosting a Boba Fundraiser to raise funds for The Network for patients living with ME/CFS and Long Covid.
Care Club will be doing their fundraiser on the UNR Campus at the Hillard Plaza on Tuesday, October 27th, from 10 AM to 2 PM.
All drinks will be sold for $6.00, boba is an additonal $1.00

10/26/2026
WPI is encouraging everyone to register or donate to The   Network to support their   campaign, Pace to the Capitol! We ...
10/26/2026

WPI is encouraging everyone to register or donate to The Network to support their campaign, Pace to the Capitol!
We recognize how important this campaign will be to spread awareness about ME/CFS, uplift voices of those who live with the condition, and to help change policies and research funding for ME/CFS and Long Covid!

Join our Pace to the Capitol! We can’t Race, but we can Pace. Register today to help change policy, culture and research funding for ME and Long COVID. https://www.meaction.net/pace-to-the-capitol-landing

“Pace to the Capitol” is a seven month campaign leading up to May 12, 2027 when we will place 200 empty beds in front of the U.S. Capitol. Two hundred reminders of the people missing from school, work, family life, and public view because of ME/CFS and Long COVID.

We are working on a number of unprecedented opportunities this year that we have never had at once, and we need to keep ME in the spotlight.

We are working with Congress to get the ME/CFS Research Roadmap funded. We are working with the Surgeon General's office to develop and disseminate ME/CFS educational materials to clinicians. We are working with The Library of Congress to recognize ME/CFS as a disability that qualifies for services. We are working with State Medicaid leaders to protect Medicaid for our community. We are working in Hollywood and have set up an event to educate TV writers and showrunners about ME/CFS.

We have lots more info coming but here is how you can join in- pick one or more!

- Washington, DC: Join us in DC for our culminating event in front of the U.S. Capitol, where we will display 200 beds to make the suffering of ME and Long COVID visible.

- In Your Community: Join the movement to place mini beds in public places and large beds in front of capitols in your state. A guide will be coming!

- From your bed: Using mini beds and creative storytelling, our community at home will speak about their own experiences living with the disease - and the necessity of pacing.

- Get your pace pack: Everyone who raises $150 or more will receive a pacing pack that is centered on the “home team” or the “hill team,” which includes minibeds and a mini cardboard cut out of the capitol building.

WPI and  will be hosting a Boba Fundraiser to raise funds for The   Network for patients living with ME/CFS and Long Cov...
10/23/2026

WPI and will be hosting a Boba Fundraiser to raise funds for The Network for patients living with ME/CFS and Long Covid.
Care Club will be doing their fundraiser on the UNR Campus at the Hillard Plaza on Tuesday October 27th from 10 AM to 2 PM.
All drinks will be sold for $6.00, boba is an additonal $1.00

Join the WPI and the  for our screening of Unrest, a 2017 feature documentary directed and produced by Jennifer Brea, te...
10/23/2026

Join the WPI and the for our screening of Unrest, a 2017 feature documentary directed and produced by Jennifer Brea, telling her personal journey with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and the global community of people living with the condition.
Please RSVP for the event as soon as possible by scanning the QR Code!

The Screening is happening on Saturday, November 17th, at the Wells Fargo Auditorium in the MIKC (basement floor). Doors open at 5:30pm, and the film begins at 6:00PM. We will have snacks and drinks available!
After the film, WPI's Engagement Team and guest speakers will be able to speak more about WPI's efforts in treating ME/CFS and research over the years.

Brea's documentary has earned multiple festival wins, nominations, and industry honors worldwide, including a Sundance Special Jury Prize for Editing and an Emmy nomination for Outstanding Editing.

Just a reminder for everyone! The Nevada Filipino Club is hosting their annual Filipino Festival on Saturday, November 7...
10/23/2026

Just a reminder for everyone! The Nevada Filipino Club is hosting their annual Filipino Festival on Saturday, November 7th, form 1:00PM to 5:00PM. Please visit our Engagement Team's table at the Festival to know more about the WPI and what we do for the ME/CFS community, here in Reno and nationwide! Get to know what other events we are planning this year, and talk with us face-to-face!

Thank you for having us at your event this year!

The WPI has put together a list of academic journals, scientific publications, and trusted newsletters about ME/CFS rese...
10/22/2026

The WPI has put together a list of academic journals, scientific publications, and trusted newsletters about ME/CFS research. Finding reliable ME/CFS info can feel overwhelming, but staying updated shouldn't be.
We hope this collection of resources will help patients and caregivers make better healthcare decisions by reading through credible resources.

  is launching their biggest   campaign yet!For the next 7 months,   is pacing to the capitol, bringing ME out of the sh...
10/19/2026

is launching their biggest campaign yet!
For the next 7 months, is pacing to the capitol, bringing ME out of the shadows and into public places across America.
In solidarity, WPI is supporting The Network USA in sharing their campaign, which helps make inroads for research funding, medical education, public policy, and cultural impact.
Your can show your support by joining the campaign and registering on the meaction.net or Donate to pace.funraise.org

This week, the WPI is spreading awareness for Invisible Disabilities Week to support the Invisible Disabilities Associat...
10/19/2026

This week, the WPI is spreading awareness for Invisible Disabilities Week to support the Invisible Disabilities Association. The WPI is proud to be a contributor of research for neuro-immune chronic illnesses and an organization that raises awareness, voices, education and support for people living with unseen conditions.

10/14/2026

The team at La Trobe University in Australia, including Dr Sarah Annesley and Dr Daniel Missailidis, have published a study acknowledging funding from ME Research UK, which provides evidence of altered lipid metabolism in ME/CFS.

Read more: https://tinyurl.com/yv4mmvtn
Read the research paper: https://tinyurl.com/5d3hbs7v

Address

1664 N Virginia Street, MS0552
Reno, NV
89557

Opening Hours

Monday 8am - 3pm
Tuesday 8am - 3pm
Wednesday 8am - 3pm
Thursday 8am - 3pm
Friday 8am - 12pm

Telephone

+17756828250

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