Tag: Parkinson’s Research Community

New Developments in Parkinson’s Diagnosis and Treatment

In two recent reports , Parkinson’s researchers describe findings that may lead to new ways of detecting early signs of the disease and a potential new treatment. In the first case, researchers in Scotland are looking at the possibility that even before a patient begins to have obvious symptoms of the ...

Read more

Patients Perspective on Parkinson’s Disease

As federal regulators listened, patients told them of their symptoms — the sleepless nights, the days with uncontrollable tremors or the little struggles simply maintaining their balance. Some of those with Parkinson’s who spoke at the special U.S. Food and Drug Administration meeting in late ...

Read more

A New Model for Discerning Parkinson’s

A team of researchers has developed a simple and non-invasive approach that uses genetic data in combination with other demographic and biomarker information to accurately distinguish those with and without Parkinson’s disease, an illness that is notoriously difficult to detect. In a study published this ...

Read more

What’s New In Parkinson’s Research

Over the last year, three promising new treatments for symptoms of Parkinson’s became available in the United States, but progress has been less hopeful on the development of drugs to modify the progression the disease, according to researchers who spoke at an annual movement disorders conference in San Diego ...

Read more

Virtual Doctor’s Visit For Parkinson’s Patients

A new study involving participants in 23andMe’s Parkinson’s Disease Community, offers hope for the future of telemedicine and the ability of clinicians to quickly and accurately assess and recruit patients for research and clinical trials. This is particularly good news for patients far removed from ...

Read more

Parkinson’s Research Challenges

Things aren’t always as they seem with Parkinson’s disease with one recent study showing as many as half those diagnosed with the disease don’t have it, according Dr. J. William Langston. At a recent visit to 23andMe, Langston, a pioneering Parkinson’s researcher as well as the founder and chief science ...

Read more

Steady On

Like all good photographers Alan Babbitt sees what’s invisible to most of us. With a steady hand and a willingness to go almost anywhere for a good shot, Alan spent decades turning his lens on people and places to create images he thought would draw the viewer in and tell a story. “I’d call it street ...

Read more

Let’s Talk About Parkinson’s

On Thursday and Friday, 23andMe will be participating in two online events hosted by the Michael J. Fox Foundation focused on Parkinson’s disease and some of the latest research into its genetic underpinning. On Thursday February 19th, at 12 pm EST, the Michael J. Fox Foundation will host a webinar titled ...

Read more

23andMe In The News

Last week was a good one for research at 23andMe with two announcements that offer more examples of the power of our research model. First was the publication of a massive Parkinson’s disease study that our scientists worked on with a consortium of 50 other organizations that were lead by researchers at ...

Read more

Debate Around Informing Research Participants

This post comes to us from our friends at the Michael J. Fox Foundation, which has worked with us through our Parkinson’s Research Community. There are many different points of view on whether to inform research participants. For 23andMe our approach has always been to give customers and research participants ...

Read more

Return to top