OMF Science Wednesday – Personalized Medicine

In honor of last week’s conference at Stanford University on Personalized Medicine, at #OMFScienceWednesday we ask the question: What is personalized health?
Whether you call it personalized medicine, precision health, or P4 medicine, we are talking about a current revolution in the way health and disease are being studied, and the way healthcare is being practiced. This means we are moving away from the one-size-fits-all approach, and towards more tailored therapies that account for individual variations at the clinical and molecular level. This means we are aiming to predict the risk and eventually prevent the onset of disease. This means a data-driven revolution, that uses the cutting-edge molecular technologies we talked about last week and sophisticated big data analysis, to predict the best ways to treat disease and maintain health in each person. This means empowering patients to take a more active role in their own healthcare. This means focusing on turning from reactive (treating disease) to proactive (maintaining wellness).

A personalized health approach to research is especially exciting in ME/CFS because of how complex and variable this disease is across patients. This is why OMF funded the big data study on severely ill patients (https://www.omf.ngo/mecfs-severely-ill-big-data-study/). We already know that different patients respond to different treatments, and personalized health research will help us not only to understand why that is, but to find even better treatments or combinations thereof. This is already starting to happen in cancer, where genome sequence information is used to select the most effective drugs for individual patients.
Much of the research OMF supports takes place at Stanford Medicine. Read more about Stanford Medicine’s commitment to precision health in research, in Dean Lloyd Minor’s Forbes op-ed: http://med.stanford.edu/…/dean-minor-on-precision-health.ht…
Dean Minor kicked off the Personalized Health conference at Stanford University, and Ron Davis spoke there about ME/CFS research on Friday afternoon. See the entire program here: https://app.certain.com/profile/web/index.cfm… and follow the live Twitter feed here: http://twitter.com/hashtag/PH17
Facebook
Twitter
WhatsApp
Email

Latest News

rectangle image with a greyish background. three white pillows stacked from smallest to largest. the words, Pillow Writers en Español in black font. the #MEAction logo in the bottom right corner.

Pillow Writers en Español

#MEAction is thrilled to announce Pillow Writers Network has expanded once again! This time with a dedicated group for Spanish speakers: Join us for our Pillow Writers En Español meetings! A place where ME/CFS/Long Covid patients are welcome to participate through writing. This #MEAction-sponsored event has been held in English for over three years. We

Read More »

Happy Juneteenth + Black Disabled Authors Reading List

Happy Juneteenth from all of us here at #MEAction! Juneteenth commemorates June 19th, 1865 when slavery of African-Americans was officially enforced. To celebrate we have put together a summer reading list of books by disabled Black authors. Keah Brown is an American author who was born with cerebral palsy. She created the popular hashtag #disabledandcute

Read More »
white rectangle with red splashes of tiny red dots in all four corners. #MEAction logo at the top. #MEAction Minnesota Helps Save Long Covid Program in red font.

Minnesota’s Long COVID Funding Saved from Elimination

We have good news! The first-in-the-nation Long COVID program run by the Minnesota Department of Health (MDH) has been saved from elimination! This means #MEAction will be able to continue its work helping Minnesotans with ME/CFS, Long COVID and related conditions access vital home and community-based support services, as part of our multi-year grant.   Last

Read More »
Scroll to Top