A Few Good Blogs

BLOGS AND OTHER RESOURCES

The number of PD bloggers has grown exponentially since I was diagnosed 11 years ago. There were only 2 that I could find. Now there are close to 100 that we know of and more popping up frequently. There is a more complete list, compiled by blogger Sherri Woodbridge of Parkinson’s Journey http://parkinsonsjourney.com/4827-2/

In no particular order:

  • Parkinson’s Diva  by Maria de Leon, M.D.
  • Living Well With Parkinsons  by Sheryl Jedlinski, well written blog with good information about living with PD
  • Mariette Robijn  Blogger from the Netherlands, often humorous, offbeat posts
  • Parkinson’s Women by Darcy Blake, Women and PD advocate
  • The Science of Parkinson’s   well written, in language the average person can understand.  By Simon Stott
  • Parkinson’s Humor  by Yuma Bev,  fun site
  • It Is What It Is  Zen and Living with Parkinson’s Disease by Tom Eckhardt
  • A Soft Voice in a Noisy World  by Karl Robb, diagnosed at 23, living with PD for over 30 years.
  • Perky Parky, Allison Smith
  • Tomorrow Edition, Benyamin Stecher
  • Parking Suns, Bruce Ballard
  • Tikvah for Parkinson, Debbie Shapiro has created an all-purpose Parkinson’s Center in Jerusalem
  • Elisabeth Ildal
  • Kathleen Kiddo Heather Kennedy
  • Tim Hague Winner of the Great Race Canada. Very inspirational
  • Parkinson Fit More of a newsletter than a blog. A lot of good information.
  • Parkinsonsecrets Dr. Michael S. Okun, a world authority on PD, co-hosts a blog with Dr. Indu Subramanian with content from a rich variety of bloggers. They provide a forum for others “to inspire faith, plant the seed of hope, help patients to discover their core values, and to share ‘secrets’ that will improve lives…Hope leads to happiness, and happiness will lead to a meaningful life.”
  • a simple island life Kai invites you to her lifestyle site where she shares about living well with parkinson’s and embracing the everyday.
  • ParkyBoy ParkyBoy is about living with Parkinson’s:  helping others with Parkinson’s by talking about it openly, to help make sense of things, and to allow me to express things that rattle around my head.