2020 Vision in 2020

New Year’s Eve, Mr. Twitchy and I went to the LA Kings Hockey game with friends. At many professional sporting events, there are giveaways of mostly useless team memorabilia. Tuesday night, the giveaway was 2020 glasses, which are just plain impossible to put on. However, like everyone else in the arena, we had to take a selfie while wearing them.

Yes, we looked like total fools, the glasses came off immediatelly after the photo, and we had a great time at the game.

So did the glasses give us 2020 vision for the new year? We won’t know until the end of the year, but lets take a look at what we can look forward to.

There are many reasons to be optimistic about the future with Parkinson’s. There is a lot of research going on in many different directions. Here are just a few of the things that popped up in the Parkinson’s news-sites this week:

At the World Parkinson Congress in Portland, in 2016, the late Tom Isaacs, in his keynote address, said that the cure is always at least 5 years away. Based on all of the recent findings, I think that maybe his theory will be proven wrong in the next year or two. In light of that, my vision for the Parkinson’s Community in the coming year is that:

  • A breakthrough is iminent, both for effective treatments that not only make our lives better, but in fact delay the disease.
  • Biomarkers will become standard early predictors of Parkinson’s so that treatment can start earlier.
  • And most important, all of the research mentioned above brings us much closer to a cure – not in 5 years – but in the next 1-2 years.

My personal vision is that I will continue to live well with PD, so that I can keep doing the things that I enjoy, which include:

  • Taking care of myself with exercise, diet and engaging in an active social life.
  • Advocating on behalf of the Parkinson’s Community and helping the newly diagnosed find their way with PD.
  • Most important of all, spending time with Mr. Twitchy, our children and grandchildren, and being thankful for all that we have.

What is your vision for the coming year? For yourself? For Parkinson’s? Please join in the conversation.


Leave a Reply

Please log in using one of these methods to post your comment:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out /  Change )

Twitter picture

You are commenting using your Twitter account. Log Out /  Change )

Facebook photo

You are commenting using your Facebook account. Log Out /  Change )

Connecting to %s

This site uses Akismet to reduce spam. Learn how your comment data is processed.

A Note To My Readers

I love to see your comments and get your emails as we share our collective experiences. But based on a couple of private questions from some of you, remember, I am just a lay person and a patient like the rest of you. For medical and similar advice, you need to talk to your own doctor

Twitchy Woman

Twitchy Women partners with the Parkinson’s Wellness Fund to ensure we have the resources to offer peer support for women with Parkinson’s.