Surge Of Urgency For Parkinson’s Disease Treatments And Cure

Illness isn’t partisan.  Both sides of the aisle are subject to health problems. Both sides are going to need more and better healthcare. Illness doesn’t care about socio-economic status, race, or anything else. It has but one mission , and that is to disrupt and challenge the patient. Life is challenging enough without illness, but when illness combines with everyday existence, life can seem overwhelming.

Lately, there has been talk by politicians and the media about colonizing the moon. Only in a comedy club would this even be funny! I am a huge NASA fan and fully support a space program. Let’s be rational. The technological costs and manpower to perform an operation like this would not only take an astronomical cost but it would require years of preparation, and for what purpose?

For the past 20+ years, I have been told that in 5 years we are going to have a cure for Parkinson’s Disease. I heard it from renowned neurologists and even former leaders in the Parkinson’s community. They assured me that a cure was in the pipeline. I was and remain skeptically hopeful. Until the cure comes, it is up to us, as patients, to do what we can for ourselves.

The United States put a man on the moon, largely to prove our abilities to the Russians during the Cold War, but the USA did it, and in a very short time period. It is this kind of focus and dedication to achievement that is needed to make a breakthrough in Parkinson’s Disease and many other illnesses.

Neurological disorders are usually chronic and degenerative, so time is critical. There ought to be a sense of urgency to uncovering the mysteries of illness on this planet before we go colonize anywhere else.

About Karl Robb

Karl Robb has had Parkinson’s disease (PD) for over thirty years. With symptoms since he was seventeen years old, Karl was diagnosed at the age of twenty-three. Now fifty-one, he is a Parkinson’s disease advocate, an entrepreneur, an inventor, an author of two books (A Soft Voice in a Noisy World: A Guide to Dealing and Healing with Parkinson’s Disease and Dealing and Healing with Parkinson’s Disease and Other Health Conditions: A Workbook for Body, Mind, and Spirit) with his wife and care partner, Angela Robb. He has blogged for ten years on his website, ASoftVoice.com. He is a Community Team Member to ParkinsonsDisease.net and is a contributor to PatientsLikeMe.com. His blog, ASoftVoice.com, has been recognized four years in a row by Healthline.com as one of The Best Parkinson’s Blogs of 2018, 2017, 2016, and 2015! Healthline.com also listed the book A Soft Voice in a Noisy World in their list of Best Parkinson’s Disease Books of 2017! FeedSpot.com has recognized ASoftVoice.com for 2018 and 2017 as a Top 50 Parkinson’s Disease blog. Karl was a blogger for the 2016 World Parkinson Congress in Portland, Oregon. He is a frequent speaker on Parkinson’s disease issues as well as an experienced advocate for Parkinson’s issues throughout the United States. He is also an advisor and consultant on Parkinson’s disease. Karl is a board member of both the Parkinson Voice Project and Parkinson Social Network based in Virginia. He was an active board member (6 years) and an advocate (18 years) with the Parkinson’s Action Network (PAN). In his free time, he is a photographer, constant writer, longtime magician, and a practicing Reiki Jin Kei Do master. Karl received a Bachelor of Arts degree in English from the University of North Carolina at Chapel Hill. He has been featured by The New York Post, BBC Radio, CBS News, National Public Broadcasting (NPR), in The New Republic magazine and NHK World Television, as well as several Washington, D.C., television stations. You may reach Karl via email at asoftvoice@gmail.com, on Facebook, or contact him via Twitter @asoftvoicepd. I’m available for speaking engagements to share my experience living with Parkinson’s disease. Please contact me at asoftvoice@gmail.com if you are interested in having me speak to your group, conference/symposium, or would like me to write an article for your newsletter or blog. I am not a medical professional and this information is my personal view. I am just sharing my medical journey with you, the reader. I encourage you to seek all avenues that can benefit your condition.

Posted on February 20, 2012, in Education & Support, Health, Media & Trends, Parkinson's Disease, Politics, Uncategorized and tagged , , , , , , , , , , , , , , , , , , , , , , , . Bookmark the permalink. 2 Comments.

  1. I guess I’m too cynical – why would a drug company want to release a “cure for PD” pill, when they’re looking at a huge revenue stream for drugs that only reduce symptoms and don’t cure? I think we should just buy their stocks and at least make some money as our PD suffering continues long into the future!

  2. You said it brother, “we need a sense of urgency.” Everyday with more frequency I am seeing emails and obits from people I share this disease with. I just call them friends. They are the fortunate ones. Not because of their passing but for them a cure did not come quick enough and now they aren’t suffering. I – We continue to live with PD and the torment continues. May God bless those who he now cares for and those still living and fighting PD everyday.

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