My Experience with Parkinson’s and What I Have Done to Positively Live the Best Life Possible

February 22, 2021

Parkinson’s is awful. But you know that already. If you are reading this, you most likely are a Person with Parkinson’s (“PwP”) or a caregiver to one. I remember getting diagnosed. Other than the hand tremor, I did not think that anything was wrong.


I don’t know how I missed it, but I did not notice my lack of facial expression, my eyes did not blink, and my handwriting was illegible. I also did not think anything of the tremor because my shaking hand just had been operated on to repair a broken thumb and I thought that the surgery caused the shaking. Interestingly, my arm did not swing when I walked which I again attributed to having a heavy cast on that hand. I was, finally, diagnosed in March of 2002.


I was just 41 years old. I was admitted into a club called, “Early Onset.” A club that I would not have joined voluntarily. The bad side is, well, you have Parkinson’s. The good side, if there is one, is that I have observed the symptoms progress more slowly than someone diagnosed who is over, let’s say, 50 years old.


So, my disease was progressing slowly and the medicine was working. I was an Ivy League educated attorney and was able to do my job as effectively as ever. In fact, maybe better. I believe that we learn or take away something valuable from every significant event in our lives. And Parkinson’s definitely is life-changing.


I was able to remain relatively symptom free for the first few years. I did not know it at the time, but Parkinson’s effects not only motor and non-motor skills, but mental abilities. I was being paid for my ability to “see beyond what is apparent” and my judgement both legal and as an executive.


Now that I look back on it, I believe that Parkinson’s (or maybe the medicine I was taking) negatively influenced a few important decisions that I made during those first six years. For example, if I had anything to say to those newly diagnosed, I would say that you may not want to disclose your condition to your employer. Talk to an employment attorney and let them help you decide what to tell your employer in light of FMLA, ADA, and any other law. Don’t give them any excuse to fire you. Simply put, they don’t want you working for them, if they can find a way to terminate you without reference to PD, they will.


Despite these mistakes, I was able to do what was necessary to oversee a huge project, the sale of the company. I was also able to teach a college night class. When I no longer worked as a full-time attorney, with sufficient rest, I was able to win what was thought to be an unwinnable trial nine years into my PD. Granted it wiped me out for weeks, but I did it and we won. I practiced for two more years when the Parkinson’s caught up with me. I was able to control my symptoms through shear will power, staying positive and focusing on my purpose. In fact, I was able to write a book on success: Decide Success, You Ain’t Dead Yet (I just released a 2020 edition that you can get by writing to me at Not only success with PD, but also success in school and at work.


Once my symptoms started to progress, I decided to turn to exercise and diet. Yes, what you eat matters. At first, I tried to do it on my own, but was not faring well. Then I met someone who was living the lifestyle that I knew would help me with my PD. First, I became a pescatarian (organic vegetables plus line-caught fish only). The second thing I did was to cut out all soda, junk food and fast food. The third thing I did was to reduce sugar and dairy from my meals. My role model did not have to change her diet as she already lived it.


Once I started to eat a healthier diet, we started to work on my exercise routine. Once a month for 30 minutes on the treadmill was not going to cut it if I was going to try and stop or even lesson the symptoms of PD. That was in 2012. Since then, I have done a combination of the following: core training, boxing fitness, hot yoga & bike training. What is most important is to find a regime that involves stretching, sweating and hopefully strengthening. I went from 215 to 170 pounds and cut my bad cholesterol in half over the next year. I also married my role model.


This lifestyle change allowed me to have more “on” time and live a high quality of life with Parkinson’s. I should say that this suspension of symptoms does not last forever. On the plus side, I am as fit as I have ever been. On the minus side, I am getting older (59) and 18 years is starting to wear on me. I can only keep up this exercise routine for so long and have needed to adjust my lifestyle. I can tell you this: I try to work out every day and put out my best effort. Sometimes I have to try several times a day and sometimes I get in a great workout.


Traditionally, rest has been a great healer. I do the limited amount of work that I can do first thing in the morning and my work time has been diminishing over time. My work is preparing to do presentations which inspire those with chronic conditions and their care partners to live the best life possible.


Water has also made a difference. Staying hydrated is extremely important. Unfortunately there is a delicate balance. I wake up several times during the night to go to the bathroom. Recently, I have woken up unable to move my arms and legs. It feels like an alien has taken over my body.


If I concentrate, I can inch my limbs to remove my covers. Sometimes, however, I don’t make it on time. Talk about embarrassing. But it is what it is. The best that I can do is to not drink water after a certain time of the day.


I have had an exciting life and made the most out of any situation. I can tell you that PD has been a test. In order to practice what I preach, I “live the best life possible.” I have brought my inspirational presentation to as many locations as possible and enjoyed visiting new (as well as old) places.


I have also traveled extensively. In living such a life, you need to recognize that you will probably live into your eighties especially if you clean up your lifestyle. I hope that you have the financial resources to sustain yourself. Before you start spending money, you should see a financial advisor. Your earning potential is likely to be impacted by PD.


Today, I do have to deal with more off periods. That is just life. I can control some things, but not everything. You just do what you can do. That’s the best advice that I can give.


I hope that this information helps. Please don’t hesitate to share it with others.


John’s message of hope, inspiration and laughter was ideal for anyone living with PD. He was extremely flexible and a delight to work with.

Leisha Phipps, MSW Program Director - Dallas Area Parkinson Society

We all felt inspired and enjoyed listening to your presentation. Even though we are not living with Parkinson’s, we felt boost of motivation to continue helping those who are living with this disease. I am motivated to make more personal phone calls to people living with PD and asking how they are doing. Sometimes that “extra” bit of kindness truly makes a difference to someone. I am also motivated to research program ideas and partner with other organizations that may have similar values.

I learned that life is unexpected and that you cannot control it. What matters is your attitude!

-Great way to end the day, brave man, thank you very much!

-Good, excellent, great, outstanding speaker, very moving!

-Inspirational who just “gets it”

-Positive thinker and very funny!

-Honest speaker but also humorous!

Parkinson’s Society of Southwest Ontario, Canada, Symposium Keynote Presentation

“whatever hand life deals you, whatever life changing adversity you have to endure, you still have some control over it.” “You don’t have to just to live well,” he advises,” but live an Amazing Life.” The formula he proposes: Faith in yourself, discipline, determination, desire, intensity, and inner strength.


Yes, you touched every person at our conference, who will in turn change and impact so many others. The feedback from our participants was overwhelmingly positive. You are the only speaker to ever receive a standing ovation. Thank you for taking time to share, motivate and inspire. We are blessed to know you.


I will be honest. During the first 10 minutes of your presentation, I started reading work related material on my laptop. For surely, I had watched your You-Tube and seen your videos and knew what to expect. Surely, as a therapist I had studied this disease, the pathological components, the psychological components, the treatment alternatives……..Surely, I understand it.

Not so much. You caught my attention and I was enthralled. You were able to couple the impairments you experience with the emotions felt. You walked us through your life with the disease through “your eyes”. A perspective that a therapist/nurse rarely has the chance to hear. We get so busy telling patients how to deal with x, y and z, but our eyes are blurred by the science of it all most of the time.

You did it through truth, Through your humor, humility and determination to tell your story. One that most deservedly needs to be shared.

I will advocate to have you share your story. I appreciate your determination, diligence and dedication.


Speaking with European Parkinson Disease Association

Two decades ago, John Baumann was a US lawyer who thrived on competition and the thrill of winning a case. Now, nearly 20 years after being diagnosed with Parkinson’s, he’s motivated by helping inspire others live to their full potential.

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