10 episodes

Park Right Here is an informational and hopefully entertaining podcast about Parkinson's disease Tom and I both want this podcast to be more than just about PD. Our desire is to give hope, to inspire and educate PWPs (people with Parkinson's), friends, family, medical professionals, physical therapists, nurses, PCMs, pharmacists, support groups, personal trainers, home health aides, pastors/spiritual advisors, occupational therapists, neighbors, and anyone who wants to support those with PD. We want to let you know that you are not alone. We want to share our personal stories with you. They can at times be funny, sad, hopefully inspiring, difficult, and life-changing. This podcast will have episodes on various topics. An important one is your diagnosis. We will share experiences, trials, and lessons that we both have learned through our journeys. We will discuss the importance of being your own best advocate or one for those you love, basic information about medication, what is and how to choose your care team, what a movement disorder specialist is, how important exercise is for PD, the latest trials and clinical research, tips and tricks on getting through the day, nutrition, the good and bad about supplements and natural remedies, the importance of a support group, what to do when you don't have a support group nearby, how to find support on social media, the importance in talking about PD with others. We both want to make it clear that WE ARE NOT medical professionals or experts in medications, treatments, or even PD. We are lay people just like you and we will be sharing OUR experiences regarding OUR journeys with PD. We want you to take what helps you and discard the rest. We also want to EMPHASIZE that if you have any questions about any medication, speak to your doctor, neurologist, movement disorder specialist, or pharmacist. We want to be transparent and honest. We will not sugarcoat how difficult dealing with PD can be or hide our bad days. What you hear and see, is what you get. We want you to know that PD affects every aspect of your life and those around you, but it shouldn't stop you from living the best life you can. We will interview people who work with and are associated with PD. For example, a movement disorder specialist, physical and occupational therapists, the CEO of LSVT, PWR (Parkinson's Wellness Recovery) PD exercise group, medical professionals, those involved in clinical research, those that work for nonprofit organizations like Michael J Fox foundation and Davis Phinney Foundation, psychologists, family and caregivers, those with PD, and the many inventors and entrepreneurs who are working on treatments and items to help improve our quality of life. Possibly even Micheal J Fox himself. An important part of this podcast is that every listener can be involved. It is our podcast. We want the ideas and questions that you have about PD. We want to hear what topics you would like to discuss. It's important to understand if you violate guidelines, use bad language, bully/troll, or are disruptive, you will be reported and blocked. If you threaten or we believe you are a danger to yourself or others, We will report any comments and posts that we deem necessary for you to get the help that you need. We are so excited to share this with you and we hope it helps you understand what PD is and how to walk through this journey with hope and joy. Thanks for listening and supporting our dream.

"Park Right Here" with Katrina Rochon and Tom Consentino...our personal journeys with Parkinson's Disease Katrina Rochon and Thomas Cosentino

    • Health & Fitness

Park Right Here is an informational and hopefully entertaining podcast about Parkinson's disease Tom and I both want this podcast to be more than just about PD. Our desire is to give hope, to inspire and educate PWPs (people with Parkinson's), friends, family, medical professionals, physical therapists, nurses, PCMs, pharmacists, support groups, personal trainers, home health aides, pastors/spiritual advisors, occupational therapists, neighbors, and anyone who wants to support those with PD. We want to let you know that you are not alone. We want to share our personal stories with you. They can at times be funny, sad, hopefully inspiring, difficult, and life-changing. This podcast will have episodes on various topics. An important one is your diagnosis. We will share experiences, trials, and lessons that we both have learned through our journeys. We will discuss the importance of being your own best advocate or one for those you love, basic information about medication, what is and how to choose your care team, what a movement disorder specialist is, how important exercise is for PD, the latest trials and clinical research, tips and tricks on getting through the day, nutrition, the good and bad about supplements and natural remedies, the importance of a support group, what to do when you don't have a support group nearby, how to find support on social media, the importance in talking about PD with others. We both want to make it clear that WE ARE NOT medical professionals or experts in medications, treatments, or even PD. We are lay people just like you and we will be sharing OUR experiences regarding OUR journeys with PD. We want you to take what helps you and discard the rest. We also want to EMPHASIZE that if you have any questions about any medication, speak to your doctor, neurologist, movement disorder specialist, or pharmacist. We want to be transparent and honest. We will not sugarcoat how difficult dealing with PD can be or hide our bad days. What you hear and see, is what you get. We want you to know that PD affects every aspect of your life and those around you, but it shouldn't stop you from living the best life you can. We will interview people who work with and are associated with PD. For example, a movement disorder specialist, physical and occupational therapists, the CEO of LSVT, PWR (Parkinson's Wellness Recovery) PD exercise group, medical professionals, those involved in clinical research, those that work for nonprofit organizations like Michael J Fox foundation and Davis Phinney Foundation, psychologists, family and caregivers, those with PD, and the many inventors and entrepreneurs who are working on treatments and items to help improve our quality of life. Possibly even Micheal J Fox himself. An important part of this podcast is that every listener can be involved. It is our podcast. We want the ideas and questions that you have about PD. We want to hear what topics you would like to discuss. It's important to understand if you violate guidelines, use bad language, bully/troll, or are disruptive, you will be reported and blocked. If you threaten or we believe you are a danger to yourself or others, We will report any comments and posts that we deem necessary for you to get the help that you need. We are so excited to share this with you and we hope it helps you understand what PD is and how to walk through this journey with hope and joy. Thanks for listening and supporting our dream.

    Tom, Katrina, and special guest Stacey M. from Misson PD

    Tom, Katrina, and special guest Stacey M. from Misson PD

    Katrina, Tom, and Stacey sit and discuss the Invention project they were involved in. It is a wonderful program for Middle School students where Tom spoke about his Parkinson's Journey they invented a special glove to help with tremors and also Stacey worked with them. It is an amazing story to hear and I hope you guys enjoy it. We also talk about Mission PD and how it's going. We also talk of course about exercise and Parkinson's. So come join us for another live Thursday podcast of Park Right Here.
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    • 1 hr 2 min
    Another day in ParaDise

    Another day in ParaDise

    Check out today's episode with Katrina, Tom, and Amy Becker of the Michael J. Fox Foundation. Today our topic is advocacy and what you can do about it. How you can get involved in letting your government officials know more about Parkinson's. Amy's role is at the Michael J. Fox Foundation and getting the word out in DC about how important Parkinson's is and the funding we need in our community. I hope you learn as much as I did and enjoy the discussion as much.
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    • 52 min
    Episode 8 with Stacey Macaluso from Mount Laurel NJ Mission PD

    Episode 8 with Stacey Macaluso from Mount Laurel NJ Mission PD

    Hello, everyone, and welcome to today's episode number 8 of the Park Right Here podcast! Welcome, as always, with me, Katrina, and Tom, and our special guest today is Stacey Macaluso from Mount Laurel, New Jersey. She runs Mission PD, a non-profit working with the Parkinson's community. We talk about her nonprofit, and we, as in Me, Katrina, and her, connected on a personal level through dance, and we both know what Body Groove is and who Misty Tripoli is!  It was a wonderful experience for me, and I hope it was wonderful for Stacy. Let's not forget Tom. Tom was outnumbered this time for a change. It was a wonderful experience, and it was nice to meet her. We talked about exercise and what it is like not having Parkinson's and working with the Parkinson's community. So come as always and Park Right 
    Here with us, and enjoy our conversation. We are live every Thursday at 2:00 pm EST on Facebook Live YouTube, and now we're trying Instagram. If you have any questions, please email us at parkrightherepodcast@gmail.com or leave a comment. See you guys next week!
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    • 1 hr 17 min
    episode 7 Parkinson's and Exercise with Kristine Meldrum BA, ACE with Jay Alberts PHD and Daniel M Corcas PHD

    episode 7 Parkinson's and Exercise with Kristine Meldrum BA, ACE with Jay Alberts PHD and Daniel M Corcas PHD

    Hello everyone! Welcome to the park right here podcast episode 7. Yes, we made it to the hump of episode 7. The big milestone of all podcasts. Today, we have a special guest, Kristine Meldrum, PhD " Parkinson's: How To Reduce Symptoms Through Exercise. She sits down with Tom and me, and we have a wonderful discussion. I tell some of my stories, and Tom tells some of his rants, and we have an actual hour-and-a-half show that is full of fun and entertainment, as always. So come with us and park right here and enjoy sometime together. Check us out on Facebook, YouTube, and Instagram.
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    • 1 hr 31 min
    Episode 6

    Episode 6

    In Park Right Here podcast episode 6, we talk to Larry, an attorney from Canada. He is also a Canadian Ambassador for the Davis Finney Foundation. We talked about employment and the laws surrounding it concerning when to let your employer know you have Parkinson's and when to possibly go on temporary disability or to start looking at permanent disability. We also talk about exercise and the importance of exercise with Parkinson's. We also discuss the importance of having a sense of humor, so come and Park Right Here with Katrina, Tom, and our guest, Larry.
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    • 59 min
    Episode 5

    Episode 5

    Today at Park Right Here podcast, it's episode 5. Our Guest is Jim Allen. He is a newly diagnosed Parkie. He is a former prosecuting attorney from Augusta, Georgia. He is now a pastor and speaker.  Tom and I enjoyed having him on the podcast today. Tom and I sat down with him and talked about being newly diagnosed, and I felt he had some great insight that I think of jaded parkies who have had it for a while we're missing. I learned a lot from him. Come park right here and enjoy episode 5! If you have any questions, put them down in the comments. Also, you can email us at Park right here podcast at gmail.com. Every Thursday at 2:00 p.m. EST, we go live on Facebook and YouTube.
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    • 59 min

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