This episode includes the second half of an interview with Dr. Ross, Mayo Clinic geneticist, about the story of Parkinson's disease (PD) genetics. This episode also has intermixed debriefing segments with Dr. Tipton & Kandice to explain why genetics is important to patients, caregivers, clinicians and the general public. Genetic studies of PD may provide the key for improved treatments and a cure. Listen to hear about this and more!
May 27, 2020•1 hr 5 min•Season 1Ep. 22
This week's episode includes the first half of an interview with Dr. Owen Ross, Mayo Clinic geneticist. This segment discusses the story of how Parkinson's disease (PD) was initially thought to have no genetic basis. We've since come a long way to now knowing 90 different genetic locations linked with PD. The episode also includes intermixed segments with Dr. Tipton & Kandice to break down the scientific elements in an easy-to-understand bite-sized pieces.
May 20, 2020•39 min•Season 1Ep. 21
This episode contains an interview with Dr. Christine Cauffield, geriatric neuropsychologist and CEO of Lutheran Services Florida (LSF) Health Systems, on how to be kind to your mind. Topics include the nuts & bolts of neuropsychology and the importance of a "whole person" approach to health. How do you know if your level of stress is an indicator of something more, such as anxiety or depression? What are the warning signs of caregiver burnout and how to deal with it? We address all of these...
May 13, 2020•53 min•Season 1Ep. 20
This episode kicks off PSP (progressive supranuclear palsy) awareness month by interviewing Zoya and her father. Zoya is a high school Freshman, whose grandfather has PSP. Hear how Zoya has turned her experience into an opportunity to inform people about this disease and fill their stomachs by starting a business called Popcorn for Parkinsons . PSP and Parkinson's disease share many symptoms, but these two diseases are actually very different. This episode delves into the differences and shares ...
May 06, 2020•48 min•Season 1Ep. 19
In this episode, Dr. Tipton & Kandice interview Nancy Tufts & Andrea Spencer from ElderSource. This is an organization that specializes in getting resources to seniors, disabled individuals, and caregivers. From virtual support groups to food services and robotic companion pets, they are well-equipped to live up to their catch phrase: "Start here for help." Listen to learn about the organization, its resources, and special offerings during the COVID19 pandemic. Contact ElderSource on Fac...
Apr 29, 2020•1 hr 5 min•Season 1Ep. 18
In this episode, Dr. Tipton and Kandice interview the Geib family. Mr. Geib was diagnosed with Parkinson's disease (PD). He an his wife tell the story from symptom onset to diagnosis. This interview delves into many of the disease complexities, such as tremors, fatigue, depression, medications and sleep. In keeping with this month's theme, "Keep Moving," we also discuss exercise and ways that those with PD can exercise even in this midst of the COVID19 quarantining.
Apr 22, 2020•1 hr 6 min•Season 1Ep. 17
In this episode, Dr. Tipton interviews Alexander Johnson, who is a linebacker for the Denver Broncos. Alexander discusses his grandmother's battle with Alzheimer's disease and provides tips for staying active during the COVID pandemic. Dr. Tipton and Alexander also talk about the importance of exercise protective role against neurodegenerative diseases like Alzheimer's and Parkinson's disease. Listen to understand the importance of Continue Believing and Keep Moving. Resources: www.chiefbeast.co...
Apr 15, 2020•43 min•Season 1Ep. 16
This episode features an interview with Katie Fahrenbruch, who is the Alzheimer's Association Program Director for Central and North Florida. The content of this interview addresses the current and major issue of adult daycare closure, which is forcing many people to work and care for their loved one simultaneously. This is one of several scenarios prompting this deep dive conversion, which provides listeners with RESOURCES. Alzheimer's Association: www.alz.org and 24/7 Caregiver hotline: 1-800-...
Apr 08, 2020•40 min•Season 1Ep. 15
In this episode, Dr. Tipton and Kandice kick off the April as Parkinson's disease (PD) awareness month. Dr. Tipton introduces the disease and then Kandice shares her recent firsthand experience with one of the most feared problems with dementia...wandering. This terrifying experience can have devastating consequences. It can be very difficult to maintain the balance between independence and supervision when caring for someone with dementia. This is a dynamic balance that can change quickly and c...
Apr 01, 2020•1 hr 7 min•Season 1Ep. 14
In this episode, Dr. Tipton answers listener questions on safety issues faced by people with multiple system atrophy (MSA). Topics include difficulties regulating ones blood pressure and urinary function, speech and swallowing difficulties, as well as a very serious issue of particular sleep disturbances. These issues are common in MSA and some can be life-threatening.
Mar 25, 2020•38 min•Season 1Ep. 13
The world is in the midst of a pandemic of epic proportion. The coronavirus has now spread to the United States and the number of infections is rising rapidly. This has resulted in heightened anxiety and economic decline. In this episode, Dr. Tipton is joined by Megan Tipton, who asks some questions about the coronavirus. Dr. Tipton discusses why COVID-19 is a big deal and what we can do to prevent it's spread. He also discusses strategies for protecting those with dementia from infection. Resou...
Mar 18, 2020•30 min•Season 1Ep. 12
In this episode, we continue the interview with Philip Fortier, who is the executive director of Defeat MSA Alliance. This episode provides details on many of the great efforts of this organization. All donations to Defeat MSA Alliance go toward the organization's 4 pillars of clinical research, patient support, public awareness, and education. Toll Free # for Defeat MSA Alliance: 1-855-KICKMSA Defeat MSA Alliance: www.defeatmsa.org Global Online Support Hub: www.brainpatient.org Defeat MSA Awar...
Mar 11, 2020•41 min•Season 1Ep. 11
In this episode of LLTB, Dr. Tipton and Kandice introduce another neurodegenerative disease called multiple system atrophy (MSA). We also have a great interview with Mr. Philip Fortier, the direct of Defeat MSA Alliance. Mr. Fortier's brother developed MSA. Mr. Fortier discusses many of the struggles that his brother faced and what it was like to watch as this disease took his independence and, eventually, his life. Check out this links mentioned in the episode: Defeat MSA Alliance: www.defeatms...
Mar 04, 2020•37 min•Season 1Ep. 10
In this episode, Dr. Tipton and Kandice discuss the stigma & social isolation associated with the diagnosis of dementia through an interview with Cari Eyre. Cari is passionate about this topic and currently works in the social responsibility office of Baptist Health. Some of her work focuses on making Jacksonville a dementia-friendly community and issues facing seniors. Social isolation is a big issue that she tackles on a daily basis.
Feb 26, 2020•43 min•Season 1Ep. 9
In this episode, Dr. Tipton formally introduces Alzheimer's disease...what it is, what causes it, the role of genetics etc. He then interviews Linda, who has had several family members with Alzheimer's disease. Linda watched as this disease slowly took her mother's memory and reverted her to child-like behavior and eventually seizures. Hear how Linda coped with these struggles as well as those that came when some of her siblings also developed dementia.
Feb 19, 2020•44 min•Season 1Ep. 8
In this episode, Dr. Tipton introduces his new co-host, Kandice Jacobs Robinson. Kandice is a licensed funeral director & embalmer in Florida and is CEO of Kandice Jacobs Creations, Inc, which has the mission to equip individuals & families to live life abundantly & leave a lasting legacy." This episode also provides a sneak peak and some of the upcoming show topics and special formats that are just around the corner on Long Live The Brains!
Feb 12, 2020•28 min•Season 1Ep. 7
In this episode, Dr. Tipton interviews Bill Wilson, who has Parkinson's disease (PD), and his wife Marilyn. Bill graciously shares his story from the first signs that something was going on with his health to eventually receiving a diagnosis of PD. Bill and Marilyn also touch on many important points such as the importance of support groups and other great activities like Rock Steady Boxing ( www.rocksteadyboxing.org ). Check out their newsletter at http://www.firstcoastpdinfo.org/newsletter.htm...
Feb 05, 2020•28 min•Season 1Ep. 6
In this episode, Dr. Tipton interviews Lynda Everman and her husband, Don Wendorff. Lynda is no stranger to Alzheimer's disease (AD). Listen as she tells the story of seeing the first signs of disease in her husband. Lynda walks us through receiving the diagnosis of mild cognitive impairment and eventually AD. During this time she learned many lifestyle habits that can help delay the progression of symptoms. For more information about Lynda, visit https://www.usagainstalzheimers.org/author/lynda...
Jan 29, 2020•46 min•Season 1Ep. 5
In this episode of Long Live The Brains, Dr. Tipton interviews Anne Martin about her encounter with Parkinson's Disease (PD). Anne is recently retired from the Mayo Clinic where she worked as a clinical research coordinator and the facilitator of the Mayo Clinic Florida Parkinson's Disease support group. Anne has seen how PD and related disorders effects the lives of countless individuals including her sister and father. Hear Anne's perspective of the issues that her sister dealt with as she pur...
Jan 22, 2020•29 min•Season 1Ep. 4
In this episode of LLTB, Dr. Tipton interviews Kandice Robinson. Kandice is a Florida licensed funeral director & embalmer, social entrepreneur & CEO of Kandice Jacobs Creations, Incorporated (KJC). Kandice has been on the front lines of neurodegenerative disease with her father who was diagnosed with Alzheimer's Disease. Listen to this interview to hear about the road to reaching a diagnosis and how Kandice faced difficult realities and handled some very touch conversations to help her ...
Jan 15, 2020•28 min•Season 1Ep. 3
In the second episode of Long Live The Brains , Dr. Tipton interviews Wade Tipton (Dr. Tipton's father) about his encounter with Parkinson's disease (PD). Wade's father was diagnosed with PD when Wade was a child. During this interview, Wade discusses what it was like growing up with a dad who was battling Parkinson's at a time when we understood much less about it. In the discussion, we talk about genetic misconceptions of the time as well as a new blockbuster drug that was released in the 1960...
Jan 08, 2020•48 min•Season 1Ep. 2
Long Live The Brains is a podcast created by Dr. Philip Tipton, a neurologist, with a passion for neurodegenerative diseases like Alzheimer's disease, Parkinson's disease, and others. Neurodegenerative disease is the epidemic of our generation and with the lack of effective treatments, the future looks bleak. Dr. Tipton uses the power of interviews to give you a close-up look at the diseases with the goal of providing accurate information to the general public. In the first episode, Dr. Tipton i...
Dec 22, 2019•42 min•Season 1Ep. 1
