Living and Loving with Parkinson’s Disease
Our Partnership Through a 45-Year Journey
Failed to add items
Add to basket failed.
Add to wishlist failed.
Remove from wishlist failed.
Adding to library failed
Follow podcast failed
Unfollow podcast failed
£0.00 for first 30 days
Living and Loving with Parkinson’s Disease
Buy Now for £14.99
No valid payment method on file.
We are sorry. We are not allowed to sell this product with the selected payment method
-
Narrated by:
-
Marcus Freeman
About this listen
Annie and Rolf Lulloff were entering an exciting stage of life in 1976 when the first signs of health issues that lie ahead for Annie began to emerge. A sudden loss of sense of smell, severe anxiety attacks, vision issues, and other neurological challenges piled up, eventually culminating in a diagnosis of Parkinson’s disease on New Year’s Eve, 1989. But the Lulloffs were not about to let Parkinson’s get the best of them.
They cultivated a special relationship as care partners while enjoying life to its fullest over the next thirty-one years. Their commitment to experiencing all that life has to offer strengthened their bond and established them as examples for others going through similar journeys.
Living and Loving with Parkinson’s Disease is part love story and part how-to guide for all participants in a care partnership. Care persons, their spouses, and extended family and friends will benefit from the tips and care suggestions Rolf has compiled from his front-row seat to the ever-changing road that is a Parkinson’s disease journey.
©2023 Rolf Lulloff (P)2023 Rolf LulloffListeners also enjoyed...
Critic reviews
"The sense of despair that often accompanies the loss of control from Parkinson’s can be overwhelming. Rolf and Annie Lulloff are great examples of how focusing on love and resilience makes it possible to enjoy a fulfilling quality of life." (Ann McKee, MD, director of the Boston University CTE Center and UNITE brain bank)
"The loving journey that Rolf and Annie Lulloff traveled together should be a model for all families dealing with Parkinson’s and other neurodegenerative diseases." (Lisa McHale, Director of Legacy Family Relations, Concussion Legacy Foundation)