If you would prefer to search for a mentor by phone, please call us at 619-373-5476. (If you are having a medical emergency, please call 911.)
Bonnie Wagner
My name is Bonnie Wagner and I am 71 years old. I retired from my corporate job as a HR Director at age 64, one year after my husband, Rusty was diagnosed with PD.
When not involved with this insidious disease, I enjoy studying the Bible, hiking, gardening, walking, traveling, entertaining, learning Spanish, and caring for our 9-month-old grandson, Luca. As you can see, there is not much room for PD.
Slowly, over the years, my role as caregiver increased greatly, until about two years ago when we brought caregivers into our home. It was a game changer.
Rusty’s needs take precedence. His major challenges are falling, fainting, shortness of breath, and cognition. He needs constant watching. However, thanks to caregivers, I try hard to protect my time for walking, going to the gym, morning devotionals, and some of the items listed above.
I consider myself to be tenacious when it comes to advocating for Rusty. That means we’ve changed physicians more than once. We’ve traveled to AZ and CA to meet specialists and flown to the east coast for specialized procedures. I obtained an assistive walking device when Medicare denied us. I search out and use non-profits to pay for Rusty’s expensive meds. I push for physical therapy in the home. I’ve advocated for those more expensive meds. All this is not to brag about my actions; rather it is to let others know that our PD experience involves work. Even when Rusty is not able or willing to seek out positive actions for himself, I need to do it rather than give in to the disease.
Other times, I’ve reached the end of my rope. I’ve given up chasing him every time he walks away from his walker, or arguing about drinking more liquid, or when he insists in walking down stairs instead of a ramp.
More than all of this, I depend upon my faith to get through each day. My God is good and guides me and the man I love.
Contact Bonnie:
Bridget Ryan
My husband was diagnosed with Parkinson’s in 2017. I retired shortly thereafter and have been focusing my attention on providing the best care I can. In addition to the prescribed medication, we focus on strength training/movement as well as mental health. We feel that this regiment has been very helpful in adapting to the disease. We have also been able to manage his freezes by understanding how and when they are likely to occur – i.e. confined spaces, thresholds etc. When these occur, we have found that counting to five after coming to a complete stop enables him to start moving again.
I would like to help other care partners try to manage the disease with what has worked for us over the years. We have been through multiple stages of the disease and have focused on adapating as best we could to these progressions.
Contact Bridget
Dorene Whitworth
Receiving a diagnosis of Parkinson’s can be scary and isolating. Doctors are not necessarily in tune with just how devastating a diagnosis of Parkinson’s can be to an individual. As a mentor and someone with Parkinson’s, I hope to alleviate some of the fears, uncertainty and anxiety that often accompanies a diagnosed by giving them someone to talk to. I would encourage them to share their experiences and concerns and I could provide them with information on a number of local resources.
Contact Dorene
Mark Lenz
I am a Reno, Nevada native, with degrees from UNR, the New England Conservatory of Music and Cornell Law School. I was diagnosed with Parkinson’s in 2005, and eventually had to retire from both my music and law careers. I have, however, remained active in retirement, with fishing and other outdoor activities, woodworking and music composition.
Contact Mark
Matt Riecken
I believe I can help newly diagnosed people with the challenges and transitions they’ll need to make, and help them develop new and constructive perspectives.
Contact Matt
Sarah Parks
I always want to help people find the positive side of Parkinson’s – the people they will meet and interact with. Diagnosed with PD in 2017 I’ve learned that fighting PD is most important and not a death sentence.
Contact Sarah:
Sharleen Phillips
I was diagnosed with Parkinson’s disease in 2012. I have many symptoms long before being diagnosed. I think I can provide information and support to someone who has Parkinson’s disease.
Contact Sharleen:
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