
37 episodes

Experiences in Caregiving Experiences in Caregiving
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- Education
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5.0 • 14 Ratings
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This podcast is in partnership with the San Diego/Imperial County chapter of the Alzheimer’s Association, and is a place where everyday people can speak on their experiences, their struggles, and the everyday highs and lows that come with their family member’s Alzheimer’s journey. The goal of this podcast is to create a space of comradery, connecting listeners with this support group and hopefully encouraging people to ask questions, give advice, and share their own stories.
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How to be an Ally
In this episode we discuss the complex nature of relationships between caregivers and those around them who may or may not also be grieving. We discuss communication styles, how best to support a caregiver, and how caregivers can compensate when their allies can’t or won’t support them.
For more information about episodes, links to resources, and to give us your thoughts and ideas for new topics, visit https://www.experiencesincaregiving.com/ -
The Impact of Caregiving on the Black Community - Part 2
With the overwhelming response to our “The Impact of Caregiving on the Black Community” episode, we’ve come back with a part 2 to further discuss the challenges of caregiving in the African American/Black community, the racial disparities in care for loved ones, support for caregivers, and access to resources.
For more information about episodes, links to resources, and to give us your thoughts and ideas for new topics, visit https://www.experiencesincaregiving.com/ -
Special Episode - The Longest Day 2023
In our newest episode we are celebrating Alzheimer’s & Brain Awareness Month so we are talking all things brain health, the Alzheimer’s Association’s “The Longest Day” fundraising initiatives, and how “The Longest Day” impacts our caregiving community.
For more information about episodes, links to resources, and to give us your thoughts and ideas for new topics, visit https://www.experiencesincaregiving.com/
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Brain Health & The Frustration of Getting a Diagnosis
This month we discuss the upcoming “era of treatment” in relation to brain health and the frustration caregivers feel when trying to get a diagnosis, in particular the correct diagnosis, so that they can make plans and get out in front of dementia with treatments, medications, etc. We also discuss ways caregivers can approach primary doctors and neurologists in hopes of getting heard and getting the info they need.
For more information about episodes, links to resources, and to give us your thoughts and ideas for new topics, visit https://www.experiencesincaregiving.com/ -
The Impact of Caregiving on the Black Community - Part 1
This month we are discussing the impact of caregiving on the African American/Black community, the racial disparities in care for loved ones, support for caregivers, and access to resources. In addition, we will discuss the unique challenges the Black community is navigating and potential ways to overcome them.
For more information about episodes, links to resources, and to give us your thoughts and ideas for new topics, visit https://www.experiencesincaregiving.com/
Related Links:
Jessica Guthrie: Instagram @CareerCaregivingCollide
Andrea Krystal: Instagram @itsandreakrystal | Website: https://www.andreakrystal.com/
Ty Lewis: Instagram and Tik Tok @iamgertrude | Website: https://www.incaseiforgetconsulting.com/
Jacquelyn Revere: Instagram and TikTok @momofmymom | Website: https://momofmymom.com/
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All About Support Groups
In this episode we’re talking about why caregivers need support groups, their benefits, what made us finally say yes to this type of support, and how to overcome some of the obstacles to support.
For more information about episodes, links to resources, and to give us your thoughts and ideas for new topics, visit https://www.experiencesincaregiving.com/
Customer Reviews
Thank you
I have been listening to your podcasts for about 6 months. I have found it extremely helpful!
Like a hug for family caregivers
Thank you for sharing diverse stories and covering the topics we are all facing. I’d say more but my mom has AD and I’m her primary caregiver so I’m beyond tired. Thanks for helping me feel less alone tho
So helpful!!
I’m a young long distance caregiver and am so grateful to hear other people’s stories. It’s comforting to know we’re not alone. Thanks so much Susan and the ALZ Association for hosting this podcast.