Elaina sits down and talks with Lisa Jamieson from Walk Right In Ministries about family caregivers, the holidays, and ways the church can better support them.
The training, content, gatherings and experiences that we’ve created for pastors, church staff and ministry volunteers produced with the assistance of like-minded colleagues serving in disability ministry have become our principal service. So much of what we’re able do to help churches welcome and support families, we accomplish by bringing together experts from other ministry organizations.
November is Caregiver Awareness Month. As someone who became one of my dad’s caregivers before I started school, I grew up thinking everyone in the world was aware of caregivers and caregiving. As a young adult my husband and I cared for a son born with a life-threatening medical condition, and his typical sibling. As members of the sandwich generation, my brother, sister, and I cared for our mother for 15 years after she was diagnosed with dementia. This explains why, when I first heard that November is Caregiver Awareness Month, I was incredulous, and I still am.
In this episode, Lauren Hickman shares her personal journey and calling to disability ministry, describing how God has guided her every step of the way to serve families impacted by disability.
In today’s episode, Sandra talks about the challenges small to normative-sized churches face in disability ministry and shares how the churches she’s been a part of have overcome these challenges.
By the numbers, Linda shouldn’t be here. Everything seemed to be stacked against her by worldly standards, and still seems that way. How could bullying, struggles with education, and psychiatric hospitalizations work for His plan? In part 2 of this series from Linda Bunk, see exactly how God is powerfully using all of these struggles to minister to people in Ukraine.
Mark Arnold belongs to the Disabled Children’s Partnership, a UK-based organization that recently released the results of a series of surveys of UK families with children and young people with disabilities. The results are stark: the impact of the 18-months of the COVID-19 pandemic has been harrowing.
The day we received an official diagnosis explaining our daughter’s struggles, my husband and I cried. Actually, I literally wailed and groaned for at least half an hour. Carly’s diagnosis triggered a heart cry that special needs parents, families and individuals living with disability commonly understand, and can benefit the whole Church.
