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.
Parents of children with special needs are often labeled negatively: ‘troublemakers,’ ‘confrontational,’ ‘needy,’ ‘over-sharing.’ The reason we (as yes, I’m one too) can sometimes pick up some of these negative labels is that we won’t take no for an answer when it comes to our child. Why do we enter into conversations, meetings and appointments with our boxing gloves firmly on? Because the world cannot understand.
