Celebrating Sasha and supporting SickKids patient and family centred interprofessional care, staff and family partnership, patient safety, palliative care and Alagille Syndrome. Thanks to family for love and visits, laid back Dr Michael Peer, Dr Jennifer Russell's tireless coordination of LFHC, GI, CCCU, Gen Surg and IGT, all the staff at Hospital for Sick Children and Max and Beatrice Wolfe Centre and final homebound team Stephen Jenkinson, Dr Russell Goldman and TCCAC.
Paediatric Hospice Palliative Care Course
Presented on our experience to a group attending day 1 of a Paediatric Hospice Palliative Care course offered by Sickkids staff Maria Rugg and Dr Christine Newman. I looked at how we differed as a couple in our desire to speak to palliative care and how we ultimately deflected palliative care for several months as Sasha was slowly diminishing. Staff may need to give some parents permission to consider that their child is dying as they certainly give parent's permission to hope for better health. I described palliative care as the elephant in the interprofessional room - Sickkids funded research suggests only 8-12% of children who would benefit from palliative care get such support. The participants included mostly nurses and students, there was only one doctor in attendance - her medical credentials from Switzerland have not been recognised.
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