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We Got Dad Back... But Nothing Went Back to Normal | Heart Failure Unfiltered

Pumping Marvellous Foundation

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We Got Dad Back... But Nothing Went Back to Normal | Heart Failure Unfiltered

227 просмотров · 1 мес. назад
Pumping Marvellous Foundation
1,87 тыс. подписчиков
227 просмотров · 1 мес. назад
Getting the diagnosis is only the beginning. So what happens to a family once the crisis passes and heart failure just... stays? In this second episode of a two-part series, Nick Hartshorn-Evans - founder and CEO of the Pumping Marvellous Foundation - sits back down with his wife Karen and daughters Natasha and Anastasia to talk about what came after his heart failure diagnosis at 39. Coming home didn't mean going back to normal. Instead, it meant a new German Shepherd puppy, a secretly renovated bedroom, missing prescriptions, a heart failure nurse who became a lifeline, and two young girls quietly growing up faster than they should have. Together they talk honestly about isolation, mental health, the confusing gap between specialist and GP care, why percentages like "ejection fraction" mean nothing without context, and what they'd say to a family just starting this journey. It's a warm, funny, and deeply honest look at the long tail of a heart failure diagnosis — for the patient and everyone around them. This is part two of a two-part series. In this episode: 00:00 — Welcome & what this episode covers 02:39 — Coming home to fish and chips (and being sick) 03:57 — The secret bedroom makeover 05:28 — The chandelier assembly saga 06:55 — What the girls actually remember coming home 07:15 — Were you being a giddy five-year-old? 08:54 — Living "institutionalised" after weeks in hospital 09:15 — Nearly giving Riggs the puppy away 09:48 — Giving a hospitalised parent's gift some thought 11:27 — Watching for symptoms with no clear playbook 12:26 — The warfarin prescription fight 13:53 — Losing hospital "cotton wool" back in primary care 14:12 — Getting back to normal vs. pacing yourself 19:17 — What heart failure changed — or "chained" — in the family 19:27 — Marvellous myth buster: does a diagnosis mean nothing improves? 21:05 — Did isolation ever creep in? 22:51 — The fall, the head bang, and the long A&E wait 24:03 — Did it make the girls grow up faster? 25:29 — "Nobody's ever talked about the charity" — until now 26:18 — What have you learned about your parents? 28:09 — What clinicians should — and shouldn't — tell young children 31:19 — Why ejection fraction percentages confuse patients 33:05 — What would you say to another child going through this? 35:20 — What Nick would tell himself in that hospital bed 36:06 — Closing thoughts and how to find support 🫀 If heart failure is part of your life, you don't have to face it alone. The Pumping Marvellous Foundation is the UK's leading heart failure charity — patient-led, trusted, and here for you. 🔗 Visit: www.pumpingmarvellous.org 💛 Donate £5 today and help someone feel less alone #HeartFailure #HeartFailureAwareness #PumpingMarvellous #HeartFailureUnfiltered #FamilyStory #HeartFailureRecovery #HeartHealth #PatientAdvocacy #CardiacCare #NHS #HealthAwareness #ChronicIllness #CaregiverSupport #HeartDisease #UKCharity #PublicHealth #MentalHealthAndIllness #HospitalStory #EjectionFraction #CardiologyCare