johnnycake23
Two-time AVR Vet
Hello out there, I've been on this site for over a decade and it has been very helpful to me (and no doubt others). But this post is not about me.
Back in November my wife caught COVID, and one of her symptoms, along with pleurisy and a persistent cough (imagine coughing for six months straight), is an arrhythmia. Before COVID, she was the picture of health, never so much as taken an aspirin. Where before she was energetic, now she tires easily; she she used to rise early but now sleeps in most mornings. She started seeing an electrophysiologist (among other docs) and he prescribed her Amiodarone and Metoprolol. These meds have helped, but only mildly. She was told that these meds are not meant for long-term care, and that if her condition doesn't improve in no more than 12 months, that an ablation or even a pacemaker must be considered. The ablation is very risky because the issue is "close to the AV Node," which means a pacemaker is the likelier option. The electro, in two visits, never even listened to her with a stethoscope; he merely read her EKGs and heart monitor data, which gives me pause as to her quality of care. Every day she takes her pills, vitamins (multivitamin, E, and Zinc), and stays well hydrated. After six months we've been told to keep waiting and hope for the best, that there's nothing else we can do.
I'm writing because I'm out of ideas, desperate, and looking to pull a rabbit. If anyone has any advice/insight as to what else we can do, I'd be most grateful. Whether it's courses of treatment, exercises, or even support sites such as this one dedicated to COVID long haulers, that would be great.
Thank you for reading.
Back in November my wife caught COVID, and one of her symptoms, along with pleurisy and a persistent cough (imagine coughing for six months straight), is an arrhythmia. Before COVID, she was the picture of health, never so much as taken an aspirin. Where before she was energetic, now she tires easily; she she used to rise early but now sleeps in most mornings. She started seeing an electrophysiologist (among other docs) and he prescribed her Amiodarone and Metoprolol. These meds have helped, but only mildly. She was told that these meds are not meant for long-term care, and that if her condition doesn't improve in no more than 12 months, that an ablation or even a pacemaker must be considered. The ablation is very risky because the issue is "close to the AV Node," which means a pacemaker is the likelier option. The electro, in two visits, never even listened to her with a stethoscope; he merely read her EKGs and heart monitor data, which gives me pause as to her quality of care. Every day she takes her pills, vitamins (multivitamin, E, and Zinc), and stays well hydrated. After six months we've been told to keep waiting and hope for the best, that there's nothing else we can do.
I'm writing because I'm out of ideas, desperate, and looking to pull a rabbit. If anyone has any advice/insight as to what else we can do, I'd be most grateful. Whether it's courses of treatment, exercises, or even support sites such as this one dedicated to COVID long haulers, that would be great.
Thank you for reading.