Podcast

Home repairs and feeling left out — how people with Long COVID, ME/CFS, POTS, and dysautonomia have to miss social gatherings and fun outings because

Discusses the loss of a colleague to Amyotrophic Lateral Sclerosis (ALS) which leads to grief and existential distress — am I doing what I was

For all of us with Long COVID, ME/CFS, POTS, dysautonomia, brain fog, severe, debilitating fatigue, significant weight gain (or loss) who feel like this entire

A topic I should have discussed way before now — tips and tricks for people with Long COVID, ME/CFS, POTS, and dysautonomia to help make

How having symptoms of Long COVID, ME/CFS, POTS, MCAS, Fibromyalgia, etc. such as debilitating fatigue, brain fog, myalgias, dysautonomia, etc. affects relationships. Please rate, review,

Overall life and disability retirement update. Also, a new mantra to help visualize acknowledging Long COVID and its effect on our life: To our old

Tips and tricks for how to make cupcakes (or just generally cook) for patients with Long COVID/post acute sequelae of COVID-19 (PASC), myalgic encephalomyelitis/chronic fatigue

Updated episode re: all the meds and supplements I am taking right now as well as why I am taking them. This episode is NOT

Laurie, a fellow long-hauler, recently participated in a study that focused on brain stimulation and using an app (BrainHQ) to play brain games to improve

I go over the Cleveland Clinic’s webpage about Postural Orthostatic Tachycardia Syndrome (POTS). Website: https://www.my.clevelandclinic.org/health/diseases/16560-postural-orthostatic-tachycardia-syndrome-pots