Podcast

A snapshot into the life of someone living through a Post-Exertional Malaise (PEM) episode after minimal exertion the previous day. Please rate, review, share, and

I was able to try putting music in the background but there is no way to adjust the volume so I was on the fence

BONUS EPISODE #4: My Infectious Disease Appointment Discusses most recent appointment to see the infectious disease physician in an attempt to get on an antiviral

This episode discusses the importance of having things to look forward to in order to keep your mental health on point. Furthermore, discusses the universal

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