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I don't experience 'brain fog' as described by others, but my cognitive issues does include focusing/concentrating. I feel ill/nauseous during this time. It feels like a lack of power/energy that isn't available to go on until I lie down, blank everything out and rest for at least an hour.

What are the differences between LC and post-COVID-19 fatigue syndrome? Why are they using 2 separate names? When did they slip "fatigue" in?

I used to pass out everytime I received a vaccine in grade school. I never knew why.

Same blood pressure, same heart rate but the flow in the brain is impaired - heart failure is not only about the heart but the brain too. https://onlinelibrary.wiley.com/doi/10.1002/ehf2.13128

General Vaccine Ingredients

If nothing else, COVID-19 represents a unique opportunity to study post-infectious autonomic syndromes, research which will hopefully lead to greater understanding of the pathogenic mechanisms of POTS.

...It's official. (The Oxford/AstraZeneca vaccine is called Covishield in India) https://thehindu.com/news/national/serum-bharat-biotech-covid-vaccine-applications-put-on-hold/article33290974.ece… The application for Covaxin was rejected too.

India's drug regulatory agency reportedly rejected the application for emergency use authorization for the Oxford/AstraZeneca covid vaccine for lack of data. (The manufacturer in India is the Serum Institute of India, not AstraZeneca)...

@Esther12 Why mention ME at all? It just continues to recycle ME into the 'mysterious' and 'unknown' pit again. It's annoying more than anything.

"The exact cause of ME is unknown, but, a viral trigger is strongly suspected" They can't call themselves 'experts' on ME either. It's quite well known now that a viral or bacterial triggers ME, at least over 70% pwME have reported this.

Here is one explanation:

Wow, a good reason not to refer to PEM as PENI (psychoendoneuroimmunology (PENI))! Laugh and be well- ugh.

We may end up there by different pathways but there’s often some kind of connection.

POTS population is 90% female. They don't yet how it will affect the long-COVID population because COVID affects children and adults in a different way.

It will be named "Chronic Covid Syndrome'.

In medical terms photophobia means extreme sensitivity to light. I used to get migraines years ago, my medical record listed 'photophobia'. It is a bit odd though.

@Jonathan Edwards No, she STILL has ME based on what she wrote: ""Simple actions like showering, brushing my teeth or making food have become monumental tasks. My Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is worse. Minimal activity increases my symptoms which makes it...

@Jonathan Edwards In the article she is describing herself as having ME. I posted the quote above. She had surgery and now she is suffering from ME and long-Covid?