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I'm confused by this article. Is this the doctor in this article? https://twitter.com/mindfuldrg?lang=en "At the beginning of 2020, when COVID-19 was still only in the peripheries of our awareness, I was recovering from neurosurgery. I have a rare neurological disease, tethered cord...

I am glad that doctors are recognising autonomic dysregulation in post-infectious illness. We need more research and treatments in this area.

Or as in the Dengvaxia vaccine, it could worsen symptoms for people not previously infected by dengue. We just don't know yet.

The UK is the first to roll them out. I'm still unsure when Canada will start. We don't have facilities in Canada to produce vaccines so we are behind in the line-up.

@Trish you will have to go back for the second jab one month later. I'm going to wait, if they offer to do house calls later I will consider it. I'm in no rush.

Re: Dengvaxia vaccine "But controversy arose after Sanofi (French pharmaceutical firm) disclosed a year later that it could worsen symptoms for people not previously infected by the dengue virus." Who is to say it won't happen with the COVID vaccine?

@Peter Trewhitt I have another issue besides adverse effects which I made have had in my ME onset. The timing of the vaccines are moving too quickly for me as I wrote in my post above.

I'm not anti-vaccine, but I will wait after watching "Vaccin, la guerre secrète" last night. They brought up the Dengue vaccine fiasco in the Philippines that brought criminal charges (reckless imprudence resulting in homicide) against a prominent pediatrician and medical researcher(Rose...

I would rather read about new COVID-19 test that could help CFS.

It's possible that some will experience permanent loss of stamina, like those who contracted EBV but never developed ME. They're still functional, but can no longer exercise like they once did before the infection.

“Hi Jonathon, I’m Charlotte, I hope you don’t mind, but I’ve got four things I’d like to discuss this morning, they’ll all be quick.” “Of course” I lied, shifting my expression from a smile of greeting to friendly concern, “Can you tell me what they are?” I would have un malaise if my GP was...

My brain/forehead literally feels sore/bruised when I'm overdoing cognitively. I feel nauseous. Is this how others without ME describe brain fog?

He's a sociopath. I'd love to call to make an appointment with him just for fun. When the receptionist asks what is the problem, I would tell her "I'm lonely". See how fast I get in to see him.

I copied this from Healthrising :

I don't think they'll find treatments to 'fix' their symptoms, but addressing autonomic issues will most likely be very helpful.

They've been living with their personalities all their lives so don't expect them to change.

I have difficulty processing, concentrating and absorbing information when I have cognitive PEM. I feel brain sick/nauseous. I've never had issues with memory though.

I didn't experience 'brain fog' until 11 years into the illness. It all started when I was improving and started exercising again.

Ughh.

It seems that doctors have become social-media 'influencers' now? I mean, where is his responsibility as a physician about using his platform to spread his ignorance and misinformation?