#4 "Long COVID looks exactly, and I mean exactly, like chronic Lyme.” MIT researcher Michal Tal has investigated the immune response in cancer, chronic Lyme disease, and long COVID.
READ MORE: lymedisease.org/long-covid-l... #LymeDisease #TopStories
Adam Price introduces the debate on ME.
63,000 people live with ME in Wales.
Watch here: www.senedd.tv/Meeting/Live...
Oh...
'The parallels seen in the experiences of those with ME/CFS and long Covid suggest ‘significant improvement’ is needed in how patients are diagnosed and cared for'
www.pulsetoday.co.uk/news/clinica...
Oh...
hhs.gov/lyme/index.html
hhs.gov/lyme/index.html
4th February 2021.
#longcovid #myalgicencephalomyelitis #myalgice #cfsme #mecfs #lymedisease #lyme #chroniclyme
4th February 2021.
#longcovid #myalgicencephalomyelitis #myalgice #cfsme #mecfs #lymedisease #lyme #chroniclyme
How do controversial ideas become accepted in medical research and medicine?
T-suppressor cells were "debunked" and then rebranded as #Tregs.
Chronic Fatigue Syndrome now ME w/ #ChronicLyme to #IACI following #LongCOVID.
I want to hear your stories!!
How do controversial ideas become accepted in medical research and medicine?
T-suppressor cells were "debunked" and then rebranded as #Tregs.
Chronic Fatigue Syndrome now ME w/ #ChronicLyme to #IACI following #LongCOVID.
I want to hear your stories!!
Nice talk
Nice talk
3/6
#Lyme
#Lymedisease
#ChronicLyme
www.medpagetoday.com/special-repo...
#Lyme
#Lymedisease
#ChronicLyme
The Press, Yorkshire, England. 19th November 2019.
#lymedisease #chroniclyme #lyme #myalgicencephalomyelitis #myalgice #cfsme #mecfs #fibromyalgia #multiplesclerosis #alzheimers #parkinsons
The Press, Yorkshire, England. 19th November 2019.
#lymedisease #chroniclyme #lyme #myalgicencephalomyelitis #myalgice #cfsme #mecfs #fibromyalgia #multiplesclerosis #alzheimers #parkinsons
For some exercise will help.
If you have ME like me, it’s a no go. Even though I know my dysautonomia could improve, it will cost me my baseline.
For some exercise will help.
If you have ME like me, it’s a no go. Even though I know my dysautonomia could improve, it will cost me my baseline.
(and am myself interested in eventually trying lumbrokinase, so will be looking forward to the results of this trial!)
NYC #pwME #pwLC and people with #chroniclyme, you could join this trial!! #LongCovid #MyalgicEncephalomyelitis
(and am myself interested in eventually trying lumbrokinase, so will be looking forward to the results of this trial!)
NYC #pwME #pwLC and people with #chroniclyme, you could join this trial!! #LongCovid #MyalgicEncephalomyelitis
Register for one or both, the only restriction is where you live.
www.massmecfs.org/news-events/...
#massmecfs #MyalgicEncephalomyelitis #chronicfatigue #longcovid #chronicillness #pots #chroniclyme #fibromyalgia
Register for one or both, the only restriction is where you live.
www.massmecfs.org/news-events/...
#massmecfs #MyalgicEncephalomyelitis #chronicfatigue #longcovid #chronicillness #pots #chroniclyme #fibromyalgia