This cartoon was in a British Newspaper…I was sent it as I don’t read that paper:-). which suggests the state of the COVID research….I suspect some of you think this is the State of MS research
SID asked
“If you get time, could you do a T4TD on why the research / medical still can’t identify an approach (treatment + lifestyle factors) which would halt the progression of this vile disease”. ….
It has…..It is called “Treat early and effectively”, the community has to buy into this…it hasn’t!…Look at the drug sales to see what is being used…… As for identifiying the approach, I would argue many approaches have been identified, but the community (funders/pharma) does not want to adopt them……..where are the studies looking at the pyramid and the holistic approach…..I haven’t seen any!
“A T4TD on what might be round the corner would bring a little bit of hope (we wouldn’t hold you to anything as we know the past has been littered with promising areas which have turned out to be damp squibs)”.
Yep happy to let ProfG put his head in the noose for that one…..however COVID-19 has made a massive dent in the finances of governments and MS charities. Will this dent their plans?……However, you know what is round the corner, because nothing is done quickly as evidence-based science is slow and it is heavily regulated and is transparent as the studies are reported in registries.
I just want to ask will there ever be a cure? Probably not! From an MS’er in Lancashire UK
Treat early and effectively is great. Unless you’re like me and it’s too late.
Neuroprotectives also swallowed by the COVID-19 cow.
This is only vaguely related as it is from a newspaper and COVID. Just wondered if you had been sent this too MD? What are the implications for MSers? It seems very scary to me as an MSer.
https://www.theguardian.com/world/2020/jul/08/warning-of-serious-brain-disorders-in-people-with-mild-covid-symptoms
I have been experiencing tingling in my left leg, ankle, foot for the past 3 days, and sudden little body jerks. I had Covid 19 for 3 weeks. I just recently got my first negative test, but now all these other things going on. My cough is back and I feel itchy often. Are these Covid after effects? Whats wrong with me, I read lots about how Covid could trigger MS symtoms. Help!! Thanks
MS and COVID there is insfficient evidence