Re:MS treatment a step closer after drug shown to repair ner...
by dmclamb on Friday September 25, 2020 @05:19PM
(#24594212)
I'm RRMS, year three on Ocrevus. I wish your wife well. MS is a cruel disease.
Re:MS treatment a step closer after drug shown to repair ner...
by baldfat on Friday September 25, 2020 @12:00PM
(#24591191)
My niece has aggressive MS and Ocrevus didn't help.
CRSPR is the true dream. No more MS.
Re:MS treatment a step closer after drug shown to repair ner...
by sterlind on Friday September 25, 2020 @12:32PM
(#24591557)
How would CRISPR prevent MS? Autoimmune diseases seem a poor fit.
Re:MS treatment a step closer after drug shown to repair ner...
by faeyanpiraat on Saturday September 26, 2020 @03:21AM
(#24597025)
Maybe it wont help you if you developed MS, but it could help you before that.
MS seems to be caused by some unknown combination of environmental factors, and genetics.
You fix the bad genes, and you may become immune.
That would be an amazing find if it works in humans. My wife was on metformin for many years (not for diabetes) before being recently diagnosed with MS. Coincidentally she experienced her first MS symptoms shortly after stopping metformin. We suspect that use of prescription steroids along with metformin might have been masking the onset of her MS for years and in an indirect way even delayed it slightly.
She just got her first half-dose infusion of Ocrevus, other half scheduled for next week. Ocrevus is such an amazing disease-modifying drug. It's very expensive but our insurance covers it and after the initial dose, she only needs one 3-4 hour infusion every 6 months. No other medication needed on a daily basis! Ocrevus helps ensure no new flare-ups happen anytime soon but it leaves her immunocompromised and there is no remyelination. If metformin + antihistamine end up producing even a little bit of remyelination that would be a game changer because she's young and has enough time to regain everything if it just involves taking a couple of pills daily.
Unrelated but just putting this out there since it's fresh on my mind - if you or loved one ever gets diagnosed with MS or equivalent, you absolutely have to be your own advocate. Best thing you can do in the US is to get an online fax# (I use redfax) and the Dropbox app. Scan every single medical document you get with the Dropbox app, convert it to PDF, and then fax it over to 100 places as needed. Also sign up for every single patient portal including Quest/Labcorp. Be sure to get a DVD of every imaging test (CT/MRI) and upload them for free to postdicom.com to share with anyone or to just see it yourself if curious.
It is a LOT of work and very stressful. But if you're technically savvy, you can avoid a lot of driving back and forth between testing, doctor, hospital, medical centers. And above all reach out to anyone you trust for assistance, even if it's just to pick up groceries. People can surprise you with their generosity.