Trustworthy sources versus otherwise
In regard to HSCT, I was purposefully and continually lied to by the MS Society UK. They told me ‘Don’t do it, you might die’ 12 years ago. I ignored them, underwent the treatment and celebrated 10 years no progression, without the need of ANY drug modifying therapies or medical intervention FOR THE LAST 10 years. In the USA, I know funding is very different, but if you’re interested in the treatment, I’d suggest you look in to https://hscthope.org.
I have posted several links below that I know you’ll find of interest . If they’re not active links, drop them in to your chosen internet provider service and prepare to be enlightened.
Christy Cruise.
https://youtu.be/MwUgzuNQZWw?si=_ZYiHcCkDa_KIWDF
Interview of 3 medical professionals in relation to the success of HSCT
https://www.aimscharity.org/hsct/meet-the-experts
Key Note speaker:
Dr Burt
https://youtu.be/Vs2q1yZlCqE?si=zc3z5a9bSUHaUgFb
Aimscharity.org
I hope everyone is doing as well as could be expected considering their situation! 🙏🏾

Excellent post
No worries. Yes it is a poor situation. I had HSCT in Mexico November 2024. NHS told me I would die (thankfully I didnt). MS nurse just followed Nuerologists advice- I would die. UK based charities for MS didn't want to know. HSCT isn't a cure, we know that, but I wasn't waiting around for further options. Also, what people fail to recognise is that after HSCT there is much work you must do on yourself to get the full benefit.