If I say anything here I am censored immediately. If you would like to see how I am doing you can catch up with me on Facebook at
just message me where you are from when you friend request.
We have some very open drag down arguments over there where people actually have to support their arguments, not just start them. Plus whatever you say won't be censored or removed. We talk about everything we can't here. You'll also notice some of the disappeared CCSVI folks as friends are on the friends list, also a couple of disappeared HiCy people...all who are doing well.
This is a great place to find out what is going on in the medical field but to actually get to vent, argue, and the ability to stick up for ones self, it is not. I am sure it is Republican ran as it censors freely.
Good luck folks I do read the info on the meds but the forums on here, well, they've lost it. I will usually read the article link that start the post but nothing after that. I need to make my own decisions not what I "should think."
My doctor just told me life is too short if the last three drugs don't work. Then I try HiCy one more time and it's done.I have been told based on the 30+ years of treating MS, not liking big pharma, and not doing anything unnecessary, told me I have 5-10 years away from complete disability. Life -especially mine, is far too short to try to defend myself and be censored over here.
I don't post here anymore at all. I did to let someone know how my neuro appointment went so they could have the last laugh. Otherwise, I and a bunch of others have left.
To those remaining, good luck to you all and I hope they find a cure for this disease before we are all dead. May not happen for me but if you are newly dx'd, get a good MS neuro, read about every drug on this page, make a decision, and never end up like me.
I'll miss some of you. I am sure this will be retyped or censored anyhow and will need to be retyped anyhow.
Chris T Young
MS Survivor and advocate