6 Nov 2017 07:57 am
I'm going to offer a bit of an apology and explanation, as a member here has pointed out he feels I've been overly critical. (I'm wearing my editor hat right now, not my cpn-patient hat.)In the past week or two, I've become highly sensitized to the blanket statements and rampant postings of a couple of prolific posters here on the site. Of late, we're seeing too many posts unrelated to cpn treatment, too many blanket statements of so-called 'facts' that aren't facts at all and a few pointless posts that belong on someone's personal blog or facebook page, but not here. I've been editing a
6 Nov 2017 07:57 am
6 Nov 2017 09:44 am
Well said Mac, I hope you will say if I ever make unhelpful posts, I can take it! Honest!
MS symptoms from 2001, DX RRMS in 2008, following, a change of hospital who sent me for an MRI, precipitated by some sight loss. Took Interferons, on and off. Prescribed chemo infusions to slow pro
Well said Mac!! We all were
Well said Mac!! We all were brain fogged once............Sarah
Completed Stratton/Wheldon regime for aggressive secondary progressive MS in June 2007, after four years, three of which intermittent. Still improving bit by bit and no relapses since finishing treatment.