MediTest
Last week, Jim finally came up with the magic number enabling me to register the cpnhelp domain name. Now the only three people who can do anything to the site are Mac, me and our new Drupal expert Joe. Once the registration has fully gone through, by the end of next week, the first thing to do in my mind, is to get Joe to put in place a new messaging system which actually works.

I am at the moment writing a new front page, cleaning up the banner with its three messy typefaces and correcting a few missing links in other places. I will let you know when the messaging is about to start.

Messaging. I miss messaging. I vaguely remember it....

The difference between what we do and what we are capable of doing would suffice to solve most of the world’s problems. Mohandas Gandhi

I hope you got the letter I forwarded from Joe, who see.s to appreciate what we have been going through. Happy days should soon be here.
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.

So glad you two are heading the new incarnation, and i’m sure Joe will be a great asset. i can’t be alone in having missed it, cpnhelp.org has become a very important friend. Jane

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

Thanks Jane, that comment is greatly appreciated by both of us!

Before even more people drift away, the site won't look vastly different, but everything will work: I think that to start with, time is of the essence. I have asked Joe to get the messaging working first and I am writing a new home page, then, because cpnhelp.org is becoming one of Joe's regular clients, we can work from there.
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.

I know it will be great, and I'm guilty of being aabsent for a while, and this site has been such a support to all of us, we really need to be a friend to it. So, we should all be talking, just as in the past. How selfish to let you do all this hard work and not be grateful and present! Fair weather friends! Jane

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

As long as all you migrating birds head home soon, it'll be fine!

The difference between what we do and what we are capable of doing would suffice to solve most of the world’s problems. Mohandas Gandhi

Hi Mack, Yes it will, and i'm dure we all will! Or where else? Jane

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