This Is MS Multiple Sclerosis Knowledge & Support Community

Great idea Arron, but I am a bit fussy about what I wear, both in colour/color and design. Have you got anything in mind?

Chris P

Welcome Bruintje :D I don't know how I missed your post until now, but you are both very welcome. I too am a PPMSer and agree with your humour policy :lol: It's the only way to keep sane. I think smiling and laughter are the best medicine and can help us all conquer this trouble, better than any med...

Hi Dawn,

I just can't believe how quiet it's been around here for the past few days, but welcome to the group.

I'm sure there is plenty for you to read without any new postings, so enjoy

All the best,
Chris P

Hi Norski, and welcome to the site

There's enough information on here to keep you going for a while, so enjoy.

All the best,
Chris P

Hi Lucy,

Welcome to the group. I'm trying to tie 'Lucy' in somehow with SSF, but perhaps I'm just ignorant, or just plain nosey!

You have so much information available here, I'm sure we'll hear from you again very shortly.

All the best,
Chris P

Hi Janice, :D Welcome to the group, You've probably already found much of the information on this site, but it grows all the time and there is always someone around to ask, when you have a question. I can't help with your drug query I'm afraid, as I've never been offered any, but I'm sure others wil...

Hi Arron, it seems fine now. Thanks for the suggestions wilson, but as I say, it seems fine now.

All the best.
Chris P

Hi Arron, thanks for the quick response. :) It seems to be hanging on to my login now, but it's still not quite right. From the Forum Index page, several forums are shown as having new messages, but by the time I get through to the individual forums, none of the messages are shown as unread. I can s...

Today I keep being logged out, purely by leaving the main forum index to go to read a post. I then become anon unless I use the back button to get to the main index again. To post this message, I had to log on again.

Chris P

Hi Sharon,

I still haven't been able to get through all these posts, I think I had better put them on paper for an easier read.

Thanks for the new information, it is appreciated.

All the best,
Chris P

Hi Nabisco,

Welcome to the group. It sounds as though you have plenty to keep you busy, but please keep coming back to visit. There is so much information here, and any questions are often quickly answered.

All the best,
Chris P

Hi SammyJo, :D I'm not trying to be critical of your survey, merely pointing out how the results might have influenced my decision of whether or not to try LDN. I may have been less concerned about the results experienced, if perhaps I knew that x% of respondents couldn't get on with the med. In rep...

"LDN did not work for me, this is my information: I am 52 years old I am male I have had PPMS for 10 years I tried LDN for 10 days on this occasion I took 3mg's per night at 2130 I obtained my LDN from Martingdales The filler used was calcium carbonate My doctor was anon in Crediton, Devon UK I...

Thanks again for your thoughts Joyce, :D Thinking about it, I'm pretty sure the post above went to the Yahoo forum, and that's one I'm thinking of losing. There are too many folks on there that think they know it all. They try to liken everyone elses situation to their own, when anyone with any expe...

chris, what exactly happened when you took LDN? Hi Arron, :D I thought I had posted here on the problems I had, but when I search for my post, I can't find it. Perhaps it was on one of my other forums - I'll copy an original post in below: >> original post follows << It's bad news for me yet again ...