Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS)


advertisement
Reply
 
Thread Tools Display Modes
Old 01-26-2010, 02:36 AM #1
fmichael's Avatar
fmichael fmichael is offline
Senior Member
 
Join Date: Sep 2006
Location: California
Posts: 1,239
15 yr Member
fmichael fmichael is offline
Senior Member
fmichael's Avatar
 
Join Date: Sep 2006
Location: California
Posts: 1,239
15 yr Member
Blank

Ouch! I totally missed that. So much for Mark and artist, too, although in light of the how she was doing when she left, I'm inclined to think she's well enough wherever she is.

I know too that some people drift off, worn down by the cycle of so much fear being ever expressed anew, impatient that the light of magic treatments at the end of the tunnel never seems to be getting any closer.

Then again, as someone whose had this for 9 years, I know that by the time I hit the 4 or 5 year mark, perhaps because of my more regimented use of meds (dosing time released analgesics on a precise schedule) or other treatments, I don't know, the pain became somewhat more managable. That or I adapted to it with the help of [whatever] so I don't mind hanging out here because I'm deep down I've become something of an optimist. To paraphrase Sartre, it's knowing that the choice is ours, whether we go to our ultimate ends - whatever those may be - as slaves (wrapped up in fear and regret) or free men and women, appreciating the moment as it arises: good or bad, no difference. Not that any of us always make the mark - I certainly don't - but just keeping the target in mind is helpful.

Still, where I'm most concerned is for those folks who appeared to be in something of a state of physical free-fall (Mark, Rosie) when last we heard from them. If anyone has information on esrtwhile members who've gone too long accounted for, even if it's not necessarily upbeat, I for one, would appreciate knowing it.

And as far as you other guys are concerned, I'm with Claudia, time to check in. Theresa too.

Mike

Last edited by fmichael; 01-27-2010 at 01:40 AM.
fmichael is offline   Reply With QuoteReply With Quote
Reply


Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off



All times are GMT -5. The time now is 08:55 AM.

Powered by vBulletin • Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise v2.7.1 (Lite) - vBulletin Mods & Addons Copyright © 2024 DragonByte Technologies Ltd.
 

NeuroTalk Forums

Helping support those with neurological and related conditions.

 

The material on this site is for informational purposes only,
and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider.


Always consult your doctor before trying anything you read here.