advertisement
Reply
 
Thread Tools Display Modes
Old 05-04-2008, 02:55 PM #21
beautytransforming's Avatar
beautytransforming beautytransforming is offline
Member
 
Join Date: Apr 2008
Location: Gulf Coast, Mississippi
Posts: 194
15 yr Member
beautytransforming beautytransforming is offline
Member
beautytransforming's Avatar
 
Join Date: Apr 2008
Location: Gulf Coast, Mississippi
Posts: 194
15 yr Member
Default

Quote:
Originally Posted by AfterMyNap View Post
BTF, in plain language, you just get used to it, one day at a time. It's not denial, fighting, accommodating or anything else, it's just living with it.

If I want to do something, I figure out how and I do it.
You make it seem so easy!!! I like your way of thinking!!

Thanks! Really, Thanks!!
__________________
Diagnosed with MS 4/3/2008
.

Had onset attack in 4/2000
.

Can stop blaming myself for symptoms now.
.


Visit me on
.
.
beautytransforming is offline   Reply With QuoteReply With Quote

advertisement
Old 05-05-2008, 02:32 AM #22
coletaterbug coletaterbug is offline
Junior Member
 
Join Date: Mar 2008
Posts: 76
15 yr Member
coletaterbug coletaterbug is offline
Junior Member
 
Join Date: Mar 2008
Posts: 76
15 yr Member
Default

I know what you mean about having nobody that you can talk to in person. I have days that I go to work tired as can be and the bad thing is I am on Bupropien and Provigil C and I am still tired.Then people come in and say man they are tired after partying the night before. I hate this disease. I sometimes live in denial. I don't want to admit that I have a disease and I that I have to take a ton of medicine a day to function and it still somedays doesn't even help with the pain. I have days where I want to take my kids to the park but can't because the heat gets to me.Optic Neuritis is keeping me from driving and they said either it will get better or it won't.That was 8 mths ago and they have gotten worse. I just get so frustrated sometimes and denial comes and goes for me.But know you are not alone
coletaterbug is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
beautytransforming (05-05-2008)
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


Similar Threads
Thread Thread Starter Forum Replies Last Post
Does anyone here have RSD in their face? Kyzyl363 Reflex Sympathetic Dystrophy (RSD and CRPS) 21 03-19-2014 10:25 PM
let's face it... ol'cs Parkinson's Disease 26 04-21-2008 04:51 PM
The new face of ALS BobbyB ALS News & Research 0 07-26-2007 09:09 AM
In search of the face of Lou Gehrig's disease BobbyB ALS 0 10-08-2006 09:34 AM
Greenbrae woman stays fearless in face of disease BobbyB ALS 0 09-15-2006 07:29 AM


All times are GMT -5. The time now is 11:46 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.