advertisement
Reply
 
Thread Tools Display Modes
Old 06-03-2009, 05:28 PM #1
kentucky_wildchild's Avatar
kentucky_wildchild kentucky_wildchild is offline
Junior Member
 
Join Date: Mar 2009
Location: kentucky
Posts: 32
15 yr Member
kentucky_wildchild kentucky_wildchild is offline
Junior Member
kentucky_wildchild's Avatar
 
Join Date: Mar 2009
Location: kentucky
Posts: 32
15 yr Member
Help Does it get any easier?

I have had MS for about 1 year now and it seems like it just keeps getting worse and worse not the ms but the dealing with the MS. I use to think that my life was over when the dr told me, but after about 2 months of nothing but self pitty i started to think that i dont feel any different then i did before. except for a couple of little thing and i'm lucky some people who have ms is in a wheel chair, or cant even get out of there bed. and so far i can walk like normal no trouble getting around just a couple seziures here and there and a little weakness on my left side. but my family still treats me like i shouldnt lift a finger. I know alot of people would love that but i want to do as much as i can while i still can. but with my family it seems impossible. when i am around my family i start feeling self pitty again. Is that normal? Has anyone else felt that way?
kentucky_wildchild is offline   Reply With QuoteReply With Quote

advertisement
Old 06-03-2009, 06:18 PM #2
dmplaura's Avatar
dmplaura dmplaura is offline
Magnate
 
Join Date: Jul 2008
Location: Moncton, NB, Canada
Posts: 2,195
15 yr Member
dmplaura dmplaura is offline
Magnate
dmplaura's Avatar
 
Join Date: Jul 2008
Location: Moncton, NB, Canada
Posts: 2,195
15 yr Member
Default

Quote:
Originally Posted by kentucky_wildchild View Post
I have had MS for about 1 year now and it seems like it just keeps getting worse and worse not the ms but the dealing with the MS. I use to think that my life was over when the dr told me, but after about 2 months of nothing but self pitty i started to think that i dont feel any different then i did before. except for a couple of little thing and i'm lucky some people who have ms is in a wheel chair, or cant even get out of there bed. and so far i can walk like normal no trouble getting around just a couple seziures here and there and a little weakness on my left side. but my family still treats me like i shouldnt lift a finger. I know alot of people would love that but i want to do as much as i can while i still can. but with my family it seems impossible. when i am around my family i start feeling self pitty again. Is that normal? Has anyone else felt that way?
Hey hun. It's tough isn't it? I've been officially diagnosed for just over a year myself.

You're absolutely right. Not necessarily the MS, but the dealing part.

We're all unique, so I can only speak for myself. I decided for the most part to ignore the MS. Yup. As much as I can. Which is tough where I have daily pain. But there's certain things I've done differently.

I got rid of most of my MS sites and bookmarks. I come here now, and don't frequent other forums, and I cut back on my time here. I made the tough decision (I don't recommend this, it's just what was right for me) to stop shooting needles into myself everyday. I changed my diet completely, eat low fat, exercise, get good sleep.

Most importantly, I got the diagnosis and was determined to keep going as long as I could, and not let things hold me back. When I returned to work and people asked if I was 'better', I answered, "I'm no worse, only I can name it now and get better medications!". Which is pretty much the case!

Keep positive, have fun with what you have, not with what you don't have, and live life to the fullest every day. Don't dwell on the 'what ifs'. Guess what? That person beside you without MS could be gone tomorrow. What's the use in worrying, you know?

Show the fam you can kick major butt. Maybe they'll never 'get' it, but spend that energy trying to get them to 'get it' elsewhere
__________________
2004 to present - Trigeminal Neuralgia
2007 to present - Burning Mouth Syndrome
March 2008 - Multiple Sclerosis DX
05/2008 - Relapse
05/2008 to 02/2009 - Copaxone
10/2011 - Relapse - Optic Neuritis developed
9/2012 - Relapse - Balance issues 1 sided
8/2012 - Erythema Nodosum - diagnosed 10/2012, reaction to Topiramate (Topamax)
April 7/14 - Raynaud's Syndrome DX
dmplaura is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Debbie D (06-04-2009)
Old 06-03-2009, 07:19 PM #3
Dejibo's Avatar
Dejibo Dejibo is offline
Elder
 
Join Date: Jan 2008
Location: New Hampshire
Posts: 7,332
15 yr Member
Dejibo Dejibo is offline
Elder
Dejibo's Avatar
 
Join Date: Jan 2008
Location: New Hampshire
Posts: 7,332
15 yr Member
Default

hang in there. Its an uphill climb, and sometimes you just have to sit down, and take a ME ME ME break. I have easier periods, and harder periods, but there is rarely a block of time that I have normalcy anymore. hugs for ya
__________________
RRMS 3/26/07
.

Betaseron 5/18/07
.

Elevated LFTs Beta DC 7/07
Copaxone 8/7/07
.



.
Dejibo is offline   Reply With QuoteReply With Quote
Old 06-03-2009, 07:23 PM #4
SallyC's Avatar
SallyC SallyC is offline
In Remembrance
 
Join Date: Sep 2006
Location: SW Ohio
Posts: 17,844
15 yr Member
SallyC SallyC is offline
In Remembrance
SallyC's Avatar
 
Join Date: Sep 2006
Location: SW Ohio
Posts: 17,844
15 yr Member
Default

No KY, dealing with the MS monster doesn't get easier, but you learn to manage your time a little better. You learn to save your energy for the important things and you learn to let people help you, when you need it.

Take care of yourself and I wish you a long remission.
__________________
~Love, Sally
.





"The best way out is always through". Robert Frost



~If The World Didn't Suck, We Would All Fall Off~
SallyC is offline   Reply With QuoteReply With Quote
Old 06-03-2009, 09:18 PM #5
NurseNancy's Avatar
NurseNancy NurseNancy is offline
Grand Magnate
 
Join Date: May 2007
Location: Florida
Posts: 4,240
15 yr Member
NurseNancy NurseNancy is offline
Grand Magnate
NurseNancy's Avatar
 
Join Date: May 2007
Location: Florida
Posts: 4,240
15 yr Member
Default

you have the right idea. to do as much for yourself as you can.
you might consider getting some basic MS reading material for your family members. call 1-800-FIGHT MS to find your local MS society. and, ask for the newly dx'd packet.

sometimes some simple education can help to allay fears.
and a loving talk about what you want can help too.
__________________
Judy
trying to be New Skinny Butt
______________________
You are a child of the universe, no less than the trees and the stars; you have a right to be here.
And whether or not it is clear to you, no doubt the universe is unfolding as it should.
--------------------------------------
"DESIDERATA" by Max Ehrmann
NurseNancy is offline   Reply With QuoteReply With Quote
Old 06-04-2009, 07:29 AM #6
Debbie D's Avatar
Debbie D Debbie D is offline
Elder
 
Join Date: Jan 2008
Location: Naperville IL
Posts: 5,169
15 yr Member
Debbie D Debbie D is offline
Elder
Debbie D's Avatar
 
Join Date: Jan 2008
Location: Naperville IL
Posts: 5,169
15 yr Member
Default

It takes time...but one thing you seem to have is the will to live as normal a life as possible...
now you need your family to get on board. You want to live a fulfilled life. Tell them this. They are scared for you, I'm sure, and don't want you to overdo...but as you learn your capabilities and your limitations, you will feel more in control.
We only get this very moment...the past is gone, the future is not here yet. Learn to appreciate the moment...and quietly go and live the life YOU want to live. Good luck!
__________________
Instant Karma's gonna get you-gonna knock you right in the head...John Lennon
Debbie D is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
dmplaura (06-04-2009)
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
At/about month 5 it is getting easier...but still different volada Multiple Sclerosis 1 08-01-2008 04:22 PM
MS tips for easier living mom23angels Multiple Sclerosis 12 06-19-2008 07:18 PM
Does this really ever get any easier?? Natalie8 Multiple Sclerosis 20 05-16-2008 11:19 AM
Do the injections get any easier? Natalie8 Multiple Sclerosis 33 04-17-2008 11:59 AM
Breathing easier.. a little easier anyway Busymommie Children's Health 5 09-30-2006 06:26 AM


All times are GMT -5. The time now is 11:09 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.