Multiple Sclerosis (MS) Support Group
This community is a place where members can discuss current events and weigh in on what's going on in the world.
This community is a place where members can discuss current events and weigh in on what's going on in the world.
People tend to be very understanding or quite ignorant ( as in 'but you look fine' and 'are you over your MS ?') And since MSers portray quite different symptoms, one can hardly be surprised when people don't 'get it'.
I found it was, and is, a journey with no definite directions. You have to accept the fact that you will need to be flexible and patient - although, I will say the most govt agencies here in Australia are very good.
All the best!!
Jill
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I was turned down the first time too; It's how it is.
A month later when another ON showed up; it was the neuro who filled out all the paperwork and started my life on disability to pay for my fun life with MS.
Whenevea the gov. tries to throw me off the disability, that I now REALLY NEED because I canNOT work a fulltime regular job because of MS anymore, I ask the neuro about doing his majic so I can still see him/ get Avonex and MRIs.
Even though others who do not understand what MS is and does, can't figure why I say I'm disabled and under 60; I say just work for as long as you are able to, but let the neuros' office make sure you get what you NEED and have disability that alot of us need!
I knew when I went out on disability that I could not go back. My fatigue was just too back. I could not function at work and do what I needed to do at home. Now I can do what I need to do at home (mostly) and could never function at a job. So that is a decision that you need to make.
Best of luck to you.
I was diagnosed in 2004
and pushed back to 1999. I was a t,Escher from ~-2012. I was fortunate to reformed SSD On the 1St try. I didn't want to stop working. Just couldn't do it any longer.
Work if you can
I have long term disability coverage that pays 66% of my salary. I look at it like this - the longer I work the more I make. The more I make now, the more I'll make monthly for the rest of my life once I have to go on the LTD/SSDI. If I can put in 5 more years it'll be well worth it later.
My advice, Work as long as you can for the financial, physical and emotional benefits. But if you can't, then you can't.
I wish I could still work but there are days I'm glad I don't. Like it was said before, only you know how you feel.
Best of Luck!
Who knows when your MS symptoms will rear it's ugly head. That's the nature of RRMS. You're in a tough position. It's a gamble and you have to ask yourself are you prepared to take that gamble going back to work? I still work, and have RRMS, but I have a super job where I work from home and can have rests periods and what nots to help me when I'm having a flare. Do you have the type of job that will work with you when you do have a flare? Do you even have a job now? (because that last question would be hard to answer if you don't). I don't know many employers who would want an employee that will be taking alot of leave. Tough question!! Harder answers!!