... I am starting to have a hard time thinking at work and multitask. I can't afford to be off work but at the same time I can't affford the problems I am having as it takes away from my young family. Does anyone feel this way? I can't even excersise because I am so weak and in pain all the time in my legs. I also feel I have gained weight and that just adds to my sadness.
Multiple Sclerosis - I have had MS for 14 years. I use Copaxone and other pill method meds?
- Posted:
- 24 Aug 2011 by FJ
- Topics:
- copaxone, multiple sclerosis
Answers (1)
24 Aug 2011
I totally understand how you feel. Earlier this year I had to take 3 weeks off b/c of my MS. I went back to work as soon as I could (maybe too soon), because I didn't want to seem as though I couldn't do my job. I also gained 35 lbs in 4 months because I was less mobile and didn't feel well enough to workout.
So here is some advice:
At Work:
1. Write lists, so you can avoid too much multitasking yet keep track of all the things your supposed to do.
2. Pace yourself at work and ask for help. As a person with a chronic condition, I believe you are protected by law and have the right to ask for reasonable assistance/accommodations.
At Home:
Search for questions
Still looking for answers? Try searching for what you seek or ask your own question.
Similar questions
How long is a person on copaxone?
My mother is 75, living in a nursing home and has had MS for 40+ yrs. Her new neorologist advised that she no longer needed to be on copaxone as she ...
Our daughter has just started Copaxone. The areas where she has given the injections are hard,?
... bruised looking. She has only been on the medication for 9 days. Massage the area was suggested, is that correct? I read that heat before and ice ...
Is it common to have new pain symptoms from copaxone a year and a half later?
I've recently started having severe lower back pain. After an injection I had severe chest pain and couldn't straighten my left leg. It ...
Can you take ampyra and copaxone at the same time?
My dr. wants to try Gelyna by I am not sure what to do. My most difficulties are walking, no sense of balance and very edgy and nervous feeling all ...
I was recently diagnosed with MS, back in December 2010. I began treatment with Avonex, but the?
... flu-like symptoms had me down for at least 2 days or more, so after 6 months, I have switched to Copaxone. My question is does anyone else get ...

I understand how you feel as well I believe we all do you are not alone!!! I worked for the first 6 years of the fatigue,numgness migraine,pain,tripping over my own feet and many more. I walked 9 hrs a day on my job me like you have a family to support bills need paid. I couldn't do it anymore! My husband does a lot to help as well as my children. It was hard fr me t except at first I have always been the caregiver and natural prretty in control of most situations. But it gets easier. I found a pain specialist who is helping me with pain my regular dr didn't understand what I go through. I have signed up for as many ms groups as I can msf (ms foundation) ms society the organization can help you with ways to get exersice and offer prgrams that are effordable and some that cost nothing they are there to help you get the thing you need to make your life more managable. Lok them up in your community they are all over you can find them on your phnebook or internet.
Expand this post...
Water exercising is a good way to do it while not putting to much stress on the body and she is right yoga and palates as well. So good luck hope this help and I wish you and your family well hope you find enjoyment in everyday