Skip to Accessibility Tools Skip to Content Skip to Footer

CWilliams’s Story

I started having chronic fatigue in approximately 2008 possibly before. I would work everyday for a few months and be okay and then I would awake one morning and just was not able to go anymore. I would have to call in to work. This cycle just kept repeating. I am a medical lab technician that works in a physician;s office and I would be seen by a doctor, have blood work with everything showing normal. In 2009, the fatigue become worse and was so overwhelming that I struggled to make it to work each day.It took until 2015 for me to be diagnosed with RRMS. I feel that I no longer have RRMS. I feel that it has progressed because unfortunately I have a lot more bad days than good. I still work full time and am usually down almost every weekend due to working all week. Fatigue has been my worst symptom however, I have blurred vision and balance issues. If anyone is having symptoms that persist and you know that it is not your normal be persistent and follow through to get an answer.If I would have kept letting myself go just because the doctors that I went to could not find anything wrong, I would still not have been diagnosed to this day. MS is a terrible disease that has no mercy. It is so unique to each individual. I think that is one of the reasons that it can be difficult to diagnose.

This article represents the opinions, thoughts, and experiences of the author; none of this content has been paid for by any advertiser. The MultipleSclerosis.net team does not recommend or endorse any products or treatments discussed herein. Learn more about how we maintain editorial integrity here.

Comments

  • Nancy W
    2 years ago

    CWilliams. Do you still have to and want to work? I struggled with fatigue and anxiety over whether I could continue working and went to part time. 3 years after diagnosis, I stopped working. I thought I would go back but never did. Since then, my quality of life is much better. I usually can pace myself and do the things that I enjoy. If I am fatigued, I can rest. I do have less money but I have enough for the essentials, I think not working wa best for me.

    Of course I was blessed with a supportive husband who has health insurance and a long term disability policy. Not everyone has the option to make that choice.

  • Meagan Heidelberg moderator
    2 years ago

    Hi CWilliams. We are so glad that you’ve shared your journey with us and our community members! You were your own advocate, and remained persistent to find out what was going on with your body. Although sometimes it does take years, as in your case, it’s good to know what the next step is. We appreciate you being a part of our community!
    Best – Meagan, MultipleSclerosis.net Team Member

  • Poll